M0505
Methylamine hydrochloride
≥98%
동의어(들):
Methanaminium chloride, Methylamine monohydrochloride, Methylammonium chloride, Monomethylammonium chloride
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3NH2 · HCl
CAS 번호:
Molecular Weight:
67.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-795-0
Beilstein/REAXYS Number:
3588822
MDL number:
Assay:
≥98%
Form:
powder or crystals
InChI key
NQMRYBIKMRVZLB-UHFFFAOYSA-N
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H
SMILES string
Cl[H].CN
assay
≥98%
form
powder or crystals
bp
225-230 °C/15 mmHg (lit.)
mp
231-233 °C (lit.)
solubility
H2O: 1 g in 10 mL, clear, colorless
Quality Level
유사한 제품을 찾으십니까? 방문 제품 비교 안내
General description
Methylamine hydrochloride is used as a buildingblock for the synthesis of various organic compounds.
Application
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
저장 등급
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
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
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
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
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