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Details

Stereochemistry RACEMIC
Molecular Formula C11H14N2OS
Molecular Weight 222.307
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-OXO-3-(2-MERCAPTOETHYL)-5-PHENYLIMIDAZOLIDINE, (±)-

SMILES

SCCN1CC(NC1=O)C2=CC=CC=C2

InChI

InChIKey=KKEBXNMGHUCPEZ-UHFFFAOYSA-N
InChI=1S/C11H14N2OS/c14-11-12-10(8-13(11)6-7-15)9-4-2-1-3-5-9/h1-5,10,15H,6-8H2,(H,12,14)

HIDE SMILES / InChI

Molecular Formula C11H14N2OS
Molecular Weight 222.307
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:31:22 GMT 2023
Edited
by admin
on Sat Dec 16 10:31:22 GMT 2023
Record UNII
AC57BIX3H8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-OXO-3-(2-MERCAPTOETHYL)-5-PHENYLIMIDAZOLIDINE, (±)-
Systematic Name English
2-OXO-3-(2-MERCAPTOETHYL)-5-PHENYLIMIDAZOLIDINE, DL-
Common Name English
LEVAMISOLE HYDROCHLORIDE IMPURITY C [EP IMPURITY]
Common Name English
OMPI
Common Name English
DL-2-OXO-3-(2-MERCAPTOETHYL)-5-PHENYLIMIDAZOLIDINE
Systematic Name English
LEVAMISOLE HYDROCHLORIDE IMPURITY C [WHO-IP]
Common Name English
(4RS)-4-PHENYL-1-(2-SULFANYLETHYL)IMIDAZOLIDIN-2-ONE
Systematic Name English
2-IMIDAZOLIDINONE, 1-(2-MERCAPTOETHYL)-4-PHENYL-
Systematic Name English
LEVAMISOLE FOR VETERINARY USE IMPURITY C [EP IMPURITY]
Common Name English
RAC-(4R)-4-PHENYL-1-(2-SULFANYLETHYL)IMIDAZOLIDIN-2-ONE [WHO-IP]
Common Name English
1-(2-MERCAPTOETHYL)-4-PHENYL-2-IMDAZOLIDINONE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID50954049
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
PUBCHEM
135446
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
CAS
32190-33-3
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
FDA UNII
AC57BIX3H8
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
PARENT -> IMPURITY
The chromatogram obtained with solution (1) may show peaks due to the following impurities eluting at the following relative retention with reference to levamisole (retention time about 3.5 minutes): impurity C about 1.5. In the chromatogram obtained with solution (1): ?the area of any peak corresponding to impurity C, when multiplied by a correction factor of 2.9, is not greater than 2 times the area of the peak due to levamisole in the chromatogram obtained with solution (4) (0.2%).
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
- for veterinary use - correction factor: for the calculation of content, multiply the peak area of impurity C by 2.9
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY