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

Details

Stereochemistry ACHIRAL
Molecular Formula C6H12O2
Molecular Weight 116.1583
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYL ACETATE

SMILES

CCCCOC(C)=O

InChI

InChIKey=DKPFZGUDAPQIHT-UHFFFAOYSA-N
InChI=1S/C6H12O2/c1-3-4-5-8-6(2)7/h3-5H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H12O2
Molecular Weight 116.1583
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Biofiltration and kinetic aspects of a biotrickling filter for the removal of paint solvent mixture laden air stream.
2008-04-15
Development and validation of a high performance liquid chromatography-tandem mass spectrometry for the determination of etodolac in human plasma.
2008-02-15
Thixotropic twin-dendritic organogelators.
2008
Comparative evaluation of biomarkers of occupational exposure to toluene.
2007-10
Predicting olfactory receptor neuron responses from odorant structure.
2007-05-04
Production of butyl acetate ester by lipase from novel strain of Rhizopus oryzae.
2007-04
Formation and durability of dithiocarbamic metals in stabilized air pollution control residue from municipal solid waste incineration and melting processes.
2007-03-01
Bioconversion of ethyl 4-chloro-3-oxobutanoate by permeabilized fresh brewer's yeast cells in the presence of allyl bromide.
2007-02
Determination of itopride in human plasma by liquid chromatography coupled to tandem mass spectrometric detection: application to a bioequivalence study.
2007-01-30
The behavior of exciplex decay processes and interplay of radiationless transition and preliminary reorganization mechanisms of electron transfer in loose and tight pairs of reactants.
2007-01-18
Functional organogel based on a salicylideneaniline derivative with enhanced fluorescence emission and photochromism.
2007
Developmental toxic effects of ethylbenzene or toluene alone and in combination with butyl acetate in rats after inhalation exposure.
2006-12-21
In situ bioremediation of nitrate and perchlorate in vadose zone soil for groundwater protection using gaseous electron donor injection technology.
2006-12
Effect of copper on the volatility of aroma compounds in a model mouth system.
2006-11-29
Changes in the volatile compounds and chemical and physical properties of Kuerle fragrant pear (Pyrus serotina Reld) during storage.
2006-11-15
New method of change in temperature coefficient delay of acoustic waves in thin piezoelectric plates.
2006-11
Biochemical kinetic behaviors between n-butyl acetate and composite bead in biofilter.
2006-11
Photoisomerization of a carbocyanine derivative in the reverse phases of a block copolymer: evidence for the existence of water droplets.
2006-08-01
Multiple microbial activities for volatile organic compounds reduction by biofiltration.
2006-07
Micro-extraction techniques in analytical toxicology: short review.
2006-06-17
Physical and reactive extraction equilibria of penicillin G in a hydrogen-bond acceptor solvent system.
2006-06-03
[Study on fluorescence spectral behavior of trimethoxyphenylflurone with gallium in microemulsion].
2006-06
Occupational exposure to airborne solvents during nail sculpturing.
2006-05
Enhanced urinary odor discrimination in female aromatase knockout (ArKO) mice.
2006-05
Spectral characteristics and nonlinear studies of crystal violet dye.
2006-03-01
Multiple headspace single-drop microextraction-a new technique for quantitative determination of styrene in polystyrene.
2006-01-13
[Determination of cotinine in human urine with gas chromatograph-mass spectrometry].
2006-01
[Changes in amino acid and fatty acid contents as well as activity of some related enzymes in apple fruit during aroma production].
2005-12
Neuropsychological effects of chronic low-dose exposure to polychlorinated biphenyls (PCBs): a cross-sectional study.
2005-10-19
Liquid chromatography-tandem mass spectrometry determination of LSD, ISO-LSD, and the main metabolite 2-oxo-3-hydroxy-LSD in forensic samples and application in a forensic case.
2005-10-15
Mathematical modeling of biofiltration in activated pine-bark charge of a biofilter.
2005-09
Injector-internal thermal desorption from edible oils. Part 1: visual experiments on sample deposition on the liner wall.
2005-08
Investigation of the micropolarity in reverse micelles of nonionic poly(ethylene oxide) surfactants using 4-nitropyridine-N-oxide as absorption probe.
2005-07-15
Interaction of cyclodextrins with aliphatic acetate esters and aroma components of La France pear.
