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Trestolone Acetate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C21H30O3
  • Melting Point 447.571 °C at 760 mmHg
  • Flash Point 194.228 °
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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.   To make more than 1 gram Trestolone Acetateat a time, simply multiply the amounts by how much you want to do.For example, this guide will demonstrate making 3 grams Trestolone Acetate at one time. The following recipe is used:   -3 grams Trestolone Acetate Powder -49.65 mL Grape Seed Oil -1.8 mL Benzyl Alcohol -6 mL Benzyl Benzoate Then you will need following items: -Trestolone Acetate Powder -Grape Seed Oil -Benzyl Alcohol -Benzyl Benzoate -Empty Vials, sealed and sterile (20mL recommended) -Large (20mL+) luer lock syringe -Regular (3mL) luer lock syringe -A few large gauge luer lock needles (21-18ga recommended) -Sterile .45u Whatman luer lock syringe filter -Unsterile .45u Whatman luer lock syringe filter -A couple small glass jars/beakers to hold your solution -A large pot/container that can hold hot water and your smaller jar -Alcohol prep pads -Paper towels or similar, mainly for cleaning   Trestolone Acetate 50mg/ml cooking step    Make sure your work area is clean. You aren’t going to perform surgery, but you don’t want excessive dirt. Wipe your empty mixing jars/beakers with an alcohol prep pad, rinse with water, and dry with a paper towel.   Add Trestolone Acetate Powder to one and set to the side. Add some GSO to the other, exceeding the amount needed for your brew. In this case, we need 49.65 mL, so use about 60 mL. Place the GSO jar in the larger container and add hot water to the larger container (NOT THE GSO). This will heat up the GSO for easier filtering.   After heating up, use the larger syringe to draw out some GSO. Screw on the unsterile Whatman filter and start filtering into the jar with the Trestolone Acetate powder.This step may take a few times to finish. For us, we need about 50 mL. The syringe used is 25mL. So, we draw in 25 mL, attach the Whatman, filter, unscrew the Whatman, draw in another 25 mL, reattach the Whatman, and filter the rest. You just need to filter the total needed for the recipe.Using the normal syringe, measure out the appropriate amounts of the Benzyl Alcohol and Benzyl Benzoate. Add to the Trest/GSO solution   At this point, you should have something that looks like mud. This is normal. The Trestolone Acetate is floating around and not much dissolving has happened. Seal off the jar, I use a screw top. Like we did with the GSO, place the Trest/GSO/BA/BB solution into a bath of hot water to heat it up. You will need to shake up the container to help the dissolving process. Trestolone powder likes to fall to the bottom and clump. Repeat as many times and needed to dissolve most of the Trestolone.

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Testosterone Enanthate CAS 315-37-7

  • Min. Order (MOQ) 10 Gram
  • M.F C26H40O3
  • M.W 400.59
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Finshed Testosterone enanthate in 10ml vials specification:   Enanject 200 (Testosterone enanthate) 200mg/ml Enanject 250 (Testosterone enanthate) 250mg/ml Enanject 400 (Testosterone enanthate) 400mg/ml Enanject 600 (Testosterone Enanthate) 600mg/ml     Testosterone enanthate descriptions:    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.   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.   Enhanced Protein Synthesis Enhanced Nitrogen Retention Increased Red Blood Cell Count Increased IGF-1 Output Inhibition of Glucocorticoids   All people who use steroids will enjoy the ultimate effect of testosterone heptanoate, regardless of their direct use. High levels of testosterone will result in greater muscle endurance. You will not be exhausted and will be able to do more work. You will also find that your overall recovery rate is greatly improved, which is essential for progress. There was no progress in the gym. When we train we actually tear off the muscle tissue. It is through recovery that we progress. This makes the compound like testosterone heptanoate not only for bodybuilders and recreational gym mice, but also for athletes. Endurance and recovery are two key elements of successful athletic performance. Contact this whatsapp number +8613027196769 to know more about details for your order . As an added benefit, high levels of testosterone will increase the strength of the individual. This is obviously an advantage of an athlete and is improved in the body of the very popular off-season cycle design. In a diet that limits calories, especially in a harsh diet of competitive bodybuilding, the individual should not expect much, if any strength increases, but he should be able to keep more.

