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Trestolone Acetate powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C21H30O3
  • Melting Point 447.571 °C at 760 mmHg

Chemically speaking, trestolone acetate(MENT) actually an alright looking drug. It doesn't show much interaction with Sex Hormone Binding Globulin, which means that a good portion ought to stay unbound and active in the blood. Also, the drug is a potent binder to the androgen receptor, while showing minimal affinity for the progesterone and mineralocorticoid receptors respectively. Since it is not able to be 5a reduced into a dihydroversion, it likely wouldn't cause many of the side effects commonly associated with Dihydrotestosterone. This is also a likely reason that it is less apt to cause prostate enlargement, and may even be indicated for the treatment of specific prostate issues.   The ability of 7 alpha-methyl-19-nortestosterone acetate (MENT) to increase the weights of ventral prostate and seminal vesicles of castrated rats was four times higher than that of testosterone, while its effect on the weights of bulbocavernosus plus levator ani muscles (muscle), was 10 times that of testosterone.   Various forms of MENT in human pharmaceutical preparations and devices for contraception and hormone therapy, specifically MENT Ac implant and MENT transdermal gel and patch formulations, are currently under clinical investigation. MENT is absorbed transdermally up to three times the rate of testosterone - 17 methyl testosterone and 17-α methyl testosterone.   MENT will have application in a wide range of indications beyond androgen replacement therapy and contraception, including, without limitation, primary hypogonadism, testicular failure, ASIH, baldness, sarcopenia, loss of bone mass, muscle wasting and cachexia, BPH, prostate cancer and of course, bodybuilding and sports performance enhancement.   Trestolone acetate is the chemical name of active ingredient in MENT. MENT is a registered trademark of Population Council, Inc. in the United States and/or other countries.   Trestolone Acetate 50mg/ml Homebrew   Basic recipe    -1 gram Trestolone Acetate Powder -16.55 mL Grape Seed Oil (GSO) -0.6 mL Benzyl Alcohol -2 mL Benzyl Benzoate   This will achieve a 20 mL solution that has a 50 mg/mL ratio. The 16.55 mL of GSO is calculated based on a 0.85 mL displacement of Trestolone when dissolved. This means that 1 gram of Trestolone Acetate will only take up about 0.85 mL of space. The BA/BB ratio is 3/10.

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Trenbolone

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Testosterone

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Nandrolone

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Boldenone

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Masteron

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Testost Enanthate Powder CAS 315-37-7

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  • M.F C26H40O3
  • M.W 400.59
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Testost 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.   Testosterone Enanthate is an anabolic steroid that is perfect for low testosterone . If your body is cannot produce enough testosterone , you could suffer from low testosterone .   The symptom for low testosterone :   Sexual hypoactivity ED (Erectile Dysfunction) Decrease in muscle mass Strength loss when you take exercise Body fat Increased Feel giddy and absent-minded     Testosterone enanthate Benefit :   Testosterone heptanoic acid ester is the perfect remedy for the treatment of low testosterone.If you have low testosterone, it just means that your body no longer produce enough of this major androgens.Because testosterone heptanoic acid ester is testosterone, it can remedy the condition of low level.All over the world millions of men suffering from some kind of low level of androgen deficiency.Only in the United States, it is estimated that more than 20 million men with androgen deficiency.Women may also suffer from low testosterone and testosterone heptanoic acid ester can treat it.However, most women will better taking alternative forms of testosterone treatment, such as containing testosterone and progestin or small testosterone implant pellet (such as Testopel) a mixture of gel.

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Testosterone Base CAS 58-22-0

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  • CAS No 58-22-0
  • Alias Test Base
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Testosterone is an injection preparation containing testosterone (no ester) in the oil base.   In the bodybuilder, "base" is known to be a very effective mass agent. It is usually listed as the most potent injectable steroid available, leading to an incredible rapid growth in muscle mass and strength. This is mainly due to the very rapid effect of the drug, since the water-based steroids begin to enter the bloodstream almost immediately after administration of the injection. Unlike longer esters, such as heptanoate or cyclopentamate, it takes several weeks for the blood to reach the maximum level of treatment, based on just a few days. Obviously, the metabolic effect of this testosterone will be much faster than what we expect for oil-based (esterification) preparations.  So the dosage of testosterone you need to concern :   It is also important to remember that 100 mg of testosterone ester is not equivalent to 100 mg of testosterone in pure testosterone (as in the matrix). When the ester is present, its weight is clearly included in the total milligram of the formulation. Look at testosterone heptanoate, 100mg of this compound is equivalent to only 72mg of raw testosterone. So the weekly use of 400mg heptanoate bodybuilders really get about 288mg of testosterone per week. This is clearly a significant increase in the average male testosterone level of the average male, which is in the range of 2.5 to 11 mg per day. The general view, however, is that during the circulation of the testosterone matrix, we usually see an even more dramatic increase in testosterone intake than usual oil. According to common recommendations, athletes usually inject 100 mg of testosterone daily, a total of 700 mg per week. This is 40 times the amount of normal men. Those who try this cycle are rarely disappointed with the results because this heavy dose of this hormone will produce significant weight gain.    The most common method of testosterone matrices is to inject drugs daily. The dosage will vary greatly depending on the needs of the individual, but is usually in the range of 50 mg to 100 mg per injection.  

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Testost Acetate Powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formula C21H30O3
  • Molecular weight 330.47
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Testost 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.   Testos 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.   Testoste 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.

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Testosterone Propionate CAS No: 57-85-2 powder

740 /Gram
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  • MF: C22H32O3
  • MW 344.49

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.   The note of testosterone propionate   1. General dose should be controlled at 0.25g / day. 2. Injection for oil, if the crystallization, can be dissolved by heating. 3. Kidney, liver dysfunction and heart disease patients with caution, found masculine and liver dysfunction when weaning; the goods on the liver less toxic. 4. Long-term application of children can affect the growth and development.   Product Usage   Thus, testosterone propionate is much faster than other testosterone esters (e.g., cyclopentaprole or heptanoate) and requires more frequent dosing regimens to maintain a stable blood level. Can be used as a pharmaceutical material. Its main function is to promote metabolism. Synthetic metabolic effects include muscle mass and intensity growth, increased bone density and intensity, as well as stimulating linear growth and bone maturation.

