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We offer a complete product range of Testosterone enanthate CAS: 315-37-7, Testosterone Sustanon 250, Boldenone Undecylenate (Equipoise) CAS No: 13103-34-9, Dianabol (Metandienone) CAS :72-63-9 and Methenolone Enanthate

Testosterone enanthate CAS: 315-37-7

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  • Min. Order (MOQ) 10 Gram
  • Country of Origin India
  • Color white
  • Appearance White to yellowish-white crystalline powder
  • Dosage Men 250-1000 mg/week
  • Half life 15-16 days

reference standard: ep5 appearance: white to yellowish-white crystalline powder dosage:average dose: men 250-1000 mg/week   testosterone enanthate is a slow acting ester with a release time between 8-10 days. Testosterone enanthate is typically injected anywhere between once every week to once every three weeks. Testosterone propionate is a fast-acting ester with a release time of 3-4 days. To keep blood levels from fluctuating greatly, testosterone propionate is usually injected between one to three times a week.  

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Testosterone Sustanon 250

  • Min. Order (MOQ) 10 Gram
  • product name Testosterone Sustanon 250
  • Appearance White powder
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Testosterone is the most important and popular anabolic steroid, and Sustanon 250 is the best-known form of injectable testosterone. It has become so popular for anabolic steroid cycles that the name now extends past the Schering brand and is often given to any steroid preparation made to the same formulation.   Sustanon 250 Recipes     Sustanon recipes 200 mg/ml   50grams powder (37.5ml) 5mL BA (2%) 50mL BB (20%) 157.5mL Grapeseed oil     Sustanon recipes 400mg/ml   100grams powder (75ml) 5mL BA (2%) 50mL BB (20%) 120mL Grapeseed oil       Our Advantage:   High quality with competitive price:   1) Standard: Enterprise Standard 2) All Purity:>=99% 3) We are manufacturer and can provide high quality products with factory price.  

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Boldenone Undecylenate (Equipoise) CAS No: 13103-34-9

  • Min. Order (MOQ) 10 Gram
  • Application Medical
  • product name Boldenone Undecylenate
  • Appearance Yellowish oily liquid
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cas no: 13103-34-9 einecs no: 236-024-5 mf: c30h44o3 mw: 452.67 description :   boldenone undecylenate is a synthetic steroid which has a similar effect as the natural steroid testosterone. It is frequently used in veterinary medicine, though it is also used in humans. The effects of this steroid are more subtle than that of many other steroids.   one of the most common uses for boldenone undecylenate is in the treatment of horses. When the drug is administered, horses show improvement in temperament and appetite. The increased appetite helps them put on additional weight which is easily converted into muscle tissue with the help of the steroid. Generally, a veterinarian administers one injection of the medication every three or four weeks.   though boldenone undecylenate aids in the creation of muscle tissue, the effects of this steroid are relatively mild. It may take a few weeks to notice any results. Muscle growth is slow, but the muscle tissue that develops tends to remain for a while after steroid use is stopped. Of course, without regular maintenance and exercise, the new muscles will eventually atrophy.   in humans, boldenone undecylenate is also used to help build small amounts of muscle slowly. The effects, as in veterinary medicine, are not extreme and generally not much more pronounced than the effects of a rigorou s workout routine. This steroid remains in the body for a long time which means that it is easily picked up by routine drug tests, even if a person has not taken a dose for weeks.   applications:   boldenone undeclynate has become a very popular steroid with athletes and bodybuilders due to the fact that it has very low side effects and has anabolic properties which promote a steady gain in quality muscle mass over time. The steroid was tagged with the name equipose? when it first became available as a veterinary steroid and was widely used in racehorses.     eq, as it is often called, can be effectively incorporated in both "cutting" and "bulking" cycles due to the well balanced effects of this anabolic substance. This steroid aromatizes very little, and therefore produces almost no estrogenic side effects such as water retention or "gyno" (the development of female tissue under the nipples in males resulting in unattractive and often painful lumps in this area), and therefore is a favorite among bodybuilders who are looking to make solid gains without the extra bloat, or are nearing contest.

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Dianabol (Metandienone) CAS :72-63-9

  • Min. Order (MOQ) 10 Gram
  • Product Name Dianabol
  • Appearance White Powder
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product name: dianabol alias: methandrostenolone cas registry number: 72-63-9 einecs no: 200-787-2 molecular formula: c20h28o2 molecular weight: 300.44 purity: >99%   description   dianabol represents one of the most popular and one of the most important anabolic steroids of all time. Without question, this is the most popular oral steroid to ever hit the market and one of the most popularsteroids in any form. While almost always found as an oral tablet, dianabol can be found as an injectable solution, but the tablets represent the primary route of administration.   why is this steroid so important? in many ways it gave birth to the age of modern performance enhancement. It was not the first anabolic steroidused for that purpose, that would belong to testosterone, but dianabol would open the door to a new wave ofsteroid use that has grown beyond what anyone expected.     dianabol represents one of the only anabolic steroids that was developed for the sole purpose of performance enhancement. The compound did carry listed therapeutic uses at one time, but performance was the true reason this steroid was given life. Through the 1940's and 50's the soviet union had begun to dominate the olympic games, and the use of testosterone by many of its athletes left the rest of the world lagging far behind. dianabol functions and traits   methandrostenolone is a testosterone derived anabolic androgenic steroid. Officially, it is a structurally altered form of the primary male androgen testosterone. Dianabol is the testosterone hormone with an added double bond at the carbon one and two position. This slight alteration reduces the hormone's androgenic nature. It also carries an added methyl group at the 17th carbon position that allows the hormone to survive oral ingestion, officially classifying dianabol as a c17-alpha alkylated steroid. An important note, injectable dianabol is also c17-alpha alkylated.   the end result gives us an anabolic steroid with an androgenic rating of 40-60 with a much lower binding affinity to the androgen receptor compared to testosterone. However, it will also share a much weaker relationship for serum binding protein, which results in an extremely powerful anabolic steroid. If there's any doubt, this is one extremely powerful anabolic steroid carrying a potent anabolic nature. on a functional basis, dianabol is one of the easier anabolic steroids to understand. This steroid will largely provide its anabolic benefits by enhancing protein synthesis, nitrogen retention and glycogenolysis. Protein synthesis represents the rate by which cells build proteins, the building blocks of muscle. Nitrogen retention, this is important as all muscle tissue is comprised of approximately 16% nitrogen. benefits of dianabol 1. As a tonic 2. Bodybuilding 3. Dianabol reduces exhaustion    

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Methenolone Enanthate

  • Min. Order (MOQ) 10 Gram
  • Product Name Methenolone Enanthate
  • Appearance White crystalline powder
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product name: methenolone enanthate alias: primobolan-depot cas no: 303-42-4 einecs no: 206-141-6 mf: c27h42o3 mw: 414.62 purity: 99%   description: methenolone enanthate is the injectable version of methenolone with a long ester attached to slow absorption of a the active methenolone compound and provide steady blood concentrations. The oral version of this compound is practically identical with the difference being the attached ether (the oral version has a shorter acetate ester attached). Both versions of methenolone are good choices for cutting cycles for men and/or women and have shown to maintain muscle while on a low-calorie diet. Methenolone enanthate provides a less frequent administration mode for methenolone and anecdotally appears to require a lower overall dose in order to be as effective as the oral acetate version.   methenolone has a reputation as being a very safe steroid and in doses of up to 200 mgs/week very little side effects are reported. Unfortunately, many users also report minor gains at best using such a low dose and more pronounced gains seem to occur at 350 mgs/week (100 mg eod) and up. While methenolone is mild without much hpta suppression, higher doses will result in negative feedback in this regard. Also, some users report hair loss while using primo so a product like finasteride may be necessary while cycling methenolone. On the plus side, because of the few side effects exhibited by primo use, an anti-estrogen is likely not necessary.   applications:   methenolone enanthate is a dihydrotestosterone based anabolic steroid, methenolone enanthate is an ester derivative of methenolone sold commonly under the brand name primobolan, methenolone enanthate is used by people who are very susceptible to estrogenic aide effect, having lower estrogenic properities than nandrolone, methenolone, in form of enanthate and acetate, methenolone has no estrogenic side effects and its effects on cholesterol, methenolone is also not overly suppressive of the hpta axis, for this reason, mang bodybuilder use methenolone in between steroid cycles.   cook recipe of methenolone enanthate   50 ml for 200mg/ml 10 grams primobolan e powder (7.5ml) 1ml ba (2%) 7.5ml bb (15%) 17ml grapeseed oil 17ml ethyl oleate   40ml for 100mg/ml 4 grams methenolone enanthate 29 ml grapeseed oil 2ml benzyl alcohol = 5% 6ml benzyl benzoate = 15%  

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Clomiphene citrate CAS: 50-41-9

  • Min. Order (MOQ) 10 Gram
  • product name Clomiphene citrate
  • Appearance White powder
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product name: clomiphene citrate cas: 50-41-9 appearance: white powder grade: pharmaceutical grade package: disguised package ; foil bag delivery date: 3-5 work days formula: c32h36clno8 molecular weight: 598.09 purity: 99%   description:   clomifene citrate is a drug treatment that stimulates your ovaries to release eggs.clomiphene is a non-steroidal fertility medicine. It causes the pituitary gland to release hormones needed to stimulate ovulation (the release of an egg from the ovary).   clomiphene is used to cause ovulation in women with certain medical conditions (such as polycystic ovary syndrome) that prevent naturally occurring ovulation.   ovulation stimulation using clomifene citrate is a well-established, effective treatment. Clomifene citrate is the most widely used of all fertility drugs.   clomid is the commonly referenced brand name for the drug clomiphene citrate. It is not an anabolic steroid, but a prescription drug generally prescribed to women as a fertility aid. This is due to the fact that clomiphene citrate shows a pronounced ability to stimulate ovulation. This is accomplished by blocking/minimizing the effects of estrogen in the body. To be more specific clomid is chemically a synthetic estrogen with both agonist/antagonist properties, and is very similar in structure and action to nolvadex. In certain target tissues it can block the ability of estrogen to bind with its corresponding receptor. Its clinical use is therefore to oppose the negative feedback of estrogens on the hypothalamic-pituitary-ovarian axis, which enhances the release of lh and fsh. This of course can help to induce ovulation.     applications :   clomid ordinarily is dosed at 50 mg/day. However, it’s important to note that clomiphene has a long half life. Where this has relevance is that when a daily dose is taken, the body will have not only that dose in it, but also an accumulated amount of about five days’ worth of previous doses as well. That’s fine: it results in correct blood levels. Where there can be a problem is when first starting use. If simply taking 50 mg/day from the beginning, there is no such buildup and levels will be low.   to account for this, 300 mg is taken on the first day, as three doses of 100 mg, or optionally six doses of 50 mg. This immediately gets levels to where they should be. Ongoing 50 mg/day dosing will maintain this level.   after day 1, doses of more than 50 mg are not needed and are not recommended. They will not improve results, but may increase adverse side effects.