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Testosterone Acetate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formula C21H30O3
  • Molecular weight 330.47
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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.   American athletes have a long and fond relationship with testosterone cypionate.While testosterone enanthate is manufactured widely throughout the world, cypionate seems to be almost exclusively an American item.But many claim this is not just a matter of simple pride, often swearing cypionate to be a superior product, providing a bit more of a "kick" than enanthate.At the same time it is said to produce a slightly higher level of water retention, but not enough for it to be easily discerned.

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Testosterone Propionate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C22H32O3
  • MW 344.49
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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.

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Testosterone Cypionate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular formula C27H40O3
  • Molecular weight 412.61
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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   testosterone cypionate application:     testosterone cypionate is a steroid hormone from the androgen and is found in mammals and other vertebrates, testosterone cypionate is primarily secreted in the tests of mails and the ovaries of female, although small amount are also secreted by the adrenal glands, testosterone cypionate is the principle male sex hormone and an anabolic steroid.

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Testosterone Phenylpropionate

INR 745 /Gram
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  • Min. Order (MOQ) 101 Gram
  • MF C28H36O3
  • MW 420.58
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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.   Nandrolone is aromatic, but in its structure has a combination of phenyl propionate, the percentage of aroma is usually lower than that of testosterone when it is used in large quantities, the effect of aromatization can be expected to occur; including men's breast development and virus. Male users will notice the enlargement of the prostate with alopecia and hair loss. The ester phenylpropionate function is to increase the concentration of norromone blood on the first day of use, allowing you to maximize the benefits of the use of Nandrolone / testosterone propionate for the first five days. You should observe your natural testosterone production using nandrolone / testosterone propylpropionate though, as it will be adversely affected.  

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Testosterone Isocaproate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • EINECS 239-307-1
  • Molecular Formula C25H38O3
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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. there are some other side effects also associated with the excess use of this isocaproate. This excess usage would cause skin diseases and hair loss. Skin diseases include formation of acne on different body parts and hair loss includes male pattern baldness. Extra growth of hair on body and face, disturbance in liver function, disturbance in immunity system and cholesterol levels are also caused due to excess usage of testosterone isocaproate. Increase in aggression, depression, swinging of moods, irritability and becoming hostile are also few side effects associated with testosterone isocaproate.

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Testosterone Decanoate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MolecularFormula C29H46O3
  • MolecularWeight 442.68
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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.   testosterone decanoate adverse drug effects   liver toxicity, which produces pressure on the liver male breast development headache gastrointestinal pain hypertension testosterone decanoate formulations as a single entity: testosteronedecanoate 250mg/ml in combination with esters: testosterone decanoate 100mg + testosterone propionate 30mg + testosterone phenylpropionate 60mg + testosterone isocaproate 60mg   testosterone-decanoate is one of the most popular testosterones on the market due to it being an imperative part of the sustanon-250 mixture. However, pure testosterone-decanoate is rarely found alone as a single ester based testosterone except under the neotest 250 name. Until neotest 250 hit the market, unless you bought your own decanoate powder and made your own testosterone-decanoate you wouldn't be able to find any.  

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Testosterone Sustanon 250

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Product 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 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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Testosterone Undecanoate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C30H48O3
  • MW 456.7
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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, 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.     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.

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17-Methyltestosterone

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C20H30O2
  • MW 302.45
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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.  

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Mestanolone

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H32O2
  • Molecular Weight 304.47
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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.

