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N-PENTADECYLPYRIDINIUM BROMIDE is a quaternary ammonium compound that functions as a cationic surfactant. It is recognized for its potent antimicrobial properties, which stem from its ability to disrupt the cell membranes of microorganisms. This makes it a versatile disinfectant and preservative, suitable for a range of applications across various industries.

53171-29-2

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53171-29-2 Usage

Uses

Used in Industrial Applications:
N-PENTADECYLPYRIDINIUM BROMIDE is used as an antimicrobial agent for its effectiveness in eliminating microorganisms and preserving the quality of products in various industries.
Used in Pharmaceutical Applications:
In the pharmaceutical sector, N-PENTADECYLPYRIDINIUM BROMIDE is used as a disinfectant to ensure the sterility of medical equipment and supplies, thereby preventing infections and promoting public health.
Used in Personal Care Products:
N-PENTADECYLPYRIDINIUM BROMIDE is used as a preservative in personal care products to prevent microbial growth, ensuring the safety and longevity of these products for consumers.
Used in Pesticide Formulations:
In agriculture, N-PENTADECYLPYRIDINIUM BROMIDE is used as an ingredient in pesticide formulations to enhance their effectiveness by controlling the growth of harmful microorganisms that can affect crop yields.
Its water solubility and low toxicity make N-PENTADECYLPYRIDINIUM BROMIDE a preferred choice for applications requiring antimicrobial properties, contributing to its widespread use across different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 53171-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,7 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53171-29:
(7*5)+(6*3)+(5*1)+(4*7)+(3*1)+(2*2)+(1*9)=102
102 % 10 = 2
So 53171-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H36N.BrH/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-21-19-16-14-17-20-21;/h14,16-17,19-20H,2-13,15,18H2,1H3;1H/q+1;/p-1

53171-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pentadecylpyridin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names N-PENTADECYLPYRIDINIUM BROMIDE

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:53171-29-2 SDS

53171-29-2Downstream Products

53171-29-2Relevant academic research and scientific papers

Relationship of Structure to Properties of Surfactants. 12. Synthesis and Surface Properties of Long-Chain 2-Pyridinium Alkanoates

Zhao, Fulin,Rosen, Milton J.

, p. 6041 - 6043 (1984)

Three surface-active 2-pyridinium alkanoates, 2-pyridinium dodecanoate, tetradecanoate, and hexadecanoate, have been synthesized and characterized.Their physical properties investigated include decomposition and Krafft points, pKa of the conjugate acids, and ultraviolet absorption.From surface tension measurements on aqueous solutions of the compounds at 25 deg C, critical micelle concentrations (cmc), surface excess concentrations, minimum area per molecule at the aqueous solution/air interface, efficiency and effectiveness of surface tension reduction, and standard free energies of adsorption (ΔG0ad) and of micellization (ΔG0mic) have been calculated.The cmc of a 2-pyridinium alkanoate is considerably smaller than that of the corresponding 2-trimethylammonium alkanoate, which may be due to the ease of packing of the planar pyridinium and carboxylate groups.At the aqueous solution/air interface, the molecules are almost close packed, with orientation perpendicular to the interface and both pyridinium and carboxylate groups in the aqueous phase.The ΔG0ad per methylene group is -3.15 kJ; the ΔG0mic per methylene group, -2.7 kJ, at 25 deg C.

BIS-PYRIDINO CONTAINING COMPOUNDS FOR USE IN THE TREATMENT OF CNS PATHOLOGIES

-

Page/Page column 38-39, (2008/06/13)

N-n-Alkylation of nicotine converts nicotine from an agonist into an antagonist specifically for neuronal nicotinic acetylcholine receptor subtypes mediating nicotine-evoked dopamine release. Conformationally restricted analogs exhibit both high affinity and selectivity at this site, and are able to access the brain due to their ability to act as substrates for the blood-brain barrier choline transporter.

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