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Furfuryl acetate

Base Information Edit
  • Chemical Name:Furfuryl acetate
  • CAS No.:623-17-6
  • Molecular Formula:C7H8O3
  • Molecular Weight:140.139
  • Hs Code.:2915.39
  • European Community (EC) Number:210-775-9
  • NSC Number:5585
  • UNII:3CJC9ALG3X
  • DSSTox Substance ID:DTXSID7025346
  • Nikkaji Number:J1.222J
  • Wikidata:Q11644408
  • Metabolomics Workbench ID:46446
  • ChEMBL ID:CHEMBL1522321
  • Mol file:623-17-6.mol
Furfuryl acetate

Synonyms:2-Furanmethanol acetate;2-Furylcarbinyl acetate;Furfuryl alcohol, acetate;5-17-03-00344 (Beilstein Handbook Reference);Acetic acid furfurylester;2-Acetoxymethylfuran;2-Furfuryl acetate;2-Furanmethanol, acetate;2-Furanmethyl acetate;FEMA No. 2490;Acetic acid furfuryl ester;2-furylmethyl acetate;

Suppliers and Price of Furfuryl acetate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Furfuryl acetate
  • 500mg
  • $ 40.00
  • TCI Chemical
  • Furfuryl Acetate >97.0%(GC)
  • 25mL
  • $ 37.00
  • TCI Chemical
  • Furfuryl Acetate >97.0%(GC)
  • 100mL
  • $ 145.00
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 10 kg
  • $ 863.00
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 10kg-k
  • $ 836.00
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 5 kg
  • $ 495.00
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 5kg-k
  • $ 480.00
  • Sigma-Aldrich
  • Furfuryl acetate analytical reference material
  • 1ml
  • $ 82.40
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 1 kg
  • $ 114.00
  • Sigma-Aldrich
  • Furfuryl acetate ≥98%, FG
  • 1kg-k
  • $ 114.00
Total 92 raw suppliers
Chemical Property of Furfuryl acetate Edit
Chemical Property:
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:1.06mmHg at 25°C 
  • Refractive Index:1.460 - 1.464 
  • Boiling Point:177 °C at 760 mmHg 
  • Flash Point:65.6 °C 
  • PSA:39.44000 
  • Density:1.12 g/cm3 
  • LogP:1.34270 
  • Storage Temp.:2-8°C 
  • Water Solubility.:0.5-1.0 g/100 mL at 23 ºC 
  • XLogP3:0.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:140.047344113
  • Heavy Atom Count:10
  • Complexity:122
Purity/Quality:

99% *data from raw suppliers

Furfuryl acetate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 24/25-37/39-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Esters, Other
  • Canonical SMILES:CC(=O)OCC1=CC=CO1
  • Description Furfuryl acetate is the ester formed by the esterification between furfuryl alcohol and acetate. It can be used as a food spices and flavoring ingredient. It can also be used as the intermediate of dye, resin and spices. It is found in alcoholic beverage. Furfuryl acetate is present in wheat bread, crisp bread, roasted onion, pork liver, beer, rum, cocoa and coffee.
  • Uses Furfuryl acetate is a flavoring ingredient. It was used in the synthesis of 5-acetoxymethyl-2-vinylfuran and 5-hydroxymethyl-2-vinylfuran via Vilsmeier-Haack and Wittig reactions.
Technology Process of Furfuryl acetate

There total 33 articles about Furfuryl acetate 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:
Guidance literature:
With tin(IV) tetraphenylporphyrin perchlorate; at 20 ℃; for 0.0833333h;
DOI:10.1081/SCC-120003629
Guidance literature:
With 1,3-dichlorotetrabutyldistannoxane; at 30 ℃; for 24h;
DOI:10.1016/S0040-4020(99)00072-1
Guidance literature:
at 20 ℃; for 0.216667h;
DOI:10.1080/10426500802336606
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