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Details

Stereochemistry ACHIRAL
Molecular Formula C7H14O2
Molecular Weight 130.1849
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl isovalerate

SMILES

CCOC(=O)CC(C)C

InChI

InChIKey=PPXUHEORWJQRHJ-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-4-9-7(8)5-6(2)3/h6H,4-5H2,1-3H3

HIDE SMILES / InChI
Molecular Formula C7H14O2
Molecular Weight 130.1849
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

1995
203
PubMed

PubMed

TitleDatePubMed
Volatile profiling reveals intracellular metabolic changes in Aspergillus parasiticus: veA regulates branched chain amino acid and ethanol metabolism.
2010-08-24
Mass spectrometry screening reveals widespread diversity in trichome specialized metabolites of tomato chromosomal substitution lines.
2010-05
Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.
2010-02
Identification of odor impact compounds of Tagetes minuta L. essential oil: comparison of two GC-olfactometry methods.
2009-09-23
Nitrogen addition influences formation of aroma compounds, volatile acidity and ethanol in nitrogen deficient media fermented by Saccharomyces cerevisiae wine strains.
2009-08
Characterization of volatile compounds contributing to naturally occurring fruity fermented flavor in peanuts.
2008-09-10
Reusability of surfactant-coated Candida rugosa lipase immobilized in gelatin microemulsion-based organogels for ethyl isovalerate synthesis.
2008-04
Quantification of selected aroma-active compounds in strawberries by headspace solid-phase microextraction gas chromatography and correlation with sensory descriptive analysis.
2007-09
Comparison of the odor-active compounds in unhopped beer and beers hopped with different hop varieties.
2006-11-15
Quantification of selected aroma-active compounds in Pinot noir wines from different grape maturities.
2006-11-01
Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols.
2006-09-20
Comparison of aroma volatiles in commercial Merlot and Cabernet Sauvignon wines using gas chromatography-olfactometry and gas chromatography-mass spectrometry.
2006-05-31
Characterization of aroma compounds of chinese "Wuliangye" and "Jiannanchun" liquors by aroma extract dilution analysis.
2006-04-05
Aroma composition of red wines by different extraction methods and Gas Chromatography-SIM/MASS spectrometry analysis.
2005-06
Application of purge and trap extraction and gas chromatography for determination of minor esters in cider.
2005-04-01
Influence of strawberry yogurt composition on aroma release.
2004-10-06
Identification of fruity/fermented odorants in high-temperature-cured roasted peanuts.
2004-07-28
Synthesis of ethyl isovalerate using Rhizomucor miehei lipase: optimization.
2003-05-21
Gas chromatographic-olfactometric characterization of aroma compounds in two types of cashew apple nectar.
2003-02-12
A study on volatile organic compounds (VOCs) produced by tropical ascomycetous yeasts.
2003
Response of plum curculio (Coleoptera: Curculionidae) to odor-baited traps near woods.
2001-12
Evaluation of individual components of plum odor as potential attractants for adult plum curculios.
2001-01
Patents

Patents

04492799
1
06462042
1
06720319
1
JPH01311191A
5
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:40:11 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:11 GMT 2025
Record UNII
9ZZ5597636
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Ethyl isovalerate
FCC   FHFI   MI  
Systematic Name English
NSC-8869
Preferred Name English
BUTANOIC ACID, 3-METHYL-, ETHYL ESTER
Systematic Name English
3-METHYLBUTANOIC ACID ETHYL ESTER
Systematic Name English
ETHYL 3-METHYLBUTYRATE
Systematic Name English
ISOVALERIC ACID, ETHYL ESTER
Common Name English
ETHYL ISOVALERATE [MI]
Common Name English
ETHYL ISOVALERATE [FCC]
Common Name English
FEMA NO. 2463
Code English
ETHYL ISOVALERATE [FHFI]
Common Name English
ISOPENTANOIC ACID ETHYL ESTER
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION ETHYL ISOVALERATE
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
Code System Code Type Description
JECFA MONOGRAPH
202
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
WIKIPEDIA
6-Carboxyfluorescein
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
CHEBI
31571
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
NSC
8869
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
SMS_ID
100000135277
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
FDA UNII
9ZZ5597636
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
PUBCHEM
7945
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
MERCK INDEX
m5141
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY Merck Index
DAILYMED
9ZZ5597636
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
EVMPD
SUB70209
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
RXCUI
1314357
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY RxNorm
ECHA (EC/EINECS)
203-602-3
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
MESH
C475857
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID3047057
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
CAS
108-64-5
Created by admin on Mon Mar 31 18:40:11 GMT 2025 , Edited by admin on Mon Mar 31 18:40:11 GMT 2025
PRIMARY
NIH
NCATS
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