395056
Methylamine solution
2.0 M in THF
Synonym(s):
Monomethylamine
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Linear Formula:
CH3NH2
CAS Number:
Molecular Weight:
31.06
Beilstein:
741851
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
23.87 psi ( 55 °C)
7.24 psi ( 20 °C)
Quality Level
form
liquid
greener alternative product characteristics
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
concentration
2.0 M in THF
density
0.861 g/mL at 25 °C
functional group
amine
greener alternative category
SMILES string
CN
InChI
1S/CH5N/c1-2/h2H2,1H3
InChI key
BAVYZALUXZFZLV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Methylamine (CH3NH2) is a simple aliphatic primary amine used as a chemical intermediate in organic synthesis. It is prominently used in the production of pesticides and solvents.
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.
Application
Methylamine can be used as a reagent in the synthesis of the following:
- Methylmorpholine from diethylene glycol.
- N-methylalkylamines from oxoamines via formation of imine, followed by hydrogenation using Ni catalyst.
- N-Methyldipropylenetriamine by reacting with acrylonitrile, followed by hydrogenation.
- N-methyl hydroxypyrrolidines from chlorohydrin in the presence of NaCNBH as a reducing agent.
- 2-(Methylamino)-6,7-dichloro-1,4-anthracenedione by reacting with 6,7-dichloro-1,4-anthracenedione.
Methylamine solution 2.0 M in THF 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 Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
<-29.2 °F - closed cup
Flash Point(C)
< -34 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Jason A Draper et al.
Organic letters, 12(18), 4034-4037 (2010-08-24)
A convergent and stereoselective synthesis of 2,5-disubstituted 3-hydroxypyrrolidines has been developed that involves reductive annulation of β-iminochlorohydrins, which are readily available from β-ketochlorohydrins, and provides rapid access to a variety of 2,5-syn-pyrrolidines. Application of this process to the concise (three-step)
Amines, aliphatic
Eller K, et al.
Ullmann's Encyclopedia of Industrial Chemistry (2000)
Synthesis and in vitro antitumor activity of substituted anthracene-1, 4-diones
Hua DH, et al.
Tetrahedron, 60(45), 10155-10163 (2004)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 395056-100ML | 4061831982923 |
| 395056-800ML | 4061837672989 |
| 395056-2L | 4061838119650 |
| 395056-4X100ML | 4061837672972 |
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service