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Mesterolone (Proviron)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H32O2
  • Molecular weight 304.47
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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.   Applications: 1 . Mesterolone can usually reverse problems of sexual disinterest and impotency, and is sometimes used to increase the sperm count. The drug does not stimulate the body to produce testosterone, but is simply an oral androgen substitute that is used to compensate for a lack of the natural male androgen.   2 . Often used as an antiestrogenic treatment and may be used by those who have had a poor reaction to testosterone treatments. The drug has shown to be beneficial in treating sexual dysfunction, impotency and low libido. Mesterolone binds to estrogen receptors, reducing their activity, which not only reduces estrogen production, but also encourages natural testosterone production in the body.   3 . The typical dosage for men is one to four 25 mg per tablets per day. This is a sufficient amount to prevent gynecomastia, the drug is often used throughout the entire cycle. As mentioned earlier, it is often combined with Nolvadex (tamoxifen citrate) or Clomid (clomiphene citrate) when heavily estrogenic steroids are being taken (Dianabol, testosterone etc.).  

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Oral Turinabol

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H27ClO2
  • Molecular Weight 334.88
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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

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C20H30O2
  • MW : 302.45
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methyl-1-testosterone is one of the oldest available oral steroids. It is quite androgenic, with minimal anabolic effects. For athletic purposes, methyltestosterone is generally only used to stimulate aggression among power lifters and those looking to boost up their workouts.   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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Clostebol Acetate (turinabol)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C21H29ClO3
  • Molecular weight 364.91
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Clostebol acetate is a mild anabolic steroid with low androgenic effects and moderate anabolic effects. It is mainly produced for cattle, but its use has been banned by many countries, although this is not due to their health problems in the treatment of animals (1, 2). The results produced in the treatment of animals as well as some studies have shown that the drug is suitable for certain treatments of humans (3) and is of interest to the athlete and bodybuilder of the compound.   Due to its low androgen and synthetic metabolic properties, most of the phenylephrine acetate is considered to be mild synthetic metabolites. It does not show the chemical composition that produces many other drug strengths and / or increased muscle mass. However, the user does not produce serious androgen or estrogen side effects. The lack of estrogen side effects is due to the insufficient ability of the compounds to aromatize the compounds due to the 4-chloro substitution in the A ring of the compound (4). This change itself eliminates the possibility that most male users have estrogen side effects. Clostebol acetate appears in several versions. Injections, oral or even topical creams have been made. However, only oral and injectable drug versions are suitable for use by powerful athletes and bodybuilders. The current production of local creams and ointments is not effective in trying to get muscle and strength.   The use of 4-chlorotestosterone acetate by farmers for cattle fattening was recently demonstrated although the use of this anabolic steroid is strictly forbidden in the European Union. We investigated the metabolism of 4-chlorotestosterone acetate in the bovine species after intramuscular and oral administration. Nineteen metabolites were detected in urine after intramuscular injection, and eight metabolites were identified. For this purpose, preparative HPLC, mass spectrometry with different ionization modes (electronic impact and chemical ionization), and different acquisition techniques were used (high resolution, selected ion monitoring, and scan measurement). Metabolite stereoisomerism was determined on the basis of retention time and organic synthesis.  

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1-Testosterone Cypiontae

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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.  

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Nandrolone

INR 745 /Gram
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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.

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Nandrolone Decanoate (deca)

INR 745 /Feet
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recipe for deca 160mg/ml @250ml 40 grams nandrolone decanoate 162.5 ml sesame oil 12.5ml ba 5% 37.5ml bb 15%     recipe for deca 50 ml @ 200 mg/ml 10 grams nandrolone decanoate 32.50 ml sesame oil 2.5ml ba 5% 7.50ml bb 15%     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)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Color WHITE POWDER
  • Product Name Nandrolone Phenypropionate

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.

