U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C4H4N2O3
Molecular Weight 128.0862
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BARBITURIC ACID

SMILES

O=C1CC(=O)NC(=O)N1

InChI

InChIKey=HNYOPLTXPVRDBG-UHFFFAOYSA-N
InChI=1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)

HIDE SMILES / InChI

Molecular Formula C4H4N2O3
Molecular Weight 128.0862
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The molecular basis of IgE antibody binding to thiopentone. Binding of IgE from thiopentone-allergic and non-allergic subjects.
1990 Sep
Determination of barbituric acid, utilizing a rapid and simple colorimetric assay.
2002 Jul 31
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:06:27 GMT 2023
Edited
by admin
on Fri Dec 15 15:06:27 GMT 2023
Record UNII
WQ92Y2793G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BARBITURIC ACID
MI  
Systematic Name English
1,2,3,4,5,6-HEXAHYDRO-2,4,6-PYRIMIDINETRIONE
Systematic Name English
FLUOROURACIL RELATED COMPOUND A [USP IMPURITY]
Common Name English
FLUOROURACIL IMPURITY A [EP IMPURITY]
Common Name English
FLUOROURACIL RELATED COMPOUND A
USP-RS  
Common Name English
FLUOROURACIL RELATED COMPOUND A [USP-RS]
Common Name English
PYRIMIDINE-2,4,6(1H,3H,5H)-TRIONE
Systematic Name English
PYRIMIDINETRIONE
Systematic Name English
MALONYLUREA
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE
Systematic Name English
BARBITURIC ACID [MI]
Common Name English
2,4,6-TRIOXOHEXAHYDROPYRIMIDINE
Systematic Name English
NSC-7889
Code English
Classification Tree Code System Code
CFR 21 CFR 862.3150
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
Code System Code Type Description
NSC
7889
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
CHEBI
31252
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID8020129
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
WIKIPEDIA
BARBITURIC ACID
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-658-0
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
FDA UNII
WQ92Y2793G
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
MERCK INDEX
m2228
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY Merck Index
PUBCHEM
6211
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
MESH
C032232
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
RS_ITEM_NUM
1279019
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
CAS
67-52-7
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
CHEBI
16294
Created by admin on Fri Dec 15 15:06:28 GMT 2023 , Edited by admin on Fri Dec 15 15:06:28 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
USP Peak Value = 0.15%
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY