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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 C17H30N
Molecular Weight 248.4268
Charge 1
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
Design, synthesis and in vitro evaluation of pyridinium ion based cyclase inhibitors and antifungal agents.
1996 Jan
Sono-electroanalysis of copper: enhanced detection and determination in the presence of surfactants.
2002 Apr
High throughput screening of transdermal formulations.
2002 May
Effects of soil fines and surfactant sorption on contaminant reduction of coarse fractions during soil washing.
2003
Nanostructures of polyelectrolyte gel-surfactant complexes in uniaxially stretched networks.
2003 Aug
The role of the surfactant head group in the emulsification process: Single surfactant systems.
2003 Jan 15
Synthesis and characterization of 2,3-di-O-alkylated amyloses: hydrophobic substitution destabilizes helical conformation.
2003 Jul
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 Sep
Soft antimicrobial agents: synthesis and activity of labile environmentally friendly long chain quaternary ammonium compounds.
2003 Sep 11
Forces between glass surfaces in mixed cationic-zwitterionic surfactant systems.
2004 May 25
Calorimetric study on the temperature dependence of the formation of mixed ionic/nonionic micelles.
2004 Oct 26
Complex formation between dodecylpyridinium chloride and multicharged anionic planar substances.
2004 Sep 14
Effect of the nature of the counterion on the properties of anionic surfactants. 4. Characterizing micelles of tetraalkylammonium dodecyl sulfate as reaction media.
2005 Apr 28
Association of cationic surfactants with maleic acid copolymers: dependence of binding on the nature of the neutral comonomer unit.
2005 Aug 1
Ionic liquid crystal precursors for inorganic particles: phase diagram and thermal properties of a CuCl nanoplatelet precursor.
2005 Aug 18
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 Aug 25
Spectrophotometric studies of anionic dye-cationic surfactant interactions in mixture of cationic and nonionic surfactants.
2005 Mar
The role of the surfactant head group in the emulsification process: binary (nonionic-ionic) surfactant mixtures.
2005 Nov 1
Surfactant-induced detachment of monodispersed hematite particles adhered on glass.
2006 Jul 1
Antifungal characteristics of N,N'-hexamethylenebis (4-carbamoyl-1-decylpyridinium bromide).
2006 Mar
Study of the interaction between Apis mellifera venom and micro-heterogeneous systems.
2006 May
C.I. Reactive Orange 16-dodecylpyridinium chloride interactions in electrolytic solutions.
2006 Sep
The Hofmeister series effect in adsorption of cationic surfactants--theoretical description and experimental results.
2006 Sep 25
Role of the ammonium group in the diffusion of quaternary ammonium compounds in Streptococcus mutans biofilms.
2007 Dec
1-Tetra-decyl-pyridinium bromide monohydrate.
2008 Nov 26
Assessment of antibacterial activity of self-etching dental adhesive systems: An in vitro study.
2008 Oct
Ultrasonic nebulization in aqueous solutions and the role of interfacial adsorption dynamics in surfactant enrichment.
2008 Sep 16
Reducing plant uptake of PAHs by cationic surfactant-enhanced soil retention.
2009 Jun
Adsorptive removal of cationic surfactants from aqueous solutions onto high-area activated carbon cloth monitored by in situ UV spectroscopy.
2010 Feb 15
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:56:02 UTC 2023
Edited
by admin
on Fri Dec 15 16:56:02 UTC 2023
Record UNII
KJM5A6A3YL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAURYLPYRIDINIUM CHLORIDE
INCI  
INCI  
Official Name English
LAURYLPYRIDINIUM CHLORIDE [INCI]
Common Name English
ELTREN
Brand Name English
PYRIDINIUM, 1-DODECYL-, CHLORIDE (1:1)
Systematic Name English
1-DODECYLPYRIDINIUM CHLORIDE
Systematic Name English
DODECYLPYRIDINIUM CHLORIDE
WHO-DD  
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 Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
PUBCHEM
7717
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
ECHA (EC/EINECS)
203-232-2
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
RXCUI
2381132
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
EPA CompTox
DTXSID7051476
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
CAS
104-74-5
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
DAILYMED
KJM5A6A3YL
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
SMS_ID
100000079261
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
NSC
35027
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
MESH
C510815
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
FDA UNII
KJM5A6A3YL
Created by admin on Fri Dec 15 16:56:02 UTC 2023 , Edited by admin on Fri Dec 15 16:56:02 UTC 2023
PRIMARY
Related Record Type Details
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