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Oral-Turinabol

HCID 98521
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
2446-23-3
Standard SMILES
C[C@]12C=CC(=O)C(Cl)=C1CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC[C@]2(C)O
InChIKey
AGUNEISBPXQOPA-XMUHMHRVSA-N
Molecular formula
C20H27ClO2
Average molar mass
334.9 g/mol
Monoisotopic mass
334.1699578

Overview

4-Chloromethandienone is a 3-hydroxy steroid. It has a role as an androgen.

Names & identifiers

Preferred name
Oral-Turinabol
IUPAC
(8R,9S,10R,13S,14S,17S)-4-chloro-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one
English name
4-Chlorodehydromethyltestosterone
Molecular formula
C20H27ClO2
Molecular weight
334.88

Names & synonyms

2446-23-3Oral turinabolOral-Turinabol4-Chloro-methandienoneDehydrochlormethyltestosteroneD-4-Chloro-17 beta-hydroxy-3-oxo-17 alpha-methylandrosta-1,4-dieneRefChem:5758074-chloro-17 alpha-methyl-17 beta-hydroxy-1,4-androstadiene-3-oneCDMT4-Chlorodehydromethyltestosterone4-Chloromethandienone4-Chlorodianabol
Show more names
StanOral turinaboTurinabol 25mg4-Chlordehydromethylturinabol-oral TbolSTOSTERONE (Turinabol)4-Chlorodehydromethyltesto
Turinabol-oralChlorodehydromethyltestosterone(8R,9S,10R,13S,14S,17S)-4-chloro-17-hydroxy-10,13,17-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-oneDehydrochloromethyltestosteroneZPZ473F40K4-Chloro-1-dehydromethyltestosteroneChlorodehydromethyl-testosterone4-chloro-17beta-hydroxy-17alpha-methylandrosta-1,4-dien-3-one

Database identifiers

CAS

Properties

Computed structural properties

XLogP
4.4
Topological polar surface area
37.3 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
2
Rotatable bonds
0
Heavy atoms
23
Formal charge
0
Complexity
636

Experimental & physicochemical properties

Drugs · 2 items

DEA NFLIS-Drug Category -> Steroids

DEA Schedule III Controlled Substance -> Anabolic steroids

Endocrine DisruptorsPotential endocrine disrupting compound
Melting Point125 - 127 °C
Physical DescriptionSolid

Physicochemical properties

Melting point
149 · 149-151 °C(Solv: acetone (67-64-1); hexane (110-54-3))
Boiling point
464.4 · 464.4±45.0 °C(Predicted)
Density
1.2 · 1.20±0.1 g/cm3(Predicted)
solubility
1 mg/ml; · Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml
form
A crystalline solid
pka
15.05 · 15.05±0.70(Predicted)
InChI
InChI=1/C20H27ClO2/c1-18-9-8-16(22)17(21)15(18)5-4-12-13(18)6-10-19(2)14(12)7-11-20(19,3)23/h8-9,12-14,23H,4-7,10-11H2,1-3H3/t12-,13+,14+,18-,19+,20+/s3

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Danger

H350 (50%): May cause cancer [Danger Carcinogenicity]

P203, P260, P263, P264, P270, P273, P280, P318, P319, P391, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory InformationDEA schedule III controlled substance
Hazard Classes and CategoriesCarc. 1B (50%)

Safety data

DEA Controlled Substances
CSCN: 4000CSA SCH: Schedule IIINARC: No

Chemistry & industry

Pharmacology

Cellular LocationsExtracellular
Applications · 4 items

Description4-Chlorodehydromethyltestosterone (CDMT; brand name Oral Turinabol), also known as Chlorodehydromethyltestosterone, is an anabolic–androgenic steroid (AAS). It is the 4-chloro-substituted derivative of metandienone (dehydromethyltestosterone). Turinabol is indicated for hormone replacement therapy in men suffering from androgen deficiency or in severe cases of catabolism.

History4-Chlorodehydromethyltestosterone is an anabolic steroid developed in the 1960s, a highly competitive time for the Olympics and national level sports, the East German experts were looking for effective steroids that would circumvent these sports'drug testing policies. The product was introduced for clinical use in 1965 and remained in use until 1994, when production was discontinued.

Uses4-Chlorodehydromethyltestosterone is a derivative of dehydrochloromethyltestosterone. Metabolite of anabolic steroids. it can produce quality gains in muscle mass as well as strength, even if these gains are not as dramatic or quick as you might get from an aromatizable, or more androgenic oral steroid.

General DescriptionDehydrochloromethyl Testosterone is an analytical reference standard that is categorized as an androgenic anabolic steroid. Anabolic steroids, including dehydrochloromethyl testosterone, have been used to enhance physical performance in athletes. Dehydrochloromethyl testosterone is regulated as a Schedule III compound in the United States. This product is intended for research and forensic applications.

Upstream & downstream products

Upstream raw materials

Methylclostebol

Suppliers100 total

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
2446-23-3
PubChem CID
98521
DTXSID
DTXSID10179216
ChEBI
CHEBI:166768
UNII
ZPZ473F40K
EC Number
962-211-2
Nikkaji
J507.800H
InChIKey
AGUNEISBPXQOPA-RFNNMYDSNA-N
SMILES
C[C@]12C=CC(=O)C(Cl)=C1CC[C@@]1([H])[C@]3([H])CC[C@@](O)(C)[C@@]3(C)CC[C@]21[H] |&1:1,11,13,17,20,24,r|
FDA UNII
473 F40K · ZPZ473F40K
DEA Controlled Substances
4000 CSA · CSCN: 4000CSA SCH: Schedule IIINARC: No
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Additional notes

DefinitionChEBI: 4-Chloromethandienone is a 3-hydroxy steroid. It has a role as an androgen.