3385-66-8

Basic information

• Product Name: [(octyloxy)methyl]oxirane
• Synonyms: [(octyloxy)methyl]oxirane;2,3-Epoxy-1-octyloxypropane;2-(octoxymethyl)oxirane
• CAS NO: 3385-66-8
• Molecular Formula: C₁₁H₂₂O₂
• Molecular Weight: 186.29118
• EINECS: 222-199-5
• Mol File: 3385-66-8.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 243.3°Cat760mmHg
• Flash Point: 104.5°C
• Appearance: /
• Density: 0.914g/cm³
• Vapor Pressure: 0.0504mmHg at 25°C
• Refractive Index: 1.445
• CAS DataBase Reference: [(octyloxy)methyl]oxirane(CAS DataBase Reference)
• NIST Chemistry Reference: [(octyloxy)methyl]oxirane(3385-66-8)
• EPA Substance Registry System: [(octyloxy)methyl]oxirane(3385-66-8)

Safety Data

• Hazardous Substances Data: 3385-66-8(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Synthetic Communications, 24, p. 3021, 1994 DOI: 10.1080/00397919408011315

InChI:InChI=1/C11H22O2/c1-2-3-4-5-6-7-8-12-9-11-10-13-11/h11H,2-10H2,1H3

Upstream product

• 126911-83-9 1-chloro-3-octyloxy-propan-2-ol 
• 111-87-5 octanol 
• 106-89-8 epichlorohydrin 
• 3132-64-7 1,2-Epoxy-3-bromopropane 
• 3295-97-4 allyl octyl ether 
• 555-31-7 aluminum isopropoxide 
• 98-67-9 p-hydoroxybenzenesulfonic acid 

Downstream Products

• 66354-56-1 1-(bis(2-hydroxyethyl)amino)-3-(octyloxy)propan-2-ol 
• 10438-94-5 3-octyloxy-1,2-propanediol 
• 134450-05-8 1-(2-Hydroxy-3-octyloxy-propoxy)-3-octyloxy-propan-2-ol 
• 198225-64-8 N-(2-Hydroxy-3-octanoxypropyl)-1,1-dimethyl-2-(4-methoxyphenyl)ethylamine 
• 1452089-79-0 C₁₁H₂₃O₆S^(1-)*Na⁽¹⁺⁾ 

Relevant articles and documents

Chemoselective Epoxidation of Allyloxybenzene by Hydrogen Peroxide Over MFI-Type Titanosilicate

The chemoselective synthesis of 2-(phenoxymethyl)oxirane from allyloxybenzene is achieved with over 90 % yield in a sustainable reaction system using titanium-substituted silicalite-1 (TS-1) as a catalyst, hydrogen peroxide (H2O2) as an oxidant, and a mixture of MeOH/MeCN as a solvent at 40 °C. No acid-catalyzed side reactions prompted by the Lewis acidity of the Ti active site in TS-1 are observed. The TS-1 catalyst can also promote the formation of oxiranes from various p-substituted allyloxybenzenes in good yields. The reaction mechanism is investigated through the reaction with other allyloxy compounds. The results, which are supported by DFT calculations, indicate that an active species of Ti peroxides formed from the reaction of TS-1 with H2O2 selectively oxidizes the allyloxybenzene to 2-(phenoxymethyl)oxirane.

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Phosphate surfactants containing ether and hydroxyl groups were prepared by a simple reaction between the corresponding epoxide and the diethyl phosphate. The relationships between the structure and colloidal properties were evaluated in terms of the critical micelle concentration (CMC), γCMC, foaming ability, and water absorbing and holding abilities. Based on these results, it was concluded that the ether and hydroxy groups synergistically worked together to decrease the CMC and increase the foaming ability. The degree of neutralization remarkably affected the colloidal properties. The highly neutralized states showed a more positive effect on water holding power but an opposite effect on the foaming ability. Copyright

LIPID COMPOUNDS FOR SUPRESSION OF TUMORIGENESIS

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