Other Chemicals

Product link to :www.astersteroids.com/99-purity-t3-triiodothyroni , ne- bodybuilding-dose-and-function-for-bodybuil , ding-cycle/ Product Name:T3 Chemical name : 3,3',5-Triiodo-L-thyronine, sodium salt CAS NO : 55-06-1 Molecular formula : C15H11I3NNaO4 EINECS : 200-223-5 Molecular Weight : 690.9706 Purity: 99% Packing: sample 10g,100g500g,1kg Storage: Shading, confined preservation Water-solubility: 4 M NH4OH in methanol: 125 g/5mL, clear, yellow-brown Usage : It affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate, such as, treatment of depressive disorders and use as a fat loss supplement. Treatment of depressive disorders The addition of triiodothyronine to existing treatments such as SSRIs is one of the most widely studied augmentation strategies for refractory depression,however success may depend on the dosage of T3. A long-term case series study by Kelly and Lieberman of 17 patients with major refractory unipolar depression found that 14 patients showed sustained improvement of symptoms over an average timespan of two years, in some cases with higher doses of T3 than the traditional 50 μg required to achieve therapeutic effect, with an average of 80 μg and a dosage span of 24 months; dose range: 25-150 μg.The same authors published a retrospective study of 125 patients with the two most common categories of bipolar disorders II and NOS whose treatment had previously been resistant to an average of 14 other medications. They found that 84% experienced improvement and 33% experienced full remission over a period of an average of 20.3 (standard deviation of 9.7). None of the patients experienced hypomania while on T3. Use as a fat loss supplement 3,5-Diiodo-L-thyronine and 3,3'-diiodo-L-thyronine are used as ingredients in certain over-the-counter fat-loss supplements, designed for bodybuilding. Several studies have shown that these compounds increase the metabolization of fatty acids and the burning of adipose fat tissue in rats.

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Product link to :www.astersteroids.com/high-quality-clomiphene-cit , rate- powder-for-men-bodybuilding-safe-shipping , / Product name:clomiphene citrate Other name:Clomifene citrate, Clomid Molecular Formula: C26H28ClNO, C6H8O7 Molecular Weight: 598.1 CAS: 50-41-9 Appearance: White or milky white crystalline powder Purity: 99% Packing: sample 10g,100g500g,1kg Storage: Shading, confined preservation Clomid was one of the original drugs used in post-cycle-therapy to stave off gynocomastia and raise the body's natural test osterone levels. There are some side effects involved with heavy prolonged use, such as vision problems, and there are more effective substances on the market that do the same thing, but Clomid is still an effective and inexpensive compound for any athlete's post-cycle-therapy. For athletic purposes, Clomid does not offer a tremendous benefit to women. In men however, the elevation in both follicle stimulating ho rmone and (primarily) luteinizing ho rmone will cause natural test osterone production to increase. Clomid and H CG are also occasionally used periodically during a stero id cycle, in an effort to prevent natural tes tosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time.

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Product link to :www.astersteroids.com/widely-used-tamoxifen-99-pu , rity- powder-for-sale-safe-shipping/ Product Name: Tamoxifen CAS 54965-24-1 MF:C32H37NO8 MW:563.64 Appeara , nce: white crystalline powder Purity: 99% Packing: sample 10g,100g500g,1kg Storage: Shading, confined preservation Usage:Applied to the treatment of advanced, recurrent breast cancer and ovarian cancer. Tamoxifen is a non steroidal anti estrogen drug, which is widely used in clinical medicine. This is a selective estrogen receptor modulator (SERM) of triphenylene series, which has the characteristics of estrogen agonists and antagonists. Therefore, it can act as estrogen in some tissues and prevent the role of estrogen in other tissues. Tamoxifen is a potent anti estrogen in breast tissue, so it is commonly used to treat hormone sensitive breast cancer in women. In some cases, it is even used as a preventive measure by women with family members with hereditary tendency of breast cancer. Among male bodybuilders and athletes, tamoxifen (unmarked) is usually used to resist the side effects caused by elevated estrogen after the use of some anabolic / androgen steroids. The main concern of the sports / bodybuilding population is the emergence of male and female breast, or the development of very ugly female breast tissue. The first thing to notice is that there may be swelling or small lump under the nipple. In the absence of surgery, if allowed to develop, it may develop into irreversible male breast development. Estrogen can also lead to an increase in the body's water content, resulting in a significant loss of muscle that begins to look smooth (or even swell) due to the retention of subcutaneous fluid. As men's estrogen levels rise, fat storage may also increase. In fact, the difference in estrogen / androgen ratio is one of the reasons why women have more body fat percentage and fat distribution (hip / thigh) than men.

