Androstenediol

CAS No. 521-17-5

Androstenediol ( 5-Adiol;Androstenediol;5-Androsten-17β,3β-diol;NSC 12163 )

Catalog No. M23110 CAS No. 521-17-5

5-Androstenediol is an analytical reference standard categorized as an anabolic androgenic steroid.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 49 In Stock
10MG 80 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Androstenediol
  • Note
    Research use only, not for human use.
  • Brief Description
    5-Androstenediol is an analytical reference standard categorized as an anabolic androgenic steroid.
  • Description
    5-Androstenediol is an analytical reference standard categorized as an anabolic androgenic steroid.5-Androstenediol is a precursor in the biosynthesis of testosterone. 5-Androstenediol is regulated as a Schedule III compound in the United States. This product is intended for research and forensic applications.
  • Synonyms
    5-Adiol;Androstenediol;5-Androsten-17β,3β-diol;NSC 12163
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    521-17-5
  • Formula Weight
    290.4
  • Molecular Formula
    C19H30O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMF: 25 mg/ml;DMSO: 15 mg/ml;DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml;Ethanol: 10 mg/ml
  • SMILES
    C[C@@]12[C@]3([H])[C@](CC=C1C[C@H](CC2)O)([H])[C@@]4([H])[C@](CC3)([C@H](CC4)O)C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Poucke, C.V., Detavernier, C., Van Cauwenberghe, R., et al. Determination of anabolic steroids in dietary supplements by liquid chromatography-tandem mass spectrometry. Anal. Chim. Acta 586(1-2), 35-42 (2007). 2. Inaba, M., and Nakao, T. Conversion of 4-androstenediol and 5-androstenediol to testosterone, and conversion of dehydroepiandrosterone to 4-androstenediol by rat testis in vitro. Endocrinol. Jpn. 13(2), 160-172 (1966).
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