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TRANS-12-OCTADECENOIC ACID (C18:1,*(TRANS-12)) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13126-38-0

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13126-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13126-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13126-38:
(7*1)+(6*3)+(5*1)+(4*2)+(3*6)+(2*3)+(1*8)=70
70 % 10 = 0
So 13126-38-0 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)/b7-6+

13126-38-0SDS

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 (12E)-12-Octadecenoic 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:13126-38-0 SDS

13126-38-0Relevant 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.

Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl grignard reagents: A practical and versatile method for preparing fatty acids

Iwasaki, Takanori,Higashikawa, Kiyokazu,Reddy, Vutukuri P.,Ho, Willbe W. S.,Fujimoto, Yukari,Fukase, Koichi,Terao, Jun,Kuniyasu, Hitoshi,Kambe, Nobuaki

, p. 2956 - 2960 (2013/03/28)

The knights who say Ni: A practical and convenient synthetic route to fatty acids involves the Ni-catalyzed alkyl-alkyl cross-coupling of bromoalkanoic acids and alkyl Grignard reagents in the presence of 1,3-butadiene as an additive (see scheme). Copyright

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