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13052-13-6

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13052-13-6 Usage

Description

[2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride is a quaternary ammonium compound characterized by its hydroxy group, trimethylammonium group, and chloride ion. It is widely recognized for its antimicrobial and antistatic properties, making it a versatile component in various household and personal care products.

Uses

Used in Disinfectant Applications:
[2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride is used as a disinfectant agent for its ability to disrupt the cell membranes of bacteria and other microorganisms, leading to their destruction. This property makes it a valuable component in disinfectant sprays and other sanitizing products.
Used in Antistatic Applications:
In the textile industry, [2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride is used as an antistatic agent to reduce static electricity in fabrics, thereby improving their softness and overall handling.
Used in Household and Personal Care Products:
[2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride is also utilized in fabric softeners and hair conditioners, where it contributes to the softening and conditioning effects of these products, enhancing their performance and user experience.
It is crucial to adhere to proper safety and handling guidelines when using products containing [2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride, as it can pose health risks if ingested or inhaled in large quantities.

Check Digit Verification of cas no

The CAS Registry Mumber 13052-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13052-13:
(7*1)+(6*3)+(5*0)+(4*5)+(3*2)+(2*1)+(1*3)=56
56 % 10 = 6
So 13052-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H18NO3.ClH/c1-5-9(12)13-7-8(11)6-10(2,3)4;/h5,8,11H,1,6-7H2,2-4H3;1H/q+1;/p-1

13052-13-6SDS

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 [2-hydroxy-3-[(1-oxoallyl)oxy]propyl]trimethylammonium chloride

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:13052-13-6 SDS

13052-13-6Downstream Products

13052-13-6Relevant articles and documents

Polymerizable quaternary ammonium cationic monomer and preparation method thereof

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Paragraph 0040; 0042; 0051-0058; 0061; 0063; 0069; 0071, (2018/04/03)

The invention relates to a preparation method of a polymerizable quaternary ammonium cationic monomer, wherein the preparation method comprises the steps: mixing a solvent and acrylic acid, dropping aNaOH saturated solution, heating up and dropping a 3-chloro-2-hydroxypropyltrimethylammonium chloride solution, and carrying out a reaction for 4-6 h at the temperature of 55-75 DEG C; after the reaction is finished, cooling, and carrying out reduced pressure distillation to remove the solvent, to obtain a monomer crude product; and cooling, then adding a benign solvent for dissolving, carrying out suction filtration, collecting a filtrate, concentrating, cooling, then adding a poor solvent, separating out a precipitate, and drying to obtain a white solid product. The solvent is one of absolute ethyl alcohol, acetonitrile, acetone or isopropanol, the volume ratio of the solvent to water is 1 to 1, the molar ratio of water to acrylic acid is 16.6 to 1, the molar ratio of acrylic acid to sodium hydroxide is 1 to 1, and the molar ratio of CHPTAC to acrylic acid is (0.8-1.3) to 1; the reaction operation is simple, the yield is relatively high, and the synthesized polymerizable qauaternaryammonium cationic monomer has the advantages of richer adsorption groups, good water solubility, and high polymerization activity, and can further enrich the types of cationic monomers for polymerization.

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