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Details

Stereochemistry ACHIRAL
Molecular Formula C8H16O2
Molecular Weight 144.2114
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYL BUTYRATE

SMILES

CCCCOC(=O)CCC

InChI

InChIKey=XUPYJHCZDLZNFP-UHFFFAOYSA-N
InChI=1S/C8H16O2/c1-3-5-7-10-8(9)6-4-2/h3-7H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H16O2
Molecular Weight 144.2114
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Differential attraction of malaria mosquitoes to volatile blends produced by human skin bacteria.
2010-12-30
Rate coefficients for reactions of OH and Cl with esters.
2010-12-17
Comparison of volatile components in Chinese traditional pickled peppers using HS-SPME-GC-MS, GC-O and multivariate analysis.
2010-12
Enzymatic reactions and synthesis of n-butyl caproate: esterification, transesterification and aminolysis using a recombinant lipase from Geobacillus thermoleovorans CCR11.
2010-09
Screening of food grade lipases to be used in esterification and interesterification reactions of industrial interest.
2010-02
Attraction and antennal response of the common wasp, Vespula vulgaris (L.), to selected synthetic chemicals in New Zealand beech forests.
2009-09
Characterization of fermentative behaviors of lactic acid bacteria in grape wines through 1H NMR- and GC-based metabolic profiling.
2009-06-10
Comparative analysis of the volatile fraction from Annona cherimola Mill. cultivars by solid-phase microextraction and gas chromatography-quadrupole mass spectrometry detection.
2009-01-15
Analysis of expressed sequence tags from Actinidia: applications of a cross species EST database for gene discovery in the areas of flavor, health, color and ripening.
2008-07-27
Immobilization of Candida antarctica lipase B by adsorption to green coconut fiber.
2008-03
Covalent attachment of Candida rugosa lipase on chemically modified hybrid matrix of polysiloxane-polyvinyl alcohol with different activating compounds.
2008-02-15
The effect of ultrasonic pre-treatment on the catalytic activity of lipases in aqueous and non-aqueous media.
2008-01-30
Enhancement of lipase activity in non-aqueous media upon immobilization on multi-walled carbon nanotubes.
2007-11-29
A new method for wide frequency range dynamic olfactory stimulation and characterization.
2007-09
Chemesthesis from volatile organic compounds: Psychophysical and neural responses.
2006-07-30
Understanding structure-stability relationships of Candida antartica lipase B in ionic liquids.
2005-05-10
Criteria to design green enzymatic processes in ionic liquid/supercritical carbon dioxide systems.
2004-06-05
Heterologous expression of the Saccharomyces cerevisiae alcohol acetyltransferase genes in Clostridium acetobutylicum and Escherichia coli for the production of isoamyl acetate.
2003-07
Lipase-catalyzed synthesis of butyl butyrate by alcoholysis in an integrated liquid-vapor system.
2003-06-07
Continuous green biocatalytic processes using ionic liquids and supercritical carbon dioxide.
2002-04-07
Esterification activity and stability of Candida rugosa lipase immobilized into chitosan.
2002
Rice straw as a support for immobilization of microbial lipase.
2001-12-12
Aromatic profile of aqueous banana essence and banana fruit by gas chromatography-mass spectrometry (GC-MS) and gas chromatography-olfactometry (GC-O).
2001-10
Selection of stabilizing additive for lipase immobilization on controlled pore silica by factorial design.
2001
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:46:29 GMT 2025
Edited
by admin
on Mon Mar 31 18:46:29 GMT 2025
Record UNII
1BHV00T1M4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTYL BUTYRATE
FCC   FHFI  
Systematic Name English
N-BUTYL N-BUTYRATE
MI  
Preferred Name English
N-BUTYL-BUTYRATE
Common Name English
BUTANOIC ACID, BUTYL ESTER
Common Name English
N-BUTYL N-BUTYRATE [MI]
Common Name English
BUTYRIC ACID N-BUTYL ESTER
Common Name English
BUTYL BUTYRATE [FHFI]
Common Name English
FEMA NO. 2186
Code English
NSC-8458
Code English
N-BUTYL BUTYRATE
Common Name English
BUTYL BUTYRATE [FCC]
Common Name English
N-BUTYL BUTANOATE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
JECFA EVALUATION BUTYL BUTYRATE
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
Code System Code Type Description
WIKIPEDIA
BUTYL BUTYRATE
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
EVMPD
SUB176719
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
MERCK INDEX
m2828
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY Merck Index
CAS
109-21-7
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
NSC
8458
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
FDA UNII
1BHV00T1M4
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
JECFA MONOGRAPH
223
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
PUBCHEM
7983
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
MESH
C022793
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
CHEBI
87429
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID7041702
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
SMS_ID
100000162741
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-656-8
Created by admin on Mon Mar 31 18:46:29 GMT 2025 , Edited by admin on Mon Mar 31 18:46:29 GMT 2025
PRIMARY