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Drostanolone Propionate (masteron)

  • Min. Order (MOQ) 10 Gram
  • MF C23H36O3
  • MW 360.53
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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:

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Drostanolone Enanthate

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

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Tamoxifen Citrate (nolvadex)

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C32H37NO8
  • Application Treatment of breast cancer.
  • MW 563.64
  • EINECS 259-415-2

(1)Similar with Clomid



Nolvadex (tamoxifen citrate) is very comparable to Clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure. It is not correct that Nolvadex reduces levels of estrogen: Rather, it blocks estrogen from estrogen receptors and, in those tissues where it is an antagonist, causes the receptor to do nothing.



(2) Bodybuilders have made excellent gains while using Nolvadex



The claim that Nolvadex reduces gains should not be taken too seriously. The fact is that any number of bodybuilders have made excellent gains while using Nolvadex.



The belief that it reduces gains seems to stem from the fact that the scientific literature reports a slight reduction from use of Nolvadex.

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Clomiphene Citrate

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Formula C32H36ClNO8
  • Molecular Weight 598.09

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.

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Exemestane (aromasin)

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C20H24O2
  • Molecular Weight 296.40

1. Exemestane is a steroidal Aromatase Inhibitor (AI) that is most commonly known as Aromasin. In fact, the Aromasin brand name is the only pharmaceutical grade brand of the Exemestane AI due to the tight patent Upjohn has maintained on the product. While tightly controlled by the pharmaceutical giant, Aromasin is available in numerous countries around the globe.



2. Aromasin was first released on the U.S. market in 2000 after shortly gaining FDA approval a few months prior in 1999. The primary purpose of use as with most AI's would be to combat breast cancer in post-menopausal women. Shortly after, the AI would begin to gain a lot of popularity among anabolic steroid users for its ability to protect against estrogenic related side effects. This action is very similar to the older and more popular AI's in Arimidex and Femara It would also gain a fair amount of popularity in Post Cycle Therapy (PCT) plans among steroid users. It was not the first AI to gain such popularity but would prove to be a little more advantageous for this purpose than most AI's.


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Formestane

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C19H26O3
  • MW 302.41

A. Formestane is a synthetic steroidal substance with antineoplastic activity. Formestane binds irreversibly to and inhibits the enzyme aromatase, thereby blocking the conversion of cholesterol to pregnenolone and the peripheral aromatization of androgenic precursors into estrogens.



B. Formestane is a drug that has been previously used in breast cancer treatment. Like most drugs which have some sort of phsyique usage, athletes eventually get a hold of it. Formestane is currently one of the best legal anti-estrogens out there. It is classified as an irreversible arromatase inhibitor, meaning, it destroys the aromatase enzyme.

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CJC1295 Peptides Growth Hormone

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C152H252N44O42
  • Molecular Weight 3367.97
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CJC-1295 is basically a peptide hormone that acts similar to growth hormone releasing hormones (GHRH), it is beneficial to athletes because it can bioconjugate with circulating albumin and increase the time it can be used for medical purposes. It achieves this by preventing degradation of its amino acids. With a single dose, it can remain in the body for quite a few days and can cause the growth hormone to be released many times per day. This reduces the frequency of injections needed.



CJC-1295 increases the production of growth hormone as well as IGF-1 - which has anabolic effects in adults. However, it does not increase the levels of prolactin - high levels of which can create impotence and mental health problems in men. By increasing these two hormones, it enhances protein production in the body, which in turn, boosts muscle mass. It also induces lipolysis - the breakdown of fat tissue, boosts recovery from injuries, increases bone density, and also reduces aging factors like skin wrinkles. It can also stimulate cell growth, due to which it can be used to treat withered tissue or organs.

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CJC1295 With DAC

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C152H252N44O42
  • Molecular Weight 3367.2
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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

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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MT-2

  • Min. Order (MOQ) 10 Gram
  • MF C50H69N15O9
  • MW 1024.18
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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

  • Min. Order (MOQ) 10 Gram
  • MF C42H50N8O5
  • MW 746.91
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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
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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.


.

