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ACRYLAMIDO BUFFER, also known as 2-Acrylamidoglycolic Acid, is a white crystalline powder with unique chemical properties. It serves as a versatile reactant in the synthesis of polymer-metal hybrids through radical polymerization, making it a valuable component in various chemical and industrial applications.

6737-24-2

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6737-24-2 Usage

Uses

Used in Chemical Industry:
ACRYLAMIDO BUFFER is used as a reactant for the preparation of polymer-metal hybrids via radical polymerization. Its ability to form stable complexes with metal ions and its compatibility with various polymerization techniques make it an essential component in the development of advanced materials with tailored properties.
Used in Material Science:
ACRYLAMIDO BUFFER is used as a building block for the synthesis of novel materials with enhanced properties. Its reactivity and ability to form stable complexes with metal ions allow for the creation of hybrid materials with improved mechanical, thermal, and electrical properties, making them suitable for various applications in the material science field.
Used in Environmental Applications:
ACRYLAMIDO BUFFER is used as a component in the development of environmental remediation technologies. Its ability to form stable complexes with metal ions can be utilized for the removal of heavy metals from contaminated water and soil, contributing to the development of sustainable and eco-friendly solutions for environmental challenges.
Used in Pharmaceutical Industry:
ACRYLAMIDO BUFFER is used as a starting material for the synthesis of drug delivery systems and other pharmaceutical applications. Its compatibility with various polymerization techniques and its ability to form stable complexes with metal ions make it a promising candidate for the development of innovative drug delivery systems with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 6737-24-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6737-24:
(6*6)+(5*7)+(4*3)+(3*7)+(2*2)+(1*4)=112
112 % 10 = 2
So 6737-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO4/c1-2-3(7)6-4(8)5(9)10/h2,4,8H,1H2,(H,6,7)(H,9,10)/p-1/t4-/m0/s1

6737-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-2-(prop-2-enoylamino)acetic acid

1.2 Other means of identification

Product number -
Other names HF 7630

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:6737-24-2 SDS

6737-24-2Relevant academic research and scientific papers

An organic silicon compound containing polymerized amide, due to their tropicalis tool and silicon-containing polymer

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Paragraph 0095; 0096, (2016/10/10)

There is provided a fast curing composition comprising an alpha, beta-unsaturated amido-containing organosilicon compound, useful in making water absorbing silicone-hydrogel films for biomedical devices, such as contact lens, and a process for producing these monomers. This invention also provides for hydrogels made from the alpha, beta-unsaturated amido-containing organosilicon compound described herein.

Process for manufacturing N-acyl derivatives of hydroxy-arylglycines

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, (2008/06/13)

Condensation of the addition product of glyoxylic acid and amides with hydroxyaryl compounds is effected by a first step, wherein the reaction is carried out hot, at a temperature below 60° C, of an aliphatic amide having at the most 4 carbon atoms selected from the group of acetamide, chloracetamide, propionamide, acrylamide and butyramide, on an aqueous solution of glyoxylic acid. Then in a second step, after the addition of acetic acid and gaseous hydrochloric acid, condensation is effected at a temperature below 35° C of the carboxamidoglycolic acid with an excess reaching 500% of hydroxyaryl compound selected from the group comprising phenol and its alkyl derivatives, their halogen derivatives, polyphenols and their ethers and betanaphthol. After the condensation of said second step, the volatile products are removed by vacuum distillation. When the hydroxyaryl compound is phenol, the crude product resulting from this distillation is taken up in nitromethane or water, which are a non-solvent of the N-acyl derivative of parahydroxyphenylglycine but a solvent of the corresponding ortho derivative; the proportion of the para derivative in the resulting compound is then of the order of 100%.

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