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Details

Stereochemistry ACHIRAL
Molecular Formula C17H30N.Cl
Molecular Weight 283.88
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAURYLPYRIDINIUM CHLORIDE

SMILES

[Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1

InChI

InChIKey=GKQHIYSTBXDYNQ-UHFFFAOYSA-M
InChI=1S/C17H30N.ClH/c1-2-3-4-5-6-7-8-9-10-12-15-18-16-13-11-14-17-18;/h11,13-14,16-17H,2-10,12,15H2,1H3;1H/q+1;/p-1

HIDE SMILES / InChI

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

Molecular Formula C17H30N
Molecular Weight 248.4268
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Adsorptive removal of cationic surfactants from aqueous solutions onto high-area activated carbon cloth monitored by in situ UV spectroscopy.
2010-02-15
Reducing plant uptake of PAHs by cationic surfactant-enhanced soil retention.
2009-06
1-Tetra-decyl-pyridinium bromide monohydrate.
2008-11-26
Assessment of antibacterial activity of self-etching dental adhesive systems: An in vitro study.
2008-10
Ultrasonic nebulization in aqueous solutions and the role of interfacial adsorption dynamics in surfactant enrichment.
2008-09-16
Role of the ammonium group in the diffusion of quaternary ammonium compounds in Streptococcus mutans biofilms.
2007-12
The Hofmeister series effect in adsorption of cationic surfactants--theoretical description and experimental results.
2006-09-25
C.I. Reactive Orange 16-dodecylpyridinium chloride interactions in electrolytic solutions.
2006-09
Surfactant-induced detachment of monodispersed hematite particles adhered on glass.
2006-07-01
Study of the interaction between Apis mellifera venom and micro-heterogeneous systems.
2006-05
Antifungal characteristics of N,N'-hexamethylenebis (4-carbamoyl-1-decylpyridinium bromide).
2006-03
The role of the surfactant head group in the emulsification process: binary (nonionic-ionic) surfactant mixtures.
2005-11-01
Effect of the nature of the counterion on the properties of anionic surfactants. 5. Self-association behavior and micellar properties of ammonium dodecyl sulfate.
2005-08-25
Ionic liquid crystal precursors for inorganic particles: phase diagram and thermal properties of a CuCl nanoplatelet precursor.
2005-08-18
Association of cationic surfactants with maleic acid copolymers: dependence of binding on the nature of the neutral comonomer unit.
2005-08-01
Effect of the nature of the counterion on the properties of anionic surfactants. 4. Characterizing micelles of tetraalkylammonium dodecyl sulfate as reaction media.
2005-04-28
Spectrophotometric studies of anionic dye-cationic surfactant interactions in mixture of cationic and nonionic surfactants.
2005-03
Calorimetric study on the temperature dependence of the formation of mixed ionic/nonionic micelles.
2004-10-26
Complex formation between dodecylpyridinium chloride and multicharged anionic planar substances.
2004-09-14
Forces between glass surfaces in mixed cationic-zwitterionic surfactant systems.
2004-05-25
Soft antimicrobial agents: synthesis and activity of labile environmentally friendly long chain quaternary ammonium compounds.
2003-09-11
N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices.
2003-09
Nanostructures of polyelectrolyte gel-surfactant complexes in uniaxially stretched networks.
2003-08
Synthesis and characterization of 2,3-di-O-alkylated amyloses: hydrophobic substitution destabilizes helical conformation.
2003-07
The role of the surfactant head group in the emulsification process: Single surfactant systems.
2003-01-15
Effects of soil fines and surfactant sorption on contaminant reduction of coarse fractions during soil washing.
2003
High throughput screening of transdermal formulations.
2002-05
Sono-electroanalysis of copper: enhanced detection and determination in the presence of surfactants.
2002-04
Design, synthesis and in vitro evaluation of pyridinium ion based cyclase inhibitors and antifungal agents.
1996-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:09 GMT 2025
Record UNII
KJM5A6A3YL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAURYLPYRIDINIUM CHLORIDE
INCI  
INCI  
Official Name English
DODECYLPYRIDINIUM CHLORIDE
WHO-DD  
Preferred Name English
ELTREN
Brand Name English
PYRIDINIUM, 1-DODECYL-, CHLORIDE (1:1)
Systematic Name English
1-DODECYLPYRIDINIUM CHLORIDE
Systematic Name English
DEHYQUART C
Brand Name English
NSC-35027
Code English
Dodecylpyridinium chloride [WHO-DD]
Common Name English
QUATERNARIO LPC
Brand Name English
Code System Code Type Description
EVMPD
SUB13644MIG
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
PUBCHEM
7717
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-232-2
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
RXCUI
2381132
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID7051476
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
CAS
104-74-5
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
DAILYMED
KJM5A6A3YL
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
SMS_ID
100000079261
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
NSC
35027
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
MESH
C510815
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
FDA UNII
KJM5A6A3YL
Created by admin on Mon Mar 31 18:38:09 GMT 2025 , Edited by admin on Mon Mar 31 18:38:09 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE