Home » Products » Pharmaceuticals » API » Methylamine hydrochloride
Assay: Min99%
Appearance: White crystalline
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Product Name |
Methylamine hydrochloride |
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Synonyms: |
Methylamine-hydrogenchloride(1/1);Methyl-ammonium;MERCURIALIN HYDROCHLORIDE;METHYLAMINE HYDROCHLORIDE;METHYLAMINE HCL;METHYLAMMONIUM CHLORIDE;AMINOMETHANE HYDROCHLORIDE;MethylaMine hydrochloride, 99% 250GR |
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Chemical Formula |
CH5N.ClH |
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Molecular Weight |
67.52/mol |
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CAS NO |
593-51-1 |
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Assay |
99.0% |
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Storage Conditions |
Protected from light,Preserve in sealed |
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Packaging |
25KG/barrel |
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Lead time |
In stock |
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Hs code |
2921110030 |
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Transport Information |
NON DG |
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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