| Identification | Back Directory | [Name]
CARBONICACID,DIPENTYLESTER | [CAS]
2050-94-4 | [Synonyms]
Dipentyl carbonate
CARBONICACID,DIPENTYLESTER | [Molecular Formula]
C11H22O3 | [MDL Number]
MFCD00068969 | [MOL File]
2050-94-4.mol | [Molecular Weight]
202.29 |
| Chemical Properties | Back Directory | [Boiling point ]
238-240 °C | [density ]
0.919±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Hexane (Slightly) | [form ]
Oil | [color ]
Clear Colorless | [InChI]
InChI=1S/C11H22O3/c1-3-5-7-9-13-11(12)14-10-8-6-4-2/h3-10H2,1-2H3 | [InChIKey]
HSNQKJVQUFYBBY-UHFFFAOYSA-N | [SMILES]
C(OCCCCC)(=O)OCCCCC |
| Hazard Information | Back Directory | [Uses]
Dipentyl Carbonate can be synthesized by transesterification using a basic ionic liquid 1-butyl-3-methylimidazolium hydroxide catalyst. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 47, p. 5209, 1982 DOI: 10.1021/jo00147a037 | [Synthesis]
The reaction apparatus was the same as in Example 1. 10 g of urea, 60 g of n-pentanol, 0.5 g of nickel acetate and 2 g of triphenylphosphine were added to a three-neck flask. The flask was heated in an oil bath at 170°C to maintain the system temperature at 140°C and reflux the reaction for 20 hours. The yield of dipentyl carbonate was 92.2% as determined by gas chromatography analysis using urea as the reference. | [References]
[1] Patent: CN108358786, 2018, A. Location in patent: Paragraph 0047
[2] Angewandte Chemie, 1980, vol. 92, # 9, p. 742 - 743 |
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| Company Name: |
Energy Chemical
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021-021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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