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Methylstenbolone/Stenbolone

  • Min. Order (MOQ) 10 Gram
  • Product Name Methylstenbolone/Stenbolone
  • Appearance White Powder
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Descriptions   1. Methy-Tren is an oral steroid that has never been sold as a prescription drug or a dietary supplement. Its only use at this point has been as a research chemical, although it does have some limited availability on the black market. Methy-Tren is basically with a C-17 methyl group making it orally bioavailable.   2. Methy-Tren is one of the strongest oral anabolic steroids ever produced. This agent is a derivative of trenbolone(trienolone), which has been c 17 alpha alkylated to allow for oral administration. This modification has created a steroid that is significantly stronger than its non-methylated cousin.   Applications   1. A potent, non-aromatizable androgen that is structurally similar to trenbolone and has been referred to as "oral tren."   2. Although they are very similar in structure, methyltrienolone is very different in effect from trenbolone. It has an anabolic to androgenic ratio of 12000/6000 in comparison to methyl-testosterone, making it possibly the most potent steroid in existence.   3. Methyltrienolone may also be the strongest androgen receptor binder of all steroids. Methyltrienolone required very small doses to see big gains in size and strength. Methyltrienolone does not convert to estrogen, but it does have progestational activity which may increase the effects of estrogen. This can be considered a "dry" compound that will not cause much if anything for subcutaneous (under the skin) water retention.   Methyl Stenbolone dosing for new users:   Week1:4-8mg / per day Week 2-3:8mg / per day     Methyl Stenbolone dosing for experienced users:   Week1:8mg / per day Week 2-3:12mg / per day Week 4:16mg / per day   Methyl Stenbolone is a recent and potent methylated prohormone   1. Along with the incredible potency of methyltrienolone comes some very strong side effects. Methyltrienolone is very androgenic and is likely to cause hair loss and severe acne in those who are prone to these effects.   2. There is some risk for gynecomastia due to the progestational effects of methyltrienolone. The biggest concern with Methyltrienolone is probably its liver toxicity. Even at very low doses, methyltrienolone can cause significant liver stress in a very short period of time. This may possibly be the most liver toxic steroid in existence, and it is definitely not recommended to use methyltrienolone for any longer than 4 weeks at a time.    

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Phenibut CAS:1078-21-3

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  • Min. Order (MOQ) 10 Gram
  • Product Name Phenibut

1.phenibut is a derivative of the naturally occurring inhibitory neurotransmitter gaba.   2.phenibut is used by bodybuilders to reduce fatigue and improve neurological functions.   3.phenibut has been and is still used medically to treat stress, relieve tension, improve sleep, and as a potentiate for other medications.   4 phenibut induce relaxation and improve mental function.   5 phenibut improve cognition and has nootropic and anxiolytic properties.   6 phenibut help with fear, anxiety, tension, congnitive disorders, and also neurotic patients and insomnia, depression and asthenia.   7 phenibut used for post-traumatic stress and vestibular problems.   function   1.phenibut is a derivative of the naturally occurring inhibitory neurotransmitter gaba.   2.phenibut is used by bodybuilders to reduce fatigue and improve neurological functions.   3.phenibut has been and is still used medically to treat stress, relieve tension, improve sleep, and as a potentiate for other medications.   phenibut hcl benefits   as a modified version of gamma-aminobutyric acid, phenibut hcl offers many of the similar potential effects and benefits as gaba. Gaba is naturally released by the brain to invoke feelings of calm and relaxation, but gaba cannot supplemented because the compound has trouble circulating from the blood to the brain or neurons on its own. Phenibut hcl has been shown to replicate many of gaba's effects, activating the same receptors. This may result in relaxaton and a distinct calming effect. phenibut dosage     the recommended serving size of phenibut is 500 - 2000mg per day, in up to two to three separate servings, depending on the desired effect.phenibut should not be consumed in amounts exceeding 4 grams total per week, and should never be taken in higher amounts on consecutive days due to rapid development of tolerance to the benefits.  

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1,3-dimethyl-butylamine citrate (AMP Citrate) CAS :318-98-9

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  • Min. Order (MOQ) 10 Gram
  • Product Name 1,3-dimethyl-butylamine citrate (AMP Citrate)
  • Appearance White powder

1, 3-dimethylbutylamine (1, 3-dmba), or simply dimethylbutylamine (dmba), is a stimulant drug structurally related to methylhexanamine (1, 3-dimethylamylamine (1, 3-dmaa)) where a butyl group replaces the amyl group. It is also known as amp citrate (4-amino-2-methylpentane citrate). The compound is an aliphatic amine. dmba has been identified as an unapproved ingredient in some over-the-counter dietary supplements, in which it is used in an apparent attempt to avoid laws prohibiting the use of methylhexanamine.  application:     (1.) as an alternative of dmaa, pharmaceutical intermediates, fine organic synthesis and catalyst, health care products, etc.   (2.) in health care, the 1, 3 - dimethyl amine hydrochloride can increase energy, refreshing, and improve the body's energy, or calorie restriction athletes gather energy particularly effective.   (3.) used in weight class where you can significantly reduce the appetite suppressing effects caused by heat. There are reports of 1, 3 - dimethyl amine hydrochloride can increase fitness, improve concentration, significantly suppress appetite, inhibit excitement.   (4.) also can be used as a other ingredients with dietary supplements.   use:   in health care, the 1, 3 - dimethyl amine hydrochloride can increase energy, refreshing, and improve the body's energy, or calorie restriction athletes gather energy particularly effective; used in weight class where you can significantly reduce the appetite suppressing effects caused by heat. There are reports of 1, 3 - dimethyl amine hydrochloride can increase fitness, improve concentration, significantly suppress appetite, inhibit excitement; also can be used as a and other ingredients with dietary supplements.   advantage: 1, has a high quality with competitive price: (1)standard: enterprise standard (2)all purity≥ 99% (3)we are manufacturer and can provide high quality products with factory price. 2, fast and safe delivery (1)parcel can be sent out in 24 hours after payment. Tracking number available (2)secure and discreet shipment. Various transportation methods for your choice. (3)customs pass rate ≥ 99% (4)we have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.

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Testosterone Acetate CAS No. 1045-69-8

  • Min. Order (MOQ) 10 Gram
  • Appearance White crystalline powder
  • Usage Testosterone Acetate is an androgenic steroid

Product nameTestosterone acetate CAS No.1045-69-8 Molecular formulaC21H30O3 Molecular weight330.47 Einecs No:213-876-6 AppearanceWhite crystalline powder Description:   Testosterone Acetate is an androgenic steroid with a pronounced anabolic effect. Most acetate treatments deliver medication to the body relatively quickly. Testosterone Acetate has very low risk of water retention. Individuals that utilize this form of Testosterone also claim that it is arguably the most painless form of Testosterone. Testosterone Acetate ester is much faster acting, and thus requires a more frequent schedule in order to keep blood levels as stable as possible.The benefit to this however, is that the steroid can be cleared from the body much more quickly after use is discontinued, thus making it a more preferable choice for tested athletes. Athletes use Testosterone Acetate to see dramatic gain in muscle size and strength, as well as an overall sense of well being and increases libido and sex drive. Testosterone acetate Under partially anaerobic conditions, production of testosterone acetate was limited, and the substrate was converted mainly to 20α-hydroxypregn-4-en-3-one. In order to clarify the role of molecular oxygen in the course of side-chain cleavage of progesterone by C. resinae, a double tracer method was applied using 18O2 as a tracer of molecular oxygen and 14C as a tracer of the steroidal substrate. After the microbiological transformation of progesterone under 18O2 atmosphere, testosterone acetate, along with the testosterone derived from the testosterone acetate by microbial esterase during the culture, and the testosterone which was chemically produced by saponification of the testosterone acetate, were obtained and subjected to mass-spectrometric analysis.     Application   Testosterone Acetate combination of Testosterone and ester acetate, Testosterone Acetate is an androgenic steroid with a pronounced anabolic effect. Most acetate treatments deliver medication to the body relatively quickly. Testosterone Acetate has very low risk of water retention. Individuals that utilize this form of also claim that it is arguably the most painless form of . Testosterone Acetate ester is much faster acting, and thus requires a more frequent schedule in order to keep blood levels as stable as possible. The benefit to this however, is that the steroid can be cleared from the body much more quickly after use is discontinued, thus making it a more preferable choice for tested athletes. Athletes use Testosterone Acetate to see dramatic gain in muscle size and strength, as well as an overall sense of well being and increases libido and sex drive.

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Testosterone Propionate CAS No: 57-85-2

  • Min. Order (MOQ) 10 Gram
  • Color White crystall powder
  • Application maintain stable blood levels
  • Purity 99%

The testosterone suspension is an injectable testosterone hormone developed and used in water for decades and is actually the first synthetical androgenic steroid. In order to build the purpose of the public, testosterone suspensions have never been exceeded because it was the first development in the 1930s. Many underground laboratories also suspend this product in propylene glycol or oil (which makes very painful injections). It has no ester attached; therefore no weight of the ester is calculated.   100 USP injections provide testosterone propionate, a major endogenous androgenic testosterone derivative, for intramuscular administration. The esterification of 17-beta-hydroxy increases the duration of testosterone action. Testosterone propionate has been prepared in an oily solution and is slowly absorbed from the liquid phase when intramuscularly injected. This allows testosterone 100 to be administered at intervals of 3-4 days. 100 contains testosterone propionate in 10 ml of solution (100 mg of testosterone propionate / ml) for injection only.   100 is a transparent, pale yellow oily solution for intramuscular injection. Testosterone Propionate is for the treatment of primary gonadal dysfunction (congenital or acquired), testicular failure in men due to cryptorchidism, bilateral torsion, orchitis, testicular syndrome or testicular resection.   Product Applications   Testosterone propionate has been used to study its effects on pregnant ewes. Testosterone propionate is the shortest ester attached to the testosterone hormone. This means that your body needs the least time to get rid of the ester and release the parent hormone into the body. Because of its short active life, testosterone propionate usually needs to be injected at least once every other day. Incredible, testosterone propionate leads to minimal side effects and minimal bloating; these side effects usually fade quickly when used to stop.   Androgen guides the development of male phenotypes during the embryogenesis and the male sterility secreted by testes. The hormone is converted to dihydrotestosterone in the target tissue, where it regulates several biological functions. Testosterone pyruvate has been obtained from plant synthesis. The product has an extended and faster effect when compared to the product.   Testosterone propionate is the shortest ester attached to testosterone. This means that your body needs the least time to get rid of the ester and release the parent hormone into the body. Due to its short active life, testosterone propionate usually needs to be injected at least every other day. Interestingly, testosterone propionate leads to minimal side effects and minimal bloating; these side effects usually fade rapidly when used to stop.

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Testosterone Cypionate CAS No: 58-20-8

  • Min. Order (MOQ) 10 Gram
  • Appearance white crystalline powder
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Testosterone cypionate; Good quality Testosterone cypionate; Test cypionate;    Testosterone cypionate CAS No: 58-20-8  Testosterone cypionate Molecular formula: C27H40O3    Testosterone cypionate Molecular weight: 412.61   Testosterone cypionate Assay: 99% min   Testosterone cypionate Appearance: white crystalline powder   Testosterone cypionate Quality standard: USP32   Testosterone cypionate Effective Dose (Men): 300-2000mg+ week   Testosterone cypionate Packing: aluminum foil bag Testosterone cypionate   Testosterone cypionate Min. order quantity: 10g Testosterone cypionate   Testosterone cypionate Payment: Western Union ;Moneygram;T/T. Testosterone cypionate  

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Testosterone phenylpropionate CAS: 1255-49-8

  • Min. Order (MOQ) 10 Gram
  • product name Testosterone phenylpropionate
  • Appearance powder
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Product Name: Testosterone Phenylpropionate Model NO.: 1255-49-8 CAS: 1255-49-8 Customized: Non-Customized Suitable for: Elderly, Children, Adult Purity: >99% Testosterone Phenylpropionate 2: Burn Fat in The Body Testosterone Phenylpropionate 4: Increase Immunity and Increase Energy   Propyl propionate has been combined with testosterone and norolone to produce steroids such as cromoglycans and gallbladder agents. Libriol is a mixture of nandrolone and methandriol, and tribolan is a mixture of nandrolone and decanoate. No phenyl propionate alone is found. Nandrolone is one of the most popular steroids in the world because it can be used to obtain and lose weight, less of the known aromatherapy effects of testosterone. Thus, Nandrolone Phenyl Propionate will also contain the effects of phenyl propionate and norethisterone.     If you want to add lean muscle and get a lot of power while in phenylpropionate will help to do so. What is the ability of the body to synthesize and store more protein. When dieting involves eating a lot of animal and plant protein, you can expect to see many changes in the volume of the user's muscles. It is important to note that phenyl propionate should be accompanied by dieting and exercise to increase muscle volume and strength. Propionate improves the amount of IGF in muscle and increases the amount of androgen receptors in muscle.

