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Laurylpyridinium iodide, also known as cetylpyridinium iodide, is a quaternary ammonium compound with the chemical formula C21H38IN. It is a cationic surfactant and a widely used antimicrobial agent. LAURYLPYRIDINIUMIODIDE is derived from the reaction of laurylamine (a derivative of dodecylamine) with pyridine and iodine. Laurylpyridinium iodide is soluble in water and has a characteristic yellowish color. It is commonly used in pharmaceuticals, as a disinfectant, and in various personal care products such as mouthwashes, throat lozenges, and hand sanitizers due to its broad-spectrum antimicrobial properties. The compound works by disrupting the cell membrane of microorganisms, leading to their death. However, it is important to note that its effectiveness can be reduced in the presence of organic matter and high levels of hardness in water.

3026-66-2

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3026-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3026-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3026-66:
(6*3)+(5*0)+(4*2)+(3*6)+(2*6)+(1*6)=62
62 % 10 = 2
So 3026-66-2 is a valid CAS Registry Number.

3026-66-2SDS

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 N-Dodecylpyridinium iodide

1.2 Other means of identification

Product number -
Other names -

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:3026-66-2 SDS

3026-66-2Downstream Products

3026-66-2Relevant academic research and scientific papers

Activation of tetrabutylammonium hydrogen difluoride with pyridine: A mild and efficient procedure for nucleophilic fluorination

Moughamir, Khadija,Atmani, Aziz,Mestdagh, Helene,Rolando, Christian,Francesch, Charlette

, p. 7305 - 7306 (2007/10/03)

The nucleophilic fluorination of alkyl iodides, bromides and tosylates and of α-bromo- or α-chloroketones is smoothly effected by tetrabutylammonium hydrogen difluoride in the presence of pyridine, in dioxane or THF, with good or satisfying substitution-to-elimination ratio.

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