241016
Methylamine hydrochloride
≥99%
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About This Item
Linear Formula:
CH3NH2 · HCl
CAS Number:
Molecular Weight:
67.52
EC Number:
209-795-0
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3588822
MDL number:
assay
≥99%
bp
225-230 °C/15 mmHg (lit.)
mp
231-233 °C (lit.)
solubility
absolute ethanol: soluble(lit.), acetone: insoluble(lit.), chloroform: insoluble(lit.), diethyl ether: insoluble(lit.), ethyl acetate: insoluble(lit.), water: soluble(lit.)
SMILES string
Cl[H].CN
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H
InChI key
NQMRYBIKMRVZLB-UHFFFAOYSA-N
General description
Methylamine hydrochloride causes the chroloplast to shrink.
Application
Methylamine hydrochloride was used in the synthesis of mephtetramine via Mannich reaction.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
flash_point_f
408.7 °F - closed cup
flash_point_c
209.3 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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S Izawa et al.
Plant physiology, 41(3), 533-543 (1966-03-01)
Whole chloroplasts isolated from the leaves of spinach (Spinacia oleracea L.) exhibit 2 types of conformational change during electron transport. Amine-uncoupled chloroplasts swell and atebrin-uncoupled chloroplasts shrink. Chloroplasts uncoupled by carbonylcyanide phenylhydrazones and by treatment with ethylenediamine tetraacetic acid do
John D Power et al.
Drug testing and analysis, 6(7-8), 668-675 (2014-02-28)
Three legal highs; nitracaine (3-(diethylamino)-2,2-dimethylpropyl 4-nitrobenzoate), methoxypiperamide (MEOP, (4-methoxyphenyl)(4-methylpiperazin-1-yl)methanone) and mephtetramine (MTTA, 2-((methylamino)methyl)-3,4-dihydronaphthalen-1(2H)-one) appeared in 2013 as new psychoactive substances (NPS) on Internet websites selling 'research chemicals'. These compounds were synthesized and analyzed via our synthesize, analyze, and metabolize (SAM)
Thomas S Hofer et al.
Molecular bioSystems, 8(11), 2891-2900 (2012-08-01)
Molecular dynamics simulations have been performed to investigate the binding of tris(hydroxymethyl)-aminomethane to the surface of the core domain of the mouse cellular tumor antigen p53 employing the GROMOS and 53A6 force field parameter sets. A close investigation of the