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Rosa hybrida

A novel pigment has been isolated from the petals of Rosa hybrida with complex chromatographic techniques and the structure was elucidated with spectroscopic methods and high resolution fast-atom bombardement mass spectrometry, lH NMR, and FTIR. Anthocyanins were extracted from 7.9 kg of petals of Rosa hybrida cv. M me Violet with 80 per cent aqueous ACN containing 0.1 per cent TFA. The extract was purified in a Sephadex LH-20 column, and the fraction eluted with 80 per cent ACN was further fractionated in a HP-20 column using water, 15, 20 and 30 per cent ACN as mobile phases. The last fraction was lyophilized and separated by preparative RP-HPLC using an ODS column (50 X 5 cm i.d.). Solvents were 0.5 per cent aqueous TFA (A) and water-methanol... [Pg.277]

Y. Fukui, T. Kusumi, K. Masuda, T. Iwashita and K. Nomoto, Structure of rosacyanin B, a novel pigment from the petals of Rosa hybrida. Tetrahedron Lett. 43 (2002) 2637-2639. [Pg.363]

Sense Rosa hybrida Flower color changed from red to pale red 390... [Pg.191]

Eiroozabady, E. et al.. Regeneration of transgenic rose Rosa hybrida) plants from embryogenic tissue. Biotechnology, 12, 609, 1994. [Pg.218]

Tanaka, Y. et al.. Molecular cloning and characterization of Rosa hybrida dihydrofiavonol 4-reductase gene. Plant Cell Physiol, 36, 1023, 1995. [Pg.218]

Two classes of dimeric anthocyanins isolated from plants (section 10.2.6) have been identified in plants for the first time. One class includes pigments where an anthocyanin and a flavone or flavonol are linked to each end of a dicarboxylic acyl unit. The other class includes four different catechins linked covalently to pelargonidin 3-glucoside. During the last decade, seven new desoxyanthocyanidins and a novel type of anthocyanidin called P)Tanoanthocyanidins have been reported (Section 10.2.2). Toward the end of the 20th century, several color-stable 4-substituted anthocyanins, pyranoanthocyanins, were discovered in small amounts in red wine and grape pomace.Recently, similar compounds have been isolated from extracts of petals of Rosa hybrida cv. M me Violet, scales of red onion, and strawberries. About 94% of the new anthocyanins in the period of this review are based on only six anthocyanidins (Table 10.2). [Pg.472]

Circadian rhythmicity in emission of volatile compounds by flowers of Rosa hybrida L. cv. Honesty. Planta 207 88-95. [Pg.171]

Fig. 8.4 The ratios of the concentrations of odor volatiles change as a function of the time period of sampling, a) Diurnal emission of individual odor volatiles by flowers of Rosa hybrida exposured to a 12-h photoperiod shaded and non-shaded area,s correspond to periods of darkness and light. Each point represents the amount of a given volatile at a 3 h sampling period, b) Representation of the odor volatiles for each 3 h sampling period over a 24 h period (shown in a dotted box on (a)). The odors are represented on the x-axis as l=geraniol, 2=nerol, 3 itrone lol, 4=e-citral, 5=z-citral, 6=methyigeranylate, 7=caryophyllene, 8= J-cubebene, 9=dihydro-B-ionone, 10=hexylacetate, 1 l=2-phenylcthanol, 12-2-phenylethyl-acetate, 13-3,5 dimethyoxy toluene. Fig. 8.4 The ratios of the concentrations of odor volatiles change as a function of the time period of sampling, a) Diurnal emission of individual odor volatiles by flowers of Rosa hybrida exposured to a 12-h photoperiod shaded and non-shaded area,s correspond to periods of darkness and light. Each point represents the amount of a given volatile at a 3 h sampling period, b) Representation of the odor volatiles for each 3 h sampling period over a 24 h period (shown in a dotted box on (a)). The odors are represented on the x-axis as l=geraniol, 2=nerol, 3 itrone lol, 4=e-citral, 5=z-citral, 6=methyigeranylate, 7=caryophyllene, 8= J-cubebene, 9=dihydro-B-ionone, 10=hexylacetate, 1 l=2-phenylcthanol, 12-2-phenylethyl-acetate, 13-3,5 dimethyoxy toluene.
Reproduced from Helsper et al., Planta, 1998, Circadian rhythmicity in emission of volatile compounds by flowers of Rosa hybrida L. Cv. Honesty, vol. 207, iss. 1, pp. 88-95, with the permission of the authors and Springer. [Pg.206]

Figure 6.1.2 GC-MS chromatogram of fragrance chemicals from Rosa hybrida (adapted from... Figure 6.1.2 GC-MS chromatogram of fragrance chemicals from Rosa hybrida (adapted from...
To give an example of the many fragrance chemicals that can be present in an extract. Figure 6.1.2 shows a GC-MS chromatogram obtained in the analysis of Rosa hybrida. [Pg.252]

Volatile compounds have been found to be synthesized de novo in the cells of the plant tissues from which they are emitted [131, 132]. In flowers, their biosynthesis occurs in the epidermal cell layers, allowing easy escape of volatiles into the atmosphere [133-135]. While in some species, including Clarkia breweri and some rose varieties (e.g. Rosa x hybrida Baronne Edmond de Rothshild , Anna , The Mac Cartney Rose ), the biosynthesis of volatile constitnents of scent is localized on either side of the petals [136, 137], in others (snapdragon, Stephanotis floribunda, Nicotiana sua-veolens and Rosa x hybrida Lady Hillingdon ),... [Pg.417]


See other pages where Rosa hybrida is mentioned: [Pg.103]    [Pg.198]    [Pg.479]    [Pg.493]    [Pg.220]    [Pg.221]    [Pg.2806]    [Pg.221]    [Pg.103]    [Pg.198]    [Pg.479]    [Pg.493]    [Pg.220]    [Pg.221]    [Pg.2806]    [Pg.221]    [Pg.692]    [Pg.419]   
See also in sourсe #XX -- [ Pg.277 ]




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