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Testoste Cypionate Powder

740 /Gram
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  • Molecular formula C27H40O3

testost cypionate powder conversion recipes:     1. Test cypionate 5 gram conversion 20ml @ 250mg/ml needed 5 grams test cyp 1ml benzyl alcohol = 5% ba 15.25 ml sesame oil syringes 3cc & 5/10cc 18 or 20 gauge needles mixing vial sterile vial whatman sterile filter 1. Weigh out 5 grams of powder. 2. Place powder in vial. 3. Add ba to the vial. 4. Heat oil in the oven to help sterilize it, heat to at least 212 degrees f. I usually heat my oil at 275 to be sure, I put the oil in a muffin pan, just fill one of the indentions this is plenty for these experiments. Also heat more oil than you need, as you will not be able to get it all out of the pan. 5. Add oil to the vial, save 2 ml of oil in the syringe for later. Gently shake vial. 6. Heat mixture if necessary. I like heating my powder products, by placing the vial in a frying pan, and placing it on the eye of the stove. 7. Place a 18 or 20 gauge needle in the sterile vial attach whatman sterile filter. 8. Place another needle in the sterile vial to relieve the pressure. 9. Draw out solution with a syringe, run though whatman filter. 10. Take other syringe with 2ml oil, run through whatman into solution. --------------------------------------------------------------------- 2. Test cypionate 10 gram conversion 40ml @ 250mg/ml 10 grams test cyp 2ml benzyl alcohol = 5% ba 30.5 ml sesame oil syringes 3cc & 5/10cc 18 or 20 gauge needles mixing vial sterile vial whatman sterile filter   ---------------------------------------------------------------------- 3. 60ml @ 250mg/ml test cypionate powder: 15 grams 42.7 ml grapeseed oil 2.8 ml 5% ba ---------------------------------------------------------------------- 4. 80mg/ml @250ml testosterone cyp powder 20g benzyl alcohol 5ml benzyl benzoate 45ml grapeseed oil 185ml 5.200mg/ml @250ml testosterone cyp powder 50g benzyl alcohol 5ml benzyl benzoate 45ml grapeseed oil 162.5ml    

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Testosteron Phenylpropionate Powder

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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.   Users will have a lot of endurance, which means they will not be as tired as ever before. They will not have muscle pain as before, they will do so while avoiding watery muscles. This means that they will be able to invest in quantity and quality in their workouts and bring more results. Propionate is achieved by increasing the amount of red blood cells in the user, which is the main cause of the treatment of anemia; a disease characterized by low red blood cell count.   It is also a wonderful fat loss. Weight gain and fat reduction are part of each other. Rarely find an athlete who wants to get muscle without reducing muscle fat. It will reduce the amount of fat, especially in the abdomen, although this is highly dependent on the amount of nandrolone / testosterone propylpropionate used; higher doses will result in higher loss of fat in the abdomen region, resulting in lower doses Lower losses in the same area. The brain will also be affected by the amount of nandrolone  testosterone phenylpropionate you use. Known to promote aggressive behavior among its users, it is positive that in this sense it will allow the user to increase his hard work and the negative sense that the aggressiveness can be directed against the wrong person. The negative impact of this situation is that users already know to participate in crime, more likely than non-users suffering from depression. Again, it also depends on the dose you use; the higher the dose, the higher your  chances of depression.

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Testosteron Isocaproate Powder

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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.   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.   As it has got many effects, it has got some side effects as well. One of its major and serious side effects in males is that as this testosterone is taken in the body, it limits the production of natural testosterone in the body. This is because when the natural production of testosterone observes that testosterones from some external source are supplied to the body, it automatically stops or lowers the production. First it limits the natural production but if the usage of external testosterone is continued for a longer period of time then natural production is stopped. Another major side effect is of aromatization. The process of conversion of Testosterone into estrogens is called as aromatization. Estrogens are basically the sex hormone of the females. These estrogens attach with the tissues of breasts of men and cause them to get bigger. Apart from this, retention of water is also common. Retention of water means collection of fluids under the skin which makes muscle look not much active.

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Testoster Decanoate powder

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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.      productapplication   testosterone decanoate is usually used for intramuscular injection, oil absorption is slow, functional and durable, can be maintained only a few days. Testosterone propionate can promote male organ development and secondary characteristics, promote protein synthesis and bone formation, estrogen, inhibit endometrial growth and ovarian and pituitary function. For testosterone, cryptorchidism, male gonadal dysfunction, gynecological diseases such as menorrhagia, uterine fibroids, senile osteoporosis and aplastic anemia.     testosterone decanoate usage and dosage   because decanoate is so long lasting, the user only needs to inject the drug once a week. The drug itself does not leave the body for 15 days. The user sometimes stacks neotest 250 with deca-durabolin and injects at the same time as they will remain in the body for the same amount of time. The dose was as low as 250 mg / week and the results were seen and an extreme dose of 1000 mg / week had been recorded with little side effects, although the use of an aromatic sugar inhibitor at extreme doses was necessary.    

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Sustano 250 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 contains for testosterone esters , per 1ml contains    30mg short-acting testosterone propionate   60 mg of testosterone phenylpropionate   60 mg of testosterone isocaproate   100 mg of testosterone decanoate       Sustanon 250 Dosages     Sustanon administration during steroid cycling should generally be divided into at least two injections per week, more preferably at least three times.       After any steroid cycle, including the Sustanon cycle, post-circulation therapy is highly desirable.       250mg per week      At a level of 250 mg / week, Sustanon essentially provided only a high level of testosterone replacement therapy. Individuals with low testosterone can see significant improvements, but many people with moderate or high natural testosterone do not see an increase in the dose level. However, Sustanon inhibits the hypothalamus and pituitary at this dose, and will significantly shut down natural testosterone production when used. Thus, the dose has a relatively small benefit of most steroid cycles, but has adverse side effects that inhibit testosterone production.       500mg per week      500 mg / week is the lowest dose level, most see good results. At this dose, the gain is usually good for the first cycle and generally does not require adjuvant drugs to control estrogen. But in many cases, estrogen control is already desirable.       750mg per week      The next step at 750 mg / week provides a significant further increase, and if the control of estrogen, the side effects are usually not significantly different from 500 mg / week.       1000mg per week      Dose 1000 mg / week is usually sufficient for intermediate or even many advanced users. In some cases even more than this. However, this is usually unnecessary, unless the result has reached 1g / week level has reached the platform.           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

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Testost Undecanoate powder

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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, restando     Testosterone undecanoate dose:   The drug on paper seems to be a great oral testosterone product. Clean, safe and the world except for other oral testosterone derivatives such as mechild testosterone. But as we always hear in life, if it looks good, it is true that it might be. Andriol certainly has some problems. The first problem is bioavailability, although the apparent world in addition to trying to take direct testosterone orally, may not be significantly next to the c17alpha alkylated mouth. Athletes often find that at doses less than 240 mg / day (6 capsules), the effect is usually not seen at all. 240mg testosterone every day, the main male androgen, only weak effect. When the dose increases, it may be 8-10 capsules (320-400mg), the new muscle grows slightly to moderate, but did not report incredible huge gains. Logic leads people to believe that only one testosterone is flowing in a way. Testosterone is a powerful hormone, no matter what the ester or form of management. If it is active in the blood, the result must be pronounced. When a person injects an oil-based testosterone ester such as cyclopentanepropionate, the dose of 400 mg per week is sufficient to see the result. 400mg daily placebo should be packaged in an incredible quantity of quality. Where is all this? Personal absorption problems may play a role here. Obviously, there is little nothing to say, except that this medicine is unpredictable by its ability to be absorbed and utilized by the body. Although one day you may get a lot of absorption, maybe the next day you become very little The study with men was no better than women, again that the drug proved to be unpredictable to absorb and use blood levels ranging from 11.5 to 60.1 nmol / L with 80 mg twice daily.

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Fluoxymesterone (Halotestin) powder

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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.     Quick Reviews of Fluoxymesteron Halotestin   1. Halotestin's benefits are very common compared to Winstrol, and in some ways this is not inaccurate, since both will be designed to increase the intensity, and both steroids can lead to more difficult physique.   2. Halo will increase the strength of unmatched Winstrol and most synthetic metabolic steroids, and in this fast way we can think in many ways it is the king of strength.   3. In a competitive bodybuilding world, especially at the elite level, Halotestin is often regarded as the staple of the last minute, in which case it does not actually have anything to do with strength. Halo has the ability to greatly harden the body, thin body.   4. Fluoxymesteron is one of the most potent synthetic metabolic steroids and one of the fastest startings. While this is still true, there are very few steroids equal to Fluoxymesteron's usual forces known as Halotestin, commonly referred to as Halo.   5. Halotestin by its nature is highly synthetically active and hyperandrogenic, but it hardly shows the androgen effect, leaving only the end of synthetic metabolism.   6. Because Halo is purely synthetically acting in the role, it is one of the best-growing steroids on the market, but it will do little in terms of quality; in fact, we can safely say that for the masses it Really do not do anything.   7. Halogen A is most commonly used in strength athletes, especially power lifters; however, it is also very popular in competitive bodybuilders, especially during the latter part of the game preparing for a diet.   8. While Halotestin is very powerful, it is also very harsh for gymnasium rats with many other options safer and more efficient to achieve their desired goals.

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17-methyltestosteron Powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram

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   A testosterone can promote male sexual organs and use for seedling stage changes. Methyl testosterone is a steroid hormone derived from androgen, present in mammals and other vertebrates. Methyl testosterone is mainly secreted in e-mail and female ovarian tests, although a small amount is also secreted by the adrenal gland, methyltestosterone is the main male sex hormone and anabolic steroids. Methyltestosterone plays a key role in male reproductive tissue such as testicular and prostate development. In addition, methyltestosterone is essential for both health and well-being and for the prevention of osteoporosis. Methylestosterone is conserved in most vertebrates, although fish are slightly different from the so-called 11-ketone testosterone.         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.     Brief Introduction   Methyl-testosterone(brand names Android, Androral, Metandren, Oraviron, Testred, Virilon), also known as 17α-methyltestosterone, is a 17α-alkylated androgenic-anabolic steroid (AAS) used to treat males with a testosterone deficiency.It bears close structural similarity to testosterone, but has a methyl group at C17α in order to increase oral bioavailability.     17-methyl testosterone dose   Methyl testosterone film GENESIS can be administered orally and rapidly absorbed in the bloodstream. It has a relatively short half-life. Although it is recommended only once a day in medical patients, some bodybuilders prefer to take twice a day.     17-methyl testosterone in male   For the treatment of androgen deficiency, the prescription guidelines require a daily dose of 10-40 mg. When used for physical or performance enhancement purposes, the most commonly used daily dose is 10-50 mg, with a duration of no more than 6-8 weeks long.

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Mestanolon Powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H32O2
  • Molecular Weight 304.47

DHT anabolic products provide excellent benefits, but they are somewhat limited in effectiveness due to the application process and breakdown in the body. Mestanolone can give you the best of a DHT product with a lot of added benefits. It is easy to take and very flexible to use. You can easily get the mental edge you have been striving for and make it through any high stress routine as if it is nothing. It is a total mind and body product that can change the way you work out and compete.   Methyldihydrotestosterone (methyl-DHT; 17alpha-methyl-17beta-hydroxy-5alpha-androstane-3-on, Mestanolone) is a DHT type steroid that you are able to ingest, rather than apply topically. It has a high androgenic effect and women are warned against using it because of that. It has such a strong androgenic power that it makes marked changes psychologically as much as it does physically. It has always been the frequent steroid choice for cutting and leaning before competitions.   The DHT type qualities mean that it does not break down into estrogen. It is perfect for reducing water weight gain, hardens muscles and leans out the muscle tissue throughout the body. It is the perfect toner and enhancer for any bodybuilder or serious weightlifter. It can be stacked with other products for the perfect cutting cycle pre-competition. It makes it that much easier to bulk up, maintain muscle mass and reduce unneeded weight.     What are the advantages of using Mestanolone over other products?   One of the favored advantages of Mestanolone is having the benefits of a DHT type anabolic in an ingestible form. It can be added to a liquid drink or sprinkled on food and eaten. You never have to worry about absorbing enough of the product, such as a gel, or take painful injections. It is both discreet and easy.   The best advantage might be the psychological boost it gives you for maintaining a high stress physical routine. It acts as a bridge to strengthening both the mind and body for optimal performance results. The patent for the product took time to note the undeniable ability of the product to awaken and stimulate the entire nervous system to create an edge in physical abilities. Those tested doing high stress physical activities simultaneously with high neurological demands did extremely well while using Mestanolone.       practical effects   Mestanolone has been a common and well used steroid with German athletes for decades. It made them very tough to beat on many fronts. It also allowed for a large pool of athletes to study and see what the real results of use are. It also gives clues to understanding how it seems to work. Studies in animals seem to show that it has a 60% androgenic effect and 25% anabolic. The importance of this is its psychological impact on the user. It creates a very immediate aggressive and energetic mental state. That makes it perfect for those that need more motivation before strenuous workouts. There were many additional benefits discovered that include: Increased stamina; Incredible levels of endurance; Zero loss of muscle with strict diet; Aggressive energy with workout; Ability to mentally block discomfort levels.