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Mibolerone

  • Min. Order (MOQ) 10 Gram
  • MF C20H30O2
  • MW 302.45

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.   Applications:     1. Use in Animal:   Cheque drops (chemical name: mibolerone) were originally developed by Upjohn for the veterinarian market. This is arguably the most liver-toxic steroid on the planet, so only 2 weeks on this AAS at a dose of 5mgs per day is enough for a user to experience very bad side-effects. In veterinarian applications, cheque drops are fed to female dogs during heat to stop ovulation   2. Use in Bodybuiolding:   Cheque Drops earned the reputation in the bodybuilding community as one of the strongest steroids ever made. Users often reported a rapid increase in strength and muscle mass and also increased aggression in the gym. The aggression caused by Cheque Drops often led the idea that it was used by some fighters and powerlifters before competing in their respective sports. Mibolerone also displays strong estrogenic characteristics and will raise the levels of estrogen in the body dramatically during use. Because of this, estrogen related side effects such as water retention, excess body fat, and gynecomastia are always a concern when using this product. Because of this, users of this product will often want to include an anti-estrogen such as arimidex or aromasin during use of this drug. It is also important to note that mibolerone displays strong progestin activity in the body. High progesterone levels can cause side effects similar to those seen from elevated estrogen levels. To help combat this, users might also consider running an agent such as cabaser or bromocripten during administration of Cheque Drops.

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Nandrolone Cypionate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MW 398.57812
  • Eiencs 210-006-7

Nandrolone Cypionate, anabolic DN is an effective compound that produces quality, lasting muscle benefits. This is because the half-life of the drug is relatively long (about 8 days).   Nandrolone cypionate is recommended as a adjuvant for the treatment of weakness when it is necessary to improve the weight, hair coat or general physical condition. Failure is usually accompanied by disease or may occur after overwork and overwork. Nandrolone improves the general state of weakness, thereby helping to correct weight loss and improve appetite. It can not replace a balanced diet. Only when using good management and feeding methods can we get the best results.     Nandrolone Cypionate is one of several synthetic estrogenic steroids containing drugs Nandrolone. Its most distinctive feature is that it is the longest lasting nandrolone because of its big ester. The user reports that Nandrolone Cypionate gives them a slow, steady muscle and power gain that has little side effects.

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Trenbolone Acetate (Finaplix H/Revalor-H)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H24O3
  • Molecular Weight 312.4

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.

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Trenbolone Enanthate

INR 745 /Gallon
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C25H34O3
  • Molecular weight 382.54

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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Boldenone Undecylenate (equipoise)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C30H44O3
  • MW 452.67

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.

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Oxymetholone (Anadrol)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF: C21H32O3
  • MW: :332.48
  • EINECS 207-098-6
  • Melting point 172-180°C

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.    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.   Anadrol has been shown to really taper down in-terms of benefits once doses start going much past 100mg per day and this negative reaction can start to occur at doses over only 50mg per day in some individuals. What this means is an extremely high dose of Anadrol will typically not yield better results than a lower more optimal dose; the only effect will be a higher level of liver damage.   The majority of Anadrol users will find their use of the steroid do be best suited for bulking cycles but only for part of the cycle for shorter periods of time than the total cycle itself. 4-6 weeks is a good rule of thumb as going past this point will not only cause undue stress to your liver but the benefits of the steroid will start to fall when you extend past the 6 week mark. The most optimal time to use this steroid will be the first 4-6 weeks of the given cycle and most will find Anadrol stacks very well with testosterone of any form with additional Deca-Durabolin for those who are really looking for a punch.  

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Oxandrolone (Anavar)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Product Anavar
  • Form White Crystalline Powder

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.  

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Stanozolol (Winstrol)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • M. F C21H32N2O
  • M. W 328.49

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.  

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Drostanolone Propionate (masteron)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Einecs No 208-303-1
  • MF C23H36O3

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.   Actual use of Masteron   Nowadays Drostanolone is a very popular anabolic steroid used mainly by athletes and bodybuilders.  

