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36214-48-9

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36214-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36214-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,1 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36214-48:
(7*3)+(6*6)+(5*2)+(4*1)+(3*4)+(2*4)+(1*8)=99
99 % 10 = 9
So 36214-48-9 is a valid CAS Registry Number.

36214-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name formaldehyde monomethylhydrazone

1.2 Other means of identification

Product number -
Other names formaldehyde methylhydrazone

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:36214-48-9 SDS

36214-48-9Downstream Products

36214-48-9Relevant academic research and scientific papers

1-Thia-3,4-diazolidine-2,5-dione Functionality: A Photochemical Synthon for the Azo Group

Squillacote, Michael,Felippis, James De

, p. 3564 - 3571 (2007/10/02)

The 1-thia-3,4-diazolidine-2,5-dione functional group was shown to yield azo compounds upon photolysis.This photoreaction when combined with the known ability of this group to react in a Diels-Alder fashion or as a dinucleophile toward alkylating agents greatly increases the utility of this functionality.The dual reactivity of this group was demonstrated in the synthesis of a number of 3,4-dialkyl-1-thia-3,4-diazolodone-2,5-diones.The photolysis of these compounds produced either thermally stable cyclic azo compounds or the decomposition products of thermally unstable azo compounds.

Cinetique de la reaction d'oxydation de la monomethylhydrazine par la monochloramine

Ferriol, Michel,Gazet, Josette,Cohen-Adad, Marie-Therese

, p. 180 - 188 (2007/10/02)

The kinetics of monomethylhydrazine oxidation by monochloramine has been investigated in terms of concentrations, pH from 11 to 13 and temperature in the range 293-308 K.The overall reaction, first order in both reagents, is the result of two competitive steps: - the first being pH independent; - the second accelerated by decreasing pH.The energy of activation for each step has been derived fom our results.In the solution and with an excess of methylhydrazine, formaldehyde monomethylhydrazone CH3NHNCH2 has been identified using mass spectrometry as a final product of the reaction.Other compounds: CH3Cl and CH3OH are also observed but the mechanism of their production is not still clearly established.A simple interpretation of the kinetic result is also proposed.

Ureas as Amine Substrate for Hydrazine and Alkylhydrazine Synthesis---Reaction of Chloramine with Monomethylurea and Formation of 1-Methyltriazane

Prakash, Hari,Sisler, Harry H.

, p. 825 - 828 (2007/10/02)

Reaction of chloramine with monomethylurea has been shown to yield monomethylhydrazine and several side products, e. g., formaldehyde monomethylhydrazone, 1,1-dimethylhydrazine, methyliminotarazane, and methanol, originating from the further oxidation of monomethylhydrazine with chloramine.Evidence for the existance of 1-methyltriazane, CH3NHNHNH2, is presented for the first time.

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