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M0505

Sigma-Aldrich

Methylamin -hydrochlorid

≥98%

Synonym(e):

Methanaminium chloride, Methylamine monohydrochloride, Methylammonium chloride, Monomethylammonium chloride

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About This Item

Lineare Formel:
CH3NH2 · HCl
CAS-Nummer:
593-51-1
Molekulargewicht:
67.52
Beilstein:
3588822
EG-Nummer:
209-795-0
MDL-Nummer:
MFCD00012849
UNSPSC-Code:
12352100
PubChem Substanz-ID:
57654342
NACRES:
NA.22

Qualitätsniveau

200

Assay

≥98%

Form

powder or crystals

bp

225-230 °C/15 mmHg (lit.)

mp (Schmelzpunkt)

231-233 °C (lit.)

Löslichkeit

H2O: 1 g in 10 mL, clear, colorless

SMILES String

Cl[H].CN

InChI

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

InChIKey

NQMRYBIKMRVZLB-UHFFFAOYSA-N

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Allgemeine Beschreibung

Methylamine hydrochloride is used as a buildingblock for the synthesis of various organic compounds.

Anwendung

Methylamine hydrochloride can be used as a reactant to synthesize:
  • Betahistine via aza-Michael reaction with 2-vinylpyridine in water.
  • Azatripyrrolic and azatetrapyrrolic macrocycles by reacting with pyrrole and formaldehyde via base-catalyzed Mannich reaction.
  • Tetrahydropyridines via Aza-Diels–Alder reaction with dienes and aldehydes.
  • N-methylsecondary arylamines from aryl chlorides via nickel-catalyzed amination reaction.

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Preisangaben

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

408.7 °F - closed cup

Flammpunkt (°C)

209.3 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCL2937
BCCM3607
BCCC2164
BCCH7800
BCCJ5999

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Jixian Xu et al.
Science (New York, N.Y.), 367(6482), 1097-1104 (2020-03-07)
Wide-band gap metal halide perovskites are promising semiconductors to pair with silicon in tandem solar cells to pursue the goal of achieving power conversion efficiency (PCE) greater than 30% at low cost. However, wide-band gap perovskite solar cells have been
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
Raymond J Ritchie
Microbial ecology, 65(1), 180-196 (2012-09-04)
Ammonia is the preferred nitrogen source for many algae including the cyanobacterium Synechococcus elongatis (Synechococcus R-2; PCC 7942). Modelling ammonia uptake by cells is not straightforward because it exists in solution as NH(3) and NH (4) (+) . NH(3) is
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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