| Beide Seiten der vorigen RevisionVorhergehende ÜberarbeitungNächste Überarbeitung | Vorhergehende Überarbeitung |
| tilia_platyphyllos_scop [2016/06/23 22:25] – andreas | tilia_platyphyllos_scop [2022/06/22 19:42] (aktuell) – andreas |
|---|
| |
| Tea from the dried flowers of Tilia cordata and Tilia platyphyllos is used traditionally as diaphoretic. \\ [[http://buecher.heilpflanzen-welt.de/BGA-Kommission-E-Monographien/tiliae-flos-lindenblueten.htm]] | Tea from the dried flowers of Tilia cordata and Tilia platyphyllos is used traditionally as diaphoretic. \\ [[http://buecher.heilpflanzen-welt.de/BGA-Kommission-E-Monographien/tiliae-flos-lindenblueten.htm]] |
| |
| "The smelling principle of linden blossom is formed by 'narcotic' fragrances such as farnesol or the erogenous esters of phenylacetic acid." \\ | |
| [Düfte. Signale der Gefühlswelt., Ohloff, G., Zürich 2004] | |
| |
| {{:26dimethyl357octatriene2ol.jpg| 2,6-dimethyl-3(E),5(Z/E),7-octatriene-2-ol }} 2,6-dimethyl-3(E),5(Z/E),7-octatriene-2-ol //(sweet floral)// | {{:26dimethyl357octatriene2ol.jpg| 2,6-dimethyl-3(E),5(Z/E),7-octatriene-2-ol }} 2,6-dimethyl-3(E),5(Z/E),7-octatriene-2-ol //(sweet floral)// |
| |
| The highly sensitive 2,6-dimethyl-3(E),5(Z),7-octatriene-2-ol and its 5(E) isomer (natural ratio 1:10, sweet floral odor) are main constituents present only in the headspace and not in extracts of the flowers of T.platyphyllos and T.cordata.\\ | The highly sensitive 2,6-dimethyl-3(E),5(Z),7-octatriene-2-ol and its 5(E) isomer (natural ratio 1:10, sweet floral odor) are main constituents present only in the headspace and not in extracts of the flowers of T.platyphyllos (and major constituents in T.cordata).\\ |
| [Trapping, Investigation and Reconstitution of Flower Scents, Roman Kaiser, in: Müller, P.M., and Lamparsky, D. eds. Perfumes: art, science and technology. Springer Science & Business Media, 2012, 213-250] | [Trapping, Investigation and Reconstitution of Flower Scents, Roman Kaiser, in: Müller, P.M., and Lamparsky, D. eds. Perfumes: Art, Science and Technology. Springer Science & Business Media, Dordrecht 1994, 213-250] but \\ |
| | Later on, headspace analysis of hyacinth flowers showed that 2,6-dimethylocta-1,3,5,7-tetraenes and 2,6-dimethylocta-3,5,7-triene-2-ols are associated with charcoal as adsorbing material. It was shown that these compounds are artefacts from ocimene which mainly arise during sampling with charcoal. |
| | [Headspace analysis of hyacinth flowers. Brunke, E. J., Hammerschmidt, F. J., Schmaus, G., Flavour and fragrance journal, Vol.9(2), 1994, 59-69] |
| |
| {{:tilia_platy.jpg|}} \\ | "The smelling principle of linden blossom is formed by 'narcotic' fragrances such as farnesol or the erogenous esters of phenylacetic acid." \\ |
| | [Düfte. Signale der Gefühlswelt., Ohloff, G., Zürich 2004] |
| | |
| | {{:tilia_platy.jpg?600}} \\ |
| Dietrich, A.G., Flora regni borussici, vol.12, t.831 (1844) [A.G. Dietrich]\\ | Dietrich, A.G., Flora regni borussici, vol.12, t.831 (1844) [A.G. Dietrich]\\ |
| [[http://plantgenera.org/species.php?id_species=1017807]] | [[http://plantgenera.org/species.php?id_species=1017807]] |
| | |
| | {{:tilia_platyphyllos_sb.jpg}} \\ |
| | Tilia platphyllos, [[https://creativecommons.org/licenses/by-sa/3.0/de/|CC BY-SA 3.0]], Author: Andreas Kraska |