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Drostanolone Enanthate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C27H44O3
  • MW 416.64

Drostanolone Enanthate is strictly an undergroundanabolic androgenic steroid that is based on the discontinued Drostanolone Propionate compound known as Masteron. Masteron is a fairly old anabolic steroid first created in 1959 by Syntex and has been sold under several other brand names such as Masteril, Drolban and Metormon with Masteron remaining the most recognizable.   During the 1970’s and 80’s Masteron enjoyed significant therapeutic success, particularly in the treatment of inoperable breast cancer. Despite its success in cancer treatment and other areas of medicine, in the late 1980’s and early 1990’s Masteron began to disappear from the U.S. and European markets and in modern times is no longer manufactured. Drostanolone is still an FDA approved anabolic steroid, but no U.S. pharmacy manufactures it. Masteron Enanthate (Drostanolone Enanthate) is a dihydrotestosterone (DHT) based anabolic steroid. Drostanolone is simply the DHT hormone structurally altered. The alteration exists through the addition of a methyl group at carbon position 2. This ensures the hormone doesn’t suffer metabolic breakdown brought on by the 3-hydroxysteroid dehydrogenase enzyme found in the skeletal muscle.   This simple structural change also makes the hormone far more anabolic, and that gives us Drostanolone. Once the hormone has been created, altered from DHT, an ester is then attached, and in this case the ester attached is Enanthate. Enanthate is not a steroid or a drug but nothing more than a timing tool used for a drug. Drostanolone enanthate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.   Drostanolone enanthate can promote increased strength while keeping body fat the same or even lowering it, something can help to prevent muscle loss while dieting.   Masteron is often an ideal choice for inclusion in a steroid stack, or in some cases for use as the sole injectable for a steroid cycle.   Drostanolone enanthate 100 USP injection provides drostanolone enanthate, a potent androgenic steroid that has similar characteristics of dihydrotestosterone. Drostanolone is incapable of aromization and therefore it doesn’t convert into oestrogen.   Both drostanolone’ anabolic and androgenic activity is far greater than methyl testosterone. The esterification of the 17-beta-hydroxyl group increases the duration of the action of drostanolone.   Drostanolone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus Drostanolone enanthate 100E can be administered at intervals of every 1-2 weeks.

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Methenolone Enanthate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C27H42O3
  • MW 414.62
  • Grade Pharmaceutical Grade
  • EINECS No 206-141-6

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.   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%   Effect Methenolone Enanthate   The effect of methenolone enanthate(10 mg kg−1 thrice-weekly) on total body nitrogen, potassium, phosphorus, and body-weight, muscle protein synthesis and food conversion efficiency was measured in Wistar rats during the period from weanling to maturity (22 to 64 days of age). Treated male rats exhibited a lower rate of weight gain, increased kidney weight and decreased testicular weight when compared with controls. No differences in total nitrogen, potassium or phosphorus were observed.    

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Methenolone Acetate/primobolan

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Einecs No 207-097-0
  • MF C22H32O3
  • MW 344.49
  • Appearance: white powder

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. Methenolone Enanthate/Primobolan Dosage   Medical prescription guidelines for Primobolan doses can be broken apart into two categories: (1)Oral Primobolan doses (2) Injectable Primobolan doses   Injectable Primobolan (Methenolone Enanthate): Medical prescription guidelines for the injectable variant of Primobolan called for an initial dose of 200mg, followed by 100mg weekly for the duration of therapy. Depending on the medical condition being treated, Primobolan doses can land anywhere in the range of 100mg every 1 - 2 weeks or 200mg every 2 - 3 weeks. There exist no separate medical dosing guidelines for female patients.   Oral Primobolan (Methenolone Acetate): Medical prescription guidelines for the oral variant of Primobolan were that of 100 - 150mg per day for no longer than a 6 - 8 week period. Just as with the injectable Primobolan prescription guidelines, there are no separate instructions for female Primobolan doses.  

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Clomiphene Citrate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Weight 598.09
  • Formula C32H36ClNO8

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.

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Toremifene Citrate

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Weight 598.09
  • Melting Point 158-164 ºC

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.

