17363-94-9

Basic information

• Product Name: OLEYL OLEATE
• Synonyms: 9-Octadecenoicacid, 9-octadecenyl ester (9CI); 9-Octadecenyl 9-octadecenoate
• CAS NO: 17363-94-9
• Molecular Formula: C₃₆H₆₈O₂
• Molecular Weight: 532.92
• Mol File: 17363-94-9.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: OLEYL OLEATE(CAS DataBase Reference)
• NIST Chemistry Reference: OLEYL OLEATE(17363-94-9)
• EPA Substance Registry System: OLEYL OLEATE(17363-94-9)

Safety Data

• Hazardous Substances Data: 17363-94-9(Hazardous Substances Data)

Usage

Description

Oleyl oleate is an ester of oleyl alcohol and oleic acid, known for its emollient properties that help to soften and smooth the skin. It is commonly used in cosmetics and personal care products as a moisturizing and conditioning agent, enhancing the spreadability and texture of skincare formulations, as well as improving the absorption of other active ingredients.

Uses

Used in Cosmetics and Personal Care Industry:
Oleyl oleate is used as a moisturizing and conditioning agent for its ability to soften and smooth the skin, making it a popular ingredient in lotions, creams, and moisturizers.
Used in Skincare Formulations:
Oleyl oleate is used to enhance the spreadability and texture of skincare products, providing a smooth and pleasant application experience.
Used in Hair Care Products:
Oleyl oleate is used as a conditioning agent in hair care products to provide detangling benefits, leaving the hair soft and manageable.
Used to Improve Absorption of Active Ingredients:
Oleyl oleate is used to improve the absorption of other active ingredients in skincare and hair care products, enhancing their overall effectiveness.

Upstream product

• 143-28-2 oleoyl alcohol 
• 142-77-8 oleic acid butyl ester 
• 111-62-6 oleic acid ethyl ester 
• 112-80-1 cis-Octadecenoic acid 
• 112-77-6 (Z)-9-octadecenoyl chloride 
• 112-62-9 Methyl oleate 

Downstream Products

• 51579-82-9 amfenac 
• 17673-49-3 (Z)-octadecyl ester 9-octadecenoic acid 
• 3739-65-9 (+/-)-(Ξ)-erythro-9,10-epoxy-octadecanoic acid-((Ξ)-erythro-9,10-epoxy-octadecyl ester) 

Relevant articles and documents

At Long Last: Olefin Metathesis Macrocyclization at High Concentration

Macrocyclic lactones, ketones, and ethers can be obtained in the High-Concentration Ring-Closing Metathesis (HC-RCM) reaction in high yield and selectivity at concentrations 40 to 380 times higher than those typically used by organic chemists for similar macrocyclizations. The new method consists of using tailored ruthenium catalysts together with applying vacuum to distill off the macrocyclic product as it is formed by the metathetical backbiting of oligomers. Unlike classical RCM, no large quantities of organic solvents are used, but rather inexpensive nonvolatile diluents, such as natural or synthetic paraffin oils. Moreover, use of a protecting atmosphere or a glovebox is not needed, as the new catalysts are perfectly moisture and air stable. In addition, some other cyclic compounds previously reported as unobtainable by RCM in neat conditions, or in high dilutions even, can be formed with the help of the HC-RCM method.

METHOD OF CYCLIC COMPOUNDS PRODUCTION IN OLEFINE METATHESIS REACTION AND USE OF RUTHENIUM CATALYSTS IN PRODUCTION OF CYCLIC OLEFINS IN OLEFINE METATHESIS REACTION

The invention relates to a method for the preparation of cyclic compounds in the metathesis of olefins from acyclic dienes comprising terminal and/or non-terminal C=C double bonds; the invention also relates to the use of homogeneous ruthenium complexes and homogeneous ruthenium complexes deposited on a solid support as catalysts and/or pre-catalysts for the preparation of cyclic olefins in olefin metathesis reactions. Formula (I)

Method For Synthesising Esters

A method for synthesising a second ester from a first ester, the method including the following steps: a) placing a first ester and a catalyst in the presence of dihydrogen such as to obtain a first alcohol and a second alcohol; b) extracting the second alcohol from the reaction medium; c) reacting the first alcohol with the catalyst of step a) in order to obtain a second ester and dihydrogen; and d) recirculating the dihydrogen obtained in step c) by injecting same into step a).