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Tesamorelin

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



It was originally tested for intranasal administration in treating female sexual dysfunction but this application was temporarily discontinued in 2008 after concerns were raised over adverse side effects of increased blood pressure. As of March, 2012, Palatin is conducting a human Phase 2B study using a new subcutaneous drug delivery system that appears to have little effect on blood pressure.

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Gonadorelin

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram

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.



Application:



Gonadorelin is a medicine that is the same as gonadotropin-releasing hormone (GnRH) that is naturally released from the hypothalamus gland.



GnRH causes the pituitary gland to release other hormones (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]). LH and FSH control development in children and fertility in adults.



Gonadorelin is used to test how well the hypothalamus and the pituitary glands are working. It is also used to cause ovulation (release of an egg from the ovary) in women who do not have regular ovulation and menstrual periods because the hypothalamus gland does not release enough GnRH.



Gonadorelin is used to test how well the hypothalamus and the pituitary glands are working. It is also used to cause ovulation (release of an egg from the ovary) in women who do not have regular ovulation and menstrual periods because the hypothalamus gland does not release enough GnRH.



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.



The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use.

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Epitalon

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Color C14H22N4O9
  • Molecular Weight 390.3459
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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.




Application:



After 12 years of taking the peptide Epitalon several weeks per year, the scientists subjects in this study, showed a lifespan 30 to 50% longer than those who didn't take it. Taking Epithalon gave them an average of 7 extra years of life in excellent health



This clinical study lasted only for 12 years, and they gained 7 extra years of life, but of course, nothing stops you from taking Epitalon forever, and live healthy for ever !



Rejuvenated cells are also the key to an efficient immune system. For that reason, taking Epitalon will also keep your body fit against all the diseases.



This small peptide is simply made of 4 amino acids, but its effect on the body is the most amazing thing that we had ever imagined and witnessed.



This amazing oral supplement is taken by numerous doctors around the world, and a few privileged patients that consult them. Now you can have it too !



These entrepreneurs decided to enlarge the circle of the privileged humans that will be able to prolong their lives without limits, by offering Epitalon in its purest form and for a much lower price than it was available to day through medical professionals. They are the first to bring this product to the public market, as it was only available to medical professionals until today.


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GDF-8

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gallon
  • MF C221H366N72O67S
  • Purity >98%
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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

  • Min. Order (MOQ) 1 Bottle(s)
  • Molecular Formula C14H22N4O9
  • Appearance White to off-white crystalline powder
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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.



follistatin 344 dosage



follistatin is recommended for research, but people who have tried it themselves typically take injection 100 mcg/day of dose via injections for 10 to 30 days. Ideally it can be taken every third day. People who have taken doses up to 200 mcg have not shown suffered from any adverse effects than the ones who have taken lower doses.


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Pentadecapeptide BPC 157

  • Min. Order (MOQ) 1 Bottle(s)
  • Molecular Formula C62H98N16O22
  • Molecular Weight 1419.53552
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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

  • Min. Order (MOQ) 10 Gram
  • MF C15H10I4NNaO4
  • MW 798.85
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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

  • Min. Order (MOQ) 10 Gram
  • Color C7H15NO3
  • MW 161.2
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1. Carnitine is a kind of b-class vitamin. Owing to its similar structure as amino acids, some people therefore also classify it as an amino acid. Its main function is to supply energy through facilitating the transport of long chain fatty acids. This prevents the fat accumulation in the heart, liver and skeletal muscle. It can control diabetes, fatty liver, and the fat metabolism disorder in heart disease. Taking carnitine can reduce damage to the heart. It can lower the level of blood triglyceride and also have certain role in boosting weight loss. Carnitine can further enhance the antioxidant effect of vitamin e and vitamin c.



2. Carnitine deficiency is sometimes congenital such as genetically deficiency of carnitine synthesis with symptoms including heartburn, muscle atrophy and obesity. Men need more carnitine than women. Vegetarian are more prone to get carnitine deficiency.


3. If the body has sufficient iron, thiamin, vitamin b6, lysine, methionine and vitamin c, carnitine would not be lacking. Carnitine-rich foods contain meat and offal.



4. Synthetic carnitine is divided into three forms including l-body, dextral and racemic with l-carnitine having the best efficacy.