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Mesterolone (Proviron) powder

740 /Gallon
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H32O2
  • Molecular weight 304.47

1 . Proviron (mesterolone) is an interesting anabolic steroid, though it is not of much value to bodybuilding.It seems that the most common reason for many to consider including it in a steroid stack is for anti-estrogenic activity. In the days before anti-aromatases and the use of SERMs (selective estrogen receptormodulators) such as Clomid and Nolvadex, there was some merit to this.   2 . An amount of aromatizing steroid marginally over the amount that would be tolerable without Proviron became tolerable with the inclusion of it. However, the effect is indeed only marginal, and much better anti-estrogenic agents now exist. When these are used, there is no need for Proviron as an anti-estrogen.   3 . Mesterolone is an orally applicable androgen, and DHT derivative, is sold under the brand proviron, In the late 70's and early 80's Mestero-lone was used with some success in controlled studies of men suffering from various forms of depression. Both the mestero-lone and placebo groups improved significantly and there were no statistically significant differences between the two groups. another, 100mg mestero-lone cipionate was administered twice monthly, Mestero-lone is a relatively weak androgen and rarely used for replacement therapies.   4 . Mesteronlone had seen widespread use in bodybuilding primarily for anti estrogenic activity in anabolic steroid stacks but such use has declined after introduction of aromatase inhibitors and SERMs. Most significant benefits of current use are considered by bodybuilders to be maintaining libido off-cycle and also relatively and temporarily improving vascularity.

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Oral Turinabo Powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H27ClO2
  • Molecular Weight 334.88

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.   4-Chlorodehydromethyltestosterone, sold under the brand name Oral Turinabol, is an anabolic steroid. It is a chlor-substituted version of methandrostenolone (Dianabol). Turinabol was the first original product of Jenapharm, an East German pharmaceutical company. The patent registration took place in 1961. The idea of combining the structures of 4-chlorotestosterone and methandrostenolone originated from the chemist Albert Stachowiak.At the time this represented a unique dissociation of anabolic and androgenic effects after oral administration. The product had been introduced for clinical use in 1965. Turinabol was the key steroid administered to approximately 10, 000 athletes from East Germany (GDR). The doping program was run by the East German Government from about 1968 until 1989 when the Berlin wall was destroyed. The doping program was known as STASI 14.25. The doping was done in secret and it was only in the 1990s when Franke and Berendonk looked closely at the original archived information was the true scope of just how well-planned and successful the doping regime had been (in terms of medal success and world record performances).  

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17a-Methyl-1-testosterone pwoder

740 /Gram
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  • Min. Order (MOQ) 10 Gram

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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CJC1295 without DAC powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C152H252N44O42
  • Molecular Weight 3367.97

CJC-1295 is basically a peptide hormone that acts similar to growth hormone releasing hormones (GHRH), it is beneficial to athletes because it can bioconjugate with circulating albumin and increase the time it can be used for medical purposes. It achieves this by preventing degradation of its amino acids. With a single dose, it can remain in the body for quite a few days and can cause the growth hormone to be released many times per day. This reduces the frequency of injections needed.   CJC-1295 increases the production of growth hormone as well as IGF-1 - which has anabolic effects in adults. However, it does not increase the levels of prolactin - high levels of which can create impotence and mental health problems in men. By increasing these two hormones, it enhances protein production in the body, which in turn, boosts muscle mass. It also induces lipolysis - the breakdown of fat tissue, boosts recovery from injuries, increases bone density, and also reduces aging factors like skin wrinkles. It can also stimulate cell growth, due to which it can be used to treat withered tissue or organs.   GHRH's are paired specifically with GHRP's in order to create a synergy between the peptides that will unlock the body's own stores of growth hormone. Even though many peptides work in some capacity by themselves, it is most beneficial to run your GHRH alongside a GHRP. This is why CJC 1295 is highly desirable, and it's one of the most widely used in the bodybuilding community. Right now, it has been debated which CJC 1295 is best to use. While MOD GRF (CJC 1295 no DAC) is commonly used with GHRP's to increase pituitary GH pulse, more frequent injections will need to be administered. The CJC 1295 with DAC will result in a series of smaller pulses; therefore, injections will be less frequent - often two to three times a week.

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CJC1295 with DAC powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formula C152H252N44O42
  • Molecular weight 3367.2

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.   CJC-1295 is a tetrasubstituted 30-amino acid peptide hormone, primarily functioning as a releasing hormone (GHRH) analog.One of the advantages of CJC-1295 over traditional GHRH is its ability to bioconjugate with serum albumin, thus increasing its half-life and therapeutic window. It accomplishes this by using protecting groups around the amino acids of GHRH typically susceptible to enzymatic degradation   The clinical research was ultimately successful for most research subjects. Ghrelin, released from the gut, which circulates and acts as a hunger hormone, has synergistic activity in the body with GHRH and also suppresses somatostatin to make way for the GHRH pulse.

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Hexarelin

740 /Gram
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  • Min. Order (MOQ) 10 Gram

When Hexarelin is given as a subcutaneous injection, it activates the pituitary via a pulse, just like GHRP-6, and helps circulate growth hormone in the body. Unlike GHRP-6, it does not induce any hunger side effects. Hexarelin has the ability to not only raise the level of GH in the body but to also suppress somatostatin, which is the main culprit that inhibits GH from being released. This means that there will be more GH in abundance. In addition, hexarelin is the strongest GHRP available, so users should notice that desensitization can come much quicker than other GHRP’s. This makes it less ideal for long term use, but with hexarelin’s ability to raise healthy levels of IGF-1 and GH it can work perfect as a PCT tool for those coming off a synthetic GH/IGF-1 cycle. The potency of this peptide should not be underestimated and it comes with an increase in cortisol production as well as prolactin. Nothing close to what might be seen in elevated levels from steroid use, but compared to other GHRP’s it has the strongest affinity to raise cortisol/prolactin.

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MGF

  • Min. Order (MOQ) 1 Bottle(s)
  • Mf C121h200n42o39
  • Grade Pharmaceutical grade

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 can also help to treat age-related muscle strength loss, resulting in increased brittleness This hormone may also be due to muscular dystrophy, amyotrophic lateral sclerosis (ALS), kidney disease or cancer and other diseases can not be intensive exercise patients. Astronauts can even help astronauts who spend a long time in space travel to slow down muscle loss.