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https://www.astersteroids.com/enclomiphene-overvie , w-of-increase- testosterone-levels-dosage-and-b , enefits/ Purity:99% HPLC Packing:10g,100g,500g and 1kg Min Order: Powder---10gram, Oil---50ml Payment:Bitcoin,Moneygram and Wester Union Lead time:24hours after received payment Safe shipping to US and most of Europe country As the Bodybuilders community grows and more people deal with the potential effects of lowering their testosterone levels, some drugs with the potential to increase testosterone, such as enclomiphene, have taken on an identity shift. This non-steroidal selective estrogen receptor modulator (SERM) is primarily designed to treat male hypogonadism. However, its ability to boost testosterone levels sparked interest among Bodybuilders, which led to enclomiphene’s renewed popularity. Name:Enclomiphene Other names:Androxal, (E)-clomifene, RMI-16289, enclomid, enclomifene citrate, enclomiphene citrate Cas Number: 15690-57-0 Formula: C26H28ClNO Molar mass:405.97 Half-life: 10H Learn how enclomiphene increases testosterone levels Testosterone is the male sex hormone that plays a vital role in male growth and the development of male characteristics. It is also responsible for muscle mass and strength, fat distribution, and libido. However, natural testosterone levels can decline for a variety of reasons, including age, stress, a person’s health, and the use of exogenous testosterone by bodybuilders. This is where enclomiphene comes into play. Enclomiphene acts as a SERM that works by blocking estrogen receptors in the brain. This blockage tricks the brain into thinking estrogen levels are low, which stimulates the production of two hormones: luteinizing hormone (LH) and follicle-stimulating hormone (FSH). These hormones then stimulate the testes to produce more testosterone, causing testosterone levels to rise. Enclomiphene Benefits for bodybuilders Enclomiphene’s ability to boost testosterone levels can provide bodybuilders with countless benefits. Elevated levels of testosterone can stimulate muscle cells to absorb more protein, which significantly promotes muscle growth. It can also improve strength by increasing the number of muscle fibers, which makes muscles contract more forcefully. Higher testosterone levels can speed up recovery time after exercise. This is because testosterone can increase the production of growth hormone, which is a key factor in tissue repair and healing. In addition, higher testosterone levels can boost energy levels, leading to a more powerful and productive workout. It can also improve mood by increasing levels of dopamine, a neurotransmitter associated with pleasure and satisfaction. In addition to boosting testosterone levels, Bodybuilders experience a degree of testosterone suppression during the use of supplements such as sarms. Adding enclomiphene to these supplements cycles helps maintain testosterone levels in the cycle.

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Product link to :https://www.astersteroids.com/oxymetholone-anadro , l- steroids-powder-injection-cycle-for-budybuil , ding-dosage-benefit-anadrol-50- cas434-07-1/ Product Name:Oxymetholonse Other Name:anapolon;anadrol;anadrol;Anapolon;Anasterone< , br>CAS:434-07-1 MF:C21H32O3 MW:332.48 EIN , ECS:207-098-6 Appearance:odorless white to creamy white crystalline powder. Specific optical rotation:+34~ +38° Usage: a synthetic male hormone (androgen or anabolic steroid) used to treat a low red blood cell count (anemia). It works by increasing the amount of the hormone () involved in the production of red blood cells. Anadrol is derived from Dihydrotestosterone (DHT), belonging to the family of Dihydrotestosterone (DHT) derived anabolic steroids. This means that Anadrol is basically Dihydrotestosterone modified. Other compounds belonging to this ‘DHT family’ of anabolic steroids include Winstrol, Primobolan, Masteron, Anavar, as well as several others which are all derivatives of the parent anabolic steroid DHT. The common factor in all of these DHT- derivative analogues is that, in one way or another, they are all modified forms of DHT and thus DHT could be considered the ‘parent’ or ‘progenitor’ hormone of these anabolic steroids. Anadrol differs from its parent hormone DHT by the addition of a methyl group attached to it, as well as a 2-hydroxymethylene group attached to a carbon in the first cycloalkane ring of the steroid structure. These modifications allow Anadrol to remain active in muscle tissue, which is where Dihydrotestosterone would normally be rendered inactive by its reduction to other metabolites once it enters muscle tissue. The enzyme responsible for doing this to Dihydrotestosterone, which is present in large amounts in muscle tissue, is 3-hydroxysteroid dehydrogenase. With the chemical modifications mentioned, this enzyme does not interact with Anadrol. This allows Anadrol to be heavily active in muscle tissue, and lends to its very strong potency. Anadrol possesses an anabolic rating of 320 (a little more than 3 times the strength of Testosterone, with its anabolic rating of 100). It has also been determined that Anadrol also possesses reduced androgenic strength compared to that of Testosterone, where Anadrol holds an androgenic rating of 45 (compared to Testosterone’s androgenic rating of 100)