5. L-carnitine is a kind of compound with various kinds of physiological activities. Its major function is to promote the beta-oxidation of fatty acid as well as regulate the acyl ratio inside mitochondrial to affect the energy metabolism. L-carnitine can participate in the transport of branched chain amino acid metabolites, and thus promoting the normal metabolism of branched chain amino acids. In addition, l-carnitine can take effect in the elimination and utilization of ketone bodies and play a role of biological antioxidants for scavenging free radicals, maintain the stability of the membrane, improve animal's immunity and the ability of anti-stress and disease resistance.

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Dmaa

  • Min. Order (MOQ) 10 Gram
  • MF C7H17N. HCl
  • MW 151.72
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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

  • Min. Order (MOQ) 10 Gram
  • MF C33H57N11O9
  • MW 751.9
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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.

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Synephrine

  • Min. Order (MOQ) 10 Gram
  • Color C9H13NO2
  • MW 167.21
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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

  • Min. Order (MOQ) 10 Gram
  • MF C22H21Cl3N4O
  • MW 463.79
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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

  • Min. Order (MOQ) 10 Gram
  • MF C29H53NO5
  • MW 495.73
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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.

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Calcium Pyruvate

  • Min. Order (MOQ) 10 Gram
  • MF C6H6CaO6
  • MW 214.19
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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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Prilocaine Hcl

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  • Min. Order (MOQ) 10 Gram
  • MF C13H20N20
  • MW 220.31
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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
  • Molecular formula C15H25ClN2O2
  • Molecular weight 300.82
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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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Ropivacaine Mesylate

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  • Min. Order (MOQ) 10 Gram
  • MF C18H30N2O4S
  • MW 370.5068
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Razivacaine Mesylate, is a new long-acting amide type local anesthetic, pure isoleine, with anesthesia and analgesic dual role, high concentrations of ropivacaine mesylate (molecular formula C17H26N2O CH4O3S, English name Ropivacaine Mesylate Injection) Resulting in surgical anesthetic effects, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline. Clinical mainly for surgical anesthesia, local anesthesia and acute pain control.




Pharmacological effects



With anesthesia and analgesic dual role, high concentration can produce surgical anesthesia, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline.

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Chloroprocaine HCl

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • M.F C13H20Cl2N2O2
  • M.W 307.21600
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Chloroprocaine hydrochloride is a short-acting spinal anesthesia performed under the waist. Anesthesia of spinal nerves using spinal anesthesia, so that patients remain sober, but in the course of surgery will not be pain.



Application



Chloroprocaine (trade name Nesacaine, Nesacaine-MPF) (usually in the form of hydrochloride in the above-mentioned trade name) is a local anesthetic administered by injection during surgery and during childbirth.


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Beta-Alanine

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C3H7NO2
  • MW 89.09
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Beta-alanine is one of the non-essential amino acids that are not readily consumed in conventional mixed diets of chicken, beef, whey or fish. Because of this fact, it can make your dosage more difficult.


When the body is absorbed, -alanine will be converted to carnosine, which will help improve your physical strength, strength and muscle development.



For those who are heavily trained, this will make them harder in the gym, which leads directly to increased muscle harvest.



How does the Beta-alanine in gym work?



It is supplemented with -alanine, which can effectively increase the level of the body's carnosine, which can be observed up to twelve weeks after continuous use.


Since you can not take carnosine alone, it is the best way to choose to add -alanine.



More specifically, what is -alanine in the body, we need to know more about its relationship with carnosine. It is through the direct role of -alanine, carnosine really play its influence, so this is the key to understanding this supplement.



Troponin can be found in two different muscle types of the body, but with a higher concentration in the second fiber, which will be more for maximum strength and intensity exercise. When high-intensity exercise occurs, our body begins to accumulate a lot of hydrogen ions, so that the body produces a more acid state. This increase in hydrogen ions can also lead to the accumulation of lactate in the body, which in the movement will cause fatigue, and eventually lead to movement completely stopped.


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L-Glutamine

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  • Min. Order (MOQ) 10 Gram
  • MF C5H10N2O3
  • MW 146.14
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L-Glutamine is an amino acid (a structural unit of protein) that is naturally found in the body.



