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Details

Stereochemistry RACEMIC
Molecular Formula C12H20N2O3
Molecular Weight 240.2988
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBERAL

SMILES

CCC1(C(C)CC(C)C)C(=O)NC(=O)NC1=O

InChI

InChIKey=KXHLANWWTKSOMW-UHFFFAOYSA-N
InChI=1S/C12H20N2O3/c1-5-12(8(4)6-7(2)3)9(15)13-11(17)14-10(12)16/h7-8H,5-6H2,1-4H3,(H2,13,14,15,16,17)

HIDE SMILES / InChI

Molecular Formula C12H20N2O3
Molecular Weight 240.2988
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of barbiturate-stimulated chloride efflux from rat brain synaptoneurosomes.
1985 Nov
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:00:45 GMT 2025
Edited
by admin
on Mon Mar 31 23:00:45 GMT 2025
Record UNII
31E1HC8I46
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-31256
Preferred Name English
DIBERAL
Common Name English
5-ETHYL-5-(1,3-DIMETHYLBUTYL) BARBITURIC ACID
Systematic Name English
DMBEB
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-(1,3-DIMETHYLBUTYL)-5-ETHYL-
Systematic Name English
PENTOBARBITAL SODIUM IMPURITY F [EP IMPURITY]
Common Name English
5-ETHYL-5-(1,3-DIMETHYLBUTYL)BARBITURIC ACID
Systematic Name English
DMBB
Common Name English
(±)-5-(1,3-DIMETHYLBUTYL)-5-ETHYLBARBITURIC ACID
Systematic Name English
5-(1,3-DIMETHYLBUTYL)-5-ETHYLBARBITURIC ACID
Systematic Name English
PENTOBARBITAL IMPURITY F [EP IMPURITY]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID301031188
Created by admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
PRIMARY
FDA UNII
31E1HC8I46
Created by admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
PRIMARY
NSC
31256
Created by admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
PRIMARY
PUBCHEM
18079
Created by admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
PRIMARY
CAS
2964-06-9
Created by admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP