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Details

Stereochemistry RACEMIC
Molecular Formula C7H14O2
Molecular Weight 130.1849
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 2-METHYLBUTYRATE

SMILES

CCOC(=O)C(C)CC

InChI

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

HIDE SMILES / InChI

Molecular Formula C7H14O2
Molecular Weight 130.1849
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Evaluation of aroma differences between hand-squeezed juices from Valencia late and Navel oranges by quantitation of key odorants and flavor reconstitution experiments.
2001 May
On-line gas chromatography combustion/pyrolysis isotope ratio mass spectrometry (HRGC-C/P-IRMS) of pineapple (Ananas comosus L. Merr.) volatiles.
2003 Dec 31
Chemical and sensorial aroma characterization of freshly distilled Calvados. 2. Identification of volatile compounds and key odorants.
2003 Jan 15
Identification of fruity/fermented odorants in high-temperature-cured roasted peanuts.
2004 Jul 28
On-line reversed-phase liquid chromatography-gas chromatography coupled to mass spectrometry for enantiomeric analysis of chiral compounds in fruit beverages.
2004 Oct 29
[Changes in amino acid and fatty acid contents as well as activity of some related enzymes in apple fruit during aroma production].
2005 Dec
Aroma composition of red wines by different extraction methods and Gas Chromatography-SIM/MASS spectrometry analysis.
2005 Jun
Impact of growing environment on chickasaw blackberry (Rubus L.) aroma evaluated by gas chromatography olfactometry dilution analysis.
2005 May 4
Characterization of aroma-active compounds in raw and cooked pine-mushrooms (Tricholoma matsutake Sing.).
2006 Aug 23
Differentiation of aroma characteristics of pine-mushrooms (Tricholoma matsutake Sing.) of different grades using gas chromatography-olfactometry and sensory analysis.
2007 Mar 21
Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
2008 Jul 23
Changes in key aroma compounds of Criollo cocoa beans during roasting.
2008 Nov 12
Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.
2010 Feb
Mass spectrometry screening reveals widespread diversity in trichome specialized metabolites of tomato chromosomal substitution lines.
2010 May
Aroma profile and volatiles odor activity along gold cultivar pineapple flesh.
2010 Nov-Dec
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:01:56 GMT 2023
Edited
by admin
on Fri Dec 15 17:01:56 GMT 2023
Record UNII
L1T4AB29DS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL 2-METHYLBUTYRATE
FCC   FHFI  
Systematic Name English
ETHYL 2-METHYLBUTYRATE [FHFI]
Common Name English
ETHYL 2-METHYL BUTYRATE
Common Name English
ETHYL 2-METHYLBUTYRATE [FCC]
Common Name English
ETHYL 2-METHYLBUTANOATE
Systematic Name English
BUTANOIC ACID, 2-METHYL-, ETHYL ESTER
Common Name English
BUTYRIC ACID, 2-METHYL-, ETHYL ESTER
Common Name English
ETHYL .ALPHA.-METHYLBUTYRATE
Systematic Name English
FEMA NO. 2443
Code English
NSC-1103
Code English
ETHYL 2-METHYLBUTANOATE, (±)-
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
JECFA EVALUATION ETHYL 2-METHYLBUTYRATE
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID3052488
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
EVMPD
SUB72088
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
RXCUI
1312568
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
231-225-4
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
NSC
1103
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
DAILYMED
L1T4AB29DS
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
JECFA MONOGRAPH
28
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
CHEBI
88452
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
FDA UNII
L1T4AB29DS
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
CAS
7452-79-1
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
SMS_ID
100000135814
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY
PUBCHEM
24020
Created by admin on Fri Dec 15 17:01:56 GMT 2023 , Edited by admin on Fri Dec 15 17:01:56 GMT 2023
PRIMARY