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1609-21-8

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1609-21-8 Usage

Chemical Class

Quaternary ammonium salts

Common Uses

Surfactant and biocide in industrial and commercial applications

Applications

Production of detergents, pesticides, and pharmaceuticals

Function as Surfactant

Reduces surface tension of liquids, increases wetting ability and solubility of substances

Function as Biocide

Effective in controlling microbial growth, preventing spread of bacteria and fungi

Safety Precautions

Handle and use with caution, harmful if ingested or inhaled, can cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 1609-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1609-21:
(6*1)+(5*6)+(4*0)+(3*9)+(2*2)+(1*1)=68
68 % 10 = 8
So 1609-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H26N.ClH/c1-2-3-4-5-6-7-8-10-13-16-14-11-9-12-15-16;/h9,11-12,14-15H,2-8,10,13H2,1H3;1H/q+1;/p-1

1609-21-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-decylpyridin-1-ium,chloride

1.2 Other means of identification

Product number -
Other names 1-Decyl-pyridinium

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1609-21-8 SDS

1609-21-8Downstream Products

1609-21-8Relevant articles and documents

Thermodynamic Properties of N-octyl-, N-decyl- and N-dodecylpyridinium Chlorides in Water

Causi, S.,Lisi, R. De,Milioto, S.

, p. 1031 - 1058 (1991)

Densities, heat capacities and enthalpies of dilution at 25 deg C and osmotic coefficients at 37 deg C were measured for N-octyl-, N-decyl- and N-dodecylpyridinium chlorides in water over a wide concentration region.Conductivity measurements were performed in order to evaluate the cmc and the degree of counterion dissociation.Partial molar volumes, heat capacities, relative enthalpies and nonideal free energies and entropies at 25 deg C were derived from the experimental data as functions of the surfactant concentration.The changes with concentration of these properties are quite regular with the exception of the heat capacities which display anomalies at about 0.9, 0.25 and 0.12 mol-kg-1 for the octyl, decyl and dodecyl compounds, respectively.At these concentrations there were also changes in the slopes of the specific conductivity and of the product of the osmotic coefficients and the molality vs. concentration.These pecularities can be ascribed to micelle structural transitions.The thermodynamic functions of micellization were graphically evaluated on the basis of the pseudo-phase transition model.These data have been compared to those for alkyltrimethylammonium bromides and alkylnicotinamide chlorides.It is shown that the introduction of the hydrophilic CONH2 group lowers the hydrophilic character of the pyridinium ring. KEY WORDS: N-octylpyridinium chloride; N-decylpyridinium chloride; N-dodecylpyridinium chloride; densities; heat capacities; enthalpies of dilution; osmotic coefficients; activity coefficients; partial molar volumes; partial molar heat capacities; partial molar relative enthalpies; nonideal free energies; nonideal entropies; thermodynamics of micellization

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