1-Ethoxy-2-methylpropane

Base Information

• Chemical Name: 1-Ethoxy-2-methylpropane
• CAS No.: 627-02-1
• Molecular Formula: C6H14O
• Molecular Weight: 102.177
• Hs Code.: 2909191800
• DSSTox Substance ID: DTXSID4074934
• Nikkaji Number: J45.671C
• Wikidata: Q29653286
• Mol file: 627-02-1.mol

Synonyms:1-Ethoxy-2-methylpropane;627-02-1;Ethyl isobutyl ether;Isobutyl ethyl ether;Ether, ethyl isobutyl;Propane, 1-ethoxy-2-methyl-;BRN 1731175;iso-Butyl ethyl ether;ethylisobutyl ether;1-ethoxy-2-methyl-propane;SCHEMBL43710;1-Ethoxy-2-methylpropane #;(CH3)2CHCH2OC2H5;DTXSID4074934;MFCD00038317;AKOS006272327;AS-76117;LS-67836;1-cyclopropylmethyl-piperazinedihydrochloride;FT-0627356;D93520;Q29653286

Chemical Property of 1-Ethoxy-2-methylpropane

Chemical Property:

• Vapor Pressure: 82.9mmHg at 25°C
• Melting Point: 125-127℃
• Refractive Index: 1.3749 (589.3 nm 20℃)
• Boiling Point: 83.8 °C at 760 mmHg
• PSA: 9.23000
• Density: 0.76 g/cm³
• LogP: 1.67890
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 102.104465066
• Heavy Atom Count: 7
• Complexity: 33.2

Purity/Quality:

98%,99%, ^*data from raw suppliers

ISO-BUTYL ETHYL ETHER 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOCC(C)C
• Uses: Isobutyl Ethyl Ether was identified in the biopreservation system formed by coupling Lactobacillus reuteri INIA P572 and glycerol.

Technology Process of 1-Ethoxy-2-methylpropane

There total 4 articles about 1-Ethoxy-2-methylpropane 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:

1,2-dimethoxyethane (110-71-4) + ethanol (64-17-5) + N-Isobutyl-N-nitrosoharnstoff (760-60-1) → butan-2-yl ethyl ester (2679-87-0) + ethyl isobutyl ether (627-02-1) + Ethyl tert-butyl ether (637-92-3) + Ethyl-(2-methylpropyl)-carbonat (35363-42-9) + 1-(2-Methoxyethoxy)-2-methylpropan (89851-42-3) + 2-(2-Methoxyethoxy)butan

Guidance literature:

With sodium hydrogencarbonate; Product distribution; Ambient temperature; further reagent: K₂CO₃, var. conc.;

Reference yield:

ethanol (64-17-5) + 2-methyl-propan-1-ol (78-83-1) → diethyl ether (60-29-7,927820-24-4) + ethyl isobutyl ether (627-02-1) + isobutene (115-11-7,15220-85-6)

Guidance literature:

Reference yield:

methylene (2465-56-7) + ethylpropylether (628-32-0) → isopropyl propyl ether (627-08-7) + butan-2-yl ethyl ester (2679-87-0) + ethyl isobutyl ether (627-02-1) + Dipropyl ether (111-43-3) + butyl ethyl ether (628-81-9)

Guidance literature:

at 20 ℃; Kinetics; Irradiation;

upstream raw materials:

ethanol

2-methyl-propan-1-ol

methylene

ethylpropylether

Downstream raw materials:

tertiary butyl chloride

isobutene

chloroethane

2-methylpropyl acetate

Refernces

• 1、 Mehta, R. K. S.. "Chemistry of Carbenes: Part III - Reaction of Methylene with Ethyl n-Propyl Ether". . p. 60 - 62. Retrieved 2007/10/02.