Mestanolone


CAS No. : 521-11-9

Mestanolone,521-11-9
Product Details
Cat No:R065162
Synonyms:17α-Methylandrostan-17β-ol-3-one, 17α-Methyldihydrotestosterone, 17β-Hydroxy-17α-methyl-5α-androstan-3-one, 5α-Androstane-17α-methyl-17β-ol-3-one, Mestaline, Mestanolone, Methylandrostanolone
Molecular Formula:C20H32O2
Molecular Weight:C20H32O2
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Appearance: Powder
Purity: 98.0%
Cat No:R065162
Cas No:521-11-9
Product-Name:Mestanolone
InChI:1S/C20H32O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h13,15-17,22H,4-12H2,1-3H3/t13-,15+,16-,17-,18-,19-,20-/m0/s1
InChIKey:WYZDXEKUWRCKOB-YDSAWKJFSA-N
SMILES:CC12CCC(=O)CC1CCC3C2CCC4(C3CCC4(C)O)C
Mestanolone (brand names Andoron, Notandron) is the 17α-methylated version of dihydrotestosterone (DHT).The systematic name of mestanolone is: 17β-hydroxy-17α-methylandrost-3-one. It is an orally bioavailable androgenic steroid that is highly androgenic while only slightly anabolic. It is incapable of aromatization and is not an agonist of the progesterone receptor.
Dosage Information
Dosages range from 10 mg to 30 mg a day for males. Women should avoid Mestanolone for it is very androgenic. Long-term use, more than 12 weeks, should be avoided do to hepatoxicity. Since Mestanolone is unable to convert to estrogen, it is very useful during cutting phases or when one wishes to avoid excess weight gain.
1: Afkhami A, Ghaedi H, Madrakian T, Nematollahi D, Mokhtari B. Electro-oxidation and voltammetric determination of oxymetholone in the presence of mestanolone using glassy carbon electrode modified with carbon nanotubes. Talanta. 2014 Apr;121:1-8. doi: 10.1016/j.talanta.2013.12.047. Epub 2013 Dec 30. PubMed PMID: 24607102.
2: Madrakian T, Afkhami A, Rahimi M, Ahmadi M, Soleimani M. Preconcentration and spectrophotometric determination of oxymetholone in the presence of its main metabolite (mestanolone) using modified maghemite nanoparticles in urine sample. Talanta. 2013 Oct 15;115:468-73. doi: 10.1016/j.talanta.2013.05.056. Epub 2013 Jun 11. PubMed PMID: 24054620.
3: Yamada M, Aramaki S, Okayasu T, Hosoe T, Kurosawa M, Kijima-Suda I, Saito K, Nakazawa H. Identification and quantification of metabolites common to 17alpha-methyltestosterone and mestanolone in horse urine. J Pharm Biomed Anal. 2007 Sep 21;45(1):125-33. Epub 2007 Jun 30. PubMed PMID: 17709226.
4: ARNOLD A, POTTS GO, BEYLER AL. THE RATIO OF ANABOLIC TO ANDROGENIC ACTIVITY OF 7:17-DIMETHYLTESTOSTERONE, OXYMESTERONE, MESTANOLONE AND FLUOXYMESTERONE. J Endocrinol. 1963 Dec;28:87-92. PubMed PMID: 14086172.
5: HARRIS LH. The protein anabolic action of mestanolone. J Clin Endocrinol Metab. 1961 Sep;21:1099-105. PubMed PMID: 13711755.
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