2-heptylcyclopropyl-1-carboxylic acid
View Patent ↗Optionally isolated and/or purified enatiomers of 2-heptylcyclopropyl-1-carboxylic acid and mixtures of two, three or all enantiomers of 2-heptylcyclopropyl-1-carboxylic acid are disclosed as perfumes and/or flavourings.
1. A formulation having a flavor or aroma comprising an isolated and/or purified enantiomer of 2-heptylcyclopropyl-1-carboxylic acid or a mixture of two, three or all enantiomers of 2-heptylcyclopropyl-1-carboxylic acid.
2. A formulation having a flavor or aroma comprising a mixture of the two enantiomers of cis-2-heptylcyclopropyl-1-carboxylic acid or the two enantiomers of trans-2-heptylcyclopropyl-1-carboxylic acid.
3. The formulation according to claim 2 , further comprising an enantiomeric excess of at least 40% of said cis-2-heptylcyclopropyl-1-carboxylic acid or said trans-2-heptylcyclopropyl-1-carboxylic acid.
4. Perfume composition and/or flavouring composition, containing an organoleptically active quantity of an isolated and/or purified enantiomer or mixture of enantiomers of claim 1 .
5. Perfume composition and/or flavouring composition, containing a proportion of at least 0.001 wt. % of an enantiomer of 2-heptylcyclopropyl-1-carboxylic acid or a mixture of two, three or all enantiomers of 2-heptylcyclopropyl-1-carboxylic acid, based on the total mass of the perfume composition or flavouring composition.
6. Flavoured foodstuff, containing an organoleptically active quantity of an isolated or purified enantiomer of 2-heptylcyclopropyl-1-carboxylic acid or a mixture of two, three or all enantiomers of 2-heptylcyclopropyl-1-carboxylic acid.
7. Body care product, cleaning agent or other product not intended for consumption, containing an organoleptically active quantity of an enantiomer of 2-heptylcyclopropyl-1-carboxylic acid or a mixture of two, three or all enantiomers of 2-heptylcyclopropyl-1-carboxylic acid.
8. A method for enhancing aroma and/or flavor sensory impression of a product by adding to said product an enantiomer or mixture of enantiomers of claim 1 .
9. Process for the production or modification of a perfume composition or flavouring composition, with the following steps:
preparing a starting composition, and
mixing the starting composition with an organoleptically active quantity of an enantiomer or mixture of enantiomers of claim 1 .
10. Process for the modification of a flavouring composition in a fresher, fruitier, fuller and/or more peel-like direction, wherein the flavouring composition is mixed with an organoleptically active quantity of an enantiomer or mixture of the two enantiomers of cis-2-heptylcyclopropyl-1-carboxylic acid.
11. Process for the selective preparation of cis- or trans-2-heptylcyclopropyl-1-carboxylic acid, wherein, a precursor with a Z- or E-configured double bond is selectively cyclopropanated to establish the cis or trans configuration of the substituents on the cyclopropane ring.
12. Perfume composition and/or flavouring composition according to claim 5 , containing a proportion of at least 0.01 wt. % of said enantiomer or of said mixture of enantiomers, based on the total mass of the perfume composition or flavouring composition.
13. Perfume composition and/or flavouring composition according to claim 12 , containing a proportion of at least 0.1 wt. % of said enantiomer or of said mixture of enantiomers, based on the total mass of the perfume composition or flavouring composition.
14. The method according to claim 8 wherein flavor of said product is enhanced by adding said enantiomer or mixture of enantiomers.
15. The method according to claim 8 wherein aroma of said product is enhanced by adding said enantiomer or mixture of enantiomers.
16. The method of claim 8 , wherein said enantiomer is a mixture of cis-2-heptylcyclopropyl-1-carboxylic acid and trans-2-heptylcyclopropyl-1-carboxylic acid.
17. The method of claim 8 , wherein said enantiomer is a racemic mixture of cis-2-heptylcyclopropyl-1-carboxylic acid, and where said enantiomer is added in an amount to impart a woody, balsamic, incense-like, green herbal, pith-like and waxy aroma.
18. The method of claim 8 , wherein said enantiomer is a racemic mixture of trans-2-heptylcyclopropyl-1-carboxylic acid.
19. The method of claim 8 , wherein said enantiomers are cis-enantiomers and are added in an amount to provide balsamic flavor without an aldehyde flavor note.
20. The method of claim 8 , wherein said enantiomers are trans-enantiomers and are added in an amount to provide a waxy, fatty or sweet perfume note to said product.