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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 Phenylpropionate

835 /Gram Get Latest Price
  • 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 Sustanon 250

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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 17-methyltestosterone, is a 17-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 c17 in order to increase oral bioavailability.


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Mestanolone

835 /Gram Get Latest Price
  • 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)

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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

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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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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

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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 Phenypropionate (Durabolin)

835 /Gram Get Latest Price
  • 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 1960s 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 wasnt long after its inception that athletes and bodybuilders found a use.



Cheque Drops is one of the most potent anabolic steroids ever made. Youll 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 its not a very common bodybuilding steroid. Well understand this steroids 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

835 /Gram Get Latest Price
  • 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 Enanthate

835 /Gallon Get Latest Price
  • 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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Oxymetholone (Anadrol)

835 /Gram Get Latest Price
  • 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)

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Form White Crystalline Powder
  • Product Anavar

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, its 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 Turners syndrome in girls. As oxandrolone is C17-alpha-alkylated there is the potential for liver damage.


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Drostanolone Propionate (masteron)

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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 1970s and 80s 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 1980s and early 1990s 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 doesnt 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 doesnt 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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Clomiphene Citrate

835 /Gram Get Latest Price
  • 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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Letrazole

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF 306.44
  • Purity >99%
  • Grade Pharmaceutical grade
  • 306.44 285.30274

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

835 /Gram Get Latest Price
  • 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)

835 /Gram Get Latest Price
  • 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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Yohimbine Hcl

835 /Gram Get Latest Price
  • 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 penis). Through its effect on minor corpus cavernosum smooth muscle relaxation, the vasodilatation caused increases blood flow to the penis 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 its 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 didnt 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

835 /Gram Get Latest Price
  • 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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MGF

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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 dont 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-2

835 /Gram Get Latest Price
  • 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

835 /Gram Get Latest Price
  • 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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Ipamorelin

835 /Gram Get Latest Price
  • 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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Tesamorelin

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C221H366N72O67S
  • Molecular Weight 5135.77794

Tesamorelin / Egrifta is a synthetic form of growth-hormone-releasing hormone which is used in the treatment of HIV-associated lipodystrophy, which consisting of all 44 amino acids of hGRF with the addition of a trans-3-Hexenoic acid group. Tesamorelin has been shown to reduce lipodystrophy in HIV-infected individuals. Lipodystrophy is a condition that causes changes in placement of body fat, including wasting and fat accumulation, and changes in metabolism. Similar to Tesamorelin is Sermorelin, which may be taken with GHRP-6 is clinical trials, that also promotes production and possible fat loss.


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PT141

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C50H68N14O10
  • MW 1025.18

PT-141 (Bremelanotide) is the first of a new class of drugs called melanocortin agonists being developed to treat sexual dysfunction. The mechanism of action of PT-141(Bremelanotide) may offer significant safety and efficacy benefits over currently available products because it acts on the pathway that controls sexual function without acting directly on the vascular system.



Clinical data indicates that PT-141(Bremelanotide) may be effective in treating a broad range of patients suffering from ED. The nasal formulation of PT-141(Bremelanotide) being developed is as convenient as oral treatments, is more patient-friendly than invasive treatments for ED, such as injections and trans-urethral pellets, and appears to result in a rapid onset of action.



About PT-141Bremelanotide (PT-141) was developed from Melanotan 2 (MT-II). PT-141 is a metabolite of MT-II that lacks the C-terminal amide function-stripping away tanning properties.



Bremelanotide (formerly PT-141) is a compound under drug development by Palatin Technologies as a treatment for female sexual dysfunction, hemorrhagic shock and reperfusion injury. It functions by activating the melanocortin receptors MC1R and MC4R, to modulate inflammation and limiting ischemia.

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Gonadorelin

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C55H75N17O13
  • MW 1182.29

Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.



GnRH is available as gonadorelin hydrochloride )and gonadorelin diacetate tetrahydrate for injectable use. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. It is also used in veterinary medicine as a treatment for cattle with cystic ovarian disease.



Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens.

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Epitalon

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formular C14H22N4O9
  • Molecular Weight 390.3459
  • Appearance White Powder
  • Specification 10mg/vial

Epitalon is a protein peptide that can stimulate the body's own natural production of telomerase within our it's cells.By doing this, it strengthens telomeres for reproduction. Your body makes telomerase, but it needs to be stimulated with the right precursors.Over time it should lengthen the telomeres of cells and refresh your entire body.



