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Methenolone Enanthate

Item No. 17148

Synonyms
Synonyms
  • NSC 64967
  • SQ 16,374
Technical Information
Formal Name
(5α,17β)-1-methyl-17-[(1-oxoheptyl)oxy]-androst-1-en-3-one
CAS Number
303-42-4
Molecular Formula
C27H42O3
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mLDMSO: 11 mg/mLEthanol: 25 mg/mL
λmax
241 nm
SMILES
C[C@@]12[C@](CC[C@@H]2OC(CCCCCC)=O)([H])[C@]3([H])CC[C@@]4([H])CC(C=C(C)[C@]4(C)[C@@]3([H])CC1)=O
InChi Code
InChI=1S/C27H42O3/c1-5-6-7-8-9-25(29)30-24-13-12-22-21-11-10-19-17-20(28)16-18(2)27(19,4)23(21)14-15-26(22,24)3/h16,19,21-24H,5-15,17H2,1-4H3/t19-,21-,22-,23-,24-,26-,27-/m0/s1
InChi Key
TXUICONDJPYNPY-FRXWOFFRSA-N
Regulatory Information
DEA Schedule
III
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Methenolone enanthate (Item No. 17148) is an analytical reference standard that is categorized as an androgenic anabolic steroid. It is an ester form of methenolone, an anabolic steroid derived from dihydrotestosterone (DHT; Item No. 15874). Formulations containing primobolan have been associated with hypothalamic-pituitary-gonadal dysfunction and damage to the heart, testes, and adrenal gland.1,2,3 Methenolone enanthate is regulated as a Schedule III compound in the United States. This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Takahashi, M., Tatsugi, Y., and Kohno, T. Endocrinological and pathological effects of anabolic-androgenic steroid in male rats. Endocr. J. 51(4), 425-434 (2004).

    2. van Breda, E., Keizer, H.A., Juipers, H., et alAndrogenic anabolic steroid use and severe hypothalamic-pituitary dysfunction: A case study. Int. J. Sports Med. 24(3), 195-196 (2015).

    3. Nieschlag, E., and Vorona, E. Mechanisms in endocrinology. Medical consequences of doping with anabolic androgenic steroids: Effects on reproductive functions. Eur. J. Endocrinol. 173(2), R47-R58 (2015).