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10595-45-6

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10595-45-6 Usage

General Description

N-[2-(diethylamino)ethyl]acrylamide is a chemical compound often used in the production of polymers and as a cross-linking agent. It is a derivative of acrylamide and contains a diethylaminoethyl group. N-[2-(diethylamino)ethyl]acrylamide is widely used in the synthesis of copolymers and as a component in the manufacture of hydrogels, which have applications in fields such as medicine and industrial processes. Due to its structural properties, N-[2-(diethylamino)ethyl]acrylamide is known for its ability to form stable and flexible polymer networks, making it a valuable component in various types of materials and formulations. However, like acrylamide, it is important to handle this compound with care due to its potential health hazards and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 10595-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10595-45:
(7*1)+(6*0)+(5*5)+(4*9)+(3*5)+(2*4)+(1*5)=96
96 % 10 = 6
So 10595-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O/c1-4-9(12)10-7-8-11(5-2)6-3/h4H,1,5-8H2,2-3H3,(H,10,12)

10595-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(N',N'-diethylaminoethyl)-acrylamide

1.2 Other means of identification

Product number -
Other names N-[2-(diethylamino)ethyl]acrylamide

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:10595-45-6 SDS

10595-45-6Downstream Products

10595-45-6Relevant articles and documents

Microspheres useful for therapeutic vascular embolization

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Page/Page column 49; 50, (2016/10/04)

Provided herein, for example, are microspheres comprising a gelatin or gelatin substitute and a copolymer of a N-tris-hydroxymethyl methylacrylamide monomer unit, a diethylaminoethylacrylamide monomer unit and a N,N-methylene-bis-acrylamide monomer unit. Also provided are methods of producing microspheres comprising a gelatin or gelatin substitute and a copolymer of a N-tris-hydroxymethyl methylacrylamide monomer unit, a diethylaminoethylacrylamide monomer unit and a N,N-methylene-bis-acrylamide monomer unit. Further provided herein, for example, are compositions comprising the microspheres and methods of using the microspheres and compositions thereof.

Process for the manufacture of α,β-unsaturated N-substituted carboxylic acid amides

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, (2008/06/13)

Process for the manufacture of α,β-unsaturated N-substituted carboxylic acid amides of the general formula STR1 in which R1 represents H or CH3 R2 represents H or CH3, and Y represents a divalent straight-chain or branched organic radical having 2-30 carbon atoms, and R3 represents H or the radical of an amine of the formula --N(R4)(R5), in which R4 and R5 represent alkyl radicals having 1 to 4 carbon atoms, by reacting β-substituted carboxylic acid amides of the formula STR2 in which Z represents OH or the radical R6 O--, in which R6 is an alkyl radical having 1 to 4 carbon atoms, with amines of the general formula at temperatures in the range of 100° to 200° C., preferably 120° to 175° C., with the elimination of ammonia, and heating the resulting N-substituted β-hydroxycarboxylic or β-alkoxycarboxylic acid amides in the presence of catalysts, water or alcohol, respectively, being split off. The water is split off at temperatures of 100°-250° C. with acidic catalysts such as phosphoric acid, or basic catalysts such as sodium hydroxide, and alcohol is split off at 70°-150° C. with basic catalysts such as sodium or potassium hydroxide. The reaction product is separated by distillation, optionally in vacuo.

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