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Details

Stereochemistry ACHIRAL
Molecular Formula C15H30O2
Molecular Weight 242.3975
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL MYRISTATE

SMILES

CCCCCCCCCCCCCC(=O)OC

InChI

InChIKey=ZAZKJZBWRNNLDS-UHFFFAOYSA-N
InChI=1S/C15H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17-2/h3-14H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C15H30O2
Molecular Weight 242.3975
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Polyamine-functional sterically stabilized latexes for covalently cross-linkable colloidosomes.
2010-12-07
Identification of compounds in the essential oil of nutmeg seeds (Myristica fragrans Houtt.) that inhibit locomotor activity in mice.
2010-11-23
Biosynthesis of monomers for plastics from renewable oils.
2010-11-03
Chronic myeloid leukemia patients sensitive and resistant to imatinib treatment show different metabolic responses.
2010-10-08
Evaluation of an oviposition-stimulating kairomone for the yellow fever mosquito, Aedes aegypti, in Recife, Brazil.
2010-06
Biosynthesis of unusual moth pheromone components involves two different pathways in the navel orangeworm, Amyelois transitella.
2010-05
The tropical brown alga Lobophora variegata: a source of antiprotozoal compounds.
2010-04-16
Chlamydomonas as a "new" organism for biodiesel production.
2010-03
Olfactory perception of oviposition-deterring fatty acids and their methyl esters by the Asian corn borer, Ostrinia furnacalis.
2009
Overexpression of the apple alcohol acyltransferase gene alters the profile of volatile blends in transgenic tobacco leaves.
2008-11
Hydroxyapatite nanoparticles as stimulus-responsive particulate emulsifiers and building block for porous materials.
2007-11-01
Effects of pH and salt concentration on oil-in-water emulsions stabilized solely by nanocomposite microgel particles.
2006-02-28
Toxicity studies of tetradecanoic acid, 2-sulfo-, 1-methylester, sodium salt (C14-MES).
2005-12
Effect of varying the oil phase on the behavior of pH-responsive latex-based emulsifiers: demulsification versus transitional phase inversion.
2004-08-31
Supercritical CO2 as a reaction medium for synthesis of capsaicin analogues by lipase-catalyzed transacylation of capsaicin.
2003-09
Characterization of Z/E11- and Z9-desaturases from the obliquebanded leafroller moth, Choristoneura rosaceana.
2002
Mannosylerythritol lipid, a yeast extracellular glycolipid, shows high binding affinity towards human immunoglobulin G.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:19:12 GMT 2025
Edited
by admin
on Mon Mar 31 19:19:12 GMT 2025
Record UNII
RG9851783C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2722
Preferred Name English
METHYL MYRISTATE
FHFI   HSDB   INCI   USP-RS  
INCI  
Official Name English
METHYL MYRISTATE [HSDB]
Common Name English
NSC-5029
Code English
TETRADECANOIC ACID, METHYL ESTER
Common Name English
MYRISTIC ACID, METHYL ESTER
Common Name English
METHYL TETRADECANOATE
Systematic Name English
METHYL MYRISTATE [USP-RS]
Common Name English
METHYL MYRISTATE [FHFI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION METHYL MYRISTATE
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
Code System Code Type Description
NSC
5029
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
CHEBI
89199
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
JECFA MONOGRAPH
211
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID5027019
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
RS_ITEM_NUM
1431501
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-680-1
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
MESH
C508363
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
CAS
124-10-7
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
FDA UNII
RG9851783C
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
HSDB
5602
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY
PUBCHEM
31284
Created by admin on Mon Mar 31 19:19:12 GMT 2025 , Edited by admin on Mon Mar 31 19:19:12 GMT 2025
PRIMARY