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Anastrozole (arimidex)

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C17H19N5
  • MW 293.37

Arimidex (anastrozole) is the aromatase inhibitor of choice. Arimidex’s mechanism of action - blocking conversion of aromatizable steroids to estrogen - is in contrast to the mechanism of action of anti-estrogens such as clomiphene (Clomid) or tamoxifen (Nolvadex), which block estrogen receptors in some tissues, and activate estrogen receptors in others.   Anastrozole, sold under the trade name Arimidex among others, is a medication used in addition to other treatments for breast cancer. Specifically it is used for hormone receptor-positive breast cancer. It has also been used to prevent breast cancer in those at high risk. It is taken by mouth.     Applications:   The drug is appropriately used when using substantial amounts of aromatizing steroids, or when one is prone to gynecomastia and using moderate amounts of such steroids. Arimidex does not have the side effects of aminoglutethimide (Cytadren) and can achieve a high degree of estrogen blockade, much moreso than Cytadren. It is possible to reduce estrogen too much with Arimidex, and for this reason blood tests, or less preferably salivary tests, should be taken after the first week of use to determine if the dosing is correct.

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Letrazole

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF 306.44
  • 306.44 285.30274
  • Purity >99%
  • Grade Pharmaceutical grade

Letrazole Is a powerful aromatase inhibitor that has been developed for the fight against breast cancer. For athletes and bodybuilders, it is a medicament for estrogen side effects against synthetic metabolic steroids, acne and celiac disease. Due to decreased estrogen in the body, can also cause elevated testosterone levels. Side effects include reduced sexual behavior and continuous use can lead to reduced lipid function and impaired immune system.   Femara is only used for women without childbearing age. Possible candidates must no longer have menstruation. Often used in patients who have received other cancer treatments, such as radiotherapy, chemotherapy, and other cancer drugs such as tamoxifen. This non-steroidal aromatase inhibitor can help prevent any remaining cancer cells from spreading.   Femara is used to treat postmenopausal breast cancer.     Product application   Letrazole Is a type II (nonsteroidal) third generation aromatase inhibitor. Clinically used for the treatment of estrogen receptor-positive or estrogen receptor unknown breast cancer in postmenopausal women. In women with breast cancer, estrogen levels have been reduced by more than 98%.   However, its use is not limited to the elimination of estrogen in women. For the bodybuilder before the game, Femara is almost necessary to eliminate water retention conditions, and to achieve in today's fitness world in the necessary torn appearance of competition. However, according to my experience, only need to use in the past 4-6 weeks to eliminate excessive estrogen and water retention. After using Femara, I recommend not to suppress any estrogen for at least a month in an attempt to normalize the body.     The use and dosing of Letrazole   Letrazole Anecdotes reported good results were observed using a dose of about 25 mgs per day to 0.5 mg daily. However, these dosages do vary widely from user to user, including dosing regimens.   

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Dapoxetine Hcl

INR 745 /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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Dutasteride (avodart)

INR 745 /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.  

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Finasteride

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula: C23H36N2O2
  • Assay 99%

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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Yohimbine Hcl

INR 745 /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.   In another study, twenty obese women underwent a three-week clinical trial to test the effects of Yohimbine on weight. They all ate a low-energy diet (1000 kcal/day) for the period of the trial. Half the women were given a placebo and the other half were given Yohimbine HCl four times per day. The Yohimbine group had a significantly better weight reduction at the end of the trial. Yohimbine also seemed to promote a healthy sympathetic system. Again, none of the women reported any side effects during the trial.  

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CJC1295 with DAC

INR 745 /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

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Usage Increased cortisol levels.
  • PURITY 99%

For starters Hexarelin is not your average GHRP. The structure of the amino acid is that of a hexapeptide known to help promote the release of growth hormone (GH). The mechanism of action is not yet fully understood by scientists. However, what we know is that hexarelin has the ability to act both on the pituitary gland and the hypothalamus. It is known to give the largest release of GH than any other GHRP.   Like other peptides, hexarelin has the ability to help promote more production of natural growth hormone, and it will not shut down the production of the body’s ability to produce GH. Hexarelin has been shown in studies to increase bone mineral density, mitosis and meiosis, fat loss, connective tissue strengthening, and improved skin elasticity.

