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Details

Stereochemistry ACHIRAL
Molecular Formula C14H31N.ClH
Molecular Weight 249.864
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Dimethyl lauramine hydrochloride

SMILES

Cl.CCCCCCCCCCCCN(C)C

InChI

InChIKey=PGQAXGHQYGXVDC-UHFFFAOYSA-N
InChI=1S/C14H31N.ClH/c1-4-5-6-7-8-9-10-11-12-13-14-15(2)3;/h4-14H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C14H31N
Molecular Weight 213.4026
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
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 synthesis of chloropropyl-functionalized silica hybrid monolithic column with modification of N,N-dimethyl-N-dodecylamine for capillary electrochromatography separation.
2010-06-25
Omp85 from the thermophilic cyanobacterium Thermosynechococcus elongatus differs from proteobacterial Omp85 in structure and domain composition.
2010-06-04
Pore expansion of highly monodisperse phenylene-bridged organosilica spheres for chromatographic application.
2010-05-15
Aqueous heavy metals removal on amine-functionalized Si-MCM-41 and Si-MCM-48.
2009-11-15
Smoothly shifting fluorescent windows: a tunable "off-on-off" micellar sensor for pH.
2009-10
Insights in the antibacterial action of poly(methyloxazoline)s with a biocidal end group and varying satellite groups.
2008-07
Nanoemulsions prepared by a two-step low-energy process.
2008-06-17
X-ray crystallographic and biochemical characterizations of a mutant photosystem II complex from Thermosynechococcus vulcanus with the psbTc gene inactivated by an insertion mutation.
2008-05
Substrate specificity of a long-chain alkylamine-degrading Pseudomonas sp isolated from activated sludge.
2008-02
Regulation of germline stem cell proliferation downstream of nutrient sensing.
2006-12-06
Spectroscopic characterization of 2-amino-N-hexadecyl-benzamide (AHBA), a new fluorescence probe for membranes.
2006-11-20
N,N-dimethyl-n-dodecylamine caused contact dermatitis.
2005-12
Synthesis and characterization of N,N-dimethyldodecylamine-capped Aucore-Pdshell nanoparticles in toluene.
2005-11-08
Influence of satellite groups on telechelic antimicrobial functions of polyoxazolines.
2005-02-23
Poly(oxazoline)s with telechelic antimicrobial functions.
2005-01-11
Effect of additives on photodegradation of 1,3,5-trichlorobenzene in aqueous surfactant solutions.
2005
Effects of low-level hydrophobic substitution on conditioning properties of cationic cellulosic polymers in shampoo systems.
2004
[Occupational dermatitis in health care personnel].
2002-09-01
[The study of amphoteric surfacant sensitizing catalytic spectrophotometric determination of Mn (II)].
2002-08
Complete mineralization of dodecyldimethylamine using a two-membered bacterial culture.
2001-02
Fatty acids and derivatives as antimicrobial agents.
1972-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:44:06 GMT 2025
Edited
by admin
on Mon Mar 31 22:44:06 GMT 2025
Record UNII
Z7D9TJC8YM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-5879
Preferred Name English
Dimethyl lauramine hydrochloride
Common Name English
1-Dodecanamine, N,N-dimethyl-, hydrochloride
Systematic Name English
Dodecyldimethylamine hydrochloride
Systematic Name English
1-Dodecanamine, N,N-dimethyl-, hydrochloride (1:1)
Systematic Name English
Dimethyldodecylamine hydrochloride
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
217-953-5
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
CAS
2016-48-0
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
NSC
5879
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID40942213
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
PUBCHEM
16222
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
FDA UNII
Z7D9TJC8YM
Created by admin on Mon Mar 31 22:44:06 GMT 2025 , Edited by admin on Mon Mar 31 22:44:06 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE