Welcome to LookChem.com Sign In|Join Free

CAS

  • or

52792-65-1

Post Buying Request

52792-65-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

52792-65-1 Usage

Description

(methylamino)(methylimino)methanesulphonic acid, also known as MMSA, is a synthetic chemical compound with the molecular formula C3H9NO3S. It possesses strong acidic properties and is known for its stability in various chemical reactions. MMSA is a versatile compound that finds applications in different industries, including pharmaceuticals, agrochemicals, and fine chemicals.

Uses

Used in Pharmaceutical Industry:
MMSA is used as a strong acid catalyst for various organic chemical reactions, particularly in the production of pharmaceuticals. Its strong acidic properties enable efficient catalysis, leading to the synthesis of a wide range of pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical industry, MMSA is employed as a catalyst in the synthesis of various agrochemicals. Its ability to catalyze reactions efficiently contributes to the production of effective and safe agrochemical products.
Used in Fine Chemicals Industry:
MMSA is utilized as a catalyst in the production of fine chemicals, which are essential for various applications, including fragrances, dyes, and specialty chemicals. Its strong acidic nature and stability make it a suitable choice for these reactions.
Used as a Corrosion Inhibitor in Metal Treatment Processes:
MMSA is used as a corrosion inhibitor in metal treatment processes, where it helps protect metals from corrosion and extends their service life. Its strong acidic properties contribute to its effectiveness as a corrosion inhibitor.
Used as a Stabilizer in Polymerization Reactions:
In the field of polymer chemistry, MMSA is employed as a stabilizer in polymerization reactions. Its strong acidic nature helps control the reaction rate and ensures the formation of stable polymers with desired properties.

Check Digit Verification of cas no

The CAS Registry Mumber 52792-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52792-65:
(7*5)+(6*2)+(5*7)+(4*9)+(3*2)+(2*6)+(1*5)=141
141 % 10 = 1
So 52792-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2O3S/c1-4-3(5-2)9(6,7)8/h1-2H3,(H,4,5)(H,6,7,8)

52792-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methylamino(methylimino)methanesulfonic acid

1.2 Other means of identification

Product number -
Other names (methylamino)(methylimino)methanesulfonic acid

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:52792-65-1 SDS

52792-65-1Upstream product

52792-65-1Downstream Products

52792-65-1Relevant articles and documents

Organosulfur oxoacids. Part 2. A novel dimethylthiourea metabolite - Synthesis and characterization of the surprisingly stable and inert dimethylaminoiminomethane sulfonic acid

Petersen, Jeffrey L.,Otoikhian, Adenike A.,Morakinyo, Moshood K.,Simoyi, Reuben H.

experimental part, p. 1247 - 1255 (2011/02/24)

A new metabolite of the biologically active thiocarbamide dimethylthiourea (DMTU) has been synthesized and characterized. DMTU's metabolic activation in the physiological environment is expected to be dominated by S-oxygenation, which produces, successively, the sulfenic, sulfinic, and sulfonic acids before forming sulfate and dimethylurea. Only the sulfinic and sulfonic acids are stable enough to be isolated. This manuscript reports on the first synthesis, isolation, and characterization of the sulfonic acid: dimethylaminoiminomethanesulfonic acid (DMAIMSOA). It crystallizes in the orthorhombic Pbca space group and exists as a zwitterion in its solid crystal form. The negative charge is delocalized over the sulfonic acid oxygens and the positive charge is concentrated over the planar N-C-N framework rather than strictly on the sp2-hybridized cationic carbon center. As opposed to its sulfinic acid analogue, DMAIMSOA is extremely inert in acidic environments and can maintain its titer for weeks at pH 6 and below. It is, however, reasonably reactive at physiological pH conditions and can be oxidized to dimethylurea and sulfate by mild oxidants such as aqueous iodine.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 52792-65-1