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MGF

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • 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

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gallon
  • M.F C121H200N42O39
  • Appearance White powder

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

INR 745 /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.

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MT-2

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Product Melanotan II
  • Function Nourishing and Balancing Nutrition

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

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MW 746.91
  • MF C42H50N8O5
  • Specification 5mg/vial; 10mg/vial
  • Source Chemical Synthesis

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

INR 745 /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.

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Ipamorelin

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C38H49N9O5
  • MW 711.853

Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world.It is a synthetic peptide that has powerful Growth Hormon releasing properties.And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat. Ipamorelin is a penta-peptide.(Aib-His-D-2-Nal-D- Phe-Lys-NH2) And, the strength it displays may very well make regular old Growth Hormon (GH) obsolete.But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other GHRP peptides? Athletes are taking Ipamorelin in a 200mcg -300mcg dosage, two or three times daily, using a tiny insulin needle to inject.They usually start with the lower dose since side effects can include headaches or what feels like a head-rush.Ipamorelin can be taken at anytime but taking it about 30-45 minutes before a workout would seem ideal because of the pulse in Growth Hormon (GH) it creates allowing for maximum growth. Studies on the effects of Ipamorelin on bone growth, body weight, and GH release showed some interesting conclusions.In one experiment, various doses were administered over the course of 15 days to test the group's reactions. There was a distinct and dose-dependent effect on body weight gain however, the treatment group did not show a change in total IGF-I levels.Nor did the treatment group produce serum markers of bone development.For example, the number of cells in the wide portion of the tibia (the shinbone) did not change significantly.This is a good thing because it suggests muscle growth with less potential for deformity of bone or cartilage.

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Oxytocin

INR 745 /Gram
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  • Min. Order (MOQ) 10 Gram
  • MF C43H66N12O12S2
  • MW 1007.19

Oxytocin is a mammalian hormone that acts primarily as a neuromodulator in the brain. Oxytocin is best known for its roles in sexual reproduction, in particular during and after childbirth. It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, and after stimulation of the nipples, facilitating breastfeeding. The word oxytocin was derived from the Greek word", meaning quick birth. The oxytocin peptide is synthesized as an inactive precursor protein from the OXT gene.   Oxytocin is a peptide of nine amino acids (a nonapeptide). Its systematic name is cysteine-tyrosine-isoleucine-glutamine-asparagine-cysteine-proline-leucine-glycine-amine (cys, tyr, ile, gln, asn, cys, pro, leu, gly - NH2, or CYIQNCPLG-NH2). The cysteine residues form a disulfide bond. Oxytocin has a molecular mass of 1007 daltons. One international unit (IU) of oxytocin is the equivalent of about 2 micrograms of pure peptide. The trust-inducing property of oxytocin might help those who suffer from social anxieties and mood disorders, but with the potential for abuse with confidence tricks and military applications.   The structure of oxytocin is very similar to that of vasopressin (cys, tyr, phe, gln, asn, cys, pro, arg, gly - NH2), also a nonapeptide with a sulfur bridge, whose sequence differs from oxytocin by two amino acids. A table showing the sequences of members of the vasopressin/oxytocin super family and the species expressing them is present in the vasopressin article. Oxytocin and vasopressin were isolated and synthesized by Vincent du Vigneaud in 1953, work for which he received the Nobel Prize in Chemistry in 1955. Oxytocin and vasopressin are the only known hormones released by the human posterior pituitary gland to act at a distance. However, oxytocin neurons make other peptides, including corticotropin-releasing hormone and dynorphin, for example, that act locally. Oxytocin has peripheral (hormonal) actions, and also has actions in the brain. Its actions are mediated by specific, high-affinity oxytocin receptors. The oxytocin receptor is a G-protein-coupled receptor that requires Mg2+ and cholesterol.  

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