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Details

Stereochemistry ACHIRAL
Molecular Formula C10H23N
Molecular Weight 157.2963
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OCTYLDIMETHYLAMINE

SMILES

CCCCCCCCN(C)C

InChI

InChIKey=UQKAOOAFEFCDGT-UHFFFAOYSA-N
InChI=1S/C10H23N/c1-4-5-6-7-8-9-10-11(2)3/h4-10H2,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Enantioselective retention of beta-blocking agents on human serum albumin and alpha 1-acid glycoprotein HPLC columns: relationships with different scales of lipophilicity.
2009-12-08
Bacteriostatic polymer film immobilization.
2006-12-15
Investigation of chiral recognition mechanism on chicken alpha(1)-acid glycoprotein using separation system.
2006-02-17
The strongest isolable acid.
2004-10-11
Pharmaceutical-grade albumin: impaired drug-binding capacity in vitro.
2004-03-29
Suppression of deleterious effects of free silanols in liquid chromatography by imidazolium tetrafluoroborate ionic liquids.
2004-03-19
Enantioselective analysis of ritalinic acids in biological samples by using a protein-based chiral stationary phase.
2003-11
Analysis and pharmacokinetics of bulaquine and its major metabolite primaquine in rabbits using an LC-UV method--a pilot study.
2003-04-24
Comparison of reversed-phase liquid chromatographic methods for the separation of new quinolones.
2002-08
Characterisation of reversed-phase stationary phases for the liquid chromatographic analysis of basic pharmaceuticals by thermodynamic data.
2002-07-26
Patents
Name Type Language
NSC-63928
Preferred Name English
OCTYLDIMETHYLAMINE
Systematic Name English
1-OCTANAMINE, N,N-DIMETHYL-
Systematic Name English
N,N-DIMETHYLOCTYLAMINE
Systematic Name English
N,N-DIMETHYL-1-OCTANAMINE
Systematic Name English
DIMETHYLOCTYLAMINE
Systematic Name English
N,N-DIMETHYL-N-OCTYLAMINE
Systematic Name English
OCTYLAMINE, N,N-DIMETHYL-
Systematic Name English
N-OCTYLDIMETHYLAMINE
Systematic Name English
1-(DIMETHYLAMINO)OCTANE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID2036299
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
MESH
C095543
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
NSC
63928
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
CAS
7378-99-6
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
PUBCHEM
16224
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
230-939-3
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY
FDA UNII
20N7H7X4SD
Created by admin on Mon Mar 31 21:32:50 GMT 2025 , Edited by admin on Mon Mar 31 21:32:50 GMT 2025
PRIMARY