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PEG MGF powder

  • Min. Order (MOQ) 1 Bottle(s)

PEG-MGF, or PEGylated Mechano Growth Factor is a new and innovative form of MGF that outperforms natural MGF many times over. MGF is a splice variant of the IGF gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural MGF is made locally and does not travel into the bloodstream. Synthetic MGF is water based and when administered intramuscularly, travels into the bloodstream. MGF is only stable in the blood stream for only a few minutes.   PEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down.   MGF exhibits local effects in skeletal muscle and without cannot travel through the body without modification. The problem with synthetic MGF is that it is introduced intramuscularly and is water based so it goes into the blood stream. When used this way, MGF only remains stable in the blood stream for a few minutes. Biologically produced MGF is made locally and does not enter the bloodstream. It is also short acting so stability is not an issue. By PEGylating the MGF it is almost as efficient as local produced MGF when used intramuscularly. This is accomplished by surrounding part of the peptide with a structure of polyethylene glycol, which can be attached to a protein molecule. The polyethylene glycol groups protect the peptide but don’t surround it completely. The active sites of the peptide are still free to do their biological function. In this case the shell is a negative charged shield against positively charged compounds that would affect the protein. TNeurological research has shown that utilizing PEGylated MGF resulted in a longer more stable acting version of the MGF peptide in serum/blood.

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MT-1 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram

Melanotan 1 (also referred to as Afamelanotide) is a synthetic peptide variant of a peptide hormone, called alpha-Melanocyte stimulating hormone or MSH that is naturally produced in the body and is responsible for stimulating melanogenesis, a peptide process for pigmentation of the skin. Alpha-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-1 sunless skin tanning effects. While Melanotan 2 and PT-141 have been studied at length as a potential remedies for the treatment of sexual dysfunction, Melanotan-1 has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.   MT-1 Description   Metallothioneins(MTs) are cysteine-rich metal-binding proteins that are potentially involved in zinc homeostasis and free radical scavenging. The expression pattern of MT-1 and the binding activity of various MT-1 promoter elements were investigated after mild focal cerebral ischemia in the rat. Transient focal ischemia was induced by occluding both common carotid arteries and the right middle cerebral artery for 30 min. By the use of real-time quantitative PCR, a 10-fold increase in MT-1 and -2 mRNA levels was found in the cortex 24 hr after reperfusion.   Product Usage   Melanotan 1 (also referred to as Afamelanotide) is a synthetic peptide variant of a peptide hormone, called alpha-Melanocyte stimulating hormone or MSH that is naturally produced in the body and is responsible for stimulating melanogenesis, a peptide process for pigmentation of the skin. Alpha-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-1 sunless skin tanning effects. While Melanotan 2 and PT-141 have been studied at length as a potential remedies for the treatment of sexual dysfunction, Melanotan-has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.

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MT-2 powder

  • Min. Order (MOQ) 1 Bottle(s)

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.

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GHRP-2 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MW 746.91
  • Specification 5mg/vial; 10mg/vial

GHRP-2, like its brother GHRP-6, is a hexapeptide that is a pure growth hormone secretagogue. In addition, GHRP-2 is a synthetic agonist of ghrelin. Unlike GHRP-6, this peptide does not bring on the heavy hunger side effects associated with GHRP-6; however, some users will notice slight increases in hunger. Somewhere in between GHRP-6 and iPamorelin, this hexapeptide has the ability to be a serious contender when considering which GHRP to use with your GHRH.   Remember way back when I addressed the amazing ability GHRP-6 has in improving the production of the hormone ghrelin in the stomach (a hormone that controls hunger and GH release)? Well let me tell you about GHRP-2 and why this peptide is one step better than its little brother GHRP-6. Unlike GHRP-6 , GHRP-2 does not come with the heavy hunger side effect, but still maintains all the benefits of activating ghrelin.

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GHRP-6 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C46H56N12O6
  • Molecular Weight 873.01

ghrp-6 is most generally used for the same purposes that gh might be used, but may be chosen where a cost advantage exists favoring ghrp-6, gh is not available, or the individual prefers the idea of stimulating his own gh production to injecting gh.   these purposes can include increased fat loss, improved muscle gain when used in combination with anabolic steroids, cosmetic improvement of the skin, and improved healing from injury.   there is no need to cycle ghrp use, and so therefore ghrp-6 may be used whenever it is thought to be useful for any of the above reasons. However, when usage is ongoing instead of short-term amplification of a steroid cycle or fat-loss program, I recommend limiting dosage to the minimum end of the suggested dosage range.   increased effect from combining ghrp-6 with a ghrh   while ghrp-6 is capable of inducing large increases in gh production when used alone, a given dose will show markedly more effect what a ghrh (growth hormone releasing hormone) peptide is taken at the same time. Alternately, when combining a ghrh with ghrp-6, only about half or a third as much ghrp-6 is needed to obtain the same increase in gh production.   for this reason, it’s a common choice to combine a ghrh with a ghrp, but excellent results are often obtained without doing so. A preferred choice of ghrh is mod grf 1-29 (also known as cjc-1295 without dac.)

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Ipamorelin powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C38H49N9O5
  • MW 711.853

Ipamorelin (or NNC 26-0161) belongs to regulatory peptides because it is GH releasing protein; Its chain is quite short and only consists of five amino acids. Its molecular mass/weight is 711.86 and its molecular formula is C38H49N9O5. Ipamorelin was synthesized as innovative and novelty mimetic of ghrelin therefore it possesses ability to enhance gastric motility. There are few ongoing clinical trials with ipamorelin at the current moment. The first studies on HGr-peptides including NNC 26-0161 started in early 1990s. Also this research compound is a selective secretagogue of G-hormone and ghrelin receptor's agonist. As other proteins ipamorelin reacts with GHRP-like receptors to release growth hormone from pituitary gland. But unlike few other peptides of hormones nature this pentapeptide doesn't release same volume of such compounds as cortisol and acetylcholine, and that makes it a very good candidate for future researches. Furthermore, NNC 26-0161 is more stable form of ghrelin and has longer half-life period, and it causes secondary effect by making neurons to become excited.

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MK-2866(Ostarine,Enobosarm) powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • 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.   For research.   Ostarine (MK-2866) is a SARM for the prevention and treatment of muscle wasting. It may eventually be a medical prescription for the prevention of cachexia, atrophy and sarcopenia as well as for Hormone or Replacement Therapy.   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 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   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.

