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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H26O2
Molecular Weight 214.3443
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL LAURATE

SMILES

CCCCCCCCCCCC(=O)OC

InChI

InChIKey=UQDUPQYQJKYHQI-UHFFFAOYSA-N
InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C13H26O2
Molecular Weight 214.3443
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Methyl laurate (methyl dodecanoate), a flavouring agent, is found in alcoholic beverages.

Approval Year

PubMed

PubMed

TitleDatePubMed
Biorefinery approach for coconut oil valorisation: a statistical study.
2010-06
Crystallization of synthetic haemozoin (beta-haematin) nucleated at the surface of lipid particles.
2010-02-07
A novel regulatory system in plants involving medium-chain fatty acids.
2009-12
Fluoride, triclosan and organic weak acids as modulators of the arginine deiminase system in biofilms and suspension cells of oral streptococci.
2009-08
Retention time prediction of compounds in Grob standard mixture for apolar capillary columns in temperature-programmed gas chromatography.
2009-01
Overexpression of the apple alcohol acyltransferase gene alters the profile of volatile blends in transgenic tobacco leaves.
2008-11
Spectra and kinetic studies of the compound I derivative of cytochrome P450 119.
2008-10-08
Direct electrochemistry and electrocatalytic activity of cytochrome c covalently immobilized on a boron-doped nanocrystalline diamond electrode.
2008-06-01
The effect of ultrasonic pre-treatment on the catalytic activity of lipases in aqueous and non-aqueous media.
2008-01-30
Gas chromatographic/mass spectrometric analysis of the essential oil of Houttuynia cordata Thunb by using on-column methylation with tetramethylammonium acetate.
2007-03-22
Enzymatic chemoselective synthesis of secondary-amide surfactant from N-methylethanol amine.
2005-12
Synthesis of a novel series of 2-methylsulfanyl fatty acids and their toxicity on the human K-562 and U-937 leukemia cell lines.
2005-10
The effect of pH and organic ester penetration enhancers on skin permeation kinetics of terbutaline sulfate from pseudolatex-type transdermal delivery systems through mouse and human cadaver skins.
2005-09-30
Alkane-induced expression, substrate binding profile, and immunolocalization of a cytochrome P450 encoded on the nifD excision element of Anabaena 7120.
2005-03-24
X-ray studies of self-assembled organic monolayers grown on hydrogen-terminated Si(111).
2004-07-20
Preparation of uniform titanium dioxide (TiO2) polystyrene-based composite particles using the glass membrane emulsification process with a subsequent suspension polymerization.
2003-01-10
Uniform titanium dioxide (TiO(2)) microcapsules prepared by glass membrane emulsification with subsequent solvent evaporation.
2002-10-25
Antitumor activity of 1-acyloxymethyl derivatives of 5-fluorouracil against L1210 leukemia.
1982-03
Fatty acids and derivatives as antimicrobial agents.
1972-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:30:32 GMT 2025
Edited
by admin
on Mon Mar 31 18:30:32 GMT 2025
Record UNII
8IPS6BI6KW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYL DODECANOATE
HSDB  
Preferred Name English
METHYL LAURATE
FHFI   II   INCI   USP-RS  
INCI  
Official Name English
DODECANOIC ACID, METHYL ESTER
Common Name English
METHYL LAURATE [FHFI]
Common Name English
LAURIC ACID METHYL ESTER
Systematic Name English
LAURIC ACID, METHYL ESTER
Common Name English
METHYL LAURATE [II]
Common Name English
NSC-5027
Code English
FEMA NO. 2715
Code English
METHYL DODECANOATE [HSDB]
Common Name English
METHYL LAURATE [USP-RS]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION METHYL LAURATE
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
Code System Code Type Description
RXCUI
1362932
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY RxNorm
NCI_THESAURUS
C83962
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
NCI_THESAURUS
C45678
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
CONCEPT Industrial Aid
RS_ITEM_NUM
1430305
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
DAILYMED
8IPS6BI6KW
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
PUBCHEM
8139
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
CHEBI
87494
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID5026889
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-911-3
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
NSC
5027
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
CAS
111-82-0
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
HSDB
5550
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
MESH
C089549
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
JECFA MONOGRAPH
209
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY
FDA UNII
8IPS6BI6KW
Created by admin on Mon Mar 31 18:30:32 GMT 2025 , Edited by admin on Mon Mar 31 18:30:32 GMT 2025
PRIMARY