According to scientific studies based on animal test subjects, Epithalon (also known as Epitalon) has been shown to function with telomeres, which are areas of repeating DNA sequences that function to prevent gene degradation near the end of chromosomes.



Over time, telomeres become too small and weak to contain the sequence because of cell division, and the DNA becomes disrupted, which signals the start of the aging process.Epithalon works to replenish the enzyme that allows telomeres to remain more stabilized and better equipped to hold DNA in place.


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IGF-1 Lr3

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Appearance: White lyophilized powder
  • Specification 1mg/vial

IGF-1 LR3 greatly boosts muscle mass by inducing a state of muscle hyperplasia (increase in number of new muscle cells) in the MUSCLE WHERE ITS INJECTED! So think of it as muscle cell proliferation, or even the splitting of the cell so 1 becomes 2. That's why its perfect on cycle when you get increased muscle cell growth too. But why is IGF better than HGH? The reason being is HGH causes IGF levels to rise in the liver first, then then the muscle, Whereas IGF-LR3 causes localized IGF levels to rocket.


Igf1-lr3 As you all know is the long acting version of Igf-1, Taking its active potential up towards 20 hours, But along with its ability to stimulate the growth of satellite muscle cells and helping them to mature into new muscle fibers it holds the ability to increase the uptake of many supplements we currently use, And it can cause the enhanced recovery of testicle size, and prevent muscle loss even in PCT. Plus another reason its so potent is because of the decreased binding of Long R3 IGF-1 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF. not so with this long acting version.

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GDF-8

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C221H366N72O67S
  • Appearance White Lyophilized Powder

Myostatin (GDF-8) is a member of the transforming growth factor-beta (TGF-beta) superfamily that is highly expressed in skeletal muscle, and myostatin loss-of-function leads to doubling of skeletal muscle mass. Myostatin-deficient mice have been used as a model for studying muscle-bone interactions, and here we review the skeletal phenotype associated with altered myostatin signaling. It is now known that myostatin is a key regulator of mesenchymal stem cell proliferation and differentiation, and mice lacking the myostatin gene show decreased body fat and a generalized increase in bone density and strength.



The increase in bone density is observed in most anatomical regions, including the limbs, spine, and jaw, and myostatin inhibitors have been observed to significantly increase bone formation. Myostatin is also expressed in the early phases of fracture healing, and myostatin deficiency leads to increased fracture callus size and strength. Together, these data suggest that myostatin has direct effects on the proliferation and differentiation of osteoprogenitor cells, and that myostatin antagonists and inhibitors are likely to enhance both muscle mass and bone strength.



GDF-8 Application



The gene encoding myostatin was discovered in 1997 by geneticists Se-Jin Lee and Alexandra McPherron who produced a strain of mutant mice that lack the gene. These myostatin "knockout" mice have approximately twice as much muscle as normal mice. These mice were subsequently named "mighty mice".



Naturally occurring deficiencies of myostatin have been identified in cattle by Ravi Kambadur, whippets, and humans; in each case the result is a dramatic increase in muscle mass. A mutation in the 3' UTR of the myostatin gene in Texel sheep creates target sites for the microRNAs miR-1 and miR-206. This is likely to cause the muscular phenotype of this breed of sheep.



Human myostatin consists of two identical subunits, each consisting of 109 (NCBI database claims human myostatin is 375 residues long) amino acid residues. Its total molecular weight is 25.0 kDa. The protein is inactive until a protease cleaves the NH2-terminal, or "pro-domain" portion of the molecule, resulting in the active COOH-terminal dimer. Myostatin binds to the activin type II receptor, resulting in a recruitment of either coreceptor Alk-3 or Alk-4. This coreceptor then initiates a cell signaling cascade in the muscle, which includes the activation of transcription factors in the SMAD family - SMAD2 and SMAD3. These factors then induce myostatin-specific gene regulation. When applied to myoblasts, myostatin inhibits their differentiation into mature muscle fibers.

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Follistatin 344

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C14H22N4O9
  • Appearance White to off-white crystalline powder

Follistatin is a single-chain gonadal protein that specifically inhibits follicle-stimulating hormone release. The single FST gene encodes two isoforms, FST317 and FST344 containing 317 and 344 amino acids respectively, resulting from alternative splicing of the precursor mRNA.



Follistatin binds directly to activin and functions as an activin antagonist. specific inhibitor of the biosynthesis and secretion of pituitary follicle stimulating hormone (fsh).



