Phlox paniculata L. - Polemoniaceae - garden phlox, Hoher Stauden-Phlox, Rispige Flammenblume, Herbstflieder
Perennial herb, 50-120cm high, native to eastern North America, along rivers and open woods, extensively cultivated as ornamental.
„The flowers, 1.5-2.5cm in diameter, often fragrant, are white, pink, red, or purple, and borne in summer through fall (autumn). The flowers are grouped in panicles, hence the specific epithet paniculata.“
Main compounds of a dynamic headspace concentrate from violet Phlox flowers were phenylacetaldehyde (20%), benzaldehyde (5%), lilac alcohols (3%), linalool (2%), and 2-phenylethanol (0.4%).
[Volatile constituents of European bird cherry flowers (Padus avium Mill.). Surburg, H., Güntert, M., Schwarze, B.,Journal of Essential Oil Research, Vol.2(6), 1990, 307-316]
The fragrant volatiles of Phlox paniculata hybrids were collected by dynamic and vacuum headspace analysis. The product of the vacuum process contained mainly 2-phenyl ethanol (12-17%) and linalool (3-9%), together with 3-hydroxy-1-phenyl-2-butanone (1-4%), 3-hydroxy-4-phenyl-2-butanone (3-7%) and 1-phenyl-2,3-butanediol (0.3-6%). Cinnamic alcohol was present only in the vaccum product. Phenylacetaldehyde (1-2%), benzaldehyde (0.3-5%) and benzyl alcohol (0.2-2%) have been found both in the dynamic headspace and in the vaccum headspace product. Furthermore, lilac alcohols, eugenol methyl ether, isoeugenol methyl ether and germacrene-D are additional volatiles of Phlox flowers.
[Surburg et al., Volatile compounds from Flowers, in: Teranishi, R.;Buttery, R. G.;Sugisawa, H. Bioactive volatile compounds from plants. (Book) 1993, 170-171]
Scent emission analysis of P.paniculata flowers showed the benzenoids, benzaldehyde (14-91 ng/hr/flower), 2-phenylacetaldehyde (14-61 ng/hr/flower) and methyl eugenol (11-47 ng/hr/flower) as main constituents, together with (E)-β-ocimene (13-28 ng/hr/flower). Other components were linalool, lilac aldehyde A, lilac aldehyde B, 2-phenyl acetonitrile, eugenol and methyl isoeugenol as well as nonanal and decanal.
[Floral odor bouquet loses its ant repellent properties after inhibition of terpene biosynthesis., Junker, R.R., Gershenzon, J., Unsicker, S.B., Journal of chemical ecology, 37(12), 2011, 1323-1331]
Step,E., Bois,D., Favourite flowers of garden and greenhouse, vol.3 t 185 (1896-1897) [D.G.J.M. Bois]
garden phlox, CC BY-SA 3.0, Author: Andreas Kraska