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Diallylaminoacetonitrile, with the molecular formula C8H12N2, is a colorless liquid chemical compound that exhibits a faint, ammonia-like odor. It is primarily recognized for its role as a monomer in the synthesis of polymers, particularly polyacrylamides. Additionally, it serves as a potential precursor for a variety of laboratory-manufactured chemicals and pharmaceuticals. Due to its potential health hazards, including risks of inhalation, ingestion, and skin or eye irritation, it is crucial to handle and store Diallylaminoacetonitrile with appropriate safety measures.

72524-91-5

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72524-91-5 Usage

Uses

Used in Polymer Production Industry:
Diallylaminoacetonitrile is utilized as a monomer for the production of polymers, specifically polyacrylamides. Its role in this industry is pivotal as it contributes to the formation of polymers with specific properties that are useful in various applications.
Used in Chemical and Pharmaceutical Industries:
As a precursor, Diallylaminoacetonitrile is employed in the synthesis of various lab-made chemicals and pharmaceuticals. Its chemical structure allows it to be a building block for the development of new compounds that can have diverse applications in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 72524-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72524-91:
(7*7)+(6*2)+(5*5)+(4*2)+(3*4)+(2*9)+(1*1)=125
125 % 10 = 5
So 72524-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-3-6-10(7-4-2)8-5-9/h3-4H,1-2,6-8H2

72524-91-5SDS

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 DIALLYLAMINOACETONITRILE

1.2 Other means of identification

Product number -
Other names diallyl cyanomethyl amine

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:72524-91-5 SDS

72524-91-5Downstream Products

72524-91-5Relevant academic research and scientific papers

Gas Phase Thermolysis of Allyl Cyanomethyl Amine, Diallyl Cyanomethyl Amine, Diethyl Cyanomethyl Amine, and Diethyl Propargyl Amine

Martin, Gonzalo,Ascanio, Julian,Rodriguez, Jesus

, p. 99 - 108 (2007/10/02)

The title amines were pyrolyzed in a stirred-flow reactor at 380 - 510 deg C, pressures of 8 - 15 torr and residence times of 0.3 - 2.4 s, using toluene as carrier gas.The substrates with an allyl group yielded propene and iminonitriles as reaction products.HCN is formed by decomposition of the iminonitriles.The first-order rate coefficients for propene formation fit the Arrhenius equations.Allyl cyanomethyl amine: k(s-1) = 1013.29 +/- 0.35exp(-189 +/- 5 kJ/mol RT) Diallyl cyanomethyl amine: k(s-1) = 1013.00 +/- 0.20exp(-183 +/- 3 kJ/mol RT) Diethyl cyanomethyl amine gave a 20:1 gas mixture of ethylene and ethane, plus HCN.The liquid product fraction contained mainly N-ethyl methanaldimine.The first-order rate coefficients for ethylene formation followed the Arrhenius equation k(s-1) = 1015.30 +/- 0.24exp(-226 +/- 3 kJ/mol RT) Diethyl propargyl amine decomposed cleanly into allene and N-ethyl ethanaldimine.The first-order rate coefficients for allene formation fit the Arrhenius equation k(s-1) = 1012.84 +/- 0.30exp(-168 +/- 4 kJ/mol RT).The results suggest that the above allyl and propargyl amines decompose unimolecularly by mechanisms involving six-center cyclic transition states.For diethyl cyanomethyl amine, a nonchain free radical mechanism is proposed.

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