| Identification | More | [Name]
Methylamine hydrochloride | [CAS]
593-51-1 | [Synonyms]
AMINOMETHANE HYDROCHLORIDE
MERCURIALIN HYDROCHLORIDE
METHYLAMINE HCL
METHYLAMINE HYDROCHLORIDE
METHYLAMMONIUM CHLORIDE
MONOMETHYLAMINE HCL
MONOMETHYLAMINE HYDROCHLORIDE
Methylamine-hydrogenchloride(1/1)
Methyl-ammonium
METHYLAMINE CHLORHYDRATE
Monomethylamin hydrochloride
METHYLAMINE HYDROCHLORIDE, 99+%
MethylAmmoniumChlorideForSynthesis
Methylamine Hydrochloride 99%
Methylaminehydrochloride,98%
Methylamine-methyl-D3HCl
Methylammoniumchlorid
Methylammonium Cloride
monomethylammonium chloride
Methylamine-methyl-D3Cl | [EINECS(EC#)]
209-795-0 | [Molecular Formula]
CH6ClN | [MDL Number]
MFCD00012849 | [Molecular Weight]
67.52 | [MOL File]
593-51-1.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light tan solid | [Melting point ]
231-233 °C(lit.)
| [Boiling point ]
225-230 °C15 mm Hg(lit.)
| [density ]
0.8306 (rough estimate) | [vapor pressure ]
0.134Pa at 25℃ | [refractive index ]
1.5500 (estimate) | [Fp ]
225-230°C/15mm | [storage temp. ]
Store below +30°C. | [solubility ]
soluble | [form ]
powder | [color ]
White crystalline | [Odor]
Odorless | [PH]
5-7 (10g/l, H2O, 20℃) | [PH Range]
5 - 7 at 10 g/l at 20 °C | [Stability:]
Stable, but may be moisture sensitive. Incompatible with strong oxidizing agents. | [Water Solubility ]
soluble | [Sensitive ]
Hygroscopic | [Merck ]
14,6014 | [BRN ]
3588822 | [InChIKey]
NQMRYBIKMRVZLB-UHFFFAOYSA-N | [LogP]
-3.82 | [CAS DataBase Reference]
593-51-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Methylammonium chloride(593-51-1) | [EPA Substance Registry System]
593-51-1(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
1
| [RTECS ]
PA0603000
| [F ]
10 | [TSCA ]
Yes | [HS Code ]
29211190 |
| Hazard Information | Back Directory | [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. | [Definition]
ChEBI: The hydrochloride formed from methylamine. | [Preparation]
Methylamine hydrochloride is prepared by heating a mixture of aqueous formaldehyde and ammonium chloride; the residual water and the formic acid produced in the reaction are removed via vacuum distillation. This leaves behind solid methylamine hydrochloride. The solid is then purified by organic extractions and additional vacuum distillations. Methylamine gas for the reaction with P2P is generated in situ by heating the hydrochloride salt with sodium hydroxide. Alternatively, methylamine can be liberated from the hydrochloride with base and collected in a cold finger or flask immersed in a dry ice bath. | [Pharmacology]
Methylamine hydrochloride reduces blood pressure in both normotensive and hypertensive individuals. It has a gradual onset of action (1/2 to 2 hours) and a long-lasting effect (usually 6 to 12 hours or more). A small oral dosage often produces a smooth and predictable reduction of blood pressure. Although this antihypertensive effect is predominantly orthostatic, the supine blood pressure is also significantly reduced. | [Solubility in organics]
Very soluble in N,N-Dimethylformamide,Soluble in methanol,Sparingly soluble inglacial acetic acid, Very slightly soluble inchloroform.
| [Solubility in water]
The experimental water solubility of Methylamine hydrochloride at 20 ℃ was 1080mg/L. Methylamine hydrochloride is highly soluble in water. | [storage]
Keep in a dry, cool and well-ventilated place. Keep container tightly close
| [Purification Methods]
Crystallise the salt from n-butanol, absolute EtOH or MeOH/CHCl3. Wash it with CHCl3 to remove traces of dimethylamine hydrochloride. Dry it under vacuum first with H2SO4 then P2O5. It is deliquescent; store it in a desiccator over P2O5. [Beilstein 4 IV 122.] |
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