• CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one

CAS 315-37-7 Androst-4-en-3-one

density
one point zero six
Melting point:
34-39℃
Boiling point:
503.9°Cat760mmHg
Refractive index:
1.4700 (estimate)
Flash point:
214.2°C
Steam pressure:
0.0±1.3 mmHg at 25°C
Form:
powder
PSA:
forty-three point three seven zero zero zero
logP:
six point four zero zero five zero
Appearance
White crystalline powder
chemical property:
White or yellowish-white, crystalline powder.
Color
white to beige
physical property:
White crystalline powder. The melting point is 34-36 ℃.
Solubility:
Almost insoluble in water, highly soluble in anhydrous ethanol, and easily soluble in fatty oils.
Storage Temperature:
2-8°C
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one
  • CAS 315-37-7  Androst-4-en-3-one

Description

Testosterone Enanthate is a synthetic derivative of the naturally occurring male sex hormone testosterone, classified as an anabolic steroid. It is characterized by its long-acting ester, which prolongs its release and activity in the body. The chemical formula for Testosterone Enanthate is C21H32O3
[Purpose 1]
Clinically used to treat male sexual dysfunction, aplastic anemia, and other conditions
[Purpose 2]
Clinically used for male dysfunction, aplastic anemia, etc.
Usage 1: Testosterone heptanoate is an important physiologically active substance secreted by the human body, which plays an extremely important role in maintaining normal physical and sexual function, extending human physiological and psychological lifespan, and so on. Clinically used to treat male sexual dysfunction, aplastic anemia, and other conditions.
The production method involves reducing 4-androstenedione (4-AD) to obtain testosterone and diol, followed by oxidation to obtain testosterone; Testosterone reacts with pyridine, heptanoic anhydride, and ethyl acetate to obtain testosterone heptanoate.