Methylamine-C hydrochloride structure
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Common Name | Methylamine-C hydrochloride | ||
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CAS Number | 60656-93-1 | Molecular Weight | 68.51070 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | CH6ClN | Melting Point | 232-234ºC(lit.) | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | methanamine,hydrochloride |
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Synonym | More Synonyms |
Melting Point | 232-234ºC(lit.) |
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Molecular Formula | CH6ClN |
Molecular Weight | 68.51070 |
Exact Mass | 68.02220 |
PSA | 26.02000 |
LogP | 1.07720 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Hazard Codes | Xi |
Risk Phrases | 36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
Precursor 0 | |
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DownStream 1 | |
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... |
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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... |
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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... |
Methylamine-13C hydrochloride |
I05-2769 |
MFCD00037597 |
Methanamine-13C,hydrochloride |