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61551-69-7

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61551-69-7 Usage

Description

2,2'-Azobis[2-methyl-N-(2-hydroxyethyl)propionamide], often shortened to 2,2'-Azobis, is an organic compound that is a derivative of azobisisobutyronitrile (AIBN). It is a white powder used as a radical polymerization initiator in the production of various polymers and plastics. It is known for its convenient decomposition rate, high yield of free radicals, and relatively low purification requirement, which contribute to the formation of crosslinking structures and certain complex molecular architectures.

Uses

Used in Polymer and Plastics Industry:
2,2'-Azobis is used as a radical polymerization initiator for the production of various polymers and plastics. Its benefits include a convenient decomposition rate, a high yield of free radicals, and a relatively low purification requirement, which are essential for the efficient synthesis of these materials.
Used in Chemical Synthesis:
2,2'-Azobis is used as a radical initiator in chemical synthesis processes, particularly for the formation of crosslinking structures and complex molecular architectures. Its ability to generate free radicals at a controlled rate makes it a valuable tool in the synthesis of advanced materials.
Safety Considerations:
Due to its association with the thermal generation of radicals, 2,2'-Azobis must be handled with proper safety measures to prevent hazardous situations. This includes following appropriate guidelines for storage, handling, and disposal to ensure the safety of workers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 61551-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,5 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61551-69:
(7*6)+(6*1)+(5*5)+(4*5)+(3*1)+(2*6)+(1*9)=117
117 % 10 = 7
So 61551-69-7 is a valid CAS Registry Number.

61551-69-7SDS

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-hydroxyethyl)-2-[[1-(2-hydroxyethylamino)-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide

1.2 Other means of identification

Product number -
Other names 2,2'-azobis[2-methyl-N-(2-hydroxyethyl)propionamide]

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:61551-69-7 SDS

61551-69-7Relevant articles and documents

2,2'-azo(2-methyl-N-(2-hydroxyethyl)propionamide) preparation method

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Paragraph 0032-0060, (2019/10/04)

The invention discloses a 2,2'-azo(2-methyl-N-(2-hydroxyethyl)propionamide) preparation method, which comprises: adding 2,2'-azobisisobutyronitrile, methanol and toluene to a reactor having a stirring and reflux device, starting stirring, slowly introducing hydrogen chloride gas under cooling, and controlling the temperature of the material and carrying out a thermal insulation reaction; after completing the reaction, adding the reaction liquid into water in a dropwise manner, carrying out a hydrolysis reaction, layering after completing the hydrolysis, adding a small amount of methanol to the organic phase, and carrying out pressure reducing distillation for a certain time; after completing the distillation, slowly adding the organic phase into a mixed solution of sodium methoxide and monoethanolamine in a dropwise manner, and carrying out thermal insulation; after completing the thermal insulation, carrying out solid-liquid separation by a centrifuge, continuously washing the solid with water, crystallizing, carrying out centrifugation until the material is dried, placing the material in a drying device, and drying; and after the drying, cooling the material to a normal temperature to obtain the 2,2'-azo(2-methyl-N-(2-hydroxyethyl)propionamide) product, wherein the product content (HPLC) is more than 98%, and the yield is 55-75%.

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