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GW501516 (GSK-516,Cardarine) powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • M.F C21h18f3no3s2
  • MW 453.5

GW501516 (GW1516 or GSK-516) is a drug that acts as a PPAR delta regulator. GW 501516 activates AMP-activated protein kinases and stimulates glucose uptake in skeletal muscle tissue, GW 501516 has been shown to reverse the metabolic abnormalities of obese men with pre-diabetic metabolic syndrome, most likely by stimulating fatty acid oxidation. Potential treatments for obesity and related disorders have been proposed, particularly when used in conjunction with the synergistic compound AICAR, since the combination has been shown to significantly enhance exercise tolerance in animal studies.   GW501516 (also known as GW-501, 516, GW1516, GSK-516 and Endurobol) are PPARδ receptors. It activates the same pathway through exercise activation, including PPARδ and AMP-activated protein kinases. Has been investigated for potential treatments for obesity, diabetes, dyslipidemia and cardiovascular disease. When combined with AICAR, GW501516 has a synergistic effect: it has been shown that the combination significantly increases exercise tolerance in animal studies compared to the use of compounds alone.  

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MK-677 (Ibutamoren)

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C27H36N4O5S.CH4O3S
  • Molecular weight 624.776

Ibutamoren mesylate (MK-677) is an orally active nonpeptide growth hormone (GH) secretagogue. Nutrobal (Mk-677) was found to be very safe. This is an amazing cutting stack with Cardarine and Andarine, which will help melt off the stubborn fat and increase your muscle mass.   MK-677, acts as a potent, orally active growth hormonesecretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It has been demonstrated to increase the release of, and produces sustained increases in plasma levels of several hormones including growth hormone and IGF-1, but without affecting cortisol levels. It is currently under development as a potential treatment for reduced levels of these hormones, such as in growth hormone deficient children or elderly adults, and human studies have shown it to increase both muscle mass and bone mineral density, making it a promising therapy for the treatment of frailty in the elderly. It also alters metabolism of body fat and so may have application in the treatment of obesity.

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S-4 (Andarine,GTX-007) powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram

Andarine (GTx-007, S-4) is an investigational selective androgen receptor modulator (SARM) developed by GTX, Inc for treatment of conditions such as muscle wasting, osteoporosis and benign prostatic hypertrophy, [1] using the non-steroidal androgen antagonist bicalutamide as a lead compound.   Application   Andarine S4 is an orally active partial agonist for androgen receptors. Andarine S4 is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.This suggests that it is able to competitively block binding of dihydrotestosterone to its receptor targets in the prostate gland, but its partial agonist effects at androgen receptors prevent the side effects associated with the anti-androgenic drugs traditionally used for treatment of BPH.

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LGD-4033 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram

LGD-4033 is a selective androgen receptor modulator (SARMS), and a novel non-steroidal oral SARM that binds to AR with high affinity (Ki of ~1 nM) and selectivity. It's in a class of androgen receptor (AR) ligands that is tissue selective, developed to treat muscle wasting associated with cancer, acute and chronic illness and age-related muscle loss. LGD-4033 is expected to produce the therapeutic benefits of testosterone with improved safety, tolerability and patient acceptance due to tissue-selective mechanism of action and an oral route of administration.   LGD is still fairly new (3-5 years), but the results have been very similar in studies and logs. LGD-4033 has undergone several recent studies and trials to find the best and safest way to use it. From these trials, the results have shown increases in lean body mass and decreases in body fat. There is also a significant increase in strength, well being, as well as healing possibilities.   Dosages   LGD-4033 should be dosed at 10 mg day, taken orally, once a day in the morning. LGD should be ran 8-12 weeks, with 12 weeks being ideal. A perfect combination for fat loss is LGD-4033 with Andarine (S-4).

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SR9009 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formular C20H24ClN3O4S
  • Molecular Weight 437.94

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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SR9011 powder

740 /Gallon
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C23H31ClN4O3S
  • Molecular Weight 479.03524

SR9011 is a trifunctional methacrylate monomer that provides exceptional adhesion to metal substrates. SR9011 is recommended for use in peroxide cured coatings, sealants, and PVC-based plastisols. Usage levels of 5% to 10% by weight are recommended.SR9011 is a potent and specific synthetic REV-ERB agonist that binds to REV-ERB- with an EC50 ~790 nM and REV-ERB-with EC50 ~560 nM.   It also has good in vivo plasma/brain exposure. The nuclear receptors REV-ERB- and REV-ERB- play an integral role in regulating the expression of core clock proteins, driving rhythms in activity and metabolism. Administration of SR9011 alters circadian behavior and the circadian pattern of core clock gene expression in the hypothalami of mice. The circadian expression pattern of an array of metabolic genes in the liver, skeletal muscle and adipose tissue was also altered, resulting in increased energy expenditure.   Treatment of diet-induced obese mice with SR9011 decreased obesity by reducing fat mass and markedly improved dyslipidaemia and hyperglycaemia. These results indicate that synthetic REV-ERB ligands that pharmacologically target the circadian rhythm may be beneficial in the treatment of sleep disorders as well as metabolic diseases.

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Rad140 powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C20H16ClN5O2
  • MW 393.826

RAD140 is a nonsteroidal selective androgen receptor modulator, or SARM, that resulted from an internal drug discovery program that began in 2005.   RAD 140 is a SARM that is designed to act as if the tissues of the body are getting a good dose of testosterone without the unwanted side effects of anabolic steroids. It has been shown to enhance speed, stamina and endurance during workouts as well as increase muscular gains within shorter periods of time.   Application of RAD-140 :   RAD140 has demonstrated potent anabolic activity on muscle and bone in preclinical studies and has completed 28-day preclinical toxicology studies in both rats and monkeys. Because of its high anabolic efficacy, receptor selectivity, potent oral activity and long duration half-life, we believe that RAD140 has clinical potential in a number of indications where the increase in lean muscle mass and/or bone density is beneficial, such as treating the weight loss due to cancer cachexia, muscle frailty and osteoporosis, and also in the treatment of breast cancer.   RAD140 is a highly effective, oral SARM (Selective Androgen Receptor Modulator) currently being studied for both anabolic and neuroprotective effects. It is in a class of androgen receptor ligands that are tissue selective, developed to treat muscle wasting associated with cancer, acute and chronic illness and age-related muscle loss. Recent research of RAD140 shows superior lean tissue selectivity, and reduced androgenic side effects when compared to competing SARM compounds.   This compound provides is being studied for neuroprotection as well; an important neural action of endogenous androgens that is relevant to neural health and resilience to neurodegenerative diseases, and to be as effective as testosterone in reducing cell death induced by apoptotic insults.   Who need Testolone (RAD140)   1. Those who have low testosterone because of health issues, or prior abuse of anabolic steroids.   2. Bodybuilders who want to bridge between steroid cycles. Imagine being able to use testosterone in between your existing anabolic steroid cycles without worrying about suppression and damaging your HPTA. This will allow you to keep more strength and muscle off cycle then you ever have before. 3. Those who want to use a performance enhancing drug, but are concerned with the possible side effects. In such situation, one could cycle RAD140 instead of anabolic steroids and not worry about shutdown or the negative health effects caused by steroids.    

