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Halotestin Fluoxymesterone Stenox Anabolic Steroid Hormones Pharmaceutical Raw Materials CAS 76-43-7

OSP007
Fluoxymesterone is a testosterone derived anabolic androgenic steroid or more specifically a structurally altered form of Methyltestosterone.
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  • Product Name:
    Halotestin (Fluoxymesterone)
  • CAS No.:
    76-43-7
  • Character:
    White crystalline powder
  • Purity:
    99%
  • Usage:
    pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones
Quantity:
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(10 KG available)
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Halotestin (Fluoxymesterone)

Fluoxymesterone Basic Info

 

Product Name Halotestin
CAS 76-43-7
EINECS 200-961-8
Molecular fomular C20H29FO3
Molecular Weight 336.44
Assay 99% min.
Packing foil bag or tin.
Delivery Express courier.
Character White crystalline powder
Usage

pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

 

Fluoxymesterone COA

 

TEST ITEMS SPECIFICATION RESULTS
Description : White or Almost White Crystalline Powder White Powder
Identification : A.B. Positive
Assay : 97.0~102.0% 98.70%
Specific Rotation : +104°~+112° +107.8°
Loss On Drying : 1.0%max 0.36%
Chromatographic Purity : single impurity:1.0%max <1.0%
  total impurities:2.0%max <2.0%
Organic Volatile Impurities : meets the requirement. Conforms
Residual Solvents : meets the requirement. Conforms
     
Conclusion The specification conform with USP30 standard

Fluoxymesterone Description:

 

Stenox also known as Halotestin (fluoxymesterone), is a halogenated derivative of 17-alpha-methyltestosterone and has an extreme androgenic effect and a very slight anabolic effect. With this combination, a person can expect a great increase in muscle hardness and strength with no real gain in size or weight. Because of the very high androgenic effect, many athletes have reported high levels of aggression making their workouts extremely intense.

 

Fluoxymesterone (trade name Halotestin) is an anabolic steroid with strong androgenic properties that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women. It is approximately 5 times as potent as methyltestosterone. The antitumor activity of fluoxymesterone appears related to reduction or competitive inhibition of prolactin receptors or estrogen receptors or production.

 

Like many C-17 alpha alkylated steroids, fluoxymesterone has poor binding to the androgen receptor. Even so, its actions are mediated by the androgen receptor, most-likely due to its prolonged plasma half-life.

 

Fluoxymesterone Dosage:

 

Usually 1 to 4 times a day, This could possibly indicate the use of up to 20mgs/day of Halotestin.

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