Anisylacetone
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Anisylacetone | ||||||||||||||||||
other names |
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Molecular formula | C 11 H 14 O 2 | ||||||||||||||||||
Brief description |
colorless liquid with a characteristic odor |
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External identifiers / databases | |||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 178.23 g mol −1 | ||||||||||||||||||
Physical state |
liquid |
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density |
1.046 g cm −3 (25 ° C) |
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Melting point |
8 ° C |
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boiling point |
152–153 ° C (20 hPa) |
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solubility |
partially soluble in water |
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Refractive index |
1.519 (20 ° C) |
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safety instructions | |||||||||||||||||||
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Toxicological data |
> 5000 mg kg −1 ( LD 50 , rabbit , transdermal ) |
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
Anisylacetone is a chemical compound from the group of ketones . It is used as an artificial aniseed flavor . According to the Flavor Ordinance , it may be added to certain foods with a maximum amount of 25 mg / kg.
Anisylacetone is also one of the sexual attractants of the melon fly ( Dacus cucurbitae ).
Individual evidence
- ↑ Entry on METHOXYPHENYLBUTANONE in the CosIng database of the EU Commission, accessed on July 8, 2020.
- ↑ a b c d Data sheet 4- (p-METHOXYPHENYL) -BUTANONE-2 (PDF) from Carl Roth , accessed on October 23, 2013.
- ↑ a b c d Data sheet 4- (4-Methoxyphenyl) -2-butanone, 98% from Sigma-Aldrich , accessed on October 23, 2013 ( PDF ).
- ↑ Werner Baltes, Reinhard Matissek: Food chemistry . Springer, 2011, ISBN 978-3-642-16538-2 , pp. 387 ( limited preview in Google Book search).
- ↑ AromV: Annex 5 (to Section 3) additives
- ↑ Wolfdietrich Eichler (Ed.): Handbuch der Insektizidkunde. Berlin 1965, p. 81.