Trestolone acetate

Base Information Edit

Chemical Name:Trestolone acetate
CAS No.:6157-87-5
Molecular Formula:C21H30O3
Molecular Weight:330.467
Hs Code.:
UNII:52XDF4N1XL
DSSTox Substance ID:DTXSID80977160
Nikkaji Number:J8.350J
Wikipedia:Trestolone_acetate
Wikidata:Q27261025
NCI Thesaurus Code:C98255
Metabolomics Workbench ID:154696
ChEMBL ID:CHEMBL452329
Mol file:6157-87-5.mol

Synonyms:17 beta-hydroxy-7 alpha-methylestr-4-en-3-one acetate;7 alpha-methyl-19-nortestosterone acetate;trestolone acetate;U 15614;U-15,614

Suppliers and Price of Trestolone acetate

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 88 raw suppliers

Chemical Property of Trestolone acetate Edit

Chemical Property:

Vapor Pressure:3.33E-08mmHg at 25°C
Melting Point:111-114 °C
Refractive Index:1.538
Boiling Point:447.571 °C at 760 mmHg
Flash Point:194.228 °C
PSA：43.37000
Density:1.117 g/cm³
LogP:4.30590
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:330.21949481
Heavy Atom Count:24
Complexity:592

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC2=CC(=O)CCC2C3C1C4CCC(C4(CC3)C)OC(=O)C
Isomeric SMILES:C[C@@H]1CC2=CC(=O)CC[C@@H]2[C@@H]3[C@@H]1[C@@H]4CC[C@@H]([C@]4(CC3)C)OC(=O)C
Description Trestolone Acetate is a synthetic and injectable anabolic and androgenic steroid (AAS) that has been derived from the famous steroid nandrolone (19-nortestosterone) that doesn’t have any medical uses but is very helpful for physique and performance enhancement purposes.This steroid has firstly been described in 1963 and although there are many people searching and using Trestolone Acetate, is not as famous as many other steroids.Trestolone Acetate is also known as MENT acetate or Ment Trestolone and this is a steroid considered really beneficial for purpose of bodybuilding and strength training. Known as a steroid that is more powerful than testosterone, Trestolone is believed to offer fast and effective results.Ment Trestolone is believed to be the only steroid that can maintain a normal male physiology in a complete absence of testosterone, even including sexual life.
Uses Trestolone is a synthetic anabolic-androgenic steroid (AAS) of the nandrolone (19-nortestosterone) group. In Vivo: Trestolone is used as trestolone acetate, which is administered via intramuscular injection and acts as a long-lasting prodrug of trestolone.

Technology Process of Trestolone acetate

There total 12 articles about Trestolone acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

: 2590-41-2
6-dehydro-19-nortestosterone acetate

: 676-58-4
methylmagnesium chloride

: 6157-87-5
7alpha-Methyl-19-nortestosterone acetate

Guidance literature:: 6-dehydro-19-nortestosterone acetate; methylmagnesium chloride; copper diacetate; In tetrahydrofuran; at -45 - -35 ℃; for 3h;

With hydrogenchloride; In tetrahydrofuran; water; at 10 ℃; for 0.5h;

Reference yield: 61.0%

: zirconocene methyl chloride

: 2590-41-2
6-dehydro-19-nortestosterone acetate

: 6157-87-5
7alpha-Methyl-19-nortestosterone acetate

Guidance literature:: zirconocene methyl chloride; With silver trifluoromethanesulfonate; copper(l) chloride; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine; In diethyl ether; dichloromethane; at 20 ℃; for 0.166667h; Darkness; Inert atmosphere;

6-dehydro-19-nortestosterone acetate; With chloro-trimethyl-silane; In diethyl ether; dichloromethane; at 20 ℃; for 15h; stereoselective reaction; Inert atmosphere; Darkness;
DOI:10.1021/acs.orglett.6b01829