426466
Methylamine solution
40 wt. % in H₂O, solution
Synonyme(s) :
Monomethylamine
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A propos de cet article
Formule linéaire :
CH3NH2
Numéro CAS:
Poids moléculaire :
31.06
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
741851
Bp:
48 °C
Vapor pressure:
280 mmHg ( 20 °C), 659 mmHg ( 40 °C)
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Methylamine solution, 40 wt. % in H2O
vapor density
1.07 (vs air)
Quality Segment
vapor pressure
280 mmHg ( 20 °C), 659 mmHg ( 40 °C)
autoignition temp.
806 °F
concentration
40 wt. % in H2O
refractive index
n20/D 1.37
bp
48 °C
density
0.897 g/mL at 25 °C
functional group
amine
SMILES string
CN
InChI
1S/CH5N/c1-2/h2H2,1H3
InChI key
BAVYZALUXZFZLV-UHFFFAOYSA-N
Application
Methylamine solution may be used as a LC-MS/MS mobile phase in the perchlorate analysis of milk and yogurt samples.
It may be used in the synthesis of the following:
It may be used in the synthesis of the following:
- 9-fluorenylmethyl N-methylcarbamate and tert-butyl N-methylcarbamate
- 7-methylamino-2-(2-quinolyl)tropone
- 2,5-meso-pyrrolidines
- 2-(4-chlorophenyl)-N-methylacetamide
- 1,3-benzoxazine derivatives from eugenol
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signalword
Danger
hcodes
target_organs
Respiratory system
Classe de stockage
3 - Flammable liquids
flash_point_f
14.0 °F - closed cup
flash_point_c
-10 °C - closed cup
ppe
Faceshields, Gloves, Goggles
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
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Zacharias Amara et al.
Organic & biomolecular chemistry, 10(35), 7148-7157 (2012-07-27)
Novel 2,5-meso-pyrrolidines have been straightforwardly synthesized from readily available symmetrical double Michael acceptors. The key step rested on an aza-Michael addition of primary alkylamines to bis-enones. Competitive Rauhut-Currier and aza-Michael reactions have been highlighted in protic solvent. Ultrasound activation associated
Orthogonally Protected N-Methyl-Substituted α-Aminoglycines.
Jiang G, et al.
Protein and peptide letters, 3(4), 219-224 (1996)
Dohyung Kim et al.
Nature communications, 10(1), 444-444 (2019-01-27)
Organic-inorganic metal halide perovskites have gained considerable attention for next-generation photovoltaic cells due to rapid improvement in power conversion efficiencies. However, fundamental understanding of underlying mechanisms related to light- and bias-induced effects at the nanoscale is still required. Here, structural