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241016

Sigma-Aldrich

Methylamine hydrochloride

≥99%

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About This Item

Linear Formula:
CH3NH2 · HCl
CAS Number:
593-51-1
Molecular Weight:
67.52
Beilstein:
3588822
EC Number:
209-795-0
MDL number:
MFCD00012849
UNSPSC Code:
12352100
PubChem Substance ID:
24854452

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P301 + P312 + P330

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

Certificates of Analysis (COA)

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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
Michaela Frybortova et al.
Journal of inorganic biochemistry, 126, 46-54 (2013-06-19)
In order to shed light on the mechanism that underlies activity of bifunctional mononuclear Pt(II) analogs of transplatin we examined in the present work a DNA binding mode of the analog of transplatin, namely trans-[Pt(CH3NH2)2Cl2], in which NH3 groups 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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