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产品名称： 三苯乙烯基酚乙氧基化物 同义词： 三苯乙烯基酚乙氧基化聚芳基酚 聚乙二 醇聚乙二醇单（三苯乙烯基

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Tristyrylphenol Ethoxylates Synonyms: Tristyrylphenol Ethoxylates Ethoxylated Polyarylphenol Polyethylene Glycol Mono(Tristyrylphenyl)Ethers Chemical Composition: Tristyrylphenol Ethoxylate+15EO,16EO,19EO,20EO,25EO,29EO,36EO,54EO , CAS No.:99734-09-5 HS Code: 34021300.90 Molecular Weight: Not available. Molecular Formula: C30H24O.(C2H4O)n Chemical Code: CC5-CZ40 EINECS No. Not available. Structural Formula: Not available. Properties and Uses: 1. Light yellow liquid or white cream. It becomes solid when the temperature is low. 2. Soluble in water and many kinds of organic solvents. 3. It has good emulsification, decontamination and moisturizing capacity. And it is an important hydrophilic group for compound agrochemical emulsifier. Packing and Transport: This product is flame resisting and nontoxic which can be shipped as an ordinary chemical product. Upload and handle with care to avoid collision. As per specific customer needs(available in bulk & small volume),the product can be made available with customized packing, like in plastic drum, galvanized iron drum, IBC drum etc… Storage: Quality guaranty period for the product is 1 year. Should be stored in dry and ventilated place. Quality Specifications: Type Appearance Water Percentage PH Value Cloud Point(°C) Remarks 601# Light yellow oily liquid ≤0.5% 5.0-7.0 60-65 1% H2O 602# Light yellow liquid or semi liquid ≤0.5% 5.0-7.0 80-85 1% H2O 603# Light yellow or white solid ≤0.5% 5.0-7.0 90-95 3% NaCl 604# Light yellow liquid or semi liquid ≤0.5% 5.0-7.0 54-56 1% H2O 605# Light yellow liquid or semi liquid ≤0.5% 5.0-7.0 70-75 1% H2O

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Peptides Ipamorelin Purity:99% HPLC Packing:2mg/vial;10vials/box Min Order: 1box Payment:Bitcoin,Moneygram and Wester Union Lead time:24hours after received payment Safe shipping to US and most of Europe country Storage:Shading, confined preservation,2-8°C Product link to :www.astersteroids.com/safe-shipping-ipamorelin-fo , r- bodybuilding-cycle-dosage-benefits-to-loss-w , eight-buy/ Product Name:Ipamorelin CAS: 170851-70-4 Formula: C38H49N9O5 MW:711.853 Purity:Above 98% Packing:2mg/vial;10vials/box Appearance: White Powder Storage Lyophilized Ipamorelin is stable at room temperature for 90 days,however it should be stored in a freezer below -8C for any extended period of time. After reconstituting Ipamorelin should be refrigerated at temperatures not to exceed 36 F. Ipamorelin has been shown to be both highly potent and very selective in vivo and vitro situations, and has also demonstrated good safety and tolerability in human clinical studies. Ipamorelin Benefits Ipamorelin has been shown to be both highly potent and very selective in vivo and vitro situations, and has also demonstrated good safety and tolerability in human clinical studies. Research has shown that Ipamorelin Benefits is hormone specific which means that the pituitary hormones such as cortisol are unaffected. In one study, it was found that young female adult rats had increased bone mass due to 12 weeks of treatment with ipamorelin. Ipamorelin Benefits compared to other Hormone Releasing Peptides ensures the benefits without having to deal with possible negative side effects. Ipamorelin Benefits in theory may increase Acetylchloine or Cortisol when used in higher dosages. However, and increase in Acetylchloine or Cortisol is even more likely with GHRP-2 and GHRP-6. In fact, in the case of Ipamorelin, there was little to no rise in Acetylcholine and Cortisol blood plasma levels even at injections more than 200 times higher than the effective dosage for comparable GH release. This clearly proves that Ipamorelin is the first successful GHRP receptor agonist or chemical that binds to a receptor of a cell and triggers a response by that cell with a specific selectivity for the promotion of GH release by itself. Another advantage to Ipamorelin is that it doesn't cause sudden spikes in prolactin or cortisol as does GHRP-2 and GHRP-6. Ipamorelin is slower in its delivery unlike GHRP's which spike GH levels at a more rapid rate. The slower release is more natural and has a more sustained effect.

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