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1,6-hexanediyl dioleate is a chemical compound derived from the reaction of 1,6-hexanediol with oleic acid, resulting in the formation of a diester. It is known for its high lubricity and ability to form stable emulsions.

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  • 21224-03-3 Structure
  • Basic information

    1. Product Name: 1,6-hexanediyl dioleate
    2. Synonyms: 1,6-hexanediyl dioleate;9-Octadecenoic acid (9Z)-, 1,6-hexanediyl ester;Bis[(Z)-9-octadecenoic acid] 1,6-hexanediyl ester;Hexamethylene dioleate
    3. CAS NO:21224-03-3
    4. Molecular Formula: C42H78O4
    5. Molecular Weight: 647.06632
    6. EINECS: 244-283-0
    7. Product Categories: N/A
    8. Mol File: 21224-03-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 678.5°Cat760mmHg
    3. Flash Point: 321.4°C
    4. Appearance: /
    5. Density: 0.903g/cm3
    6. Vapor Pressure: 2.89E-18mmHg at 25°C
    7. Refractive Index: 1.471
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,6-hexanediyl dioleate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,6-hexanediyl dioleate(21224-03-3)
    12. EPA Substance Registry System: 1,6-hexanediyl dioleate(21224-03-3)
  • 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: 21224-03-3(Hazardous Substances Data)

21224-03-3 Usage

Uses

Used in Ink Production:
1,6-hexanediyl dioleate is used as a lubricant and dispersant for improving the flow and stability of ink formulations.
Used in Coating Industry:
1,6-hexanediyl dioleate is used as a lubricant and dispersant for enhancing the performance and durability of coatings.
Used in Adhesive Industry:
1,6-hexanediyl dioleate is used as a lubricant and dispersant for improving the adhesive properties and performance of various adhesives.
Used as a Biodegradable Lubricant:
1,6-hexanediyl dioleate is studied as a biodegradable and environmentally friendly alternative to traditional lubricants, with potential applications in reducing friction and wear in mechanical systems. Further research is needed to fully understand its effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 21224-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21224-03:
(7*2)+(6*1)+(5*2)+(4*2)+(3*4)+(2*0)+(1*3)=53
53 % 10 = 3
So 21224-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C42H78O4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-33-37-41(43)45-39-35-31-32-36-40-46-42(44)38-34-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20H,3-16,21-40H2,1-2H3/b19-17-,20-18-

21224-03-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[(Z)-octadec-9-enoyl]oxyhexyl-(Z)-octadec-9-enoate

1.2 Other means of identification

Product number -
Other names 1,6-Hexanediyl dioleate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21224-03-3 SDS

21224-03-3Downstream Products

21224-03-3Relevant articles and documents

Synthesis and characterization of novel diol, diacid and Di-isocyanate from oleic acid

Raghunanan, Latchmi,Yue, Jin,Narine, Suresh S.

, p. 349 - 356 (2014)

Novel linear diol 2, diacid 3, and diisocyanate 4 with functional groups located at each end of the chain have been produced from oleic acid via a diester precursor. All the compounds were fully characterized by IR, 1H NMR, 13C NMR and Mass Spectrometry. These unbranched terminally-functionalized compounds are important monomers for the manufacture of biodegradable thermoplastic polyurethanes and polyesters. The general synthetic scheme should also prove useful for the syntheses of diols, diacids and diisocyanates from any unsaturated fatty acid.

Novel Ester Compounds, Method for the Production Thereof and Use Thereof

-

Paragraph 0205-0210, (2020/05/29)

The invention relates to novel ester compounds of the general formula (I) to a process for preparation thereof and to the use thereof. These ester compounds may contain a mixture of at least two compounds of the general formula (I).

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