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Cetylbenzyl dimethylammonium bromide (CDBAB), also known as cetyldimethylbenzylammonium bromide, is a quaternary ammonium compound that serves as a surfactant and disinfectant. It is a member of the alkyl dimethyl benzyl ammonium chloride family, known for its broad-spectrum antimicrobial activity against various bacteria and viruses. CDBAB functions by disrupting the cell membrane of microorganisms, leading to their inactivation and eventual death.

3529-04-2

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3529-04-2 Usage

Uses

Used in Disinfectant and Cleaning Products:
CETYLBENZYLDIMETHYLAMMONIUM BROMIDE is used as a disinfectant and cleaning agent for its ability to effectively inactivate and kill a wide range of microorganisms, ensuring cleanliness and reducing the risk of infections in various settings.
Used in Personal Care Products:
In the personal care industry, CETYLBENZYLDIMETHYLAMMONIUM BROMIDE is used as an ingredient in shampoos and conditioners for its antimicrobial properties, helping to maintain hygiene and prevent the growth of harmful microorganisms on the scalp and hair.
Used in Household Products:
CETYLBENZYLDIMETHYLAMMONIUM BROMIDE is used as a key component in household cleaning and disinfecting products, providing a reliable means of eliminating bacteria and viruses, thus contributing to a healthier living environment.
Used in Industrial Cleaning:
In industrial settings, CETYLBENZYLDIMETHYLAMMONIUM BROMIDE is utilized in cleaning and disinfecting processes to ensure the elimination of harmful microorganisms from surfaces and equipment, promoting a safer and more hygienic working environment.

Check Digit Verification of cas no

The CAS Registry Mumber 3529-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3529-04:
(6*3)+(5*5)+(4*2)+(3*9)+(2*0)+(1*4)=82
82 % 10 = 2
So 3529-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H46N.BrH/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-20-23-26(2,3)24-25-21-18-17-19-22-25;/h17-19,21-22H,4-16,20,23-24H2,1-3H3;1H/q+1;/p-1

3529-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl-hexadecyl-dimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names N-benzyl-N,N-dimethylhexadecane-1-ammonium 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:3529-04-2 SDS

3529-04-2Downstream Products

3529-04-2Relevant academic research and scientific papers

Synthesis, self-aggregation and biological properties of alkylphosphocholine and alkylphosphohomocholine derivatives of cetyltrimethylammonium bromide, cetylpyridinium bromide, benzalkonium bromide (C16) and benzethonium chloride

Luká?, Milo?,Mrva, Martin,Garajová, Mária,Moj?i?ová, Gabriela,Varinská, Lenka,Moj?i?, Ján,Sabol, Marián,Kubincová, Janka,Haragová, Hana,Ondriska, Franti?ek,Devínsky, Ferdinand

, p. 46 - 55 (2013/10/01)

A series of alkylphosphocholine and alkylphosphohomocholine derivatives of cetyltrimethylammonium bromide, cetylpyridinium bromide, benzalkonium bromide (C16) and benzethonium chloride have been synthesized. Their physicochemical properties were also investigated. The critical micelle concentration (cmc), the surface tension value at the cmc (γcmc), and the surface area at the surface saturation per head group (Acmc) were determined by means of surface tension measurements. The prepared compounds exhibit significant cytotoxic, antifungal and antiprotozoal activities. Alkylphosphocholines and alkylphosphohomocholines possess higher antifungal activity against Candida albicans in comparison with quaternary ammonium compounds in general. However, quaternary ammonium compounds exhibit significantly higher activity against human tumor cells and pathogenic free-living amoebae Acanthamoeba lugdunensis and Acanthamoeba quina compared to alkylphosphocholines. The relationship between structure, physicochemical properties and biological activity of the tested compounds is discussed.

Preparation of benzalkonium salts differing in the length of a side alkyl Chain

Kuca, Kamil,Marek, Jan,Stodulka, Petr,Musilek, Kamil,Hanusova, Petra,Hrabinova, Martina,Jun, Daniel

, p. 2341 - 2347 (2008/02/14)

Benzalkonium salts are widely used as disinfectants, biocides and detergents, among a variety of other applications. The cationic surface-activity of these salts determines their potential to act as a biocide on both target and non-target organisms. In this study, a quick synthesis of a complete set of the benzalkonium salts differing in the length of an alkylating chain (from C2 to C20) is described. Moreover, their 1H-NMR, HPLC-MS, TLC and HPLC analysis were recorded.

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