methanamine,hydrochloride

[ Melting Point ]:
232-234ºC(lit.)

[ Molecular Formula ]:
CH₆ClN

[ Molecular Weight ]:
68.51140

[ Exact Mass ]:
68.01590

[ PSA ]:
26.02000

[ LogP ]:
1.07720

Click to get detail MSDS

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R22

[ RIDADR ]:
NONH for all modes of transport

Methylamine utilization via the N-methylglutamate pathway in Methylobacterium extorquens PA1 involves a novel flow of carbon through C1 assimilation and dissimilation pathways.

J. Bacteriol. 196(23) , 4130-9, (2014)

Methylotrophs grow on reduced single-carbon compounds like methylamine as the sole source of carbon and energy. In Methylobacterium extorquens AM1, the best-studied aerobic methylotroph, a periplasmic...

Origin and nature of bond rotation barriers: a unified view.

J. Phys. Chem. A 117(5) , 962-5, (2013)

Bond rotations are common and important in molecular studies such as drug design and enzymatic reactions. Steric hindrance and hyperconjugation are often borrowed to justify the origin of bond rotatio...

Water adsorption at two unsolvated peptides with a protonated lysine residue: from self-solvation to solvation.

J. Phys. Chem. B 116(51) , 14788-804, (2012)

We study the initial steps of the interaction of water molecules with two unsolvated peptides: Ac-Ala(5)-LysH(+) and Ac-Ala(8)-LysH(+). Each peptide has two primary candidate sites for water adsorptio...

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