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Details

Stereochemistry ACHIRAL
Molecular Formula C16H35N
Molecular Weight 241.4558
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIOCTYLAMINE

SMILES

CCCCCCCCNCCCCCCCC

InChI

InChIKey=LAWOZCWGWDVVSG-UHFFFAOYSA-N
InChI=1S/C16H35N/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h17H,3-16H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H35N
Molecular Weight 241.4558
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The critical role of surfactants in the growth of cobalt nanoparticles.
2010-01-05
Mycolic acid cyclopropanation is essential for viability, drug resistance, and cell wall integrity of Mycobacterium tuberculosis.
2009-05-29
Simultaneous extraction and concentration of penicillin G by hollow fiber renewal liquid membrane.
2009-04-01
Identification of inhibitors of the E. coli cyclopropane fatty acid synthase from the screening of a chemical library: In vitro and in vivo studies.
2008-11
Expeditious synthesis of water-soluble, monolayer-protected gold nanoparticles of controlled size and monolayer composition.
2008-04-15
In vitro permeability and metabolic stability of bile pigments and the effects of hydrophilic and lipophilic modification of biliverdin.
2008-04-01
Inelastic electron tunneling spectroscopy of alkane monolayers with dissimilar attachment chemistry to gold.
2007-12-12
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:28:30 GMT 2025
Edited
by admin
on Mon Mar 31 18:28:30 GMT 2025
Record UNII
A7HM3062RM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-1765
Preferred Name English
DIOCTYLAMINE
Systematic Name English
RC-5632
Code English
DI-N-OCTYLAMINE
Common Name English
N-N-OCTYL-N-OCTYLAMINE
Common Name English
N,N-DIOCTYLAMINE
Systematic Name English
1-OCTANAMINE, N-OCTYL-
Systematic Name English
RC 5632
Code English
Code System Code Type Description
PUBCHEM
3094
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
FDA UNII
A7HM3062RM
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
NSC
1765
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-311-6
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID2061517
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
CAS
1120-48-5
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY
CHEBI
132284
Created by admin on Mon Mar 31 18:28:30 GMT 2025 , Edited by admin on Mon Mar 31 18:28:30 GMT 2025
PRIMARY