2005-06-29
An alcohol acyl transferase from apple (cv. Royal Gala), MpAAT1, produces esters involved in apple fruit flavor.
2005-06
Air formaldehyde and solvent concentrations during surface coating with acid-curing lacquers and paints in the woodworking and furniture industry.
2005-06
Fast, simple, and validated gas chromatographic-mass spectrometric assay for quantification of drugs relevant to diagnosis of brain death in human blood plasma samples.
2005-06
Changes in volatile emissions from apple trees and associated response of adult female codling moths over the fruit-growing season.
2005-05-18
[Determination of taxol in aril of Torreya grandis cv. merrilli].
2005-05
Derivation of a human equivalent concentration for n-butanol using a physiologically based pharmacokinetic model for n-butyl acetate and metabolites n-butanol and n-butyric acid.
2005-05
[Treatment of mix gas containing butyl acetate, n-butyl alcohol and phenylacetic acid from pharmaceutical factory by bio-trickling filter].
2005-03
Anosmia in association with occupational use of a waterproof coating chemical.
2005-03
Production of volatile organic sulfur compounds (VOSCs) by basidiomycetous yeasts.
2005-02
Effectiveness of allyl acetate as a fumigant against five stored grain beetle pests.
2005-01
Interaction forces between oil-water particle interfaces--non-DLVO forces.
2005
Novel CuS nanofibers using organogel as a template: controlled by binding sites.
2004-12-07
Annoyance and performance of three environmentally intolerant groups during experimental challenge with chemical odors.
2004-12
Peripheral nerve conduction study in workers exposed to a mixture of organic solvents in paint and lacquer industry.
2004-12
Symptoms in relation to chemicals and dampness in newly built dwellings.
2004-10
[Determining mole ratio of monomers in new adsorbent of solid-phase microextraction by infrared spectroscopy].
2004-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:45:32 GMT 2025
Edited
by admin
on Mon Mar 31 17:45:32 GMT 2025
Record UNII
464P5N1905
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTYL ACETATE
FCC   FHFI   INCI   MART.   USP-RS  
INCI  
Official Name English
N-BUTYL ACETATE
HSDB   MI  
Preferred Name English
BUTYL ACETATE [FCC]
Common Name English
BUTYL ETHANOATE
Systematic Name English
ACETIC ACID N-BUTYL ESTER
Common Name English
BUTYL ACETATE [FHFI]
Common Name English
N-BUTYL ACETATE [HSDB]
Common Name English
1-ACETOXYBUTANE
Systematic Name English
ACETIC ACID BUTYL ESTER
Systematic Name English
NSC-9298
Code English
1-BUTYL ACETATE
Systematic Name English
BUTYL ACETATE [MART.]
Common Name English
FEMA NO. 2174
Code English
BUTYL ACETATE [USP-RS]
Common Name English
N-BUTYL ACETATE [MI]
Common Name English
TRIBUTYL ACETYLCITRATE IMPURITY E [EP IMPURITY]
Common Name English
BUTYL ESTER ACETIC ACID
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
CFR 21 CFR 175.320
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
JECFA EVALUATION BUTYL ACETATE
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
Code System Code Type Description
JECFA MONOGRAPH
247
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
PUBCHEM
31272
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
CAS
123-86-4
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-658-1
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
HSDB
152
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
RS_ITEM_NUM
1082606
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
WIKIPEDIA
BUTYL ACETATE
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
EVMPD
SUB23418
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
CHEBI
31328
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
MESH
C006848
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
MERCK INDEX
m2807
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY Merck Index
NSC
9298
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
SMS_ID
100000088725
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
DAILYMED
464P5N1905
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID3021982
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
FDA UNII
464P5N1905
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY
RXCUI
1362908
Created by admin on Mon Mar 31 17:45:32 GMT 2025 , Edited by admin on Mon Mar 31 17:45:32 GMT 2025
PRIMARY RxNorm
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
EP
Related Record Type Details
ACTIVE MOIETY