3β-Hydroxyandrost-4-en-17-on | 571-44-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 3β-Hydroxyandrost-4-en-17-on
• 英文别名: 3β-Hydroxyandrost-4-en-17-one；3-beta-hydroxy-androst-4-en-17-one；(3S,10R,13S)-3-hydroxy-10,13-dimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one
• CAS: 571-44-8；2791-99-3；86420-28-2
• 化学式: C₁₉H₂₈O₂
• 分子量: 288.43
• InChiKey: VMYTXBKVYDESSJ-INNQQZFDSA-N

物化性质

• 熔点：
  144-146 °C
• 沸点：
  428.5±45.0 °C(Predicted)
• 密度：
  1.12±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  21
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.84
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• Method For DHEA Enanthate Processing
  申请人：DiMaggio Robert

  公开号：US20160362443A1

  公开（公告）日：2016-12-15

  A method is provided for producing dehydroepiandrosterone (DHEA) enanthate. The method comprises placing a portion of unprocessed DHEA into a solvent, such as Benzene, and allowing the DHEA to dissolve completely into the solvent, thereby forming a solution. The unprocessed DHEA preferably comprises unprocessed 5-DHEA, 1-DHEA, or 4-DHEA. A suitable quantity of Pyridine is then mixed into the solution. Heptanoyl Chloride is added slowly into the solution to cause a reaction of the unprocessed DHEA. Once substantially all of the unprocessed DHEA has been reacted, the addition of Heptanoyl Chloride is ceased. An effective amount of the DHEA enanthate may be administered to a human so as to improve at least one of adrenal hormonal balance, improved immune system function, reduction of adipose tissue, skeletal muscle growth, reduction of abdominal bloating, improved recovery from training, increase in strength, and increased endurance.