2-Ethylhexyl glycidyl ether

Base Information

• Chemical Name: 2-Ethylhexyl glycidyl ether
• CAS No.: 2461-15-6
• Deprecated CAS: 102640-36-8,145928-91-2,98913-53-2,388080-79-3,845755-34-2,898543-72-1,145928-91-2,388080-79-3,845755-34-2,98913-53-2
• Molecular Formula: C11H22O2
• Molecular Weight: 186.294
• Hs Code.: 29109000
• European Community (EC) Number: 219-553-6
• NSC Number: 252154
• UNII: LU1UZ98B89
• DSSTox Substance ID: DTXSID6025301
• Nikkaji Number: J216.100A
• Wikipedia: 2-Ethylhexyl_glycidyl_ether
• Wikidata: Q26841189
• ChEMBL ID: CHEMBL1412431
• Mol file: 2461-15-6.mol

Synonyms:2-ETHYLHEXYL GLYCIDYL ETHER;2461-15-6;2-Ethylhexylglycidylether;2-(2-ethylhexoxymethyl)oxirane;Glycidyl 2-ethylhexyl ether;Oxirane, [[(2-ethylhexyl)oxy]methyl]-;(((2-Ethylhexyl)oxy)methyl)oxirane;2-{[(2-ethylhexyl)oxy]methyl}oxirane;2,3-Epoxypropyl-(2-ethylhexyl) ether;((2-Ethylhexyl)methyl)oxirane;[(2-Ethylhexyl)methyl]oxirane;CCRIS 2634;Oxirane, (((2-ethylhexyl)oxy)methyl)-;Oxirane, 2-[[(2-ethylhexyl)oxy]methyl]-;Propane, 1,2-epoxy-3-((2-ethylhexyl)oxy)-;EINECS 219-553-6;2-ethylhexylglycidyl ether;NSC 252154;BRN 1236919;UNII-LU1UZ98B89;2-ethyl hexyl glycidyl ether;Ethylhexyl glycidyl ether, 2-;Oxirane, 2-(((2-ethylhexyl)oxy)methyl)-;LU1UZ98B89;DTXSID6025301;NSC-252154;2-(((2-ethylhexyl)oxy)methyl)oxirane;EC 219-553-6;DTXCID505301;[[(2-ethylhexyl)oxy]methyl]oxirane;CAS-2461-15-6;Propane, 1,2-epoxy-3-[(2-ethylhexyl)oxy]-;SCHEMBL38306;C(OCC(CC)CCCC)C1CO1;CHEMBL1412431;BBBUAWSVILPJLL-UHFFFAOYSA-;2-Ethylhexyl glycidyl ether, 98%;2-((2-ethylhexyloxy)methyl)oxirane;3-(GLYCIDYLOXYMETHYL)HEPTANE;Tox21_201983;Tox21_303126;(2-Ethylhexyloxy)-2,3-epoxypropane;MFCD00005141;NSC252154;AKOS009075740;2-Ethylhexyl 2-oxiranylmethyl ether #;LS-1056;2-(2-ETHYLHEXYLOXYMETHYL)OXIRANE;NCGC00091403-01;NCGC00091403-02;NCGC00257161-01;NCGC00259532-01;LS-14025;Propane,2-epoxy-3-[(2-ethylhexyl)oxy]-;J216.100A;CS-0315014;E0229;FT-0634299;1-(2-ETHYLHEXYLOXY)-2,3-EPOXYPROPANE;F71237;A817395;Q26841189

Chemical Property of 2-Ethylhexyl glycidyl ether

Chemical Property:

• Appearance/Colour: colourless liquid
• Vapor Pressure: 0.0209mmHg at 25°C
• Refractive Index: 1.434
• Boiling Point: 259.452 °C at 760 mmHg
• Flash Point: 96.667 °C
• PSA: 21.76000
• Density: 0.913 g/cm³
• LogP: 2.61820
• Water Solubility.: <0.1 g/100 mL at 19℃
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 186.161979940
• Heavy Atom Count: 13
• Complexity: 125

Purity/Quality:

98% ^*data from raw suppliers

2-[[(2-Ethylhexyl)oxy]methyl]oxirane-d5 ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCC(CC)COCC1CO1
• Uses: It constitutes a reactive diluent and may be used as a relatively nonvolatile chloride-scavenging agent and stabilizer for vinyl resins and rubber. 2-Ethylhexyl glycidyl ether is a used as a commercial reactive diluent. 2-Ethylhexyl glycidyl ether is also known to induce sister-chromatid exchanges in Chinese hamster cells.

Technology Process of 2-Ethylhexyl glycidyl ether

There total 6 articles about 2-Ethylhexyl glycidyl 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:

2-Ethylhexyl alcohol (104-76-7) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → 2-ethyl-hexyl glycidyl ether (2461-15-6) + 5,13-diethyl-7,11-dioxa-9-heptadecanol (59068-03-0)

Guidance literature:

2-Ethylhexyl alcohol; With tetrabutylammomium bromide; sodium hydroxide; at -40 ℃; for 0.5h; Inert atmosphere;

epichlorohydrin; at 40 ℃; for 12h; Reagent/catalyst; Temperature;

Reference yield:

2-Ethylhexyl alcohol (104-76-7) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → 2-ethyl-hexyl glycidyl ether (2461-15-6)

Guidance literature:

2-Ethylhexyl alcohol; With tetrabutylammomium bromide; sodium hydroxide; at -40 ℃; for 0.5h; Inert atmosphere;

epichlorohydrin; at 40 ℃; for 12h; Reagent/catalyst; Temperature;

Reference yield:

1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol (37961-18-5) → 2-ethyl-hexyl glycidyl ether (2461-15-6)

Guidance literature:

With potassium tert-butylate; In tetrahydrofuran; at 20 - 25 ℃; for 18h;

upstream raw materials:

1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol

2-Ethylhexyl alcohol

epichlorohydrin

Downstream raw materials:

1-O-(2-ethylhexyl)glycerin

5-(((2-ethylhexyl)oxy)methyl)-3-phenyloxazolidin-2-one

N-[2-Hydroxy-3-(2-ethyl)hexanoxypropyl]-1,1-dimethyl-2-(4-methoxyphenyl)ethylamine

C₃₃H₃₈N₂O₄

Refernces

• 1、 -. "The method for producing the epoxy compound". Paragraph 0037. . Retrieved 2017/06/29.
• 2、 -. "ORGANIC CATAYST WITH ENHANCED SOLUBILITY". Page 17-18. . Retrieved 2008/06/13.