Follistatin, specifically Follistatin 344 (FS344), quickly gained popularity in the bodybuilding community as a potential supplement to rapidly increase lean tissue mass. Another protein, follistatin-related gene (FLRG) acts on similar pathways as FS344 regarding its muscle building properties.



Application & Effects



1) Follistatin 344 / FST promote muscle growth due to the unique mechanism of action, FST joint use of steroids, IGF has better results. It only acts on muscle tissue , after use will not cause the proliferation of other tissue cells.



2) Follistatin 344 / FST works by binding to and inhibiting transforming growth factor- (TGF-) peptides such as myostatin which is responsible for regulating and limiting muscle growth



How Follistatin 344 works ?



Follistatin works by binding to and inhibiting TGF-peptides such as myostatin which is responsible


for regulating and limiting muscle growth.



Follistatin 344 also suppresses the pituitary gland synthesis and secretion of follicle-stimulating hormone (FSH).


most proteins discussed in the fitness world, follistatin has carbohydrates attached to it.

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Pentadecapeptide BPC 157

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C62H98N16O22
  • Molecular Weight 1419.53552

BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models.In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease.BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect.In addition, it significantly facilitates the healing of bone fracture in rats.This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect.BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.



BPC 157 is a pentadecapeptide made up of 15 amino acids. The amino acids sequence in BPC 157 is similar to a portion of the human BPC amino acid sequence. Human BPC is found in the gastric juice. Experiments have shown that BPC 157 enhances the healing of wounds, including tendons wounds such as transected Achilles tendons of rats. The aim of this study was to investigate the probable mechanism that BPC 157 utilizes to accelerate the healing process in an injured tendon.The results also showed that BPC 157 significantly increased the survival of cells under oxidative stress. Furthermore, the Transwell filter migration assay showed that BPC 157 significantly increased in-vitro fibroblast migration in a dose-dependent fashion. Moreover, BPC 157 accelerated the dispersal of the fibroblasts in culture dishes in a dose-dependent manner.

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T4/L-Thyroxine Sodium Salt

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C15H10I4NNaO4
  • MW : 798.85

Levothyroxine (INN, USAN) or L-Thyroxine Sodium Salt is a synthetic thyroid hormone that is chemically identical to thyroxine (T4), which is naturally secreted by the follicular cells of the thyroid gland. It is used to treat thyroid hormone deficiency, and occasionally to prevent the recurrence of thyroid cancer. Like its naturally secreted counterpart, levothyroxine is a chiral compound in the L-form. The related drug dextrothyroxine (D-thyroxine) was used in the past as a treatment for hypercholesterolemia (elevated cholesterol levels) but was withdrawn due to cardiac side effects. It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.



L-Thyroxine Sodium Salt is typically used to treat hypothyroidism, and is the treatment of choice for patients with hypothyroidism, who often require lifelong thyroid hormone therapy. It may also be used to treat goiter via its ability to lower thyroid-stimulating hormone (TSH), a hormone that is considered goiter-inducing. Levothyroxine is also used as interventional therapy in patients with nodular thyroid disease or thyroid cancer to suppress thyroid-stimulating hormone (TSH) secretion.

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L-carnitine

835 /Gallon Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C7H15NO3
  • MW MW

1. L-carnitine is a dietary supplement newly approved by China. It is mainly used to strengthen the soy-based baby food and promote the absorption and utilization of fat. D- and DL-type have no nutritional value. China states: it can be used in biscuits, drinking fluids and milk drinks with usage amount of 600 3000mg / kg; for solid drink, drinking liquid and capsules, the amount should be 250 600mg/kg; the amount of milk powder is 300 400mg / kg; the amount of use in infant formula is 70 90mg/kg (in terms of L- carnitine, 1g equivalent 0.68g L- carnitine tartrate).



2. Used in pharmaceutical, nutrient health food, functional beverages, and feed additives.



3. Used as appetite enhancers.



Prospect of Function Food



L-carnitine, as a new kind of nutritional supplements, especially as the additive of baby formula, athlete food, and food for losing weight and bodybuilding, has been currently widely applied in functional foods. The commercialized L-carnitine is mainly its hydrochloric acid salt, tartaric acid salt and citric acid magnesium salts.




1.Infant formula food



L-carnitine plays an important role in the babys metabolism process of taking fat as a source of energy. Owing to that the weak ability of baby of de no biosynthesis of L-carnitine cant meet the demands of its normal metabolism, it must be ingested exogenous L-carnitine base in order to ensure the best in body fat oxidation state and provide enough energy to maintain normal body temperature of the baby.



