Aleuritic acid
Structural formula | |||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
General | |||||||||||||||||||
Surname | Aleuritic acid | ||||||||||||||||||
other names |
|
||||||||||||||||||
Molecular formula | C 16 H 32 O 5 | ||||||||||||||||||
Brief description |
Solid |
||||||||||||||||||
External identifiers / databases | |||||||||||||||||||
|
|||||||||||||||||||
properties | |||||||||||||||||||
Molar mass | 304.43 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
||||||||||||||||||
Melting point |
97-101 ° C |
||||||||||||||||||
safety instructions | |||||||||||||||||||
|
|||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Aleuritic acid is a hydroxy fatty acid which forms part of the natural resin shellac (up to 32%).
Its chemical name is 9,10,16-trihydroxypalmitic acid.
It is used on a large scale in the manufacture of fragrances and perfumes, for example ambrettolide (for artificial musk aroma) and civetone can be obtained from aleuritic acid. Aleuritic acid is also suitable for the synthesis of pheromones and prostaglandins.
Individual evidence
- ↑ Entry on ALEURITIC ACID in the CosIng database of the EU Commission, accessed on June 9, 2020.
- ↑ a b c d Data sheet (±) -erythro-Aleuritic acid, 95% from AlfaAesar, accessed on October 8, 2014 ( PDF )(JavaScript required) .
- ↑ Oliver Türk: Material use of renewable raw materials: Basics - Materials ... Springer-Verlag, 2014, p. 316 ( limited preview in Google Book Search).
- ↑ Entry on shellac. In: Römpp Online . Georg Thieme Verlag, accessed on October 9, 2014.