426466
Methylamine solution
40 wt. % in H2O
Synonym(s):
Monomethylamine
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All Photos(2)
About This Item
Linear Formula:
CH3NH2
CAS Number:
Molecular Weight:
31.06
Beilstein:
741851
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
vapor density
1.07 (vs air)
Quality Level
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
SMILES string
CN
InChI
1S/CH5N/c1-2/h2H2,1H3
InChI key
BAVYZALUXZFZLV-UHFFFAOYSA-N
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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
related product
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
14.0 °F - closed cup
Flash Point(C)
-10 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Preparation of Tetrahydroisoquinoline-3-ones Via Cyclization of Phenyl Acetamides Using Eaton's Reagent.
Yang Q, et al.
Organic Syntheses, 44-54 (2012)
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)
Han Chen et al.
Nature, 550(7674), 92-95 (2017-09-05)
Recent advances in the use of organic-inorganic hybrid perovskites for optoelectronics have been rapid, with reported power conversion efficiencies of up to 22 per cent for perovskite solar cells. Improvements in stability have also enabled testing over a timescale of
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