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[2-(methacryloyloxy)ethyl]dimethylammonium acetate is a quaternary ammonium compound that features a methacryloyloxy group and a dimethylammonium group. It is recognized for its role as a reactant in the synthesis of polyelectrolytes and copolymers, which are utilized in the creation of biomaterials, coatings, and adhesives. Additionally, this chemical is instrumental in the production of cationic polymers for applications in water treatment, papermaking, and textile processing. The presence of the acetate counterion ensures the stability of the compound, facilitating its use in a range of polymerization and synthesis reactions. Given its reactive properties, [2-(methacryloyloxy)ethyl]dimethylammonium acetate must be handled with care and in compliance with established safety protocols.

10018-87-8

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10018-87-8 Usage

Uses

Used in Biomaterials Industry:
[2-(methacryloyloxy)ethyl]dimethylammonium acetate is used as a reactant for synthesizing polyelectrolytes and copolymers for its ability to enhance the properties of biomaterials, contributing to their structural integrity and functionality in medical applications.
Used in Coatings and Adhesives Industry:
In the coatings and adhesives sector, [2-(methacryloyloxy)ethyl]dimethylammonium acetate is utilized as a component in the formulation of polyelectrolytes and copolymers, which improve the adhesive and binding properties of these products, ensuring better performance and durability.
Used in Water Treatment:
[2-(methacryloyloxy)ethyl]dimethylammonium acetate is employed as a reactant in the production of cationic polymers for water treatment, where it aids in the flocculation and coagulation processes, thereby improving water quality and purification efficiency.
Used in Papermaking:
Within the papermaking industry, [2-(methacryloyloxy)ethyl]dimethylammonium acetate is used as a component in cationic polymers that enhance the wet strength and retention properties of paper products, leading to improved paper quality and manufacturing processes.
Used in Textile Processing:
In textile processing, [2-(methacryloyloxy)ethyl]dimethylammonium acetate is used as a reactant for cationic polymers that serve to improve the dyeability, softness, and overall quality of textiles, providing enhanced performance and durability in fabric products.

Check Digit Verification of cas no

The CAS Registry Mumber 10018-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,1 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10018-87:
(7*1)+(6*0)+(5*0)+(4*1)+(3*8)+(2*8)+(1*7)=58
58 % 10 = 8
So 10018-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO2.C2H4O2/c1-7(2)8(10)11-6-5-9(3)4;1-2(3)4/h1,5-6H2,2-4H3;1H3,(H,3,4)

10018-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,2-(dimethylamino)ethyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names EINECS 233-013-7

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:10018-87-8 SDS

10018-87-8Downstream Products

10018-87-8Relevant academic research and scientific papers

Facile incorporation of natural carboxylic acids into polymers via polymerization of protic ionic liquids

Moreno, Monica,Aboudzadeh, M. Ali,Barandiaran, Maria J.,Mecerreyes, David

, p. 1049 - 1053 (2012)

This communication reports on the facile incorporation of natural carboxylic acids such as acetic acid or oleic acid into new ionic polymers. A series of protic ionic liquid monomers derived from natural carboxylic acids and N-(2-(dimethylamino)ethyl) methacrylate were easily polymerized. This method represents route to incorporate natural products into polymer latexes.

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