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N,N-Dimethylaminoethyl methacrylamide, with the chemical formula C8H15NO2, is a water-soluble, cationic monomer that is widely used in the synthesis of polymers and copolymers. Its cationic nature allows it to impart unique properties to polymers, making it a versatile compound for various applications.

13081-44-2

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13081-44-2 Usage

Uses

Used in Adhesives and Coatings Industry:
N,N-Dimethylaminoethyl methacrylamide is used as a monomer in the production of adhesives and coatings, where its cationic properties enhance the adhesion and bonding strength of these materials.
Used in Medical Devices Industry:
In the medical field, N,N-Dimethylaminoethyl methacrylamide is used in the production of medical devices, such as drug delivery systems and gene therapy vectors, due to its biocompatibility and ability to form stable polymers.
Used in Water Treatment Industry:
N,N-Dimethylaminoethyl methacrylamide is used as a flocculant in wastewater treatment processes, where its cationic properties help in the aggregation and removal of suspended particles from water.
Used in Paper Industry:
In the paper industry, N,N-Dimethylaminoethyl methacrylamide is used for paper treatments, where its cationic nature improves the wet strength and retention properties of paper products.
Used in Dyes Industry:
N,N-Dimethylaminoethyl methacrylamide is used in the synthesis of cationic dyes, which have improved affinity and colorfastness on various substrates.
Used in Oil Recovery Industry:
In the oil industry, N,N-Dimethylaminoethyl methacrylamide is used in enhanced oil recovery processes, where its cationic properties help in the displacement of oil from reservoirs.
Used in Synthesis of Polyelectrolytes and Amphiphilic Block Copolymers:
N,N-Dimethylaminoethyl methacrylamide is used as a monomer in the synthesis of polyelectrolytes and amphiphilic block copolymers, which have applications in various fields, including drug delivery, gene therapy, and nanotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 13081-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13081-44:
(7*1)+(6*3)+(5*0)+(4*8)+(3*1)+(2*4)+(1*4)=72
72 % 10 = 2
So 13081-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N2O/c1-7(2)8(11)9-5-6-10(3)4/h1,5-6H2,2-4H3,(H,9,11)

13081-44-2SDS

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-[2-(dimethylamino)ethyl]-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names N-[2-(Dimethylamino)Ethyl]-2-Methyl-2-Propenamide

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:13081-44-2 SDS

13081-44-2Relevant academic research and scientific papers

Synthesis and structures of zwitterionic polymers to induce electrostatic interaction with PDMS surface treated by air-plasma

Tanaka, Mutsuo,Hirata, Yoshiki,Sawaguchi, Takahiro,Kurosawa, Shigeru

, p. 330 - 343 (2018/06/29)

Various zwitterionic polymers, sulfobetaine and phosphoryl choline derivatives were synthesized in order to investigate zwitterionic polymer structures toward surface modification of PDMS, where the adsorption of zwitterionic polymers on polydimethylsiloxane surface treated with air-plasma was induced by the electrostatic interaction,. The electrostatic interaction was evaluated with hydrophilicity. The results suggested that a sulfobetaine polymer with higher molecular weight, lower molecular weight distribution, and shorter alkyl chain afforded high electrostatic interaction. A sulfobetaine polymer bearing phenylazide group showed similar electrostatic interaction with the PDMS surface, and it is a promising material for surface modification ofpolydimethylsiloxane.

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