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Testosterone Isocaproate

  • Min. Order (MOQ) 10 Gram
  • product name Testosterone Isocaproate
  • Appearance White crystalline powder
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CAS NO.: 15262-86-9 EINECS: 239-307-1 Molecular Formula: C25H38O3 Assay: 99.5% Character: White crystalline powder. Testosterone Isocaproate is not found individually but it is contained in some other drugs such as in Sustanon 250 and also in Omnadren, which are easily available in the market. Testosterone Isocaproate is somewhat same to the Testosterone Caproate but with a few exceptions. It has got same number of hydrogens, carbons, oxygen and same molecular weight but its active life is one day more as compared to Testosterone Caproate. Testosterone Isocaproate is bounded with a fatty acid or an ester which causes a delay in its release in the body. As told earlier that it has got a more active life which means it will stay in the body for a longer period of time and therefore to get it in the form of an injection once or at max twice a week in enough. gear@quality-steroid.com Whats app: 8615711952876 Wickr: rawsteroid Anabolic steroid powder Testosterone Isocaproate For Bodybuilding CAS 15262-86-9   Testosterone Isocaproate will help in increasing the body weight and will also help in gaining the strength. It also helps in losing fat in the body and gives an increase in libido, red blood cells, stamina and quick recovery after heavy training. As told earlier it is very hard to be found in the market in its purest form but its raw powder form is available in the market in the form of Testosterone Cypionate and Testosterone Enanthate. Testosterone Isocaproate is useful in increasing the synthesis of protein in the body, reduction of the cortisol, increasing the ability to recover especially after heavy trainings, increasing strength and helps the person gaining more mass. It is also very efficient in both cutting and the bulking cycles. But as it is related with the family of androgen it will have aromatizing properties as well. Apart from these benefits it has got all other benefits associated with it which are also associated with any other testosterone. 

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Testosterone Decanoate

  • Min. Order (MOQ) 10 Gram
  • product name Testosterone Decanoate
  • Appearance white powder
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Product Name: testosterone decanoate MolecularFormula: C29H46O3 MolecularWeight: 442.68 EINECS: 227-226-4 Specification: 200mg/ml Packing: foilbagortin Appearance: white powder Usage: Pharmaceutical material CAS: 5721-91-5 Testosterone decanoate is a steroid hormone derived from androgen, found in mammals and other vertebrates, testosterone decanoate is mainly secreted in test mail and female ovaries, although a small amount is also secreted by the adrenal gland, but testosterone decanoate is the principle of male sex hormones and Anabolic steroids.   Testosterone decanoate plays a key role in the development of male reproductive tissues such as testes and prostate glands. In addition, testosterone decanoate is a necessary condition for the health and well-being and prevention of osteoporosis, and testosterone decanoate is retained through most vertebrates, although the fish makes a little difference.

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Testosterone Undecanoate

  • Min. Order (MOQ) 10 Gram
  • product name Testosterone Undecanoate
  • Appearance white powder
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Product name: Testosterone Undecanoate Alias: Andriol CAS No:5949-44-0 Einecs No: 227-712-6 MF: C30H48O3 MW: 456.7 Its compound contains 40 mg of testosterone undecanoate based on oil and is sealed in capsules. Minus the ester weight, which is equivalent to about 25 mg of the testosterone dose per hat. This steroid is designed to be very different from most oral steroids. Oral administration of drugs usually flows through the liver into the bloodstream. When a steroid compound is administered in this manner without any form of structural protection .   This process leaves a very small steroid intact, essentially inactivating the drug. The addition of methyl (c-17AA) to the structure is a way to protect it from the process, but the results also apply pressure to the liver. In some cases, the stress can lead to actual damage to the liver tissue, so the designer of the steroid seeks another way to protect the testosterone molecule. With Andriol, which is produced by making a form of testosterone that will be absorbed through the lymphatic system. This is due to its high fat solubility caused by the ester and its suspension in the oil. It is believed that the absorption of the compound in this way is very advantageous because it allows the steroid to bypass the destructive first pass through the liver. This should allow the compound to enter the bloodstream completely without the need for harsh chemical changes. Once the ester breaks in the circulation, it produces the pharmacokinetics of free-acting oral testosterone. In the design, this steroid appears to be undecanoic, complete liver safe and oral active form of testosterone       Testosterone undecanoate Application:   Andriol or testosterone undecanoate is an ester of testosterone which is used for the treatment of male hypogonadism, and is currently under research for use as a male contraceptive, Andriol is sold and distributed under the brand names Andriol, understor, nebido, pantestone, restandol.   Testosterone undecanoate is a version of the anabolic steroid testosterone undecanoate developed by the pharmaceutical company organon, testosterone is said to enter the body as a fat through the lymphatic system, experience from user indicates that in dose of less than 240mg per day, effects are negligible, except at every onset of use, while even in higher dose, effects are still minimal, Andriol is therefor thought that most of the steroid is somehow not making it into the blood stream.

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Fluoxymesterone (Halotestin)

  • Min. Order (MOQ) 10 Kilogram
  • product name Fluoxymesterone (Halotestin)
  • Appearance white powder
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Product Name: Fluoxymesterone  Alias: Halotestin, Halotestin  CAS No: 76-43-7 Einecs No: 200-961-8 MF: C20H29FO3 MW: 336.44 Purity: 99% Appearance: white powder. Use: Fluoxymesteron Powder For Cutting Cycles Halotestin Steroids Grade: Pharmaceutical grade Certificate: ISO 9001, USP, GMP   Product description Fluoxymesteron is an extremely powerful synthetic metabolic androgen steroid, released by Upjohn for the first time by trade name Halotestin in the late 1950s. Soon after, Ciba Pharmaceuticals will release hormones under the Ultandren name, but Halotestin is still the most well-known brand. Pharmacia, formerly known as Upjohn, now manufactures Halotestin brand names. Halotestin is one of the most powerful synthetic metabolites present. Despite its strength, it only has some favorable features for most individuals, making it a poor choice for most athletes to improve performance. The average gym mouse does not find this is a steroid he wants to include in his cycle. There is no strategic advantage, the risk is far more than the reward. The average athlete's rat can easily reach his target with the use of other compounds. Of course, some gymnasium rats try to try it, the strength of the rapid and dramatic increase sounds attractive, but it is important to remember the harsh nature of this steroid. Fluoxy is a synthetic androgen steroid hormone that can be obtained by formulation. It can be given to men who have the medical condition of women who reduce or inhibit the production of testosterone naturally or have certain forms of breast cancer. Health care providers often warn that the drug may cause various possible side effects and may not be recommended for use in certain patients, due to potentially serious side effects.     The main use of fluoruric acid is to have a lower level of androgen hormones in men, which can be observed in cases such as hypogonadism or pubertal delay. Androgens are also commonly known as male hormones and are mainly responsible for male sexual development. Testosterone, which begins to form in the womb in men and promote the development of the , testes and scrotum, is the most well-known androgen.   Product Application   Halotestin is a good compound used by athletes because it can greatly increase the power and energy output. Halotestin is the name of the Upjohn brand of steroid fluoxymesteron. Structural fluoroacrylates are derivatives of testosterone that differ from our basic androgen by three structural changes (especially the addition of 17α-methyl, 11β-hydroxy and 9-fluoro groups). The result is an effective oral steroid showing very strong androgenic properties. This has a lot of things because it is derived from testosterone and therefore has important similarities with this hormone.

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17-Methyltestosterone CAS: 58-18-4

  • Min. Order (MOQ) 10 Gram
  • product name 17-Methyltestosterone
  • Appearance white powder
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Product Name: 17-Methyltestosterone Other Name: Methyltestosterone Model NO: 58-18-4 CAS: 58-18-4 Appearance: white powder Molecular Formula: C20h30o2   Methyltestosterone (brand names:[1] Android, Androral, Oraviron, Testred, Virilon) is a 17-alpha-alkylated anabolic steroid used to treat men with a testosterone deficiency.[2] It bears close structural similarity to testosterone, but has a methyl group at C17 in order to increase oral bioavailability.It is used as a feed additive to produce predominately male populations of tilapia. Methyltestosterone is a 17-alpha-alkylated anabolic steroid used to treat men with a testosterone deficiency. It is also used in women to treat breast cancer, breast pain, swelling due to pregnancy, and with the addition of estrogen it can treat symptoms of menopause.    Produdct Applications   Methyltestosterone can promote the male sex organs and used in seedling stage sex change.   Methyltestosterone is a steroid hormone from the androgen and is found in mammals and other vertebrate, Methyltestosterone is primarily secreted in the tests of mails and the ovaries of female, although small amount are also secreted by the adrenal glands, Methyltestosterones is the principle male sex hormone and an anabolic steroid.   Methyltestosterone plays a key role in the development of male reproductive tissue such as the testis and prostates. In addition, Methyltestosterone is essential for health and well-being as well as the prevention of osteoporosis, Methyltestosterone is conserved through most vertebrates, although fish make a slightly difference from called 11-ketotestosterone.

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Oral Turinabol

  • Min. Order (MOQ) 10 Gram
  • product name Oral Turinabol
  • Appearance White or white crystalline powder
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Model NO.: 2446-23-3   Synonyms: Oral turinabol;4-ChlordehydroMethyl Testosterone;4-ChlorodehydroMethyltestosterone (oral turinabol)   Purity:99%   Molecular Formula: C20H27ClO2   Molecular Weight: 334.88   Appearance: White or white crystalline powder   Usage: Pharmaceutical raw materials   Package: 1kg/Aluminum foil bag   Description : 4-Chlorodehydromethyltestosterone, generic name for the more recognized brand Oral Turinabol, is a potent derivative of Dianabol. This oral steroid is structurally a cross between methandrostenolone and clostebol (4-chlorotestosterone), having the same base structure as Dianabol with the added 4-chloro alteration of clostebol. This alteration makes chlorodehydromethyltestosterone a milder cousin of Dianabol, the new steroid displaying no estrogenic and a much less androgenic activity in comparison to its more famous counterpart. The anabolic activity of 4-Chlorodehydromethyltestosterone is somewhat lower than that of Dianabol as well, but it does maintain a much more favorable balance of anabolic to androgenic effect. This means that at any given level of muscle-building activity, chlorodehydromethyltestosterone will be less likely to produce androgenic side effects.   Application:   Oral Turinabol, commonly referred to as OT, is a derivative of Dianabol. It is designed to work without causing water retention or estrogenic effects. As a 17-alpha alkylated steroid, however, it can be toxic to the liver.Users of OT experience slow, steady gains that give the muscle a defined look probably because of the lack of water retention. Although OT was first developed in the 1960's, it has made its way back into popularity today, probably because if its low health risks and quality muscle mass it produces.

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17a-Methyl-1-testosterone CAS: 65-04-3

  • Min. Order (MOQ) 10 Gram
  • product name 17a-Methyl-1-testosterone
  • Appearance White powder
  • Usage Used as a male hormone and anabolic hormones
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Product name: 17a-Methyl-1-testosterone Alias: Methyltestosterone ;17-Alpha-Methyl-Testosterone ;Metandren CAS: 65-04-3 MF: C20H30O2 MW: 302.45 Appearance: White powder Usage: Methyl-1-Testosterone is a derivative of dihydrotestosterone. Used as a male hormone and anabolic hormones   17a-Methyl-1-testosterone Description:   17a-Methyl-1-testosterone can promote the male sex organs and used in seeding stage sex change. 17a-Methyl-1-testosterone is a steroid hormone from the androgen and is found in mammals and other vertebrates , 17a-Methyl-1-testosterone is primarily secreted in the tests of mails and the ovaries of female, although samll amount are also secreted by the adrenal glands , 17a-Methyl-1-testosterone is the principle male sex hormone and an anabolic steroid.   The usage of 17a-Methyl-1-testosterone:   Take 17a-Methyl-1-testosterone by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.If you miss a dose of 17a-Methyl-1-testosterone, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Don't take 2 doses at once.