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AICAR (Acadesine) powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C9H14N4O5
  • MW 258.23

(1). AICAR is a peptide whose technical name is 5-Aminoimidazole-4-carboxamide ribonucleotide.It can also be known as AICA ribonucleotide, ZMP, or Acadesine.It is an intermediate contained in the generation of inosine monophosphate.It primarily functions as an AMP-activated protein kinase agonist, meaning that it has the ability to promote the operation of nutrient stores for energy production.   (2). AICAR is an adenosine analog that selectively activates AMP-activated protein kinase (AMPK). AMPK regulates lipid and glucose metabolism to maintain cellular energy homeostasis (Hardie and Carling).   (3). AICAR can play a hand in boosting these processes because it contains the ability to penetrate cardiac cells and block the production of enzymes tied to regulating glucose intake and energy expulsion.   (4). With these regulatory enzymes inhibited, the affected cells can in turn boost the amount of glucose that can be received, and it can also increase its level of energy conversion.Additionally, the peptide's presence has been determined to aid in lowering programmed cell death, a process that is also known as apoptosis.  

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Benzyl Benzoate

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formula C14H12O2
  • Molecular weight 212

Benzyl- Benzoate is a solvent. This means solutes such as Hormone Powders dissolve easily in it, and that is the main purpose of its use in Steroids. The Benzyl Benzoate is used to dissolve and suspend the Hormone Powder. If the correct amount of this solvent is not used the Hormone powder will 'undissolve' from the solution causing the Steroids to 'Crash' (get cloudy/less effective).   Some Hormone Powder dissolve more easily than others and therefore less Benzyl Benzoate is required. The fact that varying amount of the solvent are required for the Hormone Powders is why having this page as a resource is so vital.   Benzyl Benzoate (BB) is the primary solvent, which keeps the product from crashing.It is A co-solvent in steroid that serves several functions: helps dissolve the hormone, helps keep it in solution in depot (injection site), and thins the gear so it is easy to draw and inject.   Benzyl Benzoate is the next common steroid solvent on the list. It is not nearly as strong and much heavier than the benzyl alcohol so benzyl benzoate is used primarily for its latent affects in the depot. Namely it helps keep the hormone in solution at the injection site after the more water-soluble benzyl alcohol has leached from the depot. benzyl benzoate is constructed of two benzene rings bridged by a carbonyl group, this making the solvent extremely hydrophobic. It is also painless at low levels and nearly painless at 15-20% for most people.

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Grape Seed Oil

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MW 428.65
  • Appearance Pale Yellow Liquid

Grape seed oil is a rare natural high nutritional oils.Grape seed through the most advanced cold pressing method and refined, is one of the very popular in the base oil and the effect is outstanding varieties. rich in essential fatty acids, linoleic acid, rich in vitamin E, A, D and other fat-soluble vitamins and various trace element, Its nutritional value and medicinal value has been fully affirmed by scientists at home and abroad.   Grape seed oil is a natural non-toxic properties, so children, pregnant women, the elderly and athletes are applicable.Treatment for endocrine disorders caused by dry skin, reduce melanin, whitening skin, removing chloasma;to stimulate cell division and tissue regeneration, activation of the surface cells, reduce wrinkles, delay aging; antioxidant, dilute the stain: inhibit and remove the body of free radicals; anti prostate cancer, the role of anti liver tumor, and nervous system to the against damage   Grape seed oil is rich in unsaturated fatty acids, mainly oleic acid and linoleic acid, of which the content of linoleic acid up to 72%~76%. Linoleic acid is an essential fatty acid in human body, easy to be absorbed by the human body, long-term consumption of grape seed oil can reduce the human serum cholesterol, and effectively regulate the human plant nerve function.

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Ethyl Oleate

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C20H38O2
  • MW 310.51

1. Ethyl oleate is one of the fatty acid ethyl esters (FAEE) that is formed in the body after ingestion of ethanol. There is a growing body of research literature that implicates FAEEs such as ethyl oleate as the toxic mediators of ethanol in the body (pancreas, liver, heart, and brain). Among the speculations is that ethyl oleate may be the toxic mediator of alcohol infetal alcohol syndrome.   2. The oral ingestion of ethyl oleate has been carefully studied and due to rapid degradation in the digestive tract it appears safe for oral ingestion. Ethyl oleate is not currently approved by the U.S. Food and Drug Administration for any injectable use. However, it is used by compounding pharmacies as a vehicle for intramuscular drug delivery, in some cases to prepare the daily doses of progesterone in support of pregnancy. Studies which document the safe use of ethyl oleate in pregnancy for both the mother and the fetus have never been performed.     Description:   Ethyl oleate is used as a solvent for pharmaceutical drug preparations involving lipophilic substances such as steroids.It also finds use as a lubricant and a plasticizer.Ethyl oleate is regulated as a food additive by the Food and Drug Administration under "Food Additives Permitted for Direct Addition to Food for Human Consumption. Ethyl oleate is a fatty acid ester formed by the condensation of oleic acid and ethanol. It is a colorless to light yellow liquid. Ethyl oleate is produced by the body during ethanol intoxication.Ethyl oleate is used as a solvent for pharmaceutical drug preparations involving lipophilic substances such as steroids. It also finds use as a lubricant and a plasticizer.Ethyl oleate is regulated as a food additive by the Food and Drug Administration under "Food Additives Permitted for Direct Addition to Food for Human Consumption", Ethyl oleate has been identified as a primer pheromone in honeybees. Ethyl oleate is one of the fatty acid ethyl esters (FAEE) that is formed in the body after ingestion of ethanol. There is a growing body of research literature that implicates FAEEs such as ethyl oleate as the toxic mediators of ethanol in the body (pancreas, liver, heart, andbrain) Among the speculations is that ethyl oleate may be thetoxicmediator of alcohol in fetal alcohol syndrome. The oral ingestion of ethyl oleate has been carefully studied and due to rapid degradation in the digestive tract it appears safe for oral ingestion. Ethyl oleate is not currently approved by the U.S. Food and Drug Administration for any injectable use. However, it is used by compounding pharmacies as a vehicle for intramuscular drug delivery, in some cases to prepare the daily doses of progesterone in support of pregnancy. Studies which document the safe use of ethyl oleate in pregnancy for both the mother and the fetus have never been performed.