L-Glutamine is used to treat some side effects of medical treatment. For example, it is used for side effects of cancer chemotherapy, including diarrhea, pain and swelling in the mouth (mucositis), nerve pain (neuropathy), and muscle and joint pain caused by cancer drug paclitaxel. Glutamine is also used to protect the immune system and digestive system of people receiving radiotherapy for esophageal cancer. In addition, glutamine is used to improve the recovery of bone marrow or postoperative bowel surgery, increase the health of people with traumatic injury, and prevent the infection of critically ill patients.



Some people use glutamine as a digestive system disorder, such as gastric ulcer, ulcerative colitis and Crohn's disease. It is also used for depression, mood, irritability, anxiety, insomnia and enhanced exercise performance.



L-glutamine powder for health is supplied with amino acid L-glutamine. It is actually the most common amino acid in the muscle, accounting for 61% of the bone tissue, which is essential for the immune system and the health of the digestive tract. In the intestine, L-glutamine enhances the healing and repair of mucosal cells, especially in leaked intestinal conditions. Glutamine also contributes to the best muscle growth and strength, and has been shown to be particularly useful in helping to prevent muscle wasting. In intense exercise training or gastrointestinal disorders, it may become vital in context.




Prodcut application



L-glutamine powder may help to address certain symptoms associated with mild inflammation of enteritis; this is because it is possible to protect the mucosa of the gastrointestinal tract. In particular, glutamine can promote the development of intestinal cells, which are found in gastrointestinal lining to support digestion and nutrient absorption of cells.



L-glutamine powder can also maintain the strength of the immune system by supporting leukocyte function. This is important because white blood cells (macrophage neutrophils and lymphocytes) can resist infection, otherwise it will make you feel sick.


Although your body is able to produce glutamine, glutamine supplements may provide the necessary ascension when you are at high levels of physical or mental stress. This is why each L-glutamine powder provides nearly 5 grams of free form of L-glutamine.

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7-keto Dhea

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C19H26O3
  • MW 302.41
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7-Keto-DHEA (also known as 7-Keto, 7-ketodehydroepiandrosterone, or 7-oxodehydroepiandrosterone) is a steroid produced by metabolism of the prohormone It is often used as the acetate ester prodrug 7-Keto-DHEA acetate.



7-Keto is unique among other derivatives of DHEA because of its oxygenated 7-position. This molecular configuration imparts different characteristics to the molecule, and research reveals that 7-Keto DHEA has multiple distinct effects in the body.Such as, Increased metabolism/weight loss, Age-related immune enhancement

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4-androstenedione

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • M.F C19H26O2
  • M.W. 286.41
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4-Androstenedione, popularly known as Androstenedione or 4-AD, has many other names. The synonyms of 4-Androstenedione include 17-ketoestosterone, Andro, Androstene, Androst-4-ene-3, 17-dione, 4-Androstene-3, 17-dione, 4-Androstenedione, Androtex, 63-05-8, 3, 17-Dioxoandrost-4-ene, Fecundin,


4-AD, SKF 2170 etc. If you are not sure whether it is 4-Androstenedione, make sure that there is only one CAS number for it, and it is 63-05-8.



According to Wikipedia, 4-Androstenedione is a 19-carbon steroid hormone produced in the adrenal glands and the gonads as an intermediate step in the biochemical pathway that produces the androgen testosterone and the oestrogens oestrone and oestradiol. 4-Androstenedione originates either from the conversion of dehydroepiandrosterone (DHEA) or from 17- hydroxyprogesterone. Conversion of dehydroepiandrosterone to androstenedione requires 3--hydroxysteroid dehydrogenase. 17- hydroxyprogesterone, on the other hand, requires 17, 20 lyase for its synthesis. Thus, both reactions that produce androstenedione directly or indirectly depend on 17, 20 lyase. 4-Androstenedione is further converted to either testosterone or oestrogen. Conversion of 4-androstenedione to testosterone requires the enzyme 17hydroxysteroid dehydrogenase, while conversion of androstenedione to oestrogen (e.g. oestrone and oestradiol) requires the enzyme aromatase. The production of adrenal androstenedione is governed by ACTH(Adrenocorticotropic Hormone), whereas production of gonadal androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total androstendione .



