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593 51 1

Methylamine hydrochloride

CAS NO.:593-51-1

Assay: Min99%

Appearance: White crystalline

 

Product Name

Methylamine hydrochloride

Synonyms:

Methylamine-hydrogenchloride(1/1);Methyl-ammonium;MERCURIALIN HYDROCHLORIDE;METHYLAMINE HYDROCHLORIDE;METHYLAMINE HCL;METHYLAMMONIUM CHLORIDE;AMINOMETHANE HYDROCHLORIDE;MethylaMine hydrochloride, 99% 250GR

Chemical Formula

CH5N.ClH

Molecular Weight

67.52/mol

CAS NO

593-51-1

Assay

99.0%

Storage Conditions

Protected from light,Preserve in sealed

Packaging

25KG/barrel

Lead time

In stock

Hs code

2921110030

Transport Information

NON DG

Contact Info

Nicole Zhao

Nicole@coreychem.com

Description Methylamine Hydrochloride is a colorless organic solid that has an odor similar to that of fish and is used as an essential part for the synthesis of a wide variety of commercial compounds such as ephedrine, theophylline and other intermediates for a wide range of agricultural chemicals, including herbicides, fungicides, insecticides, biocides, and miticides. Methylamine hydrochloride is also a key ingredient in the synthesis of methamphetamine
Chemical Properties white to light tan solid
Uses Methylamine is used as a building block for the synthesis of other organic compounds. It is on the DEA watchlist for chemical precursors because of clandestine use in manufacture of the drug MDMA (ecstasy) and methamphetamine.
The HCl salt is in the form of white deliquescent crystals, and is frequently substitutable for the aq. soln. in many synthesis preparations. Methylamines are used directly as catalysts or as raw materials to produce other compounds with catalytic activity. Fuel additives are used to improve engine performance in a variety of ways. Trimethylamine is used to make paper chemicals. The manufacture of intermediates to make pharmaceuticals is one of the most diverse uses of methylamines.
Application Methylamine hydrochloride can be used as a reactant to synthesize:
Betahistine via aza-Michael reaction with 2-vinylpyridine in water.
Azatripyrrolic and azatetrapyrrolic macrocycles by reacting with pyrrole and formaldehyde via base-catalyzed Mannich reaction.
Tetrahydropyridines via Aza-Diels–Alder reaction with dienes and aldehydes.
N-methylsecondary arylamines from aryl chlorides via nickel-catalyzed amination reaction.

25KG/barrel Or as customer’s requirement

Samples and further technical data can be provided upon request.

Contact Manager Email:Nicole@coreychem.com

 

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