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guaiacol

740 /Gallon
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  • Min. Order (MOQ) 10 Gram
  • MF C7H8O2
  • MW 124.14

The guaiacol is a naturally occurring organic compound having the formula C 6 H 4 (OH) (OCH 3), first separated by Otto Unverdorben in 1826. Although it is biosynthetic from a variety of organisms, this light yellow aromatic oil is usually derived from guaiacol or wood creosote. After exposure to air and light, the sample becomes darker. Guaiacol is present in the wood smoke produced by pyrolysis of lignin. The compounds contribute to the flavor of many compounds, such as roasted coffee.   Guaiacol Usage   Guaiacol is a precursor of various spices, such as eugenol and vanillin. Its derivatives are used as expectorants, preservatives and local anesthetics. It can also be used as an indicator in the chemical reaction to produce oxygen. When oxygen is bound thereto, the complex becomes tan and absorbs light at about 470 nm.   Product application   Guaiacol is usually colorless to pale yellow crystal, soluble in ethanol, chloroform and other organic solvents, melting point 27 ~ 29 ℃, boiling point of 205 ℃, flash point of 82 ℃ An important fine chemical intermediates, widely used in medicine, spices, such as vanillin, artificial musk, etc.), as well as the synthesis of various dyes, can also be used as polymer and antioxidants in the food industry.   Super solvent   Guaiacol is a methyl ether of catechol, obtained by distilling callus from wood tar oil. Strong solvent is simple and simple, with a certain water-soluble, oil-soluble is also very good. Guaiacol is known as a super-solvent, which, like most high-content gears, contains guaiacol as a solvent for the production of high concentrations of concentrates. It can be more easily dissolved powder, mainly for oral steroids, such as Dianabol, Winstrol, anadrol and so on.   Guaiacol is a combustible compound, so be careful if you use open flame as a heat source. I suggest you have a nice hot plate with automatic, magnetic stir, if you are always homemade coffee.  

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Polysorbate 80 (Tween 80)

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C24H44O6
  • MW 428.600006103516

Polysorbate 80 (commercially also known as Tween 80, a registered trademark of ICI Americas, Inc. ) is a nonionic surfactant and emulsifier derived from polyethoxylated sorbitan and oleic acid, and is often used in foods. Polysorbate 80 is a viscous, water-soluble yellow liquid. The hydrophilic groups in this compound are polyethers also known as polyoxyethylene groups which are polymers of ethylene oxide. In the nomenclature of polysorbates, the numeric designation following polysorbate refers to the lipophilic group, in this case the oleic acid (see polysorbate for more detail). Polysorbate 80 is often used in food and other products as an emulsifier.   This product has excellent emulsifying, dispersing, wetting properties. In the food industry, as ice cream, bread, cakes, candies and other emulsifying agents, dispersing agents and refreshing drinks turbidity agent. In an amount of 0.1% to 0.5%, in order to prevent splashing creamy food, food aging, and improve the quality and increase the gloss, improved mouthfeel, improved softness. Especially for milk chocolate toffee significant effect anti-blooming. It can be used alone, it can also be used in conjunction with glycerides, sucrose esters and other food emulsifiers, synergy. Also widely used in high-quality cosmetics, textile, pharmaceutical industry as a solubilizing agent, also widely used in textile, paint, emulsion explosives, pesticides, printing, petroleum and other industries as emulsifiers, stabilizers, lubricants, softeners, antistatic agents.   Application :   Food use: Polysorbate 80 is used as an emulsifier in foods.   For example in ice cream, polysorbate is added up to 0.5% (v/v) concentration to make the ice cream smoother and easier to handle, as well as increasing its resistance to melting. Adding this substance prevents milk proteins from completely coating the fat droplets. This allows them to join together in chains and nets, which hold air in the mixture, and provide a firmer texture that holds its shape as the ice cream melts.   Health and beauty use: Polysorbate 80 is also used as a surfactant in soaps and cosmetics, or a solubilizer such as in a mouthwash. The cosmetic grade of polysorbate 80 may have more impurities than the food grade.

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yohimbine hcl powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C21H27ClN2O3
  • MW 390.9

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.   Yohimbine Hydrochloride`s most pronounced sexual effect appears to be in its treatment of Erectile Dysfunction in men and has shown to even increase penile girth (the width of the male ). Through its effect on minor corpus cavernosum smooth muscle relaxation, the vasodilatation caused increases blood flow to the exponentially. Continual use of Yohimbine Hydrochloride is required to achieve these results as it cannot be achieved through casual or one time usage.   One of the top advantages of Yohimbine HCl is it’s potential to help maintain a healthy weight. In one study, twenty soccer players were given Yohimbine and another twenty were given a placebo. The Yohimbine group had a significantly lower fat mass at the end of the three-week trial. It didn’t affect muscle mass or athletic performance and none of the participants noted any side effects.

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Finasterid Powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C23H36N2O2
  • Appearance: White crystalline powder

1. 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.

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Dutasteride (Avodart) powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C27H30F6N2O2
  • Molecular Weight 528.53

1. Dutasteride useful for the symptoms of benign prostatic hyperplasia (BPH); colloquially known as an "enlarged prostate".   2. In those who are being regularly screened 5-alpha-reductase inhibitor (finasteride and dutasteride) reduce the overall risk of being diagnosed with prostate cancer however there is insufficient data to determine if they have an effect on the risk of death and may increase the chance of more serious cases.   3. This class of medications increases rates of erectile dysfunction (with between 5% and 9% developing problems after starting their use). This is linked to lower quality of life and can cause stress in relationships. There is also an association with lowered sexual desire. It has been reported that these adverse sexual side effects may persist even after discontinuation of the drug.   4. The FDA has added a warning to dutasteride about an increased risk of high-grade prostate cancer. While the potential for positive, negative or neutral changes to the potential risk of developing prostate cancer with dutasteride has not been established, evidence has suggested it may temporarily reduce the growth and prevalence of benign prostate tumors, but could also mask the early detection of prostate cancer.   5. The primary area for concern is for patients who may develop prostate cancer whilst taking dutasteride for benign prostatic hyperplasia, which in turn could delay diagnosis and early treatment of the prostate cancer, thereby potentially increasing the risk of these patients developing high-grade prostate cancer.

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Dapoxetine HCL powder

740 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C21H23NO HCL
  • Molecular Weight 341.88

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.

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