Anabolic steroids are commonly utilized to treat people who have a hormone deficiency or who have muscle wasting due to cancer or HIV. They have also been utilized as performance enhancing drugs to increase muscle strength and size for competitive sports. Supplements containing androstenedione were introduced in the mid 1990s and were promoted as a natural way to help increase strength and muscle mass and to combat the effects of the aging process in older men, much of which is attributed to declining testosterone levels. Like DHEA, androstenedione is a naturally derived precursor to testosterone.


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1,4-Androstadienedione

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  • Min. Order (MOQ) 10 Gram
  • Molecular Formula 19H24O2
  • Molecular Weight : 84.39
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Androstadienedione is used for simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroid, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.



Androstadienedione is the precursor to bolde-none, and as of January 4, 2010 is a Schedule III Controlled Substance. In 2004 the United States Congress passed the Anabolic Steroid Control Act of 2005 which placed 36 steroids and over the counter pro-hormones into schedule III of the Controlled Substances Act.


Application:



4-Androstenedione is the common precursor of male and female sex hormones. Some 4-Androstenedione is also secreted into the plasma, and may be converted in peripheral tissues to testosterone and estrogens.


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Androstenedione

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  • Min. Order (MOQ) 10 Gram
  • Molecular Fomule C19H2602
  • Molecular Weight 286.41
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In the body, it is produced by the adrenal glands and gonads from dehyroepiandrosterone (DHEA or 17- alpha-hydroxyprogesterone). DHEA is converted into androstenedione an the enzyme in the gonads. Androstenedione is a precursor of testosterone. Once the androstenedione is taken orally, it makes it into the liver where it is almost destroyed completely, the amount that survives combine with the enzyme 17 beta-hydroxysteroid dehydrogenase to make testosterone as shown in the figure below. Taking androstenedione orally can increase androstenedione blood serum levels over 300 percent after about 2 hours and remaining high for 4 hours. Studies have shown that androstenedione by itself does not produce increased muscle mass but once converted into testosterone in the liver, the elevated testosterone levels may lead to muscle mass gain, but not proven.



The problem with androstenedione is that it metabolizes quickly into estrogens, estrone and estradiol as shown in the figure. These two products can stay in the body for days as opposed to the androstenedione, which diminishes within hours. Estrogens have an opposite effect than testosterone; they suppress fat-loss and tissue healing. Estrogen levels can be monitored and managed by blood and saliva testing in order to be kept under control if using the product.



A study published by the American Medical Association (AMA), investigated the anabolic effects of orally taking androstenedione with men that had none or little weight training experience. The study focused on short-term effects of a single 100 mg dose followed by a longer term of 300 mg for an eight-week program of weight training. This study proved the androstenedione increased androstenedione, estrone and estradiol levels within the body. Luteininzing Hormone (LH), folical-stimulating hormone (FSH) which are involved in the production of testosterone within the body, was unaffected as were liver enzymes. This suggests that ingesting androstenedione would not affect the body in producing testosterone as in the case where elevated levels of testosterone may affect the self-production of the testosterone. The study only stated that androstenedione can produce elevated testosterone levels, and not that the levels of testosterone were not sufficient to produce enhanced performance.

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Methoxydienone

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C20H28O2
  • MW 300.44
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Methoxydienone particular to a process of synthesis of levonorgestrel, Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception.



Methoxydienone is a progestin derived steroid and not a 17-alpha alkylated steroid. Methoxydienone is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects. Great for those needing fast weight gain and unconcerned about looking smooth or fat.

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Norandrostenedione

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C18H24O2
  • MW 272.38
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Norandrostenedione is a molecule derived from Nortestosterone. It converts to Nandrolone when assimilated into the body through absorption. Nandrolone provides a chemical foundation for Deca-Durabolin. Acting as an anabolic composite which apportioned its nutrients helps to create a leaner body mass and uses up stored fat more efficiently.



This in turn provides rapid recovery mechanism to exhausted muscle mass, with little or no side effect. Norandrostenedione does not aromatize or synthesize to estrogen when taken and was noted as being able to improve the individuals mood.



Norandrostenedione is a precursor of the anabolic steroid nandrolone. Until 2005 Norandrostenedione was available without prescription in United States, where it was marketed as a prohormone, but it is now classified as a Schedule III drug. It is also banned from use in many sports, including the Olympic Games, under the World Anti-Doping Code. Norandrostenedione is readily metabolized to nandrolone after oral administration, but its potency to transactivate the androgen receptor dependent reporter gene expression is 10 times lower as compared to dihydrotestosterone (DHT).


