1120-34-9

Usage

Uses

Used in Lubricant Industry:
ERUCIC ACID METHYL ESTER is used as a lubricant due to its high melting point and resistance to oxidation, providing efficient performance in various mechanical applications.
Used in Chemical Production:
ERUCIC ACID METHYL ESTER is used as a raw material in the production of surfactants, plasticizers, and other chemicals, contributing to the manufacturing of a wide range of products.
Used in Biofuel Industry:
ERUCIC ACID METHYL ESTER is used as a potential source of biofuel because of its high energy content and desirable properties for use in diesel engines, offering an alternative to fossil fuels.
However, it is important to note that the use of ERUCIC ACID METHYL ESTER is limited due to potential toxicity concerns. Further research is needed to fully understand its environmental and health impacts before widespread adoption in various industries.

InChI:InChI=1/C23H44O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h10-11H,3-9,12-22H2,1-2H3/b11-10-

Upstream product

• 67-56-1 methanol 
• 112-86-7 cis-13-docosenoic acid 
• 112-80-1 cis-Octadecenoic acid 
• 627-91-8 adipic acid monomethyl ester 
• 13044-38-7 (Z)-1-bromo-9-octadecene 
• 14273-85-9 methyl 4-iodobutanoate 
• 1608-77-1 methyl 12-formyldodecanoate 
• 60902-45-6 nonyltriphenylphosphonium bromide 
• 1679-53-4 10-hydroxydecanoic acid 
• 143-28-2 oleoyl alcohol 
• 112-62-9 Methyl oleate 
• 693-58-3 1-Bromononane 
• 50530-12-6 10-bromodecanoic acid 
• 71736-18-0 10-iododecanoic acid 

Downstream Products

• 124-19-6 nonan-1-al 
• 111-66-0 oct-1-ene 
• 29972-79-0 methyl 11-dodecenoate 
• 4397-81-3 1,13-docosanediol 
• 4452-45-3 docosane-1,14-diol 
• 5634-26-4 (13E)-docos-13-en-1-ol 
• 661-19-8 1-docosanol 
• 2388-99-0 methyl 13-oxodocosanoate 
• 54527-15-0 methyl 14-oxodocosanoate 
• 1610968-10-9 benzyl N-[(12Z)-henicos-12-en-1-yl]carbamate 
• 1608-77-1 methyl 12-formyldodecanoate 
• 13058-55-4 cis-13-octadecenoic acid, methyl ester 
• 58594-45-9 (Z)-13-octadecenal 
• 69820-27-5 (Z)-octadec-13-en-1-ol 

Relevant academic research and scientific papers

Fatty acid based biocarbonates: Al-mediated stereoselective preparation of mono-, di- and tricarbonates under mild and solvent-less conditions

A catalytic method for the preparation of a series of fatty acid derived biocarbonates has been developed using a binary Al-complex/PPNCl catalyst. This catalyst system allows conversion of fatty acid derived epoxides under comparatively mild reaction conditions (70-85 °C, 10 bar) while maintaining high levels of diastereospecificity with cis/trans ratios of up to 97:3 in the products. The comparative catalysis data obtained for the reactions catalysed only by the nucleophilic halide based components show that the presence of the Al-complex is crucial for the retention of the original stereochemistry.

Stereoselective Synthesis of Z Fluoroalkenes through Copper-Catalyzed Hydrodefluorination of gem-Difluoroalkenes with Water

A copper catalytic system was established for the stereoselective hydrodefluorination of gem-difluoroalkenes through C?F activation to synthesize various Z fluoroalkenes. H2O is used as the hydrogen source for the fluorine acceptor moiety. This mild catalytic system shows good-functional group compatibility, accepting a range of carbonyls as precursors to the gem-difluoroalkenes, including aliphatic, aromatic, and α,β-unsaturated aldehydes and even ketones. It serves as a powerful synthetic method for the late-stage modification of complex compounds.

Oxygenation of monoenoic fatty acids by CYP175A1, an orphan cytochrome P450 from thermus thermophilus HB27

The catalytic activity of CYP175A1 toward monooxygenation of saturated and monounsaturated fatty acids of various chain lengths (C16-C24) has been investigated to assess the enzymatic properties of this orphan thermostable cytochrome P450 enzyme. The resu

Method for selective esterification of free fatty acids in triglycerides

A method for the selective esterification of free fatty acids, alone or in triglycerides, with C1-C8 aliphatic alcohols or diols. The method uses a selective heterogeneous esterification catalyst. The catalyst is contacted with a reaction mixture containing a triglyceride having at least 0.5% free fatty acids, or a reaction mixture containing only free fatty acids, and a C1-C8 aliphatic alcohol or diol under conditions suitable for esterification.

SINGLE-STAGE ESTERIFICATION OF OILS AND FATS

A process for producing alkyl esters useful as biofuels and/or lubricants. An alkyl ester product produced by the process. The process comprises a single- stage reaction for esterifying a de-watered glyceride-containing feedstock with an anhydrous short chain alcohol in the presence of a basic esterification catalyst to produce a reaction product comprising alkyl esters and a reaction by-product comprising glycerol-containing substances and the catalyst-containing alcohol. The single-stage esterification reaction is conducted within a temperature and negative-pressure controllable vessel. The alkyl ester product is separated from the reaction by-product and may be further de-watered and/or purified. The catalyst-containing alcohol may be separated from the reaction by-product, de- watered and reused. The glycerol-containing substances may be separated from the reaction by-product and further purified. Useful glyceride-containing feedstocks include those prepared from plant or animal or fish materials, particularly those produced from seeds of mustard, canola, soybean, corn, cotton, flax and palm.

Synthesis of Very Long Fatty Acid Methyl Esters

Phosphoranes, produced by treating alkyltriphenylphosphonium bromides with lithium hexamethyldisilazide, reacted with ω-oxo esters to give modest yields of the corresponding methyl cis-alkenoates.By an alternative method, treatment of ω-iodo esters with the complexes formed from reactions of alkylcopper(I) and Grignard reagents gave methyl alkanoates, cis-alkenoates, and methylene-interrupted cis,cis-alka-dienoates and cis,cis,cis-trienoates.The stereochemical integrity of the esters was determined by 13C NMR spectroscopy.