In addition, L-carnitine also has certain effects on boosting infant growth and development and improving metabolic balance. So it is necessary to strengthen the L-carnitine in infant food, especially in soy-based infant formula. Because of the low carnitine content in soy, the limit of L-carnitine content in infant formula food is 70 90mg/kg in China. Now China has carnitine fortified infant formula milk that has entered into market.




2. Athletes Food



Decombaz J. et al have reported that after fierce exercise, the free carnitine content in human muscle tissue will decrease by 20% and the supplemental of carnitine can alleviate the fatigue of the body because L-carnitine can promote fat oxidation of the body as well as provide sufficient energy which is good for the sports endurance as well as explosiveness improvement.

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Dmaa

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF: C7H17N. HCl
  • MW 151.72

Dimethylpentylamine was discovered originally in geranium flowers. An extract was taken from the flower and transformed into a compound that is oil-based. Part of the compound had the same properties that are credited today to Dimethylpentylamine.



More investigation uncovered that the compound came from natural sources and was given the name gerananmine at that time to demonstrate the substances amine categorization and natural origin. A lot of compounds like this have a colloquial name at the start and are categorized into the IUPAC naming system later when the structure of it is uncovered completely. In this case, both Dimethylpentylamine and geranamine are considered suitable names for this substance.



By imitating the effect of epinephrine in the body, it gives users a feeling of greater focus, energy, and wellbeing. This makes Methylhexanamine an effective study aid that can help you prepare for that big test, presentation, or any other activity that necessitates high mental performance.

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Theobromine

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF: C33H57N11O9
  • MW MW: 751.9

Theobromine, formerly known as xanthate, is a bitter alkaloid of a cocoa plant with a chemical formula of C7H8N4O2. It is classified as a xanthine alkaloid, which also includes similar theophylline compounds. The degree of methylation of the compounds is different.




Application



In modern medicine, theobromine is used as a vasodilator (vasodilator), a diuretic (urinary aid) and a cardiac stimulant. Theobromine increases urine production. Because of this diuretic effect and its ability to dilate blood vessels, theobromine has been used to treat high blood pressure.



lose weight



Theobromine is a mild stimulant and diuretic. These two properties can help you lose weight by helping you lose weight by giving physical activity a little energy to help you lose weight. Theobromine can also help suppress your appetite. It can be said that the ability to lose weight, including vasodilatation, diuretic and increase energy, can be promoted in a variety of ways, although these seem to be indirect.



use



In modern medicine, theobromine is used as a vasodilator (vasodilator), a diuretic (urinary aid) and a cardiac stimulant. Theobromine increases urine production. Because of this diuretic effect and its ability to dilate blood vessels, theobromine has been used to treat high blood pressure.



The health benefits of theobromine


Theobromine also relieves the bronchial muscles of the lungs. Theobromine can be used as a cough medicine. Studies have shown that theobromine acts on the vagus nerve, which flows from the lungs to the brain.



Theobromine has a similar effect to caffeine, but about 10 times weaker. Theobromine has the effect of diuretic, excitement and relaxation. Theobromine can lower blood pressure because it can dilate blood vessels.



Theobromine is irritating and is similar to caffeine. Unlike caffeine, theobromine does not affect the central nervous system.


Theobromine also relieves the bronchial muscles of the lungs. Theobromine can be used as a cough medicine. Studies have shown that theobromine acts on the vagus nerve, which flows from the lungs to the brain.


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Synephrine

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C9H13NO2
  • MW 167.21

Synephrine, or, more specifically, p-synephrine, is an alkaloid, occurring naturally in some plants and animals, and also in approved drugs products as its m-substituted analog known as neo-synephrine.



p-Synephrine and m-synephrine are known for their longer acting adrenergic effects compared to norepinephrine. This substance is present at very low concentrations in common foodstuffs such as orange juice and other orange (Citrus species) products, both of the "sweet" and "bitter" variety. The preparations used in Traditional Chinese Medicine (TCM), also known as Zhi Shi, are the immature and dried whole oranges from Citrus aurantium (Fructus Aurantii Immaturus).



Extracts of the same material or purified synephrine are also marketed in the US, sometimes in combination with caffeine, as a weight-loss-promoting dietary supplement for oral consumption. While the traditional preparations have been in use for millennia as a component of TCM-formulas, synephrine itself is not an approved OTC drug. As a pharmaceutical, m-synephrine is still used as a sympathomimetic (i.e. for its hypertensive and vasoconstrictor properties), mostly by injection for the treatment of emergencies such as shock, and rarely orally for the treatment of bronchial problems associated with asthma and hay-fever.



