2-Propanamine, N,N,2-trimethyl-

Base Information

• Chemical Name: 2-Propanamine, N,N,2-trimethyl-
• CAS No.: 918-02-5
• Molecular Formula: C6H15 N
• Molecular Weight: 101.192
• DSSTox Substance ID: DTXSID7061277
• Nikkaji Number: J397.105H
• Wikidata: Q23995131
• Mol file: 918-02-5.mol

Synonyms:918-02-5;N,N-Dimethyl-tert-butylamine;2-Propanamine, N,N,2-trimethyl-;tert-Butyldimethylamine;N,N,2-trimethylpropan-2-amine;t-C4H9N(CH3)2;2-Propanamine,N,N,2-trimethyl-;MFCD03452796;N,N-Dimethyl-tert.-butylamine;N,N-Dimethyl-t-butylamine;t-butyldimethylamine;dimethyl-t-butyl amine;tert-butyl-dimethyl-amine;N,N Dimethyl-tert-butylamine;SCHEMBL124148;DTXSID7061277;N,N,2-Trimethyl-2-propanamine;N,N,2-Trimethyl-2-propanamine #;Ethylamine, N,N,1,1-tetramethyl-;GEO-00618;AKOS005254539;AS-75496;FT-0676587;E77722;J-660059;Q23995131

Chemical Property of 2-Propanamine, N,N,2-trimethyl-

Chemical Property:

• Vapor Pressure: 104mmHg at 25°C
• Melting Point: -90 °C
• Refractive Index: 1.4065-1.4085
• Boiling Point: 89.6-89.9 °C (740 mmHg)
• PKA: 9.99±0.50(Predicted)
• Flash Point: °C
• PSA: 3.24000
• Density: 0.75g/cm³
• LogP: 1.34650
• Storage Temp.: Flammables area
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 101.120449483
• Heavy Atom Count: 7
• Complexity: 49.7

Purity/Quality:

98%Min ^*data from raw suppliers

N,N-Dimethyl-tert-butylamine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C-F,C
• Statements: 34-11
• Safety Statements: 45-36/37/39-26-16

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)N(C)C
• Uses: N,N-Dimethyl-tert-butylamine is used in method and device for calculating acid dissociation constant, and program.

Technology Process of 2-Propanamine, N,N,2-trimethyl-

There total 6 articles about 2-Propanamine, N,N,2-trimethyl- 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: 77.0%

formaldehyd (50-00-0,30525-89-4,61233-19-0) + tert-butylamine (75-64-9) → N,N-dimethyl-tert-butylamine (918-02-5)

Guidance literature:

With [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; In hexane; water; at 50 ℃; for 5h;

DOI:10.1002/cssc.201600824

Reference yield:

N-methyl-tert-butylamine (14610-37-8) + carbon dioxide (124-38-9,18923-20-1) → N,N-dimethyl-tert-butylamine (918-02-5)

Guidance literature:

With diphenylsilane; C₂₁H₄₁N₃NiP₂; In acetonitrile; at 120 ℃; for 24h; under 2052.14 Torr; Autoclave;

DOI:10.1039/c8cc05948a

Reference yield:

carbon dioxide (124-38-9,18923-20-1) + tert-butylamine (75-64-9) → N,N-dimethyl-tert-butylamine (918-02-5)

Guidance literature:

With diphenylsilane; C₂₁H₄₁N₃NiP₂; In acetonitrile; at 120 ℃; for 24h; under 2052.14 Torr; Autoclave;

DOI:10.1039/c8cc05948a

upstream raw materials:

formaldehyd

tert-butylamine

methanol

N-methyl-tert-butylamine

Downstream raw materials:

benzyl-tert-butyl-dimethyl-ammonium; chloride

N-methyl-tert-butylamine

Tert-butylmethyl-d3-amine

4-nitro-aniline