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Methyldienedione

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C18H22O2
  • Molecular Weight 270.37
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Estra-4, 9-diene-3, 17-dione is a powerful pro-steroid chemically similar to the anabolic agent Trenbolone .



When in the body , estra-4, 9-diene-3, 17-dione completes the conversion to . Trenbolone is a potent anabolic steroid , active pharmaceutical ingredientsr which binds to specific receptors present in reproductive tissue , muscle and fat .



Estra Diene Dione (estra-4, 9-diene-3, 17-dione) is an anabolic steroid and a precursor to Estra Diene Dione . It became a controlled substance in the US on January 4, 2010, and is classified as a Schedule III anabolic steroid under the United States Controlled Substances Act. Previous to this, it was sold as a bodybuilding supplement within the United States , and often mistakenly marketed as a prohormone for trenbolone, a veterinary steroid . Prior to its scheduling , it was part of a number of supplements that were seized during FDA enforcement for selling unapproved new drugs . The actual target steroid, Estra Diene Dione has some structural similarity to trenbolone , but lacks the 11-carbon -ene bond .

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Methylepitiostanol/Epistane

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C20H32OS
  • Melting Point 168-169℃
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Epistane is not just a Pro-hormone, it is already a very powerful active compound that attaches to and activates Androgen Receptor sites.


Epistane is a designer hormone designed to provide you with very good anabolic effects and can get limited side effects from Androgens.



Epistane is a DHT derivative that is similar to epitiostanol, it is an oral active anti-estrogenic dry compound that will aid users in adding lean muscle mass as well as cutting fat. Epistane has an additional single methyl group, which helps it give a much stronger anabolic release, but does cause less damage to the liver than most methylated compounds thus allowing for slightly longer cycles (4-6 weeks). As a matter of fact, on paper it has a 1100:91 anabolic to androgenic rating. Thanks to its DHT structure, Epistane does not aromatize and is non-progestagenic, it may also reduce estrogen while on cycle, so you will not need an anti-aromatase while on cycle with Epistane. This basically means that while on Epistane, estrogen related side effects like gyno and progesterone related side effects like sensitive breast tissue are virtually non-existent. Users will experience little to no side effects while on Epistane, making it an ideal beginner prohormone.



Interestingly, epistane is very comparable to winstrol and turinabol in that it will not increase water retention at all. So the user should not expect to put on water weight on it, and if your goal is mass and moving the scale up, you will probably be disappointed with your results when taking epistane. Strength trainers can enjoy strength gains, but it would be wise to stack Epistane with some other wet compound like dianabol, which would help sustain strength gains.



Furthermore, since oestrogen is the main culprit for water retention, bloat and fat gain the anti-oestrogenic effect from. Epistane means it is a prohormone which offers a high quality look to the physique. Thus Epi is a very favourable prohormone to use during cutting phases with a calorie restricted diet. However, Epistane is also noted to greatly increase the rate of protein synthesis and adds to strength gains which means it can equally be used to add lean muscle mass without the addition of unwanted fat and subcutaneous fluid retention. Epistane is an extremely versatile prohormone suitable for both bulking cycles and cutting cycles.Generally Epistane is reserved for cutting cycles but it is strong enough to be used in bulking cycles.

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Sunifiram

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C14H18N2O2
  • Molecular Weight 246.304
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1. Sunifiram is one of the newest nootropics on the market showing very promising initial results. It falls into the ampakine family of nootropic supplements because it is an ampa agonist.some reviews have suggested that it works similarly to piracetam but it is over 1000 times more potent than piracetam for the same dosage.



2. Sunifiram is highly effective at boosting memory function as well as attention span, learning, decision making and alertness.a lot of initial reviews and user experiences suggest that sunifiram could become one of the most popular nootropic study aids for improving concentration.



3. Sunifiram has a similar chemical structure to piracetam but initial studies show that it is significantly more potent than this widely used racetam.sunifiram so far shows very positive results as memory enhancer and it is currently being investigated for potential treatment of alzheimer's and other diseases related to cognitive decline.



