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Details

Stereochemistry RACEMIC
Molecular Formula C6H12O3
Molecular Weight 132.1577
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 3-HYDROXYBUTYRATE

SMILES

CCOC(=O)CC(C)O

InChI

InChIKey=OMSUIQOIVADKIM-UHFFFAOYSA-N
InChI=1S/C6H12O3/c1-3-9-6(8)4-5(2)7/h5,7H,3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H12O3
Molecular Weight 132.1577
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Antibacterial Activity of some Medicinal Mangroves against Antibiotic Resistant Pathogenic Bacteria.
2010-03
Examples of perceptive interactions involved in specific "red-" and "black-berry" aromas in red wines.
2009-05-13
Effects of industrial storage on the bioreduction capacity of brewer's yeast.
2009-01
A substitutive substrate for measurements of beta-ketoacyl reductases in two fatty acid synthase systems.
2008-04-24
Intramolecular Prins cyclisations for the stereoselective synthesis of bicyclic tetrahydropyrans.
2008-04-07
Behavioural responses of Tribolium castaneum (Herbst) to volatiles identified from dry cocoa beans.
2007-10-15
Predicting olfactory receptor neuron responses from odorant structure.
2007-05-04
An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.
2007-04-12
Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and B.
2006-07-21
The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.
2004-08
Novel natural ligands for Drosophila olfactory receptor neurones.
2003-02
Influence of the ethanol and glucose supply rate on the rate and enantioselectivity of 3-oxo ester reduction by baker's yeast.
2001-10-05
A two-step enzymatic resolution process for large-scale production of (S)- and (R)-ethyl-3-hydroxybutyrate.
2001-08-05
Asymmetric reduction of ethyl acetoacetate to ethyl (R)-3-hydroxybutyrate coupled with nitrate reduction by Paracoccus denitrificans.
2001
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:10:04 GMT 2025
Edited
by admin
on Mon Mar 31 19:10:04 GMT 2025
Record UNII
52008C87PV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL 3-HYDROXYBUTYRATE
FHFI  
Systematic Name English
ETHYL 3-HYDROXYBUTYRATE [FHFI]
Preferred Name English
GRAPE BUTYRATE
Common Name English
ETHYL (1)-3-HYDROXYBUTYRATE
Common Name English
ETHYL .BETA.-HYDROXYBUTYRATE
Systematic Name English
DL-3-HYDROXY-N-BUTYRATE ETHYL ESTER
Common Name English
FEMA NO. 3428
Code English
(±)-3-HYDROXYBUTANOIC ACID ETHYL ESTER
Systematic Name English
3-HYDROXYBUTYRIC ACID ETHYL ESTER
Systematic Name English
ETHYL (±)-3-HYDROXYBUTANOATE
Systematic Name English
NSC-42916
Code English
3-HYDROXYBUTANOIC ACID ETHYL ESTER
Systematic Name English
ETHYL 3-HYDROXYBUTANOATE
Systematic Name English
(±)-ETHYL 3-HYDROXYBUTYRATE
Systematic Name English
ETHYL DL-3-HYDROXYBUTYRATE
Common Name English
NSC-8115
Code English
BUTANOIC ACID, 3-HYDROXY-, ETHYL ESTER
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ETHYL 3-HYDROXYBUTYRATE
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
Code System Code Type Description
MESH
C435833
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
NSC
42916
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
226-456-2
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
CHEBI
87685
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
FDA UNII
52008C87PV
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
CAS
5405-41-4
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
PUBCHEM
62572
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
NSC
8115
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
JECFA MONOGRAPH
156
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID6025305
Created by admin on Mon Mar 31 19:10:04 GMT 2025 , Edited by admin on Mon Mar 31 19:10:04 GMT 2025
PRIMARY