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1-Testosterone Cypiontae

  • Min. Order (MOQ) 10 Gram
  • product name 1-Testosterone Cypiontae
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Product Description:  1-testosterone (dihydroboldenone), or DHB for short, is an anabolic steroid that has some unique properties of interest to bodybuilders. Interestingly, in spite of the fact that the name can be confusing, in no way is DHB testosterone. In fact, it is simply the 5alpha reduced form of Equipoise (boldenone), which acts in a completely different way. Therefore, you can think of it as a dihydrotestosterone (DHT) version of equipoise. Typical cycle Users will usually kickstart their cycle off with an oral and then stack around 400-500 milligrams (mg) per week of DHB with some long estered testosterone. When you do this, you should also run an aromatase inhibitor (AI) to offset the estrogen increases from testosterone, and you should also use such support supplements as N2Guard. Female use Virilization symptoms such as deepening voice, enlarged clitoris, and facial/body hair can occur when females intentionally, or accidentally, run androgenic compounds. As stated above, although DHB on paper is as androgenic as testosterone, that doesn't mean that it will yield as much androgenic symptoms as testosterone, so females usually chose DHB over testosterone. What's more, DHB is structurally more similar to primobolan and equipoise than to testosterone, so the virilization risk is lower.   In the end I would only recommend DHB to very experienced females who are aware of the risks, as DHB is in no way a weak steroid. Female users should start low at 25 milligrams (mg) per week, and work their way up to 75mg per week at the most. Half life DHB is usually tied to the cypionate ester, hence the half life in that case would be of approximately 8-10 days. It is wise to inject every 4-6 days, and once you stop using DHB, it will take about 4-5 weeks to completely clear your system. However, DHB is also found in propionate and other ester forms as well. Therefore, the frequency of the necessary injections and the clearance time will greatly depend on the ester you use.   Recipes 50 ml @ 200 mg/ml 10g 1-test cyp powder 10cc sryinges 20g needels 25g needles .22 or .45 whatmans BA BB Cottenseed oil or GSO steirile, sealed 50ml vial unsealed 50ml vial rubber stoppers funnel glass rod to stir.

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Nandrolone CAS: 434-22-0

  • Min. Order (MOQ) 10 Gram
  • Product Name Nandrolone
  • Appearance white powder
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Product name Nandrolone CAS 434-22-0 Alias Nandrolone Base; Nandrolone Molecular Formula C19H30O2 Molecular Weight 290.44 Melting point 120-125 °C Nandrolone is most commonly found with a cypionate, laurate, decanoate or plenylpropionate ester.    The ester determines how much of the given hormone is released over a period of time. Nandrolone is a modification of testosterone, meaning it is highly anabolic (muscle building) and moderately androgenic (male characteristics).    Nandrolone is an anabolic steroid that promotes growth of various tissue, increases hemoglobin and red cell mass, as well as oxygen flowing to the blood. The drug is also used to treat osteoporosis in postmenopausal women. Our body produces a very small amount of nandrolone, therefore in order to increase its size, many bodybuilders administer this substance for greater muscle mass, increased strength and more strenuous workouts. Durabolin is also one of the oldest Nandrolone compounds and was actually released a few years ahead of Deca Durabolin. However, it has been Deca Durabolin and the overall Nandrolone Decanoate mixture that has dominated the Nandrolone market place throughout history. While Organon still makes Durabolin and there are many other pharmacies and underground labs that make NPP, it is not as commonly available. However, in recent years it has seen its demand slightly increase due to performance enhancement use. Durabolin is one of the most beneficial anabolic steroids to ever hit the market. The benefits of this steroid can easily be seen in both therapeutic and performance based circles. In a medical setting, along with testosterone this is one of the most important anabolic steroids we have, and the advantages it can provide run extremely deep.

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Nandrolone Decanoate (DECA) CAS No: 360-70-3

  • Min. Order (MOQ) 10 Gram
  • product name Nandrolone Decanoate (DECA)
  • Appearance white or oyster white to pale yellow crystalline powder
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Nandrolone Decanoate Deca Durabolin Durabol Nandrolone Decanoate CAS No: 360-70-3 Deca Einecs No: 206-639-3 Durabolin MF: C28H44O3 Durabol MW: 428.65 Deca Purity: Nandrolone Decanoate purity is 99.5% Durabolin Appearance: Nandrolone Decanoate white or oyster white to pale yellow crystalline powder Durabol Usage: Pharmaceutical material, Steroid hormone, Anabolin. Is a male hormone, anabolic hormones drugs. Nandrolone Decanoate / Deca  Description:  Nandrolone decanoate is an injectable sort of the anabolic steroid. Nandrolone decanoate displays relatively powerful anabolic attributes. Dissimilar testosterone, however, Nandrolone decanoate tissue-building action is attended by weak androgenic facilities. The modest attributes of nandrolone decanoate have made it among the most pop injectable steroids in global, highly preferred by athletes for its power to promote important strength and lean muscle mass increases without strong androgenic or estrogenic side effects. Nandrolone Decanoate / Deca  Applications:  Nandrolone decanoate is wide disposable in human andveterinary drug marketplaces. Structural. Nandrolone decanoate is a modified sort of nandrolone. Esterified steroids are proposed to prolong the window of therapeutical effect following administration, allowable for a lower periodic injection docket compared to injections of free (unesterified) steroid. Nandrolone decanoate offers a keen top in nandrolone release 24-48 hours accompanying deep intramuscular injection, which constantly goes down to near baseline points about 2 weeks later. The average depot-release half life of nandrolone decanoate is eight days.

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Nandrolone Phenypropionate (Durabolin) CAS No.: 62-90-8

  • Min. Order (MOQ) 10 Gallon
  • product name Nandrolone Phenypropionate
  • Appearance white powder
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Product Name: Nandrolone Phenypropionate Other Name: Durabolin CAS No.: 62-90-8   Procut Description: Nandrolone is a 19-nor testosterone (19-nor) synthetic androgenic androgenic. 19-nor classification refers to the structural changes of testosterone hormones because the carbon atoms have been removed at the 19th position. This simple structural change gives us Nandrolone and by adding short dipropionate we have Nandrolone phenylpropionate.   On the basis of hormone function, Nandrolone phenylpropionate is identical to Nandrolone Decanoate. Both forms consist of the same active hormone. In the case of NPP, we have a shorter ester form, which gives a larger Nandrolone outbreak after injection, but also has a much shorter half-life. This means that if the blood level is to remain stable, the adrenaline phenylpropionate must be injected more frequently than its larger ester counterpart.   Nandrolone phenylpropionate is slightly more synthetically metabolically than testosterone and has a score of 125 compared to a testosterone rating of 100. Compared with the androgen rating of 100, the androgen score is 37. Androgen reduction is due to a decrease in androgen To dihydrohydrogen (DHN) in place of dihydrotestosterone (DHT). This is one of the reasons why Nandrolone phenylpropionate is more tolerant at higher doses of testosterone in some men at higher doses.   Nandrolone phenylpropionate is also slightly less estrogen than testosterone. Both Nandrolone and testosterone are aromatized, but Nandrolone is only about 20% of the rate of testosterone. IMPORTANT: Nandrolone phenylpropionate carries progesterone properties that will affect the side effects of this hormone.  Nandrolone benzoic acid carries many positive traits similar to many synthetic metabolic steroids. However, this compound also has far more functional properties than some steroid hormones can do.

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Stanolone(Androstanolone) CAS: 521-18-6

  • Min. Order (MOQ) 10 Gram
  • product name Stanolone (Steroids powder)
  • Appearance White crystalline powder
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Stanolone (Steroids powder) Synonyms: Androstanolone Chemical Name: 5A-androstan-17ß -ol-3-one CAS: 521-18-6 EINECS: 208-307-3 Assay: 99% min. Molecular Formula: C19H30O2 Packing: Foil bag or tin. Delivery: Express courier. Description: White crystalline powder   Description: Stanolone can be used for chronic wasting disease, osteoporosis, severe infections and wounds caused by burns negative nitrogen balance. Stanolone can promote premature children and the growth of immature children and so on. Stanolone can also be used on fracture healing, hypercholesterolemia, postpartum weakness. Stanolone is DHT. it to be better than and not as problematic as many might guess, at least at moderate doses. I'd consider it as part of stack, for example as an added 100-200 mg/week, rather than being the base or the sole steroid used. There's been at least one medical study on use by injection, which went well. The oral bioavailability is very low.The propionate powder may be available.If used orally, there would be no liver harshness. No harshness at all really.DHT really does only one thing that other anabolic steroids that strongly bind the androgen receptor don't do, and that is convert to 5a-androstanediol, which itself has some adverse effect on the scalp but doesn't appear to be thought a really major player in hair loss. Still, I don't know what might happen with really high doses of DHT. There really seems no reason to do it. But for example, adding it at 100-200 mg/week, by injection, for reason of getting positive effect on the nervous system would be an interesting thing to do, and I think entirely reasonable. Oral use, I would not bother with, but if doing it, would expect to have to work up to say 200-300 mg two or three times per day, which might get expensive fast.

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Mibolerone CAS:3704-09-4

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  • Min. Order (MOQ) 10 Gram
  • product name Mibolerone
  • Appearance White Crystalline Solid
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Product Name: Miboleron CAS:3704-09-4 MF: C20H30O2 MW: 302.45 EINECS: 223-046-5 Chemical Properties: White Crystalline Solid   Procut Description:   Check Drop is the trade name of the synthetic metabolic steroid miboleronecas. Originally used to suppress exhaust, Miboleronecas is one of the most demanding steroids present. It is about 5.9 times the anabolic and 2.5 times the testosterone androgen. Check the drop on the athlete to provide a brief adrenaline attack that is used before the sporting event. Due to its hyperandrogenic nature, it is usually the cause of progesterone-related men's breast development.   Mibolerone is a veterinarian grade anabolic steroid that was released in the 1960’s by Upjohn under the brand name Cheque Drops and later as Cheque Medicated Dog Food. As with many steroid hormones, and this includes veterinarian grade, it wasn’t long after its inception that athletes and bodybuilders found a use.   Cheque Drops is one of the most potent anabolic steroids ever made.. You’ll most commonly find its use limited to pre-fight or powerlifting competitions. Some bodybuilders will use it pre-contest to aid in the final weeks or in the off-season for an extra push, but it’s not a very common bodybuilding steroid. We’ll understand this steroid’s lack of appeal to many bodybuilders as we continue.

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Trenbolone Acetate yellow crystalline powder

  • Min. Order (MOQ) 10 Gram
  • product name Trenbolone Acetate
  • Appearance Yellow to Pale yellow crystalline powder
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CAS: 10161-34-9 Assays: Above 99% MOQ: 10g Molecular Formula: C20H24O3 Molecular Weight: 312.4 Appearance: Yellow to Pale yellow crystalline powder   Description :  Tren Acetate (or Tren A, TA) has the molecular formula of C20H24O3 and has an anabolic-androgenic ratio of 500:500. It has an active life of 2-3 days and has the molecular weight of 270.3706 g/mol at the base. Trenbolone Acetate, a 19-nor steroid, is derived from the compound Nandrolone. It is characterized by strong androgenic properties and no estrogenic activity. This anabolic steroid has a binding affinity for androgen receptor five times the strength Testosterone.   Trenbolone acetate is admired globally by elite athletes as it can dramatically improve the uptake of nitrogen by muscles and improve the level of protein synthesis. Ideal for cutting cycles, Tren A does not get metabolized by aromatase or 5α-reductase into estrogenic compounds like estradiol or into Dihydrotestosterone (DHT).   Trenbolone exhibits interesting stacking behavior. Combination with either Dianabol or Anadrol gives a very strong synergistic effect. Even if the same total milligram amount of steroid is used per week, results are much better with such a combination than with any of these steroids used alone Trenbolone Acetate.   While trenbolone use is not necessary to achieve excellent results in an anabolic steroid cycle, it can be a remarkable aid towards such results.     Applications :   Bodybuilding Steroids Trenbolone Acetate is very fast acting. Therefore, bodybuilders choosing to use this substance often find that daily injections are best for keep blood levels as consistent as possible. Simply put . Trenbolone Acetate is the most powerful overall steroid in use by bodybuilders today. Tren, as it is often called, is both highly androgenic and anabolic. It is chemically unable to aromatize, and therefore produces no estrogen buildup. This, along with its high androgenic properties, makes the muscle produced by this drug very hard and defined.

