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(Z)-docos-13-enyl (Z)-docos-13-enoate is a chemical compound that consists of two long-chain fatty acid molecules, specifically docos-13-enyl and docos-13-enoate. It belongs to the ester family, formed by the reaction of an alcohol with an acid. (Z)-docos-13-enyl (Z)-docos-13-enoate is commonly found in natural sources such as plant oils and animal fats.

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  • 27640-89-7 Structure
  • Basic information

    1. Product Name: (Z)-docos-13-enyl (Z)-docos-13-enoate
    2. Synonyms: (Z)-docos-13-enyl (Z)-docos-13-enoate;ERUCYL ERUCATE;(Z)-Docos-13-enyl-(Z)-docos-13-enoat;(Z)-13-Docosenoic acid (Z)-13-docosenyl ester;13-Docosenoic acid, (13Z)-13-docosenyl ester, (13Z)-
    3. CAS NO:27640-89-7
    4. Molecular Formula: C44H84O2
    5. Molecular Weight: 645.13656
    6. EINECS: 248-587-4
    7. Product Categories: N/A
    8. Mol File: 27640-89-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 668.1°Cat760mmHg
    3. Flash Point: 15.4°C
    4. Appearance: /
    5. Density: 0.865g/cm3
    6. Vapor Pressure: 1.03E-17mmHg at 25°C
    7. Refractive Index: 1.469
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (Z)-docos-13-enyl (Z)-docos-13-enoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: (Z)-docos-13-enyl (Z)-docos-13-enoate(27640-89-7)
    12. EPA Substance Registry System: (Z)-docos-13-enyl (Z)-docos-13-enoate(27640-89-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 27640-89-7(Hazardous Substances Data)

27640-89-7 Usage

Uses

Used in Cosmetics Industry:
(Z)-docos-13-enyl (Z)-docos-13-enoate is used as an ingredient in the cosmetics industry for its moisturizing and emollient properties, which help improve the skin's texture and appearance.
Used in Pharmaceutical Industry:
(Z)-docos-13-enyl (Z)-docos-13-enoate is used as an active component in the pharmaceutical industry due to its potential health benefits, such as anti-inflammatory and antioxidant properties, making it a subject of interest for further research and development in medicine.
Used in Food Additives Industry:
(Z)-docos-13-enyl (Z)-docos-13-enoate is used as an additive in the food industry for its ability to enhance the taste, texture, and shelf life of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 27640-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,4 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27640-89:
(7*2)+(6*7)+(5*6)+(4*4)+(3*0)+(2*8)+(1*9)=127
127 % 10 = 7
So 27640-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C44H84O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39-41-43-46-44(45)42-40-38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20H,3-16,21-43H2,1-2H3/b19-17-,20-18-

27640-89-7Downstream Products

27640-89-7Relevant articles and documents

ESTERS FOR USE AS A BASE STOCK AND IN LUBRICANT APPLICATIONS

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Page/Page column 18, (2012/08/28)

This invention relates to base ester compounds and complex ester compounds that can be used as a base stock for lubricant applications or a base stock blend component for use in a finished lubricant or for particular applications, and methods of making the same. The base ester compounds and complex esters described herein comprise dimer and/or trimer esters, and their respective branched derivatives.

Liquid-liquid biphasic synthesis of long chain wax esters using the Lewis acidic ionic liquid choline chloride·2ZnCl2

Sunitha, Sadula,Kanjilal, Sanjit,Reddy, P. Srinivasa,Prasad, Rachapudi B.N.

, p. 6962 - 6965 (2008/02/13)

The first liquid-liquid biphasic synthesis of wax esters in a Lewis acidic ionic liquid, choline chloride·2ZnCl2 by the esterification of long chain carboxylic acids with long chain alcohols is described. The reported reaction system has the advantages of both homogeneous and heterogeneous catalysis with high product yield and the ease of product as well as catalyst separation without the use of an organic solvent. The ionic liquid studied plays the dual role of solvent as well as catalyst and is recycled up to six times without any significant loss of activity.

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