Welcome to LookChem.com Sign In|Join Free
  • or
2-Propenamide, N-(2-amino-2-oxoethyl)-, also known as N-(2-amino-2-oxoethyl)acrylamide, is a chemical compound with the molecular formula C4H7NO2. It is a derivative of acrylamide and is primarily used in the production of various polymers.

2479-62-1

Post Buying Request

2479-62-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2479-62-1 Usage

Uses

Used in Polymer Production:
2-Propenamide, N-(2-amino-2-oxoethyl)is used as a monomer in the synthesis of polymers, such as polyacrylamide, for its ability to form long-chain polymers with diverse applications.
Used in Food Industry:
In the food industry, 2-Propenamide, N-(2-amino-2-oxoethyl)is used as a component in the production of thickeners and gelling agents, contributing to the texture and stability of various food products.
Used in Agriculture:
2-Propenamide, N-(2-amino-2-oxoethyl)is utilized in agriculture as a component in soil conditioners and water retention agents, enhancing soil structure and water management for improved crop growth.
Used in Water Treatment Industry:
In the water treatment industry, 2-Propenamide, N-(2-amino-2-oxoethyl)is employed in the production of flocculants and coagulants, aiding in the purification process by promoting the aggregation of impurities for easier removal.
Although 2-Propenamide, N-(2-amino-2-oxoethyl)is considered to be relatively low in toxicity, it is essential to follow proper handling and safety precautions when working with this chemical to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 2479-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2479-62:
(6*2)+(5*4)+(4*7)+(3*9)+(2*6)+(1*2)=101
101 % 10 = 1
So 2479-62-1 is a valid CAS Registry Number.

2479-62-1Downstream Products

2479-62-1Relevant academic research and scientific papers

Method for stably and efficiently preparing N-acrylamide compounds

-

Paragraph 0039-0047, (2019/03/28)

The invention discloses a method for preparing N-acrylamide compounds, belonging to the field of chemical industry. The method comprises the steps of adding NH2-R2 or HCl.NH2-R2 into an alkaline aqueous solution, and then adding an organic solvent with a boiling point of lower than or equal to 85 DEG C or less so as to obtain reaction liquid; dropwise adding acryloyl chloride or methacryloyl chloride into the reaction liquid, and controlling the reaction temperature to be 5-15 DEG C and the reaction time to be 0.5-2h; carrying out rotary evaporation to remove the organic solvent and water so as to obtain a mixture of the N-acrylamide compounds and salt; precipitating the salt, and spin-drying the filtrate to obtain the N-acrylamide compounds. The method improves the stability of a reaction; furthermore, the boiling point of the mixed solvent is greatly reduced, so that the rotary evaporation with a higher dehydration speed does not cause polymerization, and the time for removing the solvent is greatly shortened. Furthermore, a purification method is optimized, so that the efficiency of a whole synthetic route is finally increased.

ASSOCIATION OF POLY(N-ACRYLOYLGLYCINAMIDE) WITH AT LEAST ONE ACTIVE PRINCIPLE

-

Paragraph 0181-0193, (2015/05/13)

The present invention relates to an association of poly (N-acryloyl glycinamide) with at least one active principle and/or at least one product which is visible in medical imaging, in a physiologically acceptable aqueous medium.

Well-defined synthetic polymers with a protein-like gelation behavior in water

Glatzel, Stefan,Badi, Nezha,Paech, Michael,Laschewsky, Andre,Lutz, Jean-Franois

supporting information; experimental part, p. 4517 - 4519 (2010/10/19)

Homopolymers of N-acryloyl glycinamide were prepared by reversible addition-fragmentation chain transfer polymerization in water. The formed macromolecules exhibit strong polymer-polymer interactions in aqueous milieu and therefore form thermoreversible physical hydrogels in pure water, physiological buffer or cell medium.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2479-62-1