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Trenbolone Enanthate CAS No.: 10161-33-8

  • Min. Order (MOQ) 10 Gram
  • product name Trenbolone Enanthate
  • Appearance pale yellow or yellow crystalline powder
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Product Name:  Trenbolone Enanthate CAS No.:  10161-33-8 Molecular Formula:  C25H34O3 Molecular weight:  382.54 Assay:  99% Appearance:  pale yellow or yellow crystalline powder Trenbolone Enanthate Description:     Trenbolone Enanthate also shines is in its ability to greatly preserve lean muscle tissue.When we diet, in-order to lose body fat, not weight but body fat we must be in a caloric deficit; we must burn more calories than we consume. As a result, as the body fights change with a desire to hang onto stored body fat due to its survival nature lean muscle tissue is often sacrificed in-order to meet its energy needs. As we lose more lean muscle tissue, this slows down the metabolic rate, and of course, it makes the physique look worse; Trenbolone Enanthate will prevent this. Of course, it gets even better; through its traits, Trenbolone Enanthate will provide the ultimate in visual conditioning effects.   Trenbolone Enanthate is a steroid that will greatly increase muscular endurance, more work can be done and you will not tire out as fast and it will also play an important role in recovery and healing.     Trenbolone Enanthate Applications:     Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.     Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds).

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Trenbolone Hexahydrobenzyl Carbonate (parabolan) CAS23454-33-3

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  • Min. Order (MOQ) 10 Gallon
  • product name Trenbolone Hexahydrobenzyl Carbonate
  • Appearance White to light yellow crystalline powder
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product name:trenbolone hexahydrobenzyl carbonate synonyms:trenbolone cyclohexylmethylcarbonate; trenbolone hexahydrobenzylcarbonate, parabolan cas:23454-33-3 mf”c26h34o4 mw:410.55 einecs:245-669-1 purity (hplc):99.00%min   appearance:white to light yellow crystalline powder product description:   1.product features one of the most powerful (and hard and expensive to obtain) substances in the trenbolone family, parabolan is considered to be a superior product in many ways. Much like finaplix, parabolan can deliver very intense, lean gains without aromatizing in the body. Its half-life is very long, so injections can be spread out over the course of a week every two to three days should be sufficient.   2.the biggest concern with parabolan is that it may be liver and kidney toxic at high doses, although most users report mild to no side effects associated with its use. On its own, parabolan won't aromatize, but when stacked with aromatizing compounds it may exaggerate gynocomastia. Adding nolvadex or winstrol will help counter this. Also, parabolan is a strong androgen receptor agonist, so using hcg at the end of a cycle is recommended.   product applications   trenbolone is a steroid used by veterinarians on livestock to increase muscle growth and appetite, to increase the half-time, trenbolone is not used in an unrefined form, but is rather administered as ester derivatives such as trenbolone acetate, trenbolone enanthate ortrenbolone cyclohexylmethylcarbonate, a normal bodybuilding dosage can range from 200mg/week to 1400mg/ week. Trenbolone acetate can be injected once a week, also trenbolone acetate is often refined to as "fina" by user, trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.

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Tibolone CAS: 5630-53-5 tibolone white powder

  • Min. Order (MOQ) 10
  • product name Tibolone
  • Character White powder
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product name: tibolone (steroids) synonyms: liviella; livial cas: 5630-53-5 einecs: 227-069-1 mf: c21h28o2 mw: 312.45 character: white powder tibolone is a synthetic estrogen steroid hormone that acts as an agonist for multiple i-type steroid receptors and therefore has weak estrogen and progestogen activity as well as some androgenic properties. The parent compound is not active but is metabolized to the active form via tissue-specific metabolism of the sulfatase, which provides estrogenic action without the need for simultaneous use of progesterone. Tibolone also appears to have reduced estrogenic activity in breast tissue. Has been proven effective against menopausal symptoms and the prevention of postmenopausal osteoporosis; it is approved in several european countries, but not the united states. Tibolone can be 1.25 and 2.5 mg tablets for livial. Side effects include vaginal bleeding, abdominal pain, weight gain, bloating, breast tenderness, genital itching and vaginitis.   tibolone application   tibolone/livial is used mainly for treatment of endometriosis, as well as hormone replacement therapy in post-menopausal women. Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for er alpha. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile. It has also been investigated as a possible treatment for female sexual dysfunction.   tibolone is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women. It is a synthetic steroid that has the same activity as the female sex hormones estrogen and progesterone and the androgen testosterone. Tibolone helps restore hormonal balance in the body.   when estrogen levels are low tissues can slowly degenerate, as is experienced during menopause. In addition, low levels of estrogen can cause distressing symptoms such as hot flushes, night sweats, mood swings, reduced sex drive and vaginal dryness. Tibolone is broken down into three compounds which act in a similar way to the natural estrogen and progesterone found in the body. It restores plasma endorphin level in post-menopausal women and acts centrally to affect the thermo-regulatory system.      

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Boldenone Acetate Cas: 2363-59-9

  • Min. Order (MOQ) 10 Gram
  • product name Boldenone Acetate
  • Appearance white powder
  • Usage indicated as a sympathicolytic and mydriatic
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Product name:Boldenone Acetate Other name:Boldenone 17-acetate CAS register number:2363-59-9 EINECS:219-112-8 Molecular formula:C21H28O3 Molecular weight:328.45 Molecular structure:CAS 2363-59-9 Boldenone Acetate Muscle Growth Steroids Raw Hormone Powders Assay:99%   Description:   Boldenone Acetate would be more intense to raises red blood cells, increasing the appetite, repairs connective tissue which is also a huge plus for bodybuilders during training. Boldenone Acetate is going to be a painful injection, this steroid is containing 25mg/ml of the hormone boldenone attatched to the acetate ester and 75mg/ml of the hormone boldenone attatched to the propiopate ester. Having Boldenone attatched to these esters allows for it to raise blood levels rather quickly and for the effects to be faster than those seen with the slower ester of traditional EQ. This will favor athletes looking to run shorter cycles and those who are worried about frequent drug testing and need to able to clear hormones from their system in a timely manner.   It can be effectively incorporated in both "cutting" and "bulking" cycles due to the well balanced effects of this anabolic substance. This steroid aromatizes very little, and therefore produces almost no estrogenic side effects such as water retention or "gyno".   Application: Boldenone Acetate can be used to front load a cycle containing Boldenone Undecylenate or Cypionate which take a few weeks to kick in. Ideal for the strength athlete in a shorter cycle. Dose like most Aces 200-500mg PW. Max 800mg. It will kick in about 3 days. Half life 3 days.     Boldenone Acetate would be more intense to raises red blood cells, increasing the appetite, repairs connective tissue which is also a huge plus for bodybuilders during training. Boldenone Acetate is going to be a painful injection, this steroid is containing 25mg/ml of the hormone boldenone attatched to the acetate ester and 75mg/ml of the hormone boldenone attatched to the propiopate ester. Having Boldenone attatched to these esters allows for it to raise blood levels rather quickly and for the effects to be faster than those seen with the slower ester of traditional EQ. This will favor athletes looking to run shorter cycles and those who are worried about frequent drug testing and need to able to clear hormones from their system in a timely manner.

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Boldenone Cypionate CAS: 106505-90-2

  • Min. Order (MOQ) 10 Gram
  • product name Boldenone Cypionate
  • Appearance white crystalline powder
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Product name: Boldenone cypionate CAS register number :106505-90-2 Molecular formula: C26H38O3 Molecular weight: 398.58 Assay: 99% Delivery time: 3-7 work days   Boldenone Cypionate description: Boldenone cypionate is an ester of boldenone and is recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. Debilitation often follows disease or may occur following overwork and overexertion.   Boldenone improves the general state of debilitated horses, thus aiding in correcting weight losses and improving appetite. It is not a substitute for a well-balanced diet. Optimal results can be expected only when good management and feeding practices are utilized. Boldenone should be considered only as adjunctive therapy to other specific and supportive therapy for diseases, surgical cases and traumatic injuries.   Boldenone 200 USP injection provides boldenone cypionate is a long acting anabolic steroid used in veterinary medicine for the treatment of horses. Boldenone possess marked anabolic properties and a minimal amount of androgenic activity. Boldenone has a rapid onset of action; this is advantageous and is preferred over frequent oral dosing or even repeated injections. The esterification of the 17-beta-hydroxyl group increases the duration of the action of boldenone. Boldenone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus Boldenone 200 can be administered at intervals of every 2-3 weeks.    Boldenone Cypionate Application:   Boldenone Cypionate is an anabolic steroid developed for veterinary use; it will increase nitrogen retention, protein synthesis, increases appetito and stimulates the release of erythropoietin in the kidneys.   Boldenone cypionate is an ester of boldenone and is recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. Debilitation often follows disease or may occur following overwork and overexertion.   Boldenone Cypionate was synthetisized in an attempt to create a long-time inject able methandienone (dianabol), in reality boldenone acts nothing like methandrostenolone. It has a very long half-life, and can show up on a steroid test for up to 1.5 years, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use.   The individual dosage of Boldenone cypionate should be determined by the veterinarian before commencement of treatment. Animals should also be kept under observation during treatment.

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Oxymetholone (Anadrol)

  • Min. Order (MOQ) 10 Kilogram
  • Product Name Oxymetholone (Anadrol)
  • Appearance white powder
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As a steroid designed to treat weight deficiency and muscle wasting disease this is one of the more prominent bulking steroids we can use for a bulking purpose. While many anabolic steroids can serve both bulking and cutting purposes most have a primary role and Anadrol makes no exception. There is one purpose for Anadrol while on a cutting cycle and we will touch on it as we go but for the majority of steroid users bulking and only bulking will be the only time they use this steroid. With its immense power, Anadrol is one of the most powerful oral steroids ever made, individuals can see their weight increase by as much as 20-30lbs in a mere few weeks of use as well as see their strength shoot through the roof. Further, as this steroid is almost always used as part of a stack and not alone, due to its low androgen binding characteristics it will allow other steroids you are taking to more aptly fill this role and more or less create a higher level of synergy between the various anabolic androgenic steroids you are taking.     Anadrol & Cutting:   It is easy to see why this steroid is perfect for bulking as its attributes lend to this end and because of these very attributes very few individuals will use Anadrol during a cutting cycle. However, there is an exception and quite a large one in competitive bodybuilding. Many competitive bodybuilders will supplement with Anadrol the last few weeks before a show; by building up a large amount of the steroid in their body over a period of weeks they are able to make greater use of their carb up at the end. Through this process the competitor will possess a much fuller look but again, caution must be applied. An individual who is very sensitive to water retention from this steroid will need to stay away from this process but if ones diet is on point and such sensitivity is not a problem, coupled with a good AI and solid contest cycle a nice full effect can be gained. Anadrol Cycles & Doses:  Anadrol almost always comes in 50mg tablets and the most common dose is simply 50mg per day. While 50mg per day will prove to be very effective 100mg per day is not uncommon; however, 100mg per day will prove to be the most anyone would ever want to take if they desire to remain in a responsible realm. It should be noted that Anadrol does not carry the same risk to reward ratio most other anabolic steroids do.   This risk to reward ratio revolves around the dose and benefits of a particular steroid; meaning, the more you take the greater the results but the more you take the greater the risk of potential side-effects.

