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395048

Sigma-Aldrich

Methylamine solution

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2.0 M in methanol

Synonym(s):

Monomethylamine

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About This Item

Linear Formula:
CH3NH2
CAS Number:
74-89-5
Molecular Weight:
31.06
Beilstein:
741851
MDL number:
MFCD00008104
UNSPSC Code:
12352302
PubChem Substance ID:
24864637
NACRES:
NA.22

vapor pressure

10.86 psi ( 55 °C)
2.07 psi ( 20 °C)

Quality Level

200

form

liquid

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concentration

2.0 M in methanol

bp

40 °C

density

0.785 g/mL at 25 °C

greener alternative category

Enabling,

SMILES string

CN

InChI

1S/CH5N/c1-2/h2H2,1H3

InChI key

BAVYZALUXZFZLV-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

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.

Signal Word

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

44.6 °F - closed cup

Flash Point(C)

7 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Katja Wosikowski et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 9(5), 1917-1926 (2003-05-10)
To avoid systemic toxicity of the cytotoxic drug methotrexate (MTX) and to improve tumor selectivity, MTX was bound to human serum albumin (HSA) as a drug carrier. To understand more about the mechanism of action of MTX conjugated to HSA
T Kokubo et al.
Journal of biomedical materials research, 24(6), 721-734 (1990-06-01)
High-strength bioactive glass-ceramic A-W was soaked in various acellular aqueous solutions different in ion concentrations and pH. After soaking for 7 and 30 days, surface structural changes of the glass-ceramic were investigated by means of Fourier transform infrared reflection spectroscopy
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