Glycidyl hexanoate

Base Information

• Chemical Name: Glycidyl hexanoate
• CAS No.: 17526-74-8
• Molecular Formula: C9H16O3
• Molecular Weight: 172.25
• Hs Code.: 2915900090
• DSSTox Substance ID: DTXSID60938638
• Nikkaji Number: J49.412G
• Mol file: 17526-74-8.mol

Synonyms:Glycidyl hexanoate;oxiran-2-ylmethyl hexanoate;17526-74-8;Glycidyl ester of hexanoic acid;Hexanoic acid, oxiranylmethyl ester;BRN 1365955;(Oxiran-2-yl)methyl hexanoate;HEXANOIC ACID, 2,3-EPOXYPROPYL ESTER;Hexanoic acid oxiranylmethyl ester;starbld0003436;caproic acid glycidyl ester;SCHEMBL2318734;DTXSID60938638;LS-75272

Chemical Property of Glycidyl hexanoate

Chemical Property:

• Vapor Pressure: 0.0675mmHg at 25°C
• Refractive Index: 1.4249 (estimate)
• Boiling Point: 230°Cat760mmHg
• Flash Point: 97.3°C
• PSA: 38.83000
• Density: 1.025g/cm³
• LogP: 1.50870
• Storage Temp.: Refrigerator
• Solubility.: Chloroform (Sparingly), Ethyl Acetate (Slightly)
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 172.109944368
• Heavy Atom Count: 12
• Complexity: 145

Purity/Quality:

99% ^*data from raw suppliers

Glycidyl Hexanoate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCCC(=O)OCC1CO1
• Uses: Glycidyl Hexanoate is used as a plasticizer for polyvinyl butyral resin composition. Glycidyl Hexanoate is also an antioxidant-rust inhibitor used in the preparation of lubricating oils for refrigerators.

Technology Process of Glycidyl hexanoate

There total 2 articles about Glycidyl hexanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 76.0%

allyl hexanoate (123-68-2) → 2-oxiranylmethyl hexanoate (17526-74-8)

Guidance literature:

With 2-Picolinic acid; manganese(II) triflate; In acetonitrile; at 0 ℃; for 0.0833333h; Reagent/catalyst;

DOI:10.1021/acs.orglett.6b00518

Reference yield:

→ 2-oxiranylmethyl hexanoate (17526-74-8)

Guidance literature:

Propanol (VIII), Caproylchlorid;

DOI:10.1016/0009-3084(76)90003-7

upstream raw materials:

allyl hexanoate

Refernces