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About This Item
Linear Formula:
CH3NH2 · HCl
CAS Number:
Molecular Weight:
67.52
Beilstein:
3588822
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
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
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General description
Methylamine hydrochloride causes the chroloplast to shrink.
Application
Methylamine hydrochloride was used in the synthesis of mephtetramine via Mannich reaction.
replaced by
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
408.7 °F - closed cup
Flash Point(C)
209.3 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Jing-Jing Fang et al.
Waste management (New York, N.Y.), 32(7), 1401-1410 (2012-04-07)
This study investigated the odor compounds from different areas in a landfill site, which included the municipal solid waste (MSW)-related area, the leachate-related area and the sludge-related area. Nine sampling points were placed and 35 types of odorous substances were
Nicolas Fleury-Brégeot et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(31), 9564-9570 (2012-07-07)
Ammoniomethyl trifluoroborates are very powerful reagents that can be used to access biologically relevant aryl- and heteroaryl-methylamine motifs via Suzuki-Miyaura cross-couplings. Until now, this method was limited to the production of tertiary and primary amines. The synthesis of a large
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