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

Details

Stereochemistry RACEMIC
Molecular Formula C5H10O3
Molecular Weight 118.1311
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYVALERIC ACID

SMILES

CC(O)CCC(O)=O

InChI

InChIKey=FMHKPLXYWVCLME-UHFFFAOYSA-N
InChI=1S/C5H10O3/c1-4(6)2-3-5(7)8/h4,6H,2-3H2,1H3,(H,7,8)

HIDE SMILES / InChI

Molecular Formula C5H10O3
Molecular Weight 118.1311
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Enatiomerically pure hydroxycarboxylic acids: current approaches and future perspectives.
2010-06
High-titer production of monomeric hydroxyvalerates from levulinic acid in Pseudomonas putida.
2009-01-01
Evolution, ecology and the engineered organism: lessons for synthetic biology.
2009
Characterization and pharmacology of the GHB receptor.
2008-10
Comparative analysis of gamma-hydroxybutyrate and gamma-hydroxyvalerate using GC/MS and HPLC.
2007-03
Applications of ion mobility spectrometry (IMS) to the analysis of gamma-hydroxybutyrate and gamma-hydroxyvalerate in toxicological matrices.
2006-10
Chemical composition and structure of the microcrystals formed between silver(I) and gamma-hydroxybutyric acid and gamma-hydroxyvaleric acid.
2006-07
Analysis of GHB and 4-methyl-GHB in postmortem matrices after long-term storage.
2005-04-06
Comparison of the behavioral effects of gamma-hydroxybutyric acid (GHB) and its 4-methyl-substituted analog, gamma-hydroxyvaleric acid (GHV).
2005-04-04
The involvement of survival signaling pathways in rubella-virus induced apoptosis.
2005-01-04
Porphyrins with exocyclic rings. 16. Synthesis and spectroscopic characterization of fluoranthoporphyrins, a new class of highly conjugated porphyrin chromophores.
2001-05-04
Development of a process for the biotechnological large-scale production of 4-hydroxyvalerate-containing polyesters and characterization of their physical and mechanical properties.
2001
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:01:07 GMT 2025
Edited
by admin
on Mon Mar 31 22:01:07 GMT 2025
Record UNII
58B139Q3RL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-HYDROXYVALERIC ACID
Systematic Name English
.GAMMA.-HYDROXYVALERIC ACID
Preferred Name English
PENTANOIC ACID, 4-HYDROXY-
Systematic Name English
4-HYDROXYPENTANOIC ACID
Systematic Name English
.GAMMA.-METHYL-.GAMMA.-HYDROXYBUTYRIC ACID
Systematic Name English
VALERIC ACID, 4-HYDROXY-
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-.gamma.-Hydroxyvaleric acid
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID60928958
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
PRIMARY
PUBCHEM
114539
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
236-884-1
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
PRIMARY
CAS
13532-37-1
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
PRIMARY
FDA UNII
58B139Q3RL
Created by admin on Mon Mar 31 22:01:07 GMT 2025 , Edited by admin on Mon Mar 31 22:01:07 GMT 2025
PRIMARY