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(17beta)-3-methylandrosta-3,5-dien-17-ol, also known as methylstenbolone, is a chemical compound with the molecular formula C19H28O. It is a derivative of testosterone and is classified as an androgen. (17beta)-3-methylandrosta-3,5-dien-17-ol is known for its anabolic properties, making it popular among athletes and bodybuilders for its potential to enhance muscle growth and performance.

60397-35-5

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60397-35-5 Usage

Uses

Used in Sports and Bodybuilding:
(17beta)-3-methylandrosta-3,5-dien-17-ol is used as an anabolic agent for enhancing muscle growth and performance. Its anabolic properties make it popular among athletes and bodybuilders seeking to improve their physical abilities.
However, it is important to note that the use of methylstenbolone is banned in most sports organizations due to its potential for abuse and adverse health effects. Individuals should use (17beta)-3-methylandrosta-3,5-dien-17-ol under the guidance of a medical professional to avoid any potential risks associated with its usage.

Check Digit Verification of cas no

The CAS Registry Mumber 60397-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60397-35:
(7*6)+(6*0)+(5*3)+(4*9)+(3*7)+(2*3)+(1*5)=125
125 % 10 = 5
So 60397-35-5 is a valid CAS Registry Number.

60397-35-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (8R,9S,10R,13S,14S,17S)-3,10,13-trimethyl-2,7,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-ol

1.2 Other means of identification

Product number -
Other names (17|A)-3-methylandrosta-3,5-dien-17-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60397-35-5 SDS

60397-35-5Downstream Products

60397-35-5Relevant academic research and scientific papers

Androstene-3,5-dienes as ER-β selective SERMs

Blizzard, Timothy A.,Gude, Candido,Morgan II, Jerry D.,Chan, Wanda,Birzin, Elizabeth T.,Mojena, Marina,Tudela, Consuelo,Chen, Fang,Knecht, Kristin,Su, Qin,Kraker, Bryan,Mosley, Ralph T.,Holmes, Mark A.,Rohrer, Susan P.,Hammond, Milton L.

, p. 6295 - 6298 (2008/09/17)

A series of androstene-3,5-diene derivatives were prepared. Despite lacking the C-3 hydroxyl previously believed necessary for ER activity, some of the analogs retained surprising affinity for ER-β. For example, diene 4 retained excellent selectivity and potency as an ER-β agonist and was more selective for ER-β over the androgen receptor (AR).

ESTROGEN RECEPTOR MODULATORS

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Page/Page column 33, (2008/06/13)

The present invention relates to compounds and derivatives thereof, their synthesis, and their use as estrogen receptor modulators. The compounds of the instant invention are ligands for estrogen receptors and as such may be useful for treatment or prevention of a variety of conditions related to estrogen functioning including: bone loss, bone fractures, osteoporosis, metastatic bone disease, Paget’s disease, periodontal disease, cartilage degeneration, endometriosis, uterine fibroid disease, hot flashes, increased levels of LDL cholesterol, cardiovascular disease, impairment of cognitive functioning, cerebral degenerative disorders, restenosis, gynecomastia, vascular smooth muscle cell proliferation, obesity, incontinence, inflammation, inflammatory bowel disease, sexual dysfunction, hypertension, retinal degeneration and cancer, in particular of the breast, uterus and prostate.

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