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Oxandrolone (Anavar) CAS No.: 53-39-4

  • Min. Order (MOQ) 10 Gram
  • Product Name Oxandrolone (Anavar)
  • Appearance White Crystalline Powder
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Anavar (Oxanabol) , unlike most oral compounds is categorized as a Class I anabolic steroid, most efficiently stacked with Class II compounds such as Dianabol or Anadrol. It adds little if anything to high-dose use of Class I anabolic steroids such as or to high-dose , which is classified as having mixed activity. It can be an aid, albeit an expensive one, to moderate dose testosterone usage. Anavar is an intriguing drug. It seems to defy the definition and limitations of oral steroids. You have read about its “clean gains” and relative safety. Curiously, it’s so safe that unlike other steroids, which were used for malnutrition and anemia, Anavar was originally prescribed mainly for burn victims. In a randomized, double-blind study, patients with 40% total body surface area burns were selected to receive standard burn care plus oxandrolone, or without oxandrolone. Oxandrolone was used to help regain weight lost after surgery, severe trauma, or chronic infections. Those treated with oxandrolone showed quickened healing, improved body composition, preserved muscle mass and reduced catabolism and consequently lessened hospital stay time.   Oxandrolone is rapidly absorbed from the gastrointestinal tract, resulting in a maximum plasma concentration between 30 and 90 minutes and a plasma half-life of about 9 hours. Oxandrolone has been given orally in the treat-ment of constitutional delayed growth and puberty in boys. Courses of treatment are short (about 3 to 4 months) because of the risk of epiphyseal closure. Oxandrolone has been prescribed to post-menopausal women in the treatment of osteoporosis. Oxandrolone is also under investigation in the treatment of Turner’s syndrome in girls. As oxandrolone is C17-alpha-alkylated there is the potential for liver damage.   Application   Anavar has often been called a weak steroid. Part of the reason for this is that use of a Class I steroid alone never is maximally effective. The other cause is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids.     Usage Among bodybuilders Anavar is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results. Oxandrolone can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the showphysique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone.

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Stanozolol (Winstrol) CAS : 10418-03-8

  • Min. Order (MOQ) 10 Gram
  • Product Name Stanozolol (Winstrol)
  • Appearance white powder
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Product name: Stanozolol (Winstrol) CAS : 10418-03-8 M. F: C21H32N2O M. W: 328.49   Description: Stanozolol Winstrol is one of the most popular anabolic steroids. Stiprolol Winstrol may be administered orally or intramuscularly. Some of its therapeutic uses include treatment for aplastic anemia and hereditary angioedema. It is also indicated as adjunctive therapies for the treatment of various other medical disorders such as vascular disease and growth failure.     Like many synthetic metabolic steroids, Stanozolol Winstrol is used to treat muscle wasting disorders, burn subjects, exposure to corticosteroids and osteoporosis. It is also used to help fracture healing, even in the presence of hormonal imbalance is also successfully used for obesity treatment. Breast cancer specific forms of treatment of angioedema and even some forms of delayed growth treatment for children have been shown to be successful. Unlike many synthetic metabolic steroids in the United States, Stanozolol Winstrol has never lost FDA approval. Semi-finished Injectable / Oral steroids   Test prop-----------100mg/ml 200mg/ml Test enan-----------250mg/ml 300mg/ml 400mg/ml 500mg/ml 600mg/ml Test cyp------------200mg/ml 250mg/ml 300mg/ml Test Sustanon-------200mg/ml 250mg/ml 300mg/ml 400mg/ml Deca----------------200mg/ml 250mg/ml Equipoise-----------200mg/ml 300mg/ml Tren ace------------100mg/ml 200mg/ml Tren enan-----------100mg/ml 200mg/ml Dianabol------------50mg/ml Winstrol------------50mg/ml Masteron------------100mg/ml 150mg/ml Primobolone---------100mg/ml Supertest-----------450mg/ml Anomass ------------400mg/ml Ripex---------------225mg/ml Tritren-------------180mg/ml Tri Test------------300mg/ml Tri Deca------------300mg/ml Test Blend----------450mg/ml 500mg/ml Nandro Test---------225mg/ml Mass----------------500mg/ml Cut Depot-----------400mg/ml Tren Test-----------225mg/ml Nandro Test Depot---------450mg/ml Equi Test-----------------450mg/ml Rip Cut-------------------175mg/ml Tren Test Depot-----------450mg/ml

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Drostanolone Propionate (Masteron) CAS No: 521-12-0

  • Min. Order (MOQ) 10 Gram
  • Product Name Drostanolone Propionate (Masteron)
  • Appearance white crystalloid powder and yellow liquid
  • Usage combating advanced inoperable breast cancer in postmenopausal women.
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CAS No: 521-12-0 Einecs No: 208-303-1 MF: C23H36O3 MW: 360.53   Description:   Originally Dromostanolone (abbreviated to Drostanolone) known by trade name Masteron is an injectable oil-based anabolic steroid, derived from Dihydrotestosterone (DHT). It is a member of the DHT-derived family of anabolic steroids. Other known DHT-derivatives include: Winstrol, Anadrol, Anavar, Primobolan, and a few more. Drostanolone (Masteron) is considered a moderate strength anabolic steroid with anabolic rating: 62 - 130 and low androgenic strenght: 25 - 40.   There are two different variants of Masteron:   Drostanolone Propionate Drostanolone Enanthate     All anabolic steroid analogues and derivatives are derivates of the three natural anabolic steroids found in the human body:   Testosterone Dihydrotestosterone Nandrolone   Drostanolone is injected into the body as an ester (bonded to either Propionate or Enanthate). Enzymes cleave off the ester from the Masteron molecule - which takes varying amount of time depending on which ester was used. This process causes the gradual release rate and extended half-life of the steroid. Drostanolone Propionate has a half-life of 2.5 days, while Drostanolone Enanthate has a half-life of 10 days.   Intended use of Drostanolone / Masteron   Masteron was initially marketed as a treatment of female breast cancer. Because it pronounced male characteristics in women and because more effective breast cancer treatments were invented, Drostanolone was gradually phased out.   The dosage of Masteron    The right combination of anabolic steroids, Masteron is quite low dose can produce results.However, high doses of steroids can produce very big effect. But for many young men , they needed the high dose products to use .There are many different products and different suppliers in this market , you need to know the market and your supplier . The dose may be different because of the different supplier , so you need to find the best dose for yourself .   ① The most basic dose is 200~300mg per week , this dose is suitable for the most people . It will not produce the strong result , but it can enhance your condition . You can also use the low dose of testosterone (100mg/ml) and the basic Masteron dose to provide the needed for anti-estrogenic protection .   ② The normal dose is 300~400mg per week or an average of 350mg per week , this can enhace the hardness of muscles .   ③ The high dose is 800mg per week , this dose works well , but the side effect exsits 

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Methenolone Acetate/primobolan

  • Min. Order (MOQ) 10 Gram
  • Product Name Methenolone Acetate/Primobolan
  • Appearance white powder.
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CAS No: 434-05-9 Einecs No: 207-097-0 MF: C22H32O3 MW: 344.49 Purity: 99% Description:   Methenolone acetate(primobolan), all things being equal, is an excellent oral steroid drug. Unlike most other oral steroids, Primobolan is not 17alkylated and does not have liver toxicity problems.   Methenolone is perhaps only half as potent by the oral route as by injection, so dosages need to be high, at least 100 and preferably 200-300 mg per day, but if that can be afforded it is an excellent drug. It is unusual among oral steroids as being Class I, binding well to the androgen receptor.   Primobolan Depot is the injectable version of the steroide methenolone. It is the same compound as the one in Primobolan Orals (methenolone acetate), both produced by Schering. In this injectable version, an enanthate ester is added to the steroide, which makes for a slow and gradual release from the site of injection.   Its length of activity would thus be quite similar to Testosterone enanthate, with blood levels remaining elevated for approximately two weeks. Methenolone itself is a long acting anabolic, with extremely low androgenic properties.   It's anabolic effect is also quite mild, its potency is considered to be slightly less than DecaDurabolin (nandrolones decanoate) on a milligram for milligram basis.   For this reason, Primobolan is most commonly used during cutting cycles when a mass increase is not the main goal. Some athletes do prefer to combine a mild anabolic like "Primo" with bulking drugs such as Dianabols, Anadrol, or testosterone however, presumably to lower the overall androgen dosage and minimize uncomfortable side effects. When choosing between Primobolan versions, the injectable is preferred over the oral, as it is much more cost effective.   Applications:   Methenolone Acetate is very strong, the synthesis of the metabolism and male characteristics is very low, making it the best choice for the game. The drug for women is very good!   For men, 50-100 mgs Methenolone Acetate /day is the accurate as well actual measure by mouth, while for women, 10-25 mgs Methenolone Acetate /day is the finest quantity. If you have to administrate them as injections, the top dose for Primobolan (Methenolone Acetate) injection is 350-600 mg Methenolone Acetate /week for men. Women have to use 100 mg Methenolone Acetate weekly of this medication.

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Tamoxifen CAS: 54965-24-1

  • Min. Order (MOQ) 10 Gram
  • Product Name Tamoxifen
  • Appearance powder
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CAS:54965-24-1 MF:C32H37NO8 MW:563.64 EINECS:259-415-2   Tamoxifen Citrate description:   Tamoxifen Citrate is a Selective Estrogen Receptor Modulator (SERM) that was created in 1961 by ICI now known as AstraZenaca. There are numerous brands including generic forms of Tamoxifen Citrate on the market, but Nolvadex is the most well known. Often referred to as an anti-estrogen, Tamoxifen Citrate is actually both an antagonist and agonist. This means it will act as an anti-estrogen in certain areas of the body while acting as an estrogen in other areas.   Tamoxifen Citrate has been used medically for decades and has been highly successful in breast cancer treatment, specifically hormone-responsive breast cancer. It is also a medication that is used by many anabolic steroid users, but it is not a steroid. This is a drug steroid users will sometimes use during steroid use to help with estrogenic related side effects brought on by specific steroids. However, it is most commonly used during Post Cycle Therapy (PCT). PCT is the 3-6 week period following steroid use that is implemented in order to help with natural testosterone production that is suppressed during anabolic steroid use.   Tamoxifen Citrate Functions & Traits   Tamoxifen Citrate is a SERM that acts as both antagonist and agonist in relation to the estrogen hormone. It is an anti-estrogen in that it binds to estrogen receptors in certain parts of the body, particularly in the mammary tissue. This action prevents estrogen from acting on its originally intended point of binding. This makes Tamoxifen Citrate valuable to breast cancer patients as breast cancer feeds off of estrogen. And it’s valuable to steroid users as increased estrogen levels can bind to the mammary tissue and lead to gynecomastia.   The relationship Tamoxifen Citrate has in being an anti-estrogen is fairly straightforward and well understood by many, but it’s its relationship to being an estrogen in other areas that’s surprising to some. Tamoxifen Citrate acts as an estrogen on the liver. Liver related estrogenic activity has been shown to improve cardiovascular health, particularly as it relates to cholesterol. This can be very advantageous for the bodybuilding steroid user as most steroids have a negative impact on cholesterol levels.   Beyond its estrogen related activity Tamoxifen Citrate possesses strong testosterone stimulating properties. The use of Tamoxifen Citrate will stimulate the pituitary to increase its production of Luteinizing Hormone (LH) and Follicle Stimulating Hormone (FSH) with a strong emphasis on LH. LH and FSH are the gonadotropins that signal to the testicles to produce testosterone. Without LH and FSH there is no testosterone production.  

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Toremifene citrate CAS: 89778-27-8

  • Min. Order (MOQ) 10 Gram
  • Product Name Toremifene citrate
  • Appearance White or almost white powder
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Description   Toremifene Citrate is the chemical name of active ingredient in Fareston. Toremifene citrate is very similar to Nolvadex (Tamoxifen Citrate) and Clomid (Clomiphene Citrate), Fareston is medically used to treat breast cancer in post-menopausal women. Toremifene Citrate is also used in many performance enhancing circles for side effect protection and post cycle therapy plans. This does not make Fareston an anabolic steroid; however, it is commonly used by steroid users in order to enhance the safety and efficiency of their steroid use. Anabolic steroid users often use Fareston in order to prevent estrogenic related side effects that may be caused by the use of aromatizing steroids. The most common estrogenic issues include gynecomastia and water retention. High blood pressure can also occur when water retention gets out of hand, but Toremifene Citrate can help with all of these things.   Toremifene Citrate exerts its effects by antagonizing the estrogen receptor in some tissues, and agonizing it in others. In this way, certain estrogenic pathways are activated and others are blockaded. It seems to exert estrogenic effects on blood lipids, reducing LDL and total cholesterol, as well as estrogenic effects on bone, improving density. It would also appear to exert anti-estrogenic effects in breast tissue,   Application   Toremifene citrate is an oral selective estrogen receptor modulator (SERM) which helps oppose the actions of estrogen in the body. Licensed in the United States under the brand name Fareston, toremifene citrate is FDA-approved for use in advanced (metastatic)breast cancer. It is also being evaluated for prevention of prostate cancer under the brand name Acapodene.   Used for Metastatic breast cancer in postmenopausal women. PO 60 mg once daily with or without food. Treatment is generally continued until disease progression is observed.

