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12-Octadecenoic acid, also known as oleic acid, is a monounsaturated fatty acid with the chemical formula C18H34O2. It is a common component of various plant and animal fats and oils, and is particularly abundant in olive oil, which is why it is often referred to as the "olive oil fatty acid." This 18-carbon chain fatty acid has a double bond at the 9th carbon from the end, which gives it its monounsaturated status. Oleic acid plays a crucial role in human health, as it is known to help lower bad cholesterol (LDL) levels and increase good cholesterol (HDL) levels, thus contributing to cardiovascular health. It is also used in the food industry as an emulsifier and in the production of soaps and cosmetics due to its emollient properties.

7378-88-3

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7378-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7378-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7378-88:
(6*7)+(5*3)+(4*7)+(3*8)+(2*8)+(1*8)=133
133 % 10 = 3
So 7378-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7H,2-5,8-17H2,1H3,(H,19,20)

7378-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-octadec-12-enoic acid

1.2 Other means of identification

Product number -
Other names octadecenic acid

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:7378-88-3 SDS

7378-88-3Relevant academic research and scientific papers

NOVEL GLYCINE TRANSPORT INHIBITORS FOR THE TREATMENT OF PAIN

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Page/Page column 54; 55, (2018/08/12)

The present invention relates to novel glycine transport inhibitor compounds and their use for treating pain.

Synthesis and Characterization of Novel Acyl-Glycine Inhibitors of GlyT2

Mostyn, Shannon N.,Carland, Jane E.,Shimmon, Susan,Ryan, Renae M.,Rawling, Tristan,Vandenberg, Robert J.

, p. 1949 - 1959 (2017/09/26)

It has been demonstrated previously that the endogenous compound N-arachidonyl-glycine inhibits the glycine transporter GlyT2, stimulates glycinergic neurotransmission, and provides analgesia in animal models of neuropathic and inflammatory pain. However, it is a relatively weak inhibitor with an IC50 of 9 μM and is subject to oxidation via cyclooxygenase, limiting its therapeutic value. In this paper we describe the synthesis and testing of a novel series of monounsaturated C18 and C16 acyl-glycine molecules as inhibitors of the glycine transporter GlyT2. We demonstrate that they are up to 28 fold more potent that N-arachidonyl-glycine with no activity at the closely related GlyT1 transporter at concentrations up to 30 μM. This novel class of compounds show considerable promise as a first generation of GlyT2 transport inhibitors.

New biobased tetrabutylphosphonium ionic liquids: Synthesis, characterization and use as a solvent or co-solvent for mild and greener Pd-catalyzed hydrogenation processes

Hayouni, Safa,Robert, Anthony,Ferlin, Nadège,Amri, Hassen,Bouquillon, Sandrine

, p. 113583 - 113595 (2016/12/16)

Phosphonium-based Ionic Liquids (PhosILs) with natural organic derived anions (l-lactate, l-tartrate, malonate, succinate, l-malate, pyruvate, d-glucuronate, d-galacturonate, ferulate, p-coumarate) were easily prepared by acid-base method from tetrabutylphosphonium hydroxide and an excess of the corresponding acid with good yields. Their characterization was realized through classical NMR, IR and elemental analysis techniques; their viscosity and ATG parameters were also determined. These ionic liquids showed good performance and recyclability in the selective Pd-catalyzed hydrogenation of alkenes, polyenes like linoleic acid and enantioselective hydrogenation of unsaturated ketones such as isophorone at room temperature under atmospheric H2 pressure. Furthermore, NMR studies leading to computational calculations were performed to establish easily the composition of the resulting mixture obtained through the hydrogenation of linoleic acid.

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