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Details

Stereochemistry ACHIRAL
Molecular Formula C10H20O2
Molecular Weight 172.2646
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL NONANOATE

SMILES

CCCCCCCCC(=O)OC

InChI

InChIKey=IJXHLVMUNBOGRR-UHFFFAOYSA-N
InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-10(11)12-2/h3-9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C10H20O2
Molecular Weight 172.2646
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Production of a new glycolipid biosurfactant from marine Nocardiopsis lucentensis MSA04 in solid-state cultivation.
2010-06-15
Microbial community structure of leaf-cutter ant fungus gardens and refuse dumps.
2010-03-29
Chlamydomonas as a "new" organism for biodiesel production.
2010-03
Large-scale chemical and chemo-enzymatic synthesis of a spacer-containing Pk-trisaccharide.
2004-04-28
Enzymatic synthesis of a capsinoid by the acylation of vanillyl alcohol with fatty acid derivatives catalyzed by lipases.
2002-02
Palladium(II)-catalyzed oxidation of aldehydes and ketones. 1. Carbonylation of ketones with carbon monoxide catalyzed by palladium(II) chloride in methanol.
2001-01-12
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:29:00 GMT 2025
Edited
by admin
on Mon Mar 31 19:29:00 GMT 2025
Record UNII
7XKD6QOH68
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYL PELARGONATE
INCI  
INCI  
Preferred Name English
METHYL NONANOATE
FHFI  
Systematic Name English
METHYL NONANOATE [FHFI]
Common Name English
METHYL NONYLATE
Common Name English
METHYL N-NONANOATE
Common Name English
NONANOIC ACID METHYL ESTER
Systematic Name English
NONANOIC ACID, METHYL ESTER
Common Name English
FEMA NO. 2724
Code English
PELARGONIC ACID METHYL ESTER
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION METHYL NONANOATE
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
Code System Code Type Description
DRUG BANK
DB01631
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
ECHA (EC/EINECS)
217-052-7
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
CAS
1731-84-6
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID8061921
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
FDA UNII
7XKD6QOH68
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
PUBCHEM
15606
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
JECFA MONOGRAPH
208
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY
CHEBI
44499
Created by admin on Mon Mar 31 19:29:00 GMT 2025 , Edited by admin on Mon Mar 31 19:29:00 GMT 2025
PRIMARY