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Details

Stereochemistry RACEMIC
Molecular Formula C14H17NS2.ClH
Molecular Weight 299.882
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMETHYLTHIAMBUTENE HYDROCHLORIDE

SMILES

Cl.CC(C=C(C1=CC=CS1)C2=CC=CS2)N(C)C

InChI

InChIKey=OBFGNODOJKVYIR-UHFFFAOYSA-N
InChI=1S/C14H17NS2.ClH/c1-11(15(2)3)10-12(13-6-4-8-16-13)14-7-5-9-17-14;/h4-11H,1-3H3;1H

HIDE SMILES / InChI
Dimethylthiambutene is the synthetic narcotic analgesic agent. It has analgesic effect similar to those of meperidine. The (+)-enantiomer of dimethylthiambutene is more active than the (-)-isomer. Dimethylthiambutene clinically compared with meperidine (pethidine), but maintains the dependence-producing capability of morphine. It has had illicit use in Japan in the past. Dimethylthiambutene is under international control according to the UN Single Convention 1961 and its amendments, Schedule I.

Approval Year

Patents
Name Type Language
OHTON HYDROCHLORIDE
Preferred Name English
DIMETHYLTHIAMBUTENE HYDROCHLORIDE
MI  
Common Name English
3-DIMETHYLAMINO-1,1-BIS(2-THIENYL)-1-BUTENE HYDROCHLORIDE
Systematic Name English
3-BUTEN-2-AMINE, N,N-DIMETHYL-4,4-DI-2-THIENYL-, HYDROCHLORIDE
Systematic Name English
ALLYLAMINE, N,N,1-TRIMETHYL-3,3-DI-2-THIENYL-, HYDROCHLORIDE
Systematic Name English
DIMETHYLTHIAMBUTENE HYDROCHLORIDE [MI]
Common Name English
Code System Code Type Description
FDA UNII
ZI2995I73Y
Created by admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
PRIMARY
PUBCHEM
22028
Created by admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
PRIMARY
CAS
5786-77-6
Created by admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
PRIMARY
MERCK INDEX
m1119
Created by admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID20973449
Created by admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
PRIMARY