10143-60-9

Basic information

• Product Name: DI(2-ETHYLHEXYL) ETHER
• Synonyms: OCTYL ETHER;2-ETHYLHEXYL ETHER;DI(2-ETHYLHEXYL) ETHER;DIOCTYL ETHER;BIS(2-ETHYLHEXYL) ETHER;1,1’-oxybis(2-ethyl-hexan;3,3’-[oxybis(methylene)]bis-heptan;3,3’-[oxybis(methylene)]bis-Heptane
• CAS NO: 10143-60-9
• Molecular Formula: C₁₆H₃₄O
• Molecular Weight: 242.44
• EINECS: 233-412-6
• Mol File: 10143-60-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: -7.6°C (estimate)
• Boiling Point: 126 °C / 8mmHg
• Flash Point: 107.5 °C
• Appearance: /
• Density: 0,8 g/cm3
• Vapor Pressure: 0.00762mmHg at 25°C
• Refractive Index: 1.4320-1.4380
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: DI(2-ETHYLHEXYL) ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: DI(2-ETHYLHEXYL) ETHER(10143-60-9)
• EPA Substance Registry System: DI(2-ETHYLHEXYL) ETHER(10143-60-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RTECS: KN3175000
• Hazardous Substances Data: 10143-60-9(Hazardous Substances Data)

Usage

Uses

Derivative of Ethylhexyl Oxide over Nafion-H are highly efficient solid perfluoroalkanesulfonic acid catalyst.

InChI:InChI=1/C16H34O/c1-5-9-11-15(7-3)13-17-14-16(8-4)12-10-6-2/h15-16H,5-14H2,1-4H3

Upstream product

• 104-76-7 2-Ethylhexyl alcohol 
• 123-05-7 d,l-2-ethylhexanal 
• 122-78-1 phenylacetaldehyde 
• 100-52-7 benzaldehyde 
• 645-62-5 2-ethylhexenal 

Relevant articles and documents

Silver(I)-Catalyzed Reductive Cross-Coupling of Aldehydes to Structurally Diverse Cyclic and Acyclic Ethers

A range of medium-sized cyclic ethers (5 to 11 membered) have been effectively synthesized through intramolecular reductive coupling of dialdehydes initiated by 50 ppm to 0.5% of AgNTf2 with hydrosilane at 25 °C. The catalytic system is also suitable for the coupling of two different monoaldehydes to provide unsymmetrical ethers. This protocol features broad functional group compatibility, high product diversity, high efficiency, and utility in the late-stage modification of complex biorelevant molecules.

HIGHLY EFFICIENT METHOD FOR PRODUCING SATURATED HOMOETHER FROM UNSATURATED CARBONYL COMPOUND

PROBLEM TO BE SOLVED: To provide a method for efficiently producing a saturated homoether from an unsaturated carbonyl compound. SOLUTION: The method for producing an unsaturated homoether uses an unsaturated carbonyl compound and hydrogen as a raw material, uses a catalyst comprising a metal supported on an acidic catalyst carrier and performs at least once a pressure reduction operation so that a differential pressure from a reaction pressure is 0.01 MPa or more. In the method, the metal of the catalyst is, for example, palladium and the carrier of the catalyst is alumina, silica, silica-alumina or the like. The unsaturated carbonyl compound serving as a raw material is 2-butenal, 2-ethyl-2-hexenal, 2-ethyl-2-butenal, 2-hexenal or the like and the produced saturated homoether is dibutyl ether, bis(2-ethylhexyl)ether, bis(2-ethylbutyl)ether, dihexyl ether or the like. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT