56401-30-0

Usage

Uses

Used in Chemical Synthesis:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as an intermediate in the synthesis of various chemical compounds. Its unique structure allows it to be a valuable building block for the creation of more complex molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as a precursor for the development of new drugs. Its chemical structure can be modified to create compounds with potential therapeutic applications, such as anti-inflammatory, analgesic, or anti-cancer agents.
Used in Food Industry:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is used as an intermediate in the synthesis of Ethyl 11,14-Diepoxyeicosanoate (E916000), which is a standard used to determine epoxidized soybean oil in foods. This application helps ensure the quality and safety of food products containing epoxidized soybean oil.
Used in Cosmetics Industry:
In the cosmetics industry, 9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)can be used as a component in the formulation of various cosmetic products. Its unique properties may contribute to the development of products with improved skin hydration, anti-aging, or anti-inflammatory effects.
Used in Research and Development:
9,12-Octadecadien-1-ol, 4-methylbenzenesulfonate, (9Z,12Z)is also used in research and development for the study of its chemical properties and potential applications. This can lead to the discovery of new compounds and technologies that can benefit various industries.

Upstream product

• 506-43-4 Linoleyl alcohol 
• 98-59-9 p-toluenesulfonyl chloride 
• 96895-24-8 1-O-linolenoyl-2-O-linoleoyl-3-O-oleoyl glycerol 
• 544-35-4 ethyl (9Z,12Z)-9,12-octadecadienoate 
• 112-63-0 Methyl linoleate 

Downstream Products

• 2091-39-6 (Z,Z)-11,14-eicosadienoic acid 
• 107356-52-5 2-Methyl-3-linoleyloxy-7-ethoxycarbonylmethylthio-pyrazolo[4,3-d]pyrimidine 
• 871258-12-7 DlinDMA 
• 74685-29-3 (Z)-9-henicosene 
• 66-25-1 hexanal 
• 112-54-9 Dodecanal 
• 112-95-8 icosane 

Relevant academic research and scientific papers

Cationic lipid compound and its preparation method

The invention discloses cationic lipid compounds and a preparation method thereof. The molecular structure general formula of the compounds is shown as the description, wherein R is alkyl groups of C6 to C24, alkylenes of C6 to C24 and acyl groups of C6 t

Tuning the Thermo-Sensitivity of Micellar Systems through a Blending Approach

This paper reports an original and easy route toward thermosensitive micelles based on a lipidic core and with adjustable cloud point temperatures (TCP) through a simple blending approach between two copolymers of different TCP. The cationic ring-opening polymerization (CROP) of various 2-alkyl-2-oxazoline monomers was first investigated from both mesylated and tosylated lipoinitiators and different lipid-b-poly(2-methyl-2-oxazoline), lipid-b-poly(2-ethyl-2-oxazoline), lipid-b-poly(2-isopropyl-2-oxazoline) and lipid-b-poly((2-ethyl-2-oxazoline)-co-(2-isopropyl-2-oxazoline)) copolymers were synthesized. Blending of lipid-b-p(EtOx) and lipid-b-p(iPrOx) copolymers in various proportions were then prepared and their TCP investigated through UV-visible spectroscopy. Very interesting results were obtained as the blends exhibit a single TCP ranging from 35 to 45 °C. Furthermore, the blends TCP correspond to those of the statistical lipid-b-p((EtOx)-co-(iPrOx)) for the same p(EtOx)/p(iPrOx) content up to 52 wt % of p(EtOx). The blending approach is then an attractive strategy to control the TCP of micellar systems through a simple and easy formulation approach rather than fastidious syntheses.

Synthesis of phosphatidylcholine having a very long chain polyunsaturated fatty acid

A phosphatidylcholine 9 bearing icosadienoyl and docosahexaenoyl groups at the 1-and 2-positions respectively was synthesized. The synthetic route involves carbon chain elongation of linoleic acid via malonic ester synthesis, preparation of lyso-phosphatidylcholine via lipase-catalyzed mono-acylation of 2-O-methoxyethoxymethylglycerol and phosphodiester synthesis, and finally DCC-mediated esterification.

Polyene Pheromone Components from an Arctiid Moth (Utetheisa ornatrix): Characterization and Synthesis

In our earlier study of the female sex attractant from an arctiid moth (Utetheisa ornatrix), the occurence of an uncharacterized C-21 tetraene was noted along with (Z,Z,Z)-3,6,9-heneicosatriene, the major pheromone constituent.The sex attractant glands of females from other populations of this moth have now yielded this C-21 tetraene as a major component, accompanied by a new C-21 diene.Spectral and chemical studies of these two EAG-active compounds led to their characterization as (Z,Z,Z)-1,3,6,9-heneicosatetraene and (Z,Z)-6,9-heneicosadiene.These structures and configurations were confirmed by synthesis.