Ethanamine, N-methyl-

Base Information

• Chemical Name: Ethanamine, N-methyl-
• CAS No.: 624-78-2
• Molecular Formula: C3H9N
• Molecular Weight: 59.1112
• Hs Code.: 29211990
• European Community (EC) Number: 210-862-1
• UNII: AE3IIW7JBO
• DSSTox Substance ID: DTXSID8060793
• Nikkaji Number: J1.679I
• Wikipedia: Ethylmethylamine
• Wikidata: Q6036777
• Metabolomics Workbench ID: 146983
• ChEMBL ID: CHEMBL1232589
• Mol file: 624-78-2.mol

Synonyms:N-Ethylmethylamine;624-78-2;N-Methylethylamine;Ethanamine, N-methyl-;Methylethylamine;Ethyl(methyl)amine;N-METHYLETHANAMINE;Ethylmethylamine;Nmea;N-Methyl-N-ethylamine;Ethylamine, N-methyl-;N-ethyl methyl amine;Methylaminoethane;ethyl-methyl-amine;N-Ethyl-N-methylamine;AE3IIW7JBO;EINECS 210-862-1;N-ethylmethyl amine;methyethylamine;ethylmethylannine;ethyl methylamine;ethyl-methylamine;methyl-ethylamine;methylethyl amine;N-Ethylmethylamne;methyl ethyl amine;N-Mthylmethylamine;methyl-N-ethylamine;N-ethyl-methylamine;N-methyl ethylamine;N-methyl-ethanamine;N-methyl-ethylamine;ethyl-(methyl)amine;MFCD00009030;n-ethyl-n-methyl-amine;UNII-AE3IIW7JBO;ALEMA30;N-Ethylmethylamine, 97%;(CH3)(C2H5)NH;CHEMBL1232589;DTXSID8060793;STR03903;AKOS000145747;DB02396;A8636;E0729;FT-0651636;EN300-33324;J-523568;J-640370;Q6036777;F2158-0955

Chemical Property of Ethanamine, N-methyl-

Chemical Property:

• Appearance/Colour: clear colorless to light yellow liquid
• Vapor Pressure: 8.53 psi ( 20 °C)
• Melting Point: -70.99°C (estimate)
• Refractive Index: n20/D 1.374(lit.)
• Boiling Point: 36.7 °C at 760 mmHg
• PKA: pK1:4.23(＋1) (25°C)
• Flash Point: <?30°F
• PSA: 12.03000
• Density: 0.68 g/cm³
• LogP: 0.61660
• Storage Temp.: 0-6°C
• Sensitive.: Hygroscopic
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 59.073499291
• Heavy Atom Count: 4
• Complexity: 7.2

Purity/Quality:

99%+, ^*data from raw suppliers

N-Ethylmethylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F; C
• Hazard Codes: F,C
• Statements: 11-20/21/22-35-34
• Safety Statements: 26-36/37/39-45-16

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Nitrogen Compounds -> Amines, Aliphatic
• Canonical SMILES: CCNC
• Uses: N-Ethylmethylamine has been used in the synthesis of N-ethyl-methyl acrylamide via reaction with acryloyl chloride.

Technology Process of Ethanamine, N-methyl-

There total 58 articles about Ethanamine, N-methyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

N-(benzylidene)ethylamine (6852-54-6) + dimethyl sulfate (77-78-1) → N-Ethylmethylamine (624-78-2)

Guidance literature:

at 80 ℃; under 0 Torr; Temperature;

Reference yield: 90.0%

acetaldehyde (75-07-0,9002-91-9) + methylamine (74-89-5) → N-Ethylmethylamine (624-78-2)

Guidance literature:

With hydrogen; sodium hydroxide; Raney nickel; at 65 - 67 ℃; for 4.3h; under 22502.3 Torr; Product distribution / selectivity; Autoclave; Industry scale;

Reference yield: 80.0%

N-ethylidenemethylamine (6898-67-5) → N-Ethylmethylamine (624-78-2)

Guidance literature:

With hydrogen; platinum(IV) oxide; In ethanol;

DOI:10.1002/ardp.19843170306

upstream raw materials:

pyridine

N,N-diethylnmethylamine

dibenzoyl peroxide

diethyl ether

Downstream raw materials:

5-(ethyl-methyl-amino)-pentan-2-one

N-ethyl-N-methylbenzylamine

3-(ethylmethylamino)-propan-1-ol

ethyltrimethylammonium iodide

Refernces

• 1、 -. "ORGANOMETALLIC COMPOUNDS FOR THE DEPOSITION OF HIGH PURITY TIN OXIDE AND DRY ETCHING OF THE TIN OXIDE FILMS AND DEPOSITION REACTORS". Paragraph 0118. . Retrieved 2021/03/05.
• 2、 Matzel, Philipp,Krautschick, Lukas,H?hne, Matthias. "Photometric Characterization of the Reductive Amination Scope of the Imine Reductases from Streptomyces tsukubaensis and Streptomyces ipomoeae". . p. 2022 - 2027. Retrieved 2017/10/07.