4. User reviews and sunifiram logs point to the fact that this supplement makes information recall much easier and helps you think more clearly. Sunifiram is being compared to noopept quite a bit because of their similar potency levels.initial observations suggest that sunifiram is better as a memory booster while noopept might have an edge on increasing focus and alertness.


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Noopept

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C17H22N2O4
  • MW 318.37
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Noopept is a very potent Ampakine nootropic drug, and the nootropics brand name for the research peptide "N-phenylacetyl-L-prolyglycine ethyl ester." Noopept capsules is an entirely synthetic molecule, and has a similar effect to Piracetam, though its effects are quoted as up to 1000 times stronger. Effects are very much like a "mega dose" of piracetam (when a nootropic is taken in dosages up to 8 times the usual amount) and even provides a slight psycho stimulatory effect when taken in low to moderate dosages. Typical dosages of Noopept range from 10mg at the lower end, to a maximum effective dosage of 30mg per day. When higher dosages are taken then this, tiredness can result, negating many of Noopept's benefits, alongside tolerance and an increase in Noopept's negative side effects. Noopept, for best results, should be taken 3 times daily (preferably once with each meal) and should be taken with a choline source (preferably CDP Choline) for maximum results. Noopept, like Piracetam, displayed many neuroprotective effects in rats and mice during testing. More studies are needed to confirm exactly what causes Noopept's supposed neuroprotective effect.


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Pramiracetam

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C14H27N3O2
  • MW 269.38
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Pramiracetam is a lipid-soluble nootropic that is found within the racetam group. Although it has a structure very similar to Aniracetam, it is much stronger. Many researchers believe that the potency of Pramiracetam is actually 15 to 20 times stronger than Piracetam. Some studies have even reported that Pramiracetam is 30 times more potent.



Like all other nootropics, Pramiracetam is a cognitive enhancer. It goes by the name; Remen, Pramistar, or Neupramir. Pramiracetam is one of the strongest Nootropics available, as it increases both mental performance and certain aspects of intelligence.



Since this supplement is so potent, a lot less is needed in order to achieve a desired effected. It is believed to increase long-term memory making it a possible treatment option for Alzheimer's patients.



Nootropics are a category of chemicals that are referred to as Smart Drugs, which are proving to be advantageous as memory, neural, intelligences and cognitive enhancers, that are beneficial as supplements as well as therapeutic in the treating of certain diseases.

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Aniracetam

8,433.50 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C12H13NO3
  • Molecularweight 219.24
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Aniracetam seems to enhance the results of corticol GABAergic hang-up separate from NMDA. Aniracetam definitely seems to be in a position to potentiate signalling through nicotinic 42 receptors with 3.1nM through friendships with GS healthy proteins, separate from necessary protein kinases.



Aniracetam has been shown with 50mg/kg oral consumption (subjects) to lower the particular turn over prices for dopamine within the striatum and minimizing dopamine levels in the hypothalamus gland as well as striatum; serotonin levels lowered in the hypothalamus gland however improved inside the cortex along with striatum, exactly where it reduced return (hypothalamus gland) and also boost return (cortex, striatum, brain base).[ Aniracetam seems to be able to reduce destruction implemented to memory and also studying incapacity brought on by various real estate agents along with shock to the system including cholinergic antagonists, cerebral ischaemia along with electroconvulsive shock.


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Oxiracetam

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Formula C6H10N2O3
  • Purity 99%
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Oxiracetam and piracetam, aniracetam is currently commonly used in clinical three kinds of metabolic improvement of drugs for the pyrrolidone derivatives, by the Italian company Skebiqim in 1974, successfully developed, listed in 1987 . The mechanism of action of oxiracetam is similar to that of piracetam, which can promote the synthesis of phosphorylcholine and phosphoryl ethanolamine, increase the ratio of ATP / ADP in the brain, increase the synthesis of protein and nucleic acid in the brain, and improve the senile dementia And memory impairment in patients with memory and learning function. In animal experiments, it can be found in a variety of behavioral experiments can improve memory function and learning performance, can reduce the brain electrical shock caused by memory impairment, antagonistic spontaneously hypertensive cerebrovascular injury in rats learning ability reduction, it can Increased acetylcholine in the cortex and hippocampus of the rat was enhanced in favor of choline uptake. For brain damage and caused by neurological deficits, memory and treatment of mental retardation.


