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3026-66-2

3026-66-2 | Pyridinium, 1-dodecyl-, iodide (1:1)

CAS No: 3026-66-2 Catalog No: AG002ZEF MDL No:

Product Description

Catalog Number:
AG002ZEF
Chemical Name:
Pyridinium, 1-dodecyl-, iodide (1:1)
CAS Number:
3026-66-2
Molecular Formula:
C17H30IN
Molecular Weight:
375.3313
IUPAC Name:
1-dodecylpyridin-1-ium;iodide
InChI:
InChI=1S/C17H30N.HI/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
InChI Key:
GZNACENTEXAZDR-UHFFFAOYSA-M
SMILES:
CCCCCCCCCCCC[n+]1ccccc1.[I-]

Properties

Complexity:
161  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
375.142g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
375.338g/mol
Monoisotopic Mass:
375.142g/mol
Rotatable Bond Count:
11  
Topological Polar Surface Area:
3.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0

Literature

Title Journal
Effect of a cationic surfactant on the volatilization of PAHs from soil. Environmental science and pollution research international 20120601
The mechanism of sonochemical degradation of a cationic surfactant in aqueous solution. Ultrasonics sonochemistry 20110301
Surfactant-facilitated remediation of metal-contaminated soils: efficacy and toxicological consequences to earthworms. Environmental toxicology and chemistry 20110101
Reducing plant uptake of PAHs by cationic surfactant-enhanced soil retention. Environmental pollution (Barking, Essex : 1987) 20090601
C.I. Reactive Orange 16-dodecylpyridinium chloride interactions in electrolytic solutions. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20060901
Antifungal characteristics of N,N'-hexamethylenebis (4-carbamoyl-1-decylpyridinium bromide). Biocontrol science 20060301
Complex formation between dodecylpyridinium chloride and multicharged anionic planar substances. Langmuir : the ACS journal of surfaces and colloids 20040914
Development of subtype-selective ligands as antagonists at nicotinic receptors mediating nicotine-evoked dopamine release. Bioorganic & medicinal chemistry letters 20040419
Ultrastructure of the dentin-adhesive interface after acid-base challenge. The journal of adhesive dentistry 20040101
N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices. The Journal of pharmacology and experimental therapeutics 20030901
Sorption and desorption kinetics of surfactants TX-100 and DPC on different fractions of soils. Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering 20030601
High throughput screening of transdermal formulations. Pharmaceutical research 20020501

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