Functionalization at the Double-Bond Region of Jojoba Oil. 3. Hydroxylic Derivatives

Arnon Shani

doi:10.1021/i300009a027

Functionalization at the Double-Bond Region of Jojoba Oil. 3. Hydroxylic Derivatives

Arnon Shani

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

The apolar and hydrophobic nature of jojoba oil has been altered to slightly more hydrophylic by epoxidation, hydrolysis, and alcoholysis at the double bonds, thus forming hydroxylic derivatives. Some inorganic esters, derived from SOCl₂, POCl₃, and (C₂H₅O)₃P, have been prepared. Exposure of the oil to direct sunlight in the presence of a photosensitizer (via ¹O₂) yielded some oxidized products.

Original language	English
Pages (from-to)	121-123
Number of pages	3
Journal	Industrial & Engineering Chemistry Product Research and Development
Volume	22
Issue number	1
DOIs	https://doi.org/10.1021/i300009a027
State	Published - 1 Mar 1983

ASJC Scopus subject areas

General Chemistry
General Chemical Engineering
General Engineering
Industrial and Manufacturing Engineering

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abstract = "The apolar and hydrophobic nature of jojoba oil has been altered to slightly more hydrophylic by epoxidation, hydrolysis, and alcoholysis at the double bonds, thus forming hydroxylic derivatives. Some inorganic esters, derived from SOCl2, POCl3, and (C2H5O)3P, have been prepared. Exposure of the oil to direct sunlight in the presence of a photosensitizer (via 1O2) yielded some oxidized products.",

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AB - The apolar and hydrophobic nature of jojoba oil has been altered to slightly more hydrophylic by epoxidation, hydrolysis, and alcoholysis at the double bonds, thus forming hydroxylic derivatives. Some inorganic esters, derived from SOCl2, POCl3, and (C2H5O)3P, have been prepared. Exposure of the oil to direct sunlight in the presence of a photosensitizer (via 1O2) yielded some oxidized products.

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Functionalization at the Double-Bond Region of Jojoba Oil. 3. Hydroxylic Derivatives

Abstract

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