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Details

Stereochemistry ACHIRAL
Molecular Formula C7H12O3
Molecular Weight 144.1684
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL LEVULINATE

SMILES

CCOC(=O)CCC(C)=O

InChI

InChIKey=GMEONFUTDYJSNV-UHFFFAOYSA-N
InChI=1S/C7H12O3/c1-3-10-7(9)5-4-6(2)8/h3-5H2,1-2H3

HIDE SMILES / InChI

Approval Year

1981
138
PubMed

PubMed

TitleDatePubMed
Effects of material hydrophobicity on physical properties of polymeric microspheres formed by double emulsion process.
2002 Dec 5
Antioxidant activity in common beans (Phaseolus vulgaris L.).
2002 Nov 20
Determination of tyramine in cheese by LC-UV.
2003 Apr 10
Determination of multiclass pesticides in food commodities by pressurized liquid extraction using GC-MS/MS and LC-MS/MS.
2005 Dec
[Detection of furadan in biological fluids].
2005 Sep-Oct
Partitioning and inhibition of lipid oxidation in mechanically separated turkey by components of cranberry press cake.
2006 Aug 23
New qualitative approach in the characterization of antioxidants in white wines by antioxidant free radical scavenging and NMR techniques.
2008 Nov 12
3-Carb-oxy-2-methoxy-phenyl-boronic acid.
2008 Sep 20
Conversion of furfuryl alcohol into ethyl levulinate using solid acid catalysts.
2009
Synthesis of a photo-caged aminooxy alkane thiol.
2009 Dec 7
N-Benzoyl-N'-(2-chloro-3-pyrid-yl)thio-urea.
2009 Jul 18
Genetic manipulation of palmitoylethanolamide production and inactivation in Saccharomyces cerevisiae.
2009 Jun 16
Comment on processes for the direct conversion of cellulose or cellulosic biomass into levulinate esters.
2010 Dec 17
Crystal and electronic structure of a mixed-valent Np(IV)-Np(V) compound: [BuMeIm]5[Np(NpO2)3(H2O)6Cl12].
2010 Mar 1
A three-step synthetic approach to asymmetrically functionalized 4H-cyclopenta[2,1-b:3,4-b']dithiophenes.
2010 Nov 5
Flavan-3-ol compounds from wine wastes with in vitro and in vivo antioxidant activity.
2010 Oct
Patents

Patents

05053422
4
06114358
2
Name Type Language
ETHYL LEVULINATE
FCC   FHFI   MI  
Systematic Name English
4-OXOPENTANOIC ACID ETHYL ESTER
Systematic Name English
ETHYL LEVULINATE [FCC]
Common Name English
ETHYL LEVULINATE [MI]
Common Name English
LEVULINATE
Common Name English
NSC-24876
Code English
PENTANOIC ACID, 4-OXO-, ETHYL ESTER
Common Name English
LEVULINIC ACID, ETHYL ESTER
Common Name English
ETHYL LEVULINATE [FHFI]
Common Name English
ETHYL 4-OXOVALERATE
Systematic Name English
FEMA NO. 2442
Code English
ETHYL 4-KETOVALERATE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION ETHYL LEVULINATE
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
LOINC 79484-2
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
LOINC 79504-7
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
Code System Code Type Description
CAS
539-88-8
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
WIKIPEDIA
Ethyl levulinate
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
MERCK INDEX
m5144
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY Merck Index
RXCUI
1358175
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
ALTERNATIVE
JECFA MONOGRAPH
465
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
CHEBI
39150
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
MESH
C542586
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
DAILYMED
7BU24CSS2G
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
PUBCHEM
10883
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
SMS_ID
100000151945
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
FDA UNII
7BU24CSS2G
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
RXCUI
1313748
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID8047058
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-728-2
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
NSC
24876
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
EVMPD
SUB126382
Created by admin on Fri Dec 15 16:45:45 GMT 2023 , Edited by admin on Fri Dec 15 16:45:45 GMT 2023
PRIMARY
SUBSTANCE RECORD
Structure of ETHYL LEVULINATE
NIH
NCATS
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DISCLAIMER
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