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Coluracetam (MKC-231)

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • Molecular Weight 341.4042
  • Molecular Formula: C19H23N3O3
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Coluracetam is a nootropic drug of the racetam family. Coluracetam was initially developed and tested by the Mitsubishi Tanabe Pharma Corporation for Alzheimer's disease. After the drug failed to reach endpoints in its clinical trials it was in-licensed by BrainCells Inc for investigations into major depression disorder (MDD), after being awarded a "Qualifying Therapeutic Discovery Program Grant" by the state of California.



Findings from its Phase 2a clinical trials have suggested that it would be an ideal medication for co-morbid MDD with generalized anxiety disorder (GAD). BrainCells Inc is currently out-licensing the drug for this purpose. It may also have potential use in prevention and treatment of ischemic retinopathy and retinal and optic nerve injury.



Coluracetam (MKC-231) is a synthetic Racetam drug purported to be a Nootropic compound. It does not have a large body of evidence investigating it, but the mechanisms of action (as well as structute) appear to be very distinct from other racetam compounds like Piracetam or Aniracetam.

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Carphedon

835 /Gram Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MW 218.25
  • MF C12H14N2O2
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Carphedon is a relatively new suppository supplements, which are said to be 60 times higher than piracetam's strength.



The effect of Carphedon is roughly the same as that observed when using piracetam: improving learning, memory, focus and mood.



Other benefits can include increased creativity, better solving problems and reasoning, enhancing awareness and improving physical fitness.



Carphedon is particularly effective in improving energy levels and improving power, which is why it is often used as a research drug.



May even benefit adults with ADD or ADHD as well as individuals with chronic low energy and fatigue.



This push oot agent is known for providing doping effects rather than actually doping, which is why many people like it as a substitute for Adderall.




Carphedon application



Carphedon seems to be a model of recommended drugs for the body and brain.



Although many mental supplements can have a positive effect on physical performance and psychological performance, in fact, Caldorfen was originally developed for athletes to use.



The first to use this medicine is to increase the body's cold and painful threshold. By stimulating the dopamine receptor in the brain, it may reduce the body's sensitivity to pain.



The chi-square is also considered to improve the neuromuscular connection, leading to better sporting activity and coordination. Some bodybuilders and athletes still use this compound as a supplement before exercise.


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Phenibut

835 /Gallon Get Latest Price
  • Min. Order (MOQ) 10 Gram
  • MF C10H14ClNO2
  • C10H14ClNO2 215.68
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1.Phenibut is a derivative of the naturally occurring inhibitory neurotransmitter GABA.



2.Phenibut is used by bodybuilders to reduce fatigue and improve neurological functions.



3.Phenibut has been and is still used medically to treat stress, relieve tension, improve sleep, and as a potentiate for other medications.



4 Phenibut Induce relaxation and improve mental function.



5 Phenibut improve cognition and has nootropic and anxiolytic properties.



6 Phenibut Help with fear, anxiety, tension, congnitive disorders, and also neurotic patients and insomnia, depression and asthenia.



7 Phenibut Used for post-traumatic stress and vestibular problems.



Function



1.Phenibut is a derivative of the naturally occurring inhibitory neurotransmitter GABA.



2.Phenibut is used by bodybuilders to reduce fatigue and improve neurological functions.



3.Phenibut has been and is still used medically to treat stress, relieve tension, improve sleep, and as a potentiate for other medications.

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ADRAFINIL

  • Min. Order (MOQ) 10 Gram
  • MF C15H15NO3S
  • MW 289.35
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Adrafinils (Olmifon) is a Nootropic compound, considered to be a eugeroic.




In addition to being able to produce cognitive benefits, Adrafinils and other eugeroics act as stimulants.


Adrafinils is particularly considered to be effective for increasing daytime wakefulness and alertness as well as positively affecting mood, energy levels, motivation and reaction time.


Adrafinil is a mild central nervous system stimulant drug used to relieve excessive sleepiness and inattention in elderly patients. It is also used off-label by individuals wishing to avoid fatigue, such as night workers or others who need to stay awake and alert for long periods of time.

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