It is important to distinguish between studies concerning synephrine as a single chemical entity (and even here it should be borne in mind that synephrine can exist in the form of either of two stereoisomers, d- and l-synephrine, which are chemically and pharmacologically distinct), and synephrine which is mixed with other drugs and/or botanical extracts in a "Supplement", as well as synephrine which is present as only one chemical component in a naturally-occurring mixture of phytochemicals such as the rind or fruit of a bitter orange. Mixtures containing synephrine as only one of their chemical components (regardless of whether these are of synthetic or natural origin) should not be assumed to produce exactly the same biological effects as synephrine alone.

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Rimonabant

835 /Inch Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C22H21Cl3N4O
  • MW 463.79

Rimonabant / Acomplia selectively blocks the CB1 receptors that are present in the brain and other peripheral organs important in fat/lipid and glucose metabolism, including muscle, gastrointestinal tract, liver and adipose tissue. Basically, it switches off those brain circuits that are responsible for making people hungry while smoking . Acomplia, along with CB1 receptors, reduces the EC system's over-activity.



Rimonabant / Acomplia is said to have reduced the overall body fat by 10% in one out of three users. Also, it is reported that those users did not gain back more than a kilo over the next two years if the patients remained on Rimonabant. Rimonabant was recommended for those with a BMI of 30 or greater, who were considered obese, and is most successful when combined with exercise and a proper diet.

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Orlistat

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gallon
  • MF C29H53NO5
  • MW 495.73

Orlistat blocks some of the fat which you eat, keeping it from being absorbed because of your body. Orlistat is used to aid in weight reduction, or to lessen the risk of regaining weight lost.



This medicine is employed together with a reduced-calorie diet. Orlistat is good for use only in grown-ups. Orlistat (prescription and nonprescription) is utilized with an individualized low-calorie, low-fat eating and working out program to help lose weight. Prescription orlistat is used in overweight people who can also have high blood pressure, diabetes, high-cholesterol, or coronary disease.



Orlistat is also used after weight-loss to help keep from gaining back that weight. Orlistat is within a class of medications called lipase inhibitors. It functions by preventing a number of the fat in foods eaten from being absorbed from the intestines. This unabsorbed fat will be removed from our bodies in the stool.



Orlistat is currently internationally recognized as a new type of weight loss lipid-lowering drugs with the marketed product being under the name of Xenical. It was first listed in New Zealand in 1998 with annual sale of $ 146 million at that time. In 2007, the sale reaches $ 538 million, Orlistat occupy 80% of the market share of the global weight-loss market with the annual sale of only China Hong Kong year reaching 80 million US dollars.



Orlistat is a long-acting and potent specific inhibitor of gastrointestinal tract lipase, appearing as white or white-like powder at room temperature and being insoluble in water, soluble in chloroform and easily soluble in ethanol. It can form covalent bonds with the active serine sites of the gastric lipase and the pancreatic lipase in the stomach and small intestine cavity, resulting in inactivation of the enzymes. Fat in food cant be broken down into free fatty acids and monoacylglycerols so that the fat cant be absorbed and utilized, thereby having reduced the body's calorie intake to control the body weight.

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Calcium Pyruvate

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C6H6CaO6
  • MW 214.19
  • 214.19 White powder
  • EINECS 257-599-9

Pyruvate is a 3-carbon energy intermediate produced in cells from glucose, en route to creating ATP (the main energy currency of working cells). Pyruvate supplementation has been proposed to enhance work output and weight loss by providing more efficient energy that bypasses the ability of the body to store glucose as body fat.



Many claim that calcium pyruvate can help with weight and/or fat loss. In theory, since it is the raw material for cellular respiration, supplementing with calcium pyruvate should increase the amount of energy burned, therefore allowing for more fat burning. The question is whether this is actually the case.



A study done by Dr. Ronald Stanko at the University of Pittsburgh concluded that calcium pyruvate does have this fat burning effect. Obese women were put on a 1, 000-calorie diet for 21 days during this study. The group receiving calcium pyruvate experienced 48 percent higher fat loss, amounting to 3.2 extra pounds.

