395048
Methylamine solution
2.0 M in methanol
동의어(들):
Monomethylamine
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3NH2
CAS 번호:
Molecular Weight:
31.06
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
741851
Concentration:
2.0 M in methanol
Form:
liquid
InChI
1S/CH5N/c1-2/h2H2,1H3
SMILES string
CN
InChI key
BAVYZALUXZFZLV-UHFFFAOYSA-N
vapor pressure
10.86 psi ( 55 °C), 2.07 psi ( 20 °C)
form
liquid
greener alternative product characteristics
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concentration
2.0 M in methanol
bp
40 °C
density
0.785 g/mL at 25 °C
functional group
amine
greener alternative category
Quality Level
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General description
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Methylamine solution is an aqueous solution of Methylamine. It is used to synthesize amino-terminated monolayers of phthalimide on silicon surfaces.
Methylamine solution is an aqueous solution of Methylamine. It is used to synthesize amino-terminated monolayers of phthalimide on silicon surfaces.
Application
Methylamine solution 2.0 M in methanol can be used as a precursor that facilitates the synthesis of perovskite based materials. It can also be used as a deactivating agent to study the catalytic performance of acidic macroporous ion exchange resins. It can be annealed to reduce impurity in the grain boundaries, improve the stability and efficiency of the perovskite solar cells.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 1 - STOT SE 3
target_organs
Eyes,Central nervous system, Respiratory system
저장 등급
3 - Flammable liquids
wgk
WGK 2
flash_point_f
44.6 °F - closed cup
flash_point_c
7 °C - closed cup
ppe
Faceshields, Gloves, Goggles
Preparation of amino-terminated monolayers via hydrolysis of phthalimide anchored to Si (1 1 1)
Ara, Masato and Tsuji
Surface Science, 601, 5098-5510 (2007)
Post-annealing of MAPbI 3 perovskite films with methylamine for efficient perovskite solar cells
Jiang Y, et al.
Materials Horizons, 3(6), 548-555 (2016)
Deactivation of ion exchange catalysts by acetonitrile and methylamine
Gonzalez R, et al.
Topics in Catalysis, 54(16-18), 1054-1054 (2011)
Xin Yu Chin et al.
Nature communications, 6, 7383-7383 (2015-06-26)
Despite the widespread use of solution-processable hybrid organic-inorganic perovskites in photovoltaic and light-emitting applications, determination of their intrinsic charge transport parameters has been elusive due to the variability of film preparation and history-dependent device performance. Here we show that screening
Jeff O'Sullivan et al.
Neurotoxicology, 25(1-2), 303-315 (2003-12-31)
The semicarbazide-sensitive amine oxidases (SSAO) (EC 1.4.3.6) were believed to be detoxifying enzymes, primarily involved in the oxidative deamination of endogenous amines, such as methylamine and aminoacetone, together with some xenobiotic amines. However, it appears that the reaction products may
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