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Merck
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Documenti

241016

Sigma-Aldrich

Methylamine hydrochloride

≥99%

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About This Item

Formula condensata:
CH3NH2 · HCl
Numero CAS:
593-51-1
Peso molecolare:
67.52
Beilstein:
3588822
Numero CE:
209-795-0
Numero MDL:
MFCD00012849
Codice UNSPSC:
12352100
ID PubChem:
24854452

Saggio

≥99%

P. eboll.

225-230 °C/15 mmHg (lit.)

Punto di fusione

231-233 °C (lit.)

Solubilità

absolute ethanol: soluble(lit.)
acetone: insoluble(lit.)
chloroform: insoluble(lit.)
diethyl ether: insoluble(lit.)
ethyl acetate: insoluble(lit.)
water: soluble(lit.)

Stringa SMILE

Cl[H].CN

InChI

1S/CH5N.ClH/c1-2;/h2H2,1H3;1H
NQMRYBIKMRVZLB-UHFFFAOYSA-N

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Descrizione generale

Methylamine hydrochloride causes the chroloplast to shrink.

Applicazioni

Methylamine hydrochloride was used in the synthesis of mephtetramine via Mannich reaction.

Sostituito da

N° Catalogo
Descrizione
Determinazione del prezzo

M0505

Methylamine hydrochloride, ≥98%

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Consigli di prudenza

P301 + P312 + P330

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

408.7 °F - closed cup

Punto d’infiammabilità (°C)

209.3 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (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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