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Exemestane (Aromasin) CAS: 89778-27-8

  • Min. Order (MOQ) 10 Gram
  • Product Name Exemestane Aromasin
  • Appearance white powder
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Product: Exemestane Aromasin CAS: 89778-27-8 Molecular Formula: C20H24O2 Molecular Weight: 296.40   Product Description   1. Exemestane is a steroidal Aromatase Inhibitor (AI) that is most commonly known as Aromasin. In fact, the Aromasin brand name is the only pharmaceutical grade brand of the Exemestane AI due to the tight patent Upjohn has maintained on the product. While tightly controlled by the pharmaceutical giant, Aromasin is available in numerous countries around the globe.   2. Aromasin was first released on the U.S. market in 2000 after shortly gaining FDA approval a few months prior in 1999. The primary purpose of use as with most AI's would be to combat breast cancer in post-menopausal women. Shortly after, the AI would begin to gain a lot of popularity among anabolic steroid users for its ability to protect against estrogenic related side effects. This action is very similar to the older and more popular AI's in Arimidex and Femara It would also gain a fair amount of popularity in Post Cycle Therapy (PCT) plans among steroid users. It was not the first AI to gain such popularity but would prove to be a little more advantageous for this purpose than most AI's.   3. Aromasin is officially classified as a steroidal suicide Aromatase Inhibitor, and carries the ability to inhibit the aromatase enzyme, which is responsible for the production or conversion of testosterone to estrogen. Aromasin has the ability to block aromatization, which in turn inhibits the production of estrogen, and thereby lowers the body's serum estrogen levels. This will prove useful to breast cancer patients as breast cancer often feeds off the estrogen hormone. It will also prove useful to the anabolic steroid user.   Applications:   The third generation aromatase inhibitors, used in the treatment of metastatic breast cancer and used as aid in the treatment of early breast cancer.   Many breast cancers are stimulated to grow by the female sex hormones oestrogen and progesterone. These breast cancers are called hormone sensitive or hormone receptor positive and can be treated with drugs that block the effects of these hormones.   In women who have had their menopause, oestrogen is mainly produced by changing androgens (sex hormones produced by the adrenal glands) into oestrogens. This process is called aromatisation and happens mainly in the fatty tissues, muscle and the skin. It needs a particular enzyme called aromatase. Exemestan blocks the process of aromatisation. So it lowers the amount of oestrogen in the body. In early breast cancer, taking exemestanes can help to stop breast cancer coming back. In advanced breast cancer the cancer cells may grow more slowly or stop growing completely.

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Formestane CAS:566-48-3

  • Min. Order (MOQ) 10 Gram
  • Product Name Formestane
  • Appearance White Powder
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CAS:566-48-3 Molecular formula:C19H26O3 MW:302.41   Purity:99%   Product Description:   A. Formestane is a synthetic steroidal substance with antineoplastic activity. Formestane binds irreversibly to and inhibits the enzyme aromatase, thereby blocking the conversion of cholesterol to pregnenolone and the peripheral aromatization of androgenic precursors into estrogens.   B. Formestane is a drug that has been previously used in breast cancer treatment. Like most drugs which have some sort of phsyique usage, athletes eventually get a hold of it. Formestane is currently one of the best legal anti-estrogens out there. It is classified as an irreversible arromatase inhibitor, meaning, it destroys the aromatase enzyme.   C. Formestane is often used to suppress estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosterone, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor. Formestane has poor oral bioavailability and as such is no longer popular as many orally active aromatase inhibitors have been identified.   Application:   Formestane has a very long active life on the order of 24-36 hours.This amount will usually last you about 3-4 weeks at a sufficient dosage of 200-400mg per day.I have found 200mg a day to be perfect for on cycle anti-estrogen usage and for post-cycle recovery of natural testosterone.Formestane has zero negative feedback (even though it is an androgen by definition) and serves to elevate natural testosterone as well as any anti-estrogen/anti-aromatase drug out there, next to clomid.   Formestane attacks the aromatase enzyme and is therefore a first line inhibitor.So if you need immediate relief of estrogen during your cycle, you need a second class drug (estrogen receptor blocker) such as nolvadex or clomid.Formestane is a lot like arimidex in its mechanism of action in attacking the aromatase enzyme itself.    

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Vardenafil hydrochloride (Levitra) CAS No.: 224785-91-5

  • Min. Order (MOQ) 10 Gram
  • Product Name Vardenafil hydrochloride (Levitra)
  • Appearance White powder
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Product name: VARDENAFIL HYDROCHLORID Alias: Valdenafil.HCl , VARDENAFIL, HYDROCHLORIDE SALT CAS No.: 224785-91-5 Assay: 99%   Description :   Vardenafil hydrochloride is a prescription medicine with another name vardenafil HCl. It helps those men who have impotence(erectile dysfunction). This medicine will not help you to cure your erectile dysfunction. This drug is needed to be taken only when you want to have a sexual intercourse. "Vardenafil hydrochloride" is a brand name that doesn't mean anything. It was just made up. A new group of drugs was discovered to treat erectile dysfunction. One of the first PDE5 inhibitors that were released for this treatment was . The second similar drug that is available in United States is Vardenafil hydrochloride.Cialis is the third and soon will be on the market. In Europe you may find all three of these drugs.   Application : Vardenafil hcl is used in the management of erectile dysfunction in men above the age of 18. Erectile dysfunction is a condition wherein the person cannot get proper erections and maintain it for long duration to facilitate sexual intercourse. Although Vardenafil hcl is indicated for erectile dysfunction, it is not effective without proper sexual stimulation. The drug is known to work even in persons who are suffering from other conditions such as hypertension, diabetes or high cholesterol.   Dosage :   Patients taking Levitra are usually started on a 10 mg dose, which they take no more than once daily, about one hour before sexual activity. It can take as little as 30 minutes for Levitra to work in some patients. Like with , Levitra dosages are adjusted depending on a person's reaction, with doctors generally decreasing doses to to 2.5 mg or increasing them to no more than 20 mg once a day.   Vardenafil, as with all PDE5 inhibitors, should not be used by men taking nitrate medications, because combining them with Vardenafil might provoke potentially life-threatening hypotension (low blood pressure).    

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Dapoxetine HCL CAS NO.: 119356-77-3

  • Min. Order (MOQ) 10 Gram
  • Appearance light yellow powder
  • product name Dapoxetine HCL
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cas no.: 119356-77-3 assay: 99% molecular formula: c21h23no hcl molecular weight: 341.88   description :   hydrochloride is an oral drug for the treatment of ed, used in the treatment of erectile dysfunction and premature ejaculation, erectile function impairment and premature ejaculation has very significant improvements. There are over 1500 documents to prove the caused by different causes impotence premature ejaculation, knew the success rate is above 80%, and show its reliable curative effect, through the use of more than 20 million people worldwide, proved its long-term stability, the safety of 25 to 60 minutes of work function to coincide with a time needed for foreplay, knew the time adjustment in the highest drug concentration time, help both husband and wife a satisfactory sex life.   initially, hydrochloride is given as a 30 mg tablet one to three hours before sexual intercourse. The dose may be increased by the prescribing doctor to 60 mg, depending on response and tolerance.   applications :   1. Treat male premature ejaculation and erectile dysfunction., marketed as (among and other brands) is the first compound developed specially for the treatment of premature ejaculation (pe) for men at the age of 18-64 years old. Works by inhibiting the serotonin transporter, increasingserotonin’s action at the post synaptic cleft, so as to delay ejaculation. As a member of selective serotonin reuptake inhibitor (ssri) family, was initially created as an antidepressant. However, unlike other ssris, is absorbed and eliminated rapidly in the body. Its fast response makes it suitable for the treatment of pe but not as an antidepressant.     2. Due to the lack of specific approval treatment for pe in the us and some other countries, other ssris such as fluoxetine, paroxetine, sertraline, fluvoxamine, and citalopram have been used as clinical drugs to treat pe. Waldinger’s meta analysis shows that the use of these conventional antidepressants increases ielt from two to nine times above base line in comparison of three to eight times when  is used. However, these ssris must be taken daily in order to achieve meaningful efficacy, and the long half-life increases the risk of the drug accumulation and as a consequence an increased adverse effects such as decreasing sexual libido and causing erectile dysfunction. , on the other hand, is a fast-acting ssri. It is rapidly absorbed and eliminated from the body within a few hours. This favorable pharmacokinetics minimizes the risk of the drug’s accumulation in the body, and therefore reducing side effects.   usage :   hydrochloride is a drug that is used to treat premature ejaculation in men. It is available by prescription and is taken orally, prior to sexual intercourse. The drug belongs to the class called serotonin reuptake inhibitors (ssris), which have mainly been used to treat depression.

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Finasteride CAS:98319-26-7

  • Min. Order (MOQ) 10 Gram
  • Product Name Finasteride
  • Appearance White crystalline powder
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Finasteride is a popular anti-androgen medication manufactured by Merck most commonly known as either Proscar or Propecia. Based on the progesterone skeleton, Finasteride belongs to a class of medications known as 5alpha-reductase inhibitors and as such is used for the treatment revolving around type 2 5-AR based occurrences.This is important for performance enhancers as DHT based anabolic steroids have specific side-effects that may occur that can largely be remedied with the use of a 5-AR inhibitor such as Finasteride.   2. As a type 2 5-AR inhibitor Finasteride was designed for the purpose of treating hair-loss, prostate enlargement, as well as prostate cancer.Finasteride is very common among those who supplement with anabolic steroids yet fear hair-lossbut there are important things you need to understand before you consider Finasteride use. As an androgen suppressor Finasteride can seriously inhibit the gains made while on cycle, severely and on that basis it is not highly recommended for on-cycle hair preservation. The 2005 Prostate Cancer Prevention Trial (PCPT) showed at a dosage of 5 mg per day, as is commonly prescribed for BPH, participants taking finasteride were 25% less likely to have developed prostate cancer at the end of the trial compared to those taking a placebo. It appeared (incorrectly) that finasteride increased the specificity and selectivity of prostate cancer detection, thus creating an apparently increased rate of high Gleason grade tumor.   3. A 2008 update of this study found that finasteride reduces the incidence of prostate cancer by 30%. In the original study, the smaller prostate caused by finasteride facilitated detection of cancer nests and aggressive-looking cells. Most of the men in the study who had both low and high-grade prostate cancer chose to be treated, and many had their prostates removed. A pathologist then carefully examined each of those 500 prostates and compared the kinds of cancers found at surgery to those initially diagnosed at biopsy. This study concluded that finasteride did not increase the risk of high-grade prostate cancer.    Finasteride Applications   1. Benign prostatic hyperplasia Physicians use finasteride for the treatment of benign prostatic hyperplasia (BPH), informally known as an enlarged prostate.The FDAapproved dose is 5 mg once a day. Six months or more of treatment with finasteride may be required to determine the therapeutic results of treatment. If the drug is discontinued, any therapeutic benefits reverse within about 6 to 8 months. Finasteride may improve the symptoms associated with BPH such as difficulty urinating, getting up during the night to urinate, hesitation at the start of urination, and decreased urinary flow.   2. Male pattern baldness Finasteride is used to treat male pattern hair loss (androgenetic alopecia) in men only. Treatment provides about 30% improvement in hair loss after six months of treatment, and effectiveness only persists as long as the drug is taken.

