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19803-43-1

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19803-43-1 Usage

General Description

Ammonium methyl sulphate is a chemical compound with the formula (CH3)2NH2S04. It is a white crystalline solid that is soluble in water. Ammonium methyl sulphate is used as a reagent in organic chemical reactions, as well as in the production of pharmaceuticals and agrochemicals. It is also used as a catalyst in various chemical processes. Ammonium methyl sulphate is considered to be a moderately hazardous substance, and proper precautions should be taken when handling and storing it. Overall, it is an important compound in the chemical industry with a variety of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19803-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,0 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19803-43:
(7*1)+(6*9)+(5*8)+(4*0)+(3*3)+(2*4)+(1*3)=121
121 % 10 = 1
So 19803-43-1 is a valid CAS Registry Number.
InChI:InChI=1/CH4O4S.H3N/c1-5-6(2,3)4;/h1H3,(H,2,3,4);1H3

19803-43-1SDS

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 Sulfuric acid, methyl ester ammonium salt

1.2 Other means of identification

Product number -
Other names amine methylsulfate

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:19803-43-1 SDS

19803-43-1Upstream product

19803-43-1Relevant articles and documents

Oxidation of Aromatic Aldehydes to Esters: A Sulfate Radical Redox System

Guo, Ya-Fei,Mahmood, Sajid,Xu, Bao-Hua,Yao, Xiao-Qian,He, Hong-Yan,Zhang, Suo-Jiang

, p. 1591 - 1599 (2017)

A mild oxidative esterification of various aromatic aldehydes by sulfate radical redox system was presented. In the reaction pathway exploration, the transiency of MeOSO3- was disclosed, which was generated from esterification between the in situ generated HSO4- and MeOH, a rate-limiting step in the process. More importantly, the selectivity-controlling step was represented by the subsequent nucleophilic displacement between MeOSO3- and aldehydes. The ionic oxidant 1a ((NH4)2S2O8) with more N-H numbers in the cation, as compared with 1c ((n-Bu4N)2S2O8) and 1d ((PyH)2S2O8), has better performance in the oxidative esterification of aldehydes.

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