Chemistry:Pentyl propanoate
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Names | |
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Preferred IUPAC name
Pentyl propanoate | |
Other names
Pentyl propionate
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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UNII | |
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Properties | |
C8H16O2 | |
Molar mass | 144.22 g/mol |
Appearance | Sweet fruity odor of apricot pineapple [1] |
Density | 0.870 g/cm3 |
Melting point | −75 °C (−103 °F; 198 K) |
Boiling point | 168 °C (334 °F; 441 K) |
Related compounds | |
Related Esters
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Propyl propanoate Butyl propanoate Hexyl propanoate Pentyl acetate Pentyl butanoate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Pentyl propanoate (also known as amyl propionate) is an organic ester formed by the condensation of pentan-1-ol and propanoic acid.[2] It is a colorless liquid with an apple-like odor, that floats on water.[3]
References
- ↑ Reference Book on Fragrance Ingredients.pdf A Reference Book on Fragrance Ingredients[yes|permanent dead link|dead link}}]
- ↑ "Amyl Propionate". Chemland21. http://www.chemicalland21.com/specialtychem/nd/AMYL%20PROPIONATE.htm. Retrieved 15 December 2012.
- ↑ "N-Pentyl Propionate". CAMEO Chemicals. NOAA. http://cameochemicals.noaa.gov/chemical/24060. Retrieved 15 December 2012.
External links
Original source: https://en.wikipedia.org/wiki/Pentyl propanoate.
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