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Yohimbine HCL CAS:65-19-0

  • Min. Order (MOQ) 10 Gram
  • Appearance White to slightly yellow powder
  • Product Name Yohimbine HCL
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CAS:65-19-0 EINECS:200-600-4 MF:C21H27ClN2O3 MW:390.9   Description :  Yohimbine Hydrochloride has shown to rapidly increase the Libido of both men and women and its properties as an aphrodisiac are well known throughout the scientific world. Yohimbine Hydrochloride increases the sex drive of men and is even used to treat hypoactive sexual desire disorder (under active libido) in women. Applications : 1). Sexual dysfunction--------The NIH states that yohimbine hydrochloride is the standardized form of yohimbine that is available as a prescription medicine in the United States, and that it has been shown in human studies to be effective in the treatment of male erectile dysfunction. Yohimbine has been shown to be effective in the treatment of orgasmic dysfunction in men. Yohimbine has also been used to treat hypoactive sexual desire disorder (under active libido) in women.   2). Fat loss--------Yohimbine has shown to increase lipolysis in multiple studies.Administered prior to exercise, it boosts lipolysis and serum FFA levels both during and following exercise; blockade of adipocyte alpha-2 adrenoreceptors makes at least a modest contribution to this pro-lipolytic activity. Pre-exercise yohimbine administration has the potential to down-regulate the lipoprotein lipase activity of visceral adipocytes, increase lipolysis in refractory gynoid fat depots, and improve the impaired lipolytic response to exercise in the elderly   Dosage : First, Yohimbine HCl must NOT be taken with food or vitamin supplements of any kind. It must be taken by itself on an empty stomach in between meals or in a fasted state when you first wake up in the morning. It also is best to spread dosing throughout the day as this also helps with its appetite suppressing effects which will help maximize your weight loss when taking it.   The minimum dosing is set at 5 mg per day, with 2.5 mg taken 2 times per day on an empty stomach in between meals as described above. Wait at least 20-30 minutes until you eat after administration.   Maximum Results: In order to achieve the maximum effects when taking this supplement, the following dosing guidelines should be met.   Dosages of 0.2mg/kg bodyweight have been successfully used to increase fat burning without significant implications on cardiovascular parameters like heart rate and blood pressure. This results in a dosage of: 14 mg for a 150lb person, 18 mg for a 200lb person, and 22 mg for a 250lb person.   Recipe : 1g yohimbine hcl. 1ml BA as an anaesthetic, but it also makes it bacstat. 9ml of ethyl alcohol. 90ml of distilled water.   Let dissolve in the BA and EA for 10 min and then add water it will look cloudy after the water is added, but that doesn't matter because it will look the same after it goes through a 0.22 syringe filter.

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MK-2866(Ostarine,Enobosarm) CAS 841205-47-8

  • Min. Order (MOQ) 10 Kilogram
  • product name MK-2866
  • Appearance Almost white or white powder
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CAS 841205-47-8 MF C19H14F3N3O3 MW 389.3279696 As a research chemical, Ostarine belongs to a class of chemicals know as SARMS or selective androgen receptor modulators. SARMS create selective anabolic activity at certain androgen receptors. In comparison to testosterone and other anabolic steroids, the advantage of SARMS, is they do not have androgenic activity in non-skeletal muscle tissues. Ostarine is effective in maintaining and increasing lean body mass. Application :   Selective androgen receptor modulators may be used by athletes to assist in training and increase physical stamina and fitness, potentially producing effects similar to anabolic steroids. Usage of MK-2866 :   1. Lean muscle gains (bulking)   Ostarine is the most anabolic of any SARMS, making its first and foremost use for wanting to gain lean muscle. The gains in total weight will not be comparable to bulking steroids, however the total gains will almost entirely be lean muscle.   The gains that are made on ostarine are very keepable and users generally see an increase of up to 7 lbs. of lean body mass over and 8 week cycle at 25mg day (diet dependent). The most common dosage is 25 mg for 8 weeks. The side effects that one encounters with steroid use will not be present on cycle.   Generally, with ostarine, the higher the dosage, the more suppression. Although suppression is minimal and is nowhere comparable to suppression that one encounters on steroids, any cycle of ostarine over a 4 weeks period requires a 3 week mini pct. A serm is not required in this pct.   2. Losing Bodyfat (cutting)   Ostarine would primarily fit into a cutting protocol for the maintenance of muscle mass while reducing calories. One of the most disheartening outcomes of cutting is the loss hard earned muscle mass. The drop in metabolic rate and hormone levels (T3, IGF, Testosterone etc) with the lack of calories is a perfect catabolic environment for loss of muscle tissue. As Ostarine has anabolic effects, the dieter can cut calories without having to worry about muscle or strength loss. Ostarine has also shown noticeable nutrient partitioning effects among users, another reason why it can be of great help when cutting.   A 15-20 mg dosing protocol for 6-8 weeks is good for cutting with Ostarine without undergoing any side effects or high suppression. However it must be stated that due to the lack of androgenicity, muscle hardness and overall results are not as prominent as with the SARM S-4.

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SR9009

  • Min. Order (MOQ) 10 Gram

Name:  SR9009 Synonyms:  Stenabolic CAS No.:  1379686-30-2 Molecular formular:  C20H24ClN3O4S Molecular Weight:  437.94 Appearance:  White powder Purity:  99%   Sr9009 Description:      SR9009 is a research drug that was developed by Professor Thomas Burris of the Scripps Research Institute as an agonist ofRev-ErbA (i.e., increases the constitutive repression of genes regulated by Rev-ErbA)with a half-maximum inhibitory concentration (IC50) = 670 nM for Rev-ErbAα and IC50 = 800 nM for Rev-ErbAβ. Activation of Rev-erb-α by in mice SR9009 increases exercise capacity in mice by increasing mitochondria in skeletal muscle.   SR9009 Function:     A new compound called SR9009 increases metabolism, fat burning, and muscle growth in the lab. Scientists at The Scripps Research Institute (TSRI) have successfully tested a drug, called SR9009, in mice that kickstarts metabolism and results in increased muscle development. Essentially, it's an exercise regime in a pill.   SR9009 alters the metabolic profile of skeletal muscle in a manner similar to the changes observed [in] animals [that] are endurance trained. Basically, the drug sends a signal to the muscle to tell it to modify its metabolism.   Half of the mice studied showed improved running endurance in terms of both time and distance. What was clearly interesting was that a small, drug-like molecule could increase metabolic rate in skeletal muscle and increase exercise endurance  

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CJC1295 with DAC

  • Min. Order (MOQ) 10 Gram

Product name:CJC-1295 with DAC Other name:Cjc-1295, CJC-1295 with DAC CAS:863288-34-0 Molecular formula:C152H252N44O42 Molecular weight:3367.2 Related substance:2.0% purity:98.0% Appearance:White powder Description     CJC 1295 with dac (synonym CJC1295/DAC, changed kind (GRF 1-29) with drug affinity complex) belongs to category of tetrasubtituted amide endocrines and contains thirty amino acids; conjointly it is represented as analog of GH emotional hormone. Its formula is C165H269N47O46 and its molecular mass is 3647.28. Application     CJC-1295 DAC and CJC-1295 (also known as Modified GRF 1-29) are both Releasing Hormones (GHRH). Their action in the human body is identical but the difference between the two peptides are the span of the half-life. Modified GRF 1-29 and Sermorelin have a very short acting half-life of about 30 minutes, while CJC-1295 DAC has a half-life that can last up to approximately 8 days. Many a scientist have reported that the short half-life of Sermorelin and Modified GRF 1-29 is considered to be much more natural as they produce a short pulse of Human. What are the cjc-1295 side effects?     CJC-1295 side effects are related to its stimulation of the pituitary gland. First, a surge of growth hormone (GH) will occur, sometimes causing vasodilation which is felt as a headrush or euphoria that lasts 30 minutes to 2 hours post injection. Mild irritation such as itching, redness, and pain is frequently noticed at the injection site and is not severe in most cases. At the cellular level, CJC-1295 raises HGH, and research shows subjects have increased fat metabolism, increased muscular mass and strength, and improved skin tone and muscular definition. Diet and exercise in conjunction with CJC-1295 will enhance effects. CJC-1295 Doses Modified GRF 1-29(cjc1295 w/o DAC):   Dose per injection: 100mcg Injections per vial: 20 x 100mcg dosages   Amount to Inject: If you have used 1ml of water for mixing then a 100mcg dosage = 0.05ml (or 5 units on Insulin Syringe). If you have used 2ml of water for mixing then 100mcg = 0.10ml (or 10 units) and if you have used 3ml of water for mixing, then 100mcg = 0.15ml (or 15 units).

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MGF

  • Min. Order (MOQ) 10 Gram

PEG-MGF Description   PEG-MGF is a muscle change caused by strict exercise and muscle damage. Structural differences in liver tissue synthesis of IGF-1 and other factors, MGF into the muscle fiber repair skeletal muscle tissue, to prevent damage to cell death. It adds stem cells to the muscle and is triggered by a stimulus pulse after a significant mechanical stress is experienced in the muscle tissue. With age, MGF gene transcription is small, which is why the elderly muscle mass decline, some diseases will also affect its production.   According to a study in the UK, older people who exercise and accept hormones called "mechanical growth factor" (MGF) show an increase in muscle mass. PEG-MGF Application   PEG-MGF is used to enhance the purpose of websites and systems by increasing lean muscle and fat reduction   PEG-MGF may benefit: PEG-MGF stimulates muscle growth (hypertrophy); increases muscle growth from training; rapid repair of existing muscle cells; increases muscle cell count (proliferation); reduces protein breakdown; increases muscle repair after injury Speed and degree   Consumption method 1: Immediately after exercise immediately into the muscle   Consumption method 2: subcutaneous injection into fat layer   Injection preparation: 1 ml (100 IU) of sterile solution was added to the PEG-MGF vial. Each 200mcg is equal to 0.1ml (10IU). PEG-MGF at a dose of 1: 200 mcg (10 IU) of PEG-MGF was separated on both sides of the newly cultured muscle, i.e. 100 mcg left, 100 mcg PEG-MGF was injected into the abdominal fat at a dose of 2: 200 mcg (10 IU) of PEG-MGF PEG-MGF dose per vial: 10 x 200 mcg dose (10 doses per vial)  PEG MGF Usage   The Mechano factor (MGF) exhibits a local effect in skeletal muscle and does not pass through the body without change. The problem of synthetic Mechano factor (MGF) is intramuscular introduction and is water-based, so it enters the bloodstream. When used in this way, the Mechano factor (MGF) remains stable only in the blood for a few minutes. The bio-made MGF is made locally and does not enter the blood.   PEG-MGF function   I G F-1 is a hormone consisting essentially of 70 amino acids that are structurally similar to insulin.

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MT-2

  • Min. Order (MOQ) 10 Gram

Description   Melanotan 2 (also referred to as Melanotan II) is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis, a process responsible for pigmentation of the skin. This peptide hormone, called alpha-Melanocyte stimulating hormone or MSH, activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido via these melanocortin receptors. As a result, Melanotan 2 has been shown in studies to exhibit appetite suppressant, lipolytic, and libido-enhancing effects in addition to promoting skin tanning. Melanotan 2 has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.   Additionally, Melanotan 2 and a similar synthetically produced variant, known as PT-141, have been studied at length as a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction.     When to use Melanotan II   Melanotan II requires cumulative dosing to be effective. Depending on the individual, needed cumulative dose will typically be from 10 to 40 mg, with fairer individuals usually requiring amounts at the higher end of the range. Depending on the total amount needed and the daily dosing suitable for the individual, MT-II injections will need to begin at least a week prior to a need for improved tanning. More typically, MT-II use should begin at least a month prior to such need.   Melanotan II can also be used on a cycled basis to maintain improved ability to tan.   Further, Melanotan II can be used on occasion for prosexual effect. Melanotan II is an effective injectable peptide product to enhance ability to tan. Dosing is typically 0.5 to 1.0 mg/day, and the total amount needed for good effect is typically 30-40 mg, though for individuals of medium darkness already, it may be as low as 10 mg for significant effect. MT-II can also be used to enhance tendency to penile erection, but frequency of such use needs to be limited to avoid excessive total effect on skin pigmentation.

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