Ethyl isopropyl ether

Base Information

• Chemical Name: Ethyl isopropyl ether
• CAS No.: 625-54-7
• Molecular Formula: C5H12O
• Molecular Weight: 88.1497
• European Community (EC) Number: 210-900-7
• DSSTox Substance ID: DTXSID5060805
• Nikkaji Number: J43.311J
• Wikidata: Q24764257
• Mol file: 625-54-7.mol

Synonyms:ETHYL ISOPROPYL ETHER;2-Ethoxypropane;625-54-7;Propane, 2-ethoxy-;Ether, ethyl isopropyl;Isopropyl ethyl ether;EINECS 210-900-7;BRN 1730945;Methylather;ethylisopropyl ether;Ethyl iso-propyl ether;(CH3)2CHOC2H5;DTXSID5060805;MFCD00043532;LS-67838;E0416;FT-0612222;D90509;Q24764257

Chemical Property of Ethyl isopropyl ether

Chemical Property:

• Vapor Pressure: 183mmHg at 25°C
• Melting Point: -117.26°C (estimate)
• Refractive Index: 1.374
• Boiling Point: 63.5 °C at 760 mmHg
• PSA: 9.23000
• Density: 0.748 g/cm³
• LogP: 1.43130
• Storage Temp.: 0-10°C
• Water Solubility.: 24.09g/L(temperature not stated)
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 88.088815002
• Heavy Atom Count: 6
• Complexity: 25.1

Purity/Quality:

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

Ethyl Isopropyl Ether >98.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(C)C

Technology Process of Ethyl isopropyl ether

There total 35 articles about Ethyl isopropyl ether 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: 98.0%

Isopropyl acetate (108-21-4) → 2-butyl ethyl ether (625-54-7)

Guidance literature:

With hydrogenchloride; trichlorosilane; at 60 ℃; Irradiation;

DOI:10.1016/0022-328X(89)85276-3

Reference yield: 93.2%

diazomethane (186581-53-3,908094-01-9,334-88-3) + ethylpropylether (628-32-0) → Dimethyl ether (115-10-6,157621-61-9) + ethyl methyl ether (540-67-0) + methyl propyl ether (557-17-5) + 2-butyl ethyl ether (625-54-7)

Guidance literature:

Product distribution; Mechanism; Ambient temperature; Irradiation;

DOI:10.1021/jo00186a007

Reference yield: 92.5%

ethylpropylether (628-32-0) + diazomethane-d2 (14621-84-2) → Dimethyl ether (115-10-6,157621-61-9) + ethyl methyl ether (540-67-0) + methyl propyl ether (557-17-5) + 2-butyl ethyl ether (625-54-7)

Guidance literature:

Product distribution; Mechanism; Ambient temperature; Irradiation; deuterium distribution;

DOI:10.1021/jo00186a007

upstream raw materials:

diazomethane

diethyl ether

ethyl bromide

sodium isopropylate

Downstream raw materials:

methyl 2-hydroxy-3-(4-methoxyphenyl)-3-(2-nitrophenylthio)propionate

2-iodo-propane

ethanol

ethyl iodide

Refernces

• 1、 Babiak, Peter,Němcová, Adriana,Rulí?ek, Lubomír,Beier, Petr. "On the miscibility of ethers and perfluorocarbons. An experimental and theoretical study". . p. 397 - 401. Retrieved 2008/12/21.
• 2、 Oka, Kunio,Nakao, Ren. "γ-Ray-induced reduction of sterically hindered alkyl carboxylates with trichlorosilane in the presence of hydrogen chloride. Two-step mechanism for the formation of alkanes via the alkyl chloride". . p. 31 - 35. Retrieved 2007/10/02.