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Benzocaine

835 /Gallon Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C9H11NO2.ClH
  • MW 201.65

Benzocaine hydrochloride is a local anesthetic in the form of hydrochloride salt benzocaine, pharmacological effects with benzocaine, procaine than anesthetic effect is weak. Part of the absorption is slow and lasting effect. Because they are insoluble in water, can not be used for anesthesia, relieve pain, anti-itching, drugs are usually made of powder or oil paste for the treatment of wound clinical, ulcers, burns, skin abrasions and hemorrhoids.

Benzocaine is also known as aminobenzoate, cenuxacin.

Benzocaine HCL acts by creating a chemical barrier that prevents the accumulation of sodium, and when the nerve endings are stimulated by pain, sodium accumulates. When the sodium accumulates, the electrical signal will also increase the nerve endings. These are eventually passed to the brain, which interprets the signal as pain.

Benzocaine Hcl is also known as ethyl aminobenzoate, colorless or white diagonal needle-like crystals or crystalline powders. Benzocaine hydrochloride is the hydrochloride form of local anesthesia benzocaine, and benzocaine has the same pharmacological effect and weaker anesthesia compared to procaine. Local absorption is slow, sustained effect. Because it is insoluble in water, can not be used for anesthesia. Can be used for pain and itching.

Benzazacaine hydrochloride is usually made into powder or ointment for the treatment of wounds, ulcers, burns, skin abrasions and hemorrhoids.

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Lidocaine HCl

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C14H23ClN2O
  • Molecular Weight 270.7982

lidocaine hydrochloride is chemically designated as acetamide, 2 - (diethylamino)-n-(2, 6-dimethyl) -, monohydrochloride and has a molecular weight of 270.8. the molecular formula is c14h22n2o.hcl. for lidocaine hydrochloride solutions containing epinephrine, which is chemically designated as (-) -3, 4-dihydroxy--[(methylamino) methyl] benzyl alcohol and has the molecular weight of 183 21. its molecular formula is c9h13no3. lidocaine sterile lidocaine hydrochloride with epinephrine hydrochloride solution of lidocaine hydrochloride injections are sterile pyrogen-free solutions, water containing a local anesthetic with or without epinephrine and are administered intravenously injection.dosage forms listed as xylocaine-mpf indicates a single dose solutions are methyl araben ree p f (mpf).



lidocaine hydrochloride application



lidocaine hydrochloride (lid-oh-kane hi-droh-clor-ride) is a medicine which is used in local anesthesia and heart rhythm disorders.



the information in this medicine guide for lidocaine hydrochloride varies according to the condition being treated and the special preparation used.



lidocaine hydrochloride stops the feeling of pain. it can be used during medical procedures. lidocaine hydrochloride also can be used to treat un certain types of irregular heartbeats.



lidocaine hcl used topically to relieve itching, burning and pain of inflamed skin inhibit ion fluxes across membranes, particularly sodium transport across the cell membrane, increase decreases depolarization phase action potential blocking nerve action potential.


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Prilocaine Hcl

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C13H20N20
  • MW 220.31

Propitocaine hydrochloride is a local anesthetic of the amino amide type first prepared by Claes Tegner and Nils L? Fgren. In its injectable form, it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used forintravenous regional anaesthesia.


In some patients, a metabolite of prilocaine may cause the unusual side effect of methemoglobinemia, which may be treated with methylene blue.



Local anesthetic is a substance that causes loss of sensation only to the area to which it is applied without affecting consciousness. Most local anesthetics structures have amino-ester or an amino-amide group which are linked to hydrophilic (secondary or tertiary amine) and to hydrophobic group (aromatics) on the other side.



Local anesthetics, long duration, lower toxicity, chemicals that are also small Suitable for epidural anesthesia, block anesthesia and infiltration anesthesia, etc.

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Tetracaine Hcl

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • EINECS 205-248-5
  • Molecular formula C15H25ClN2O2
  • Molecular weight 300.82
  • Appearance White crystalline powder

Tetracaine HCL is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.



Tetracaine, also known as Amethocalne, Dlcalne, Pontocaine, Decicaine, is a kind of Local Anesthetic. It is highly soluable in Non-polar solvent, and combines with Plasma protein by 85%.



Tetracaine takes effect very fast. It just needs 1-2 min. Usually, its half life is 5-10 min. And it can lasts for 20 40min.



It is widely used as pain-killer in Mucosal surface anesthesia, Conduction anesthesia, Epidural anesthesia, Spinal anesthesia, Ophthalmic topical anesthesia and so on.



Tetracaine is more efficient than Procaine. It is 10-15 times more effective than it.

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