Glycidyl Oleate - ≥95% , CAS No.5431-33-4

CAS: 5431-33-4 Cat. No.: G343615 Molecular Weight: 338.52 EC Number: 226-588-0

GRADE & PURITY ≥95%

Synonyms

Oleic acid-glycidyl ester 100 microg/mL in Acetonitrile | Q27155965 | 9-Octadecenoic acid (9Z)-, oxiranylmethyl ester | G0I0157S14 | Oxiranyl methyl ester 9-octadecenoic acid | Solsolona [inj.] | Oleic acid,3-epoxypropyl ester | Oxiran-2-ylmethyl oleate |

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview

Glycidyl Oleate is used for preparation of Lysophosphatidic acid analogs as agonists of the edg2 lysophosphatidic acid receptor.

Specifications

Synonyms

Oleic acid-glycidyl ester 100 microg/mL in Acetonitrile | Q27155965 | 9-Octadecenoic acid (9Z)-, oxiranylmethyl ester | G0I0157S14 | Oxiranyl methyl ester 9-octadecenoic acid | Solsolona [inj.] | Oleic acid, 3-epoxypropyl ester | Oxiran-2-ylmethyl oleate |

Specifications & Purity

≥95%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Canonical Smiles: CCCCCCCCC=CCCCCCCCC(=O)OCC1CO1
• IUPAC Name: oxiran-2-ylmethyl (Z)-octadec-9-enoate
• InChIKey: VWYIWOYBERNXLX-KTKRTIGZSA-N
• INCHI: 1S/C21H38O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(22)24-19-20-18-23-20/h9-10,20H,2-8,11-19H2,1H3/b10-9-
• Isomeric SMILES: CCCCCCCC/C=C\CCCCCCCC(=O)OCC1CO1
• Molecular Weight: 338.52
• Reaxy-Rn: 39337455
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=39337455&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Glycidol esters
• Alternative Parents: Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Glycidol ester - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as glycidol esters. These are compounds containing an ester derivative of glycidol (2,3-Epoxy-1-propanol).
• External Descriptors: carboxylic ester - epoxide

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Faah Anandamide amidohydrolase (3907 Activities)

Discover Target: Faah

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Molecular Weight: 338.500 g/mol
• XLogP3: 7.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 18
• Exact Mass: 338.282 Da
• Monoisotopic Mass: 338.282 Da
• Topological Polar Surface Area: 38.800 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 325.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1