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2566-97-4

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2566-97-4 Usage

Description

LINOLELAIDIC ACID METHYL ESTER, also known as Methyl trans,trans-9,12-Octadecadienoate, is a synthetic intermediate derived from linoleic acid. It is characterized by its chemical structure, which includes a methyl ester group and two trans double bonds at the 9 and 12 positions. LINOLELAIDIC ACID METHYL ESTER is known for its potential applications in various industries due to its unique properties.

Uses

Used in Chemical Synthesis:
LINOLELAIDIC ACID METHYL ESTER is used as a synthetic intermediate for the preparation of various compounds, such as (±)-trans-9,10-Epoxy-12(E)-octadecenoic acid methyl ester and (±)-trans-12,13-Epoxy-12(E)-octadecenoic acid methyl ester. These compounds are valuable in the chemical industry for their diverse applications.
Used in Biodiesel Industry:
LINOLELAIDIC ACID METHYL ESTER is used as a biodiesel component to enhance the lubricity of the fuel. Its presence in biodiesel formulations helps improve the fuel's performance and reduce wear and tear on engine components, leading to better engine efficiency and longevity.

Check Digit Verification of cas no

The CAS Registry Mumber 2566-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2566-97:
(6*2)+(5*5)+(4*6)+(3*6)+(2*9)+(1*7)=104
104 % 10 = 4
So 2566-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3/b8-7+,11-10+

2566-97-4 Well-known Company Product Price

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  • Supelco

  • (46951-U)  trans-9,12-Octadecadienoicacidmethylester  certified reference material, 10 mg/mL in heptane

  • 2566-97-4

  • 46951-U

  • 453.96CNY

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2566-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Linolelaidic acid-methyl ester

1.2 Other means of identification

Product number -
Other names Linolelaidic Acid Methyl Ester

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:2566-97-4 SDS

2566-97-4Relevant articles and documents

Branched alkyl sulfonate anionic surfactant and preparation process thereof

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Paragraph 0090-0091, (2021/02/10)

The invention discloses a branched alkyl sulfonate anionic surfactant and a preparation process thereof, and belongs to the field of fine chemical surfactants. The method comprises the steps of (1) conducting a esterification carboxyl-terminated reaction, specifically, catalyzing oleic acid or linoleic acid and fatty alcohol to be subjected to esterification reaction by adopting organic acid as acatalyst to prepare an alkyl oleate or alkyl linoleate compound; and (2) conducting a double bond addition sulfonation reaction, specifically, in the presence of the catalyst, carrying out sulfonationreaction with the alkyl oleate compound or the alkyl linoleate compound obtained in the step (1) by taking low-carbon alcohol and deionized water as solvents and sodium hydrogen sulfite as a sulfonation reagent to prepare the branched alkyl sulfonate anionic surfactant. The synthesized branched alkyl sulfonate anionic surfactant product can effectively reduce the surface tension of an aqueous solution, and is good in solubility, large in initial foaming amount, high in defoaming speed and excellent in surfactant performance. The method has the advantages of simple process operation, few sidereactions, energy saving and environmental protection.

Metathesis of renewable polyene feedstocks – Indirect evidences of the formation of catalytically active ruthenium allylidene species

Kovács, Ervin,Sághy, Péter,Turczel, Gábor,Tóth, Imre,Lendvay, Gy?rgy,Domján, Attila,Anastas, Paul T.,Tuba, Róbert

supporting information, p. 213 - 217 (2017/09/12)

Cross-metathesis (CM) of conjugated polyenes, such as 1,6-diphenyl-1,3,5-hexatriene (1) and α-eleostearic acid methyl ester (2) with several olefins, including 1-hexene, dimethyl maleate and cis-stilbene as model compounds has been carried out using (1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)-dichloro(o-isopropoxyphenylmethylene)ruthenium (Hoveyda-Grubbs 2nd generation, HG2) catalyst. The feasibility of these reactions is demonstrated by the observed high conversions and reasonable yields. Thus, regardless of the relatively low electron density, =CH–CH= conjugated units of molecules, including compound 2 as a sustainable, non-foodstuff source, can be utilized as building blocks for the synthesis of various value-added chemicals via olefin metathesis. DFT-studies and the product spectrum of the self-metathesis of 1,6-diphenyl-1,3,5-hexatriene suggest that a Ru η1-allylidene complex is the active species in the reaction.

ADDUCTS OF LEVULINIC DERIVATIVES WITH EPOXIDIZED FATTY ACID ESTERS AND USES THEREOF

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Page/Page column 19-20, (2010/11/27)

The present disclosure relates to methods of preparation of compounds resulting from the reaction of levulinic esters and epoxidized unsaturated fatty acid esters. The compounds are useful as renewable biomass-based plasticizers for a variety of polymers. Mono-, di- and tri-ketal adducts formed in a reaction between alkyl esters of levulinate and epoxidized unsaturated fatty acid esters derived from vegetable oils are also disclosed.

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