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Trestolone Acetate

HCID 10246085
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Basic information

CAS
6157-87-5
Standard SMILES
CC(=O)O[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@H]1CCC(=O)C=C1C[C@H]3C
InChIKey
IVCRCPJOLWECJU-XQVQQVTHSA-N
Molecular formula
C21H30O3
Average molar mass
330.5 g/mol
Monoisotopic mass
330.21949481

Overview

Trestolone acetate is a synthetic and injected anabolic–androgenic steroid (AAS) and a derivative of nandrolone (19-nortestosterone) which was never marketed. It is an androgen ester – specifically, the C17 acetate ester of [DB05830].

Names & identifiers

Preferred name
Trestolone Acetate
IUPAC
[(7R,8R,9S,10R,13S,14S,17S)-7,13-dimethyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate
English name
trestolone acetate
Molecular formula
C21H30O3
Molecular weight
330.47

Names & synonyms

TRESTOLONE ACETATE6157-87-5Orgasteron acetateMENT ACETATENSC-6994817beta-Hydroxy-7alpha-methylestr-4-en-3-one acetateU-15,61452XDF4N1XLCDB-903U-1561419-Nortestosterone, 7alpha-methyl-, acetateDTXSID80977160
Show more names
Trestolone acetate (MENT)Trestolone Acetate(Ment A)IVCRCPJOLWECJU-XQVQQVTHSA-Ntrestolone acetate USP/EP/BPTrestolone acetate (MENT) 50mg/mlTrestolone Acetate (Ment) (62)-1 gram4-ESTREN-7α-METHYL-17β-OL-3-ONE ACETATE
17 beta-hydroxy-7 alpha-methylestr-4-en-3-one acetateCDB 9037alpha-Methyl-19-nortestosterone acetateEstr-4-en-3-one, 17beta-hydroxy-7alpha-methyl-, acetateNSC699487 alpha-methyl-19-nortestosterone acetateRefChem:190771DTXCID201527887

Database identifiers

CAS
6157-87-5
PubChem CID
10246085

Properties

Computed structural properties

XLogP
3.4
Topological polar surface area
43.4 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
3
Rotatable bonds
2
Heavy atoms
24
Formal charge
0
Complexity
592

Experimental & physicochemical properties

DrugsPharmaceuticals -> Listed in ZINC15
Endocrine DisruptorsPotential endocrine disrupting compound

Physicochemical properties

Melting point
111 · 111-114 °C
Boiling point
447.6 · 447.6±45.0 °C(Predicted)
Density
1.11 · 1.11±0.1 g/cm3(Predicted)
solubility
30 mg/ml; · DMF: 30 mg/ml; DMSO: 25 mg/ml; Ethanol: 30 mg/ml
form
A crystalline solid
InChI
InChI=1/C21H30O3/c1-12-10-14-11-15(23)4-5-16(14)17-8-9-21(3)18(20(12)17)6-7-19(21)24-13(2)22/h11-12,16-20H,4-10H2,1-3H3/t12-,16+,17-,18+,19+,20-,21+/s3
InChIKey
IVCRCPJOLWECJU-KHRPLIIWNA-N
SMILES
C[C@@H]1CC2=CC(=O)CC[C@]2([H])[C@@]2([H])CC[C@@]3([C@@H](OC(=O)C)CC[C@@]3([H])[C@]12[H])C |&1:1,9,11,15,16,23,25,r|
FDA UNII
52 XDF4N1XL · 52XDF4N1XL

Chemistry & industry

Applications · 2 items

DescriptionTrestolone 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.

UsesTrestolone 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.

Upstream & downstream products

Upstream raw materials

Dehydronandrolone AcetateMethylmagnesium chloride

Additional notes

DefinitionTrestolone acetate is a synthetic and injected anabolic–androgenic steroid (AAS) and a derivative of nandrolone (19-nortestosterone) which was never marketed. It is an androgen ester – specifically, the C17 acetate ester of [DB05830].

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
DTXSID
DTXSID80977160
ChEMBL
CHEMBL452329
UNII
52XDF4N1XL
Nikkaji
J8.350J