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(3-cyano-2-hydroxypropyl)trimethylammonium chloride, also known as CHPTAC, is an organochemical compound characterized by its cationic properties. This quaternary ammonium compound is widely used in various applications due to its primary function as a cationic etherification agent. Structurally, it comprises a cyano group, a hydroxy group, and a trimethylammonium chloride group. The chloride anion in the compound significantly improves its solubility in water, making it suitable for applications that necessitate water solubility.

18933-33-0

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18933-33-0 Usage

Uses

Used in Paper Industry:
(3-cyano-2-hydroxypropyl)trimethylammonium chloride is used as a cationic modifier for natural and synthetic polymers, enhancing their properties for use in paper production. This modification improves the paper's wet strength, printability, and resistance to microbial degradation.
Used in Textile Industry:
In the textile industry, (3-cyano-2-hydroxypropyl)trimethylammonium chloride is used as a cationic finishing agent to impart specific characteristics to textiles, such as softness, anti-static properties, and improved dye uptake. The cationic nature of the compound allows for better interaction with the negatively charged textile fibers.
Used in Water Treatment:
(3-cyano-2-hydroxypropyl)trimethylammonium chloride is used as a coagulant or flocculant in water treatment processes. Its cationic properties enable it to neutralize negatively charged particles in water, facilitating their aggregation and removal, thus improving water quality.
Used in Personal Care Products:
In personal care products, (3-cyano-2-hydroxypropyl)trimethylammonium chloride is used as a conditioning agent, providing benefits such as hair detangling, skin softening, and improved manageability. Its cationic nature allows it to interact with the hair and skin, enhancing their texture and feel.
Used in Other Industries:
(3-cyano-2-hydroxypropyl)trimethylammonium chloride is also used in various other industries as a cationic modifier for polymers, offering benefits such as improved adhesion, corrosion inhibition, and enhanced compatibility with other materials. Its versatility and water solubility make it a valuable component in the formulation of products across different sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 18933-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18933-33:
(7*1)+(6*8)+(5*9)+(4*3)+(3*3)+(2*3)+(1*3)=130
130 % 10 = 0
So 18933-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N2O/c1-9(2,3)6-7(10)4-5-8/h7,10H,4,6H2,1-3H3/q+1

18933-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-cyano-2-hydroxypropyl)trimethylammonium chloride

1.2 Other means of identification

Product number -
Other names carnitinenitrile hydrochloride

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:18933-33-0 SDS

18933-33-0Relevant academic research and scientific papers

Preparation method of levocarnitine

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Paragraph 0030; 0031; 0032; 0033, (2017/08/29)

The invention provides a preparation method of levocarnitine. The preparation method comprises the following steps: taking epoxy chloropropane as a starting material, then carrying out amination, cyaniding and carrying out ester exchange under the action of lipase CALB to obtain corresponding chiral ester, then carrying out alkaline hydrolysis and acidification, and then removing chlorine ions under the action of strongly alkaline resin, so that the levocarnitine finished product is obtained. In the invention, acid resin is used in an ester exchange process, and recemization can be realized, so that yield and optical purity of the levocarnitine are improved.

PROCESS FOR PRODUCTION OF BETAINE

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Page/Page column 22, (2009/09/26)

According to the present invention, by using 4-halogeno-3-hydroxybutanamide as a substrate in quaternary amination reaction with trialkylamine which is an important step in betaine (such as carnitine) preparation processes, it becomes possible to reduce the production of crotonic acid derivatives (the major by-product) greatly compared to conventional processes. Consequently, it becomes possible to prepare a betaine, such as carnitine, at a high yield. The present invention also relates to a process for preparing a betaine represented by formula (1) below, comprising a step of quaternary aminating an amide represented by formula (2) below: wherein A1, A2 and A3 individually represent a C1-C20 hydrocarbon group which may have a substituent(s); and X1 is a halogen atom.

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