Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Camelina sativa

Lein, m. flax linseed, -dotter,/. gold-of-pleas-ure, dodder seed (Camelina sativa, the seeds of which yield an oil) sometimes, dodder (Cuscuta). -dotterfil, n. cameline oil. [Pg.275]

Camelina sativa I O-leaf wash stim d. radicle elongation in presence of -fix. bacteria 104... [Pg.311]

The amino acid composition of storage proteins differs from that of the complete sprout [12, 13]. At least in the case of oilseed rape, alfalfa (Medicago sativa L.) and Camelina sativa, amino acids in the sprout are used mainly, either directly or indirectly, for the synthesis of the Rubisco proteins. Computer analysis shows that the amino acid composition of cruciferin and napin is completely different to the amino acid composition of Rubisco. This indicates that amino acids released from the seed storage proteins must be converted into other amino acids prior to Rubisco synthesis. [Pg.41]

Camelina sativa, a rare and unexploited crop plant Camelina sativa is grown as a crop plant only in Finland and Ireland. Because it is a self-pollinating plant the risk of inadvertently transferring the new trait to naturally occurring plant relatives in the environment is low. Camelina sativa has not been extensively used in plant breeding, which means that there are only few varieties of the plant... [Pg.53]

Oilcrops Oilseed rape, safflower, Camelina sativa Oil-body purification, sprouting system Lower biomass yields, oil bodies incompatible with glycosylation... [Pg.193]

The leaf flavonoids of the cruciferous species such as Camelina sativa, Crambe abyssinica, Crambe hispanica, Thlaspi arvense, Brassica napus and Sinapis alba were separated and identified with the combination of HPLC, TLC and paper chromatography. Llavonoid aglycones were extracted by cutting fresh three-week-old leaves in tiny pieces and boiled in 50 ml of 2 M HC1 for 45 min. [Pg.144]

J. Onyilagha, A. Bala, R. Hallett, M. Gruber, J. Soroka and N. Westcott, Leaf flavonoids of the cruciferous species, Camelina sativa, Crambe spp., Thlaspi arvense and several other genera of the family Brassicacaea. Biochem. Syst. Ecol. 31 (2003) 1309-1322. [Pg.355]

Cruciferous species, in which the glucosinolates are biologically active compounds (44), have been studied in both of the latter categories. In Australia, allelopathy has been associated with introduced crucifers such as Brassica tournefortii Gouan (wild turnip) and a more complete study has been made of Camelina sativa (L.) Grants (false flax). [Pg.162]

Camelina sativa, usually known in English as gold-of-pleasure or false flax, also occasionally linseed dodder and Siberian oilseed, is a flowering plant in the family brassicaceae, which also includes rapeseed. The crop is now being... [Pg.207]

Camelia oil. See Camellia sinensis oil Camelina sativa. See Gold of pleasure (Camelina sativa) oil Camellia oil. See Camellia sinensis oil Camellia oleifera. See Camellia oleifera extract Camellia oleifera extract CAS 84650-60-2... [Pg.728]

Cropure Evening Primrose. See Evening primrose (Oenothera biennis) oil Cropure Gold of Pleasure. See Gold of pleasure (Camelina sativa) oil Cropur Grapeseed. See Grape (Vitis vinifera) seed oil... [Pg.1091]

Gold of pleasure oil. See,Gold of pleasure (Camelina sativa) oil... [Pg.1945]

Balsam copaiba (Copaifera officinalis) Balsam copaiba (Copaifera officinalis) oil Behenamidopropyl dimethylamine Benzyl laurate Boron nitride Butyl octyl benzoate C10-30 cholesterol/lanosterol esters Dicocodimethylamine dimerate Distearyidimethylamine dilinoleate Gold of pleasure (Camelina sativa) oil Hexyldecyl benzoate Hyaluronic acid Isopropyl stearate Linoleamidopropyl dimethylamine Macadamia ternifolia nut oil Octyidodecyl stearoyl stearate Oleyl oleate PEG/PPG-8/3 diisostearate PEG-14 tallate Polymethylsilsesquioxane Polyquaternium-22 PPG-26-buteth-26 Sodium/TEA-lauroyl hydrolyzed keratin Stearamide DEA Stearamidoethyl ethanolamine... [Pg.5450]

Prepared from Camelina sativa seed oil. Cryst. (pet. [Pg.610]

Constit. of the seed oil of Camelina sativa. Isol. from rice plant, Fukuyuki. Inhibits rice blast fungus, [a] +0.27 (c, 1.5 in CHCI3). [Pg.631]

Figure 2.8 Supercritical fluid chromatography, with use of a miniaturized evaporative lightscattering detector, of seed extracts from (a) an autumn rapeseed (b) Camelina sativa (triacyl-glycerides containing long-chain monoenes have not been identified because reference substances are not available). SFE/SFC was off-line. Column as in Fig. 2.2. Separation conditions temperature 140°C pressure 160 atm, after 1 min programmed at -10°Cmin to 100°C and 25 atm min" to 260 atm, then programmed at -l°Cmin to 75°C and at 2 atm min to 260 atm. Extraction conditions temperature 90°C, pressure 160 atm. Abbreviations L = linoleate Ln = linolenate 0 = oleate P = palmitate S = stearate SFC = supercritical fluid chromatography SFE = supercritical fluid extraction. Figure 2.8 Supercritical fluid chromatography, with use of a miniaturized evaporative lightscattering detector, of seed extracts from (a) an autumn rapeseed (b) Camelina sativa (triacyl-glycerides containing long-chain monoenes have not been identified because reference substances are not available). SFE/SFC was off-line. Column as in Fig. 2.2. Separation conditions temperature 140°C pressure 160 atm, after 1 min programmed at -10°Cmin to 100°C and 25 atm min" to 260 atm, then programmed at -l°Cmin to 75°C and at 2 atm min to 260 atm. Extraction conditions temperature 90°C, pressure 160 atm. Abbreviations L = linoleate Ln = linolenate 0 = oleate P = palmitate S = stearate SFC = supercritical fluid chromatography SFE = supercritical fluid extraction.
A. Hebard, Camelina sativa — a pleasurable experience or another false hope, Lipid Technology, 1998, 10, 81-83. E.C. Leonard, Camelina oil a-linolenic source, INFORM, 1998, 9, 830-938. [Pg.32]

Calonyction aculeatum 89 Camelina 110 Camelina sativa 109 Canavalia ensiformis (Jack bean) 26 Cannabis 25... [Pg.283]

Abramovic, H., Terpinc, R, Polak, T., UMh, N. R 2011. Effect of heat treatment of cam-ehna (Camelina sativa) seeds on the antioxidant potential of their extracts. J Agric Food Chem. 59(16) 8639-8645. [Pg.56]

Plastid Camelina sativa Seeds PHB 29 9 Patterson et al. (2011a,b)... [Pg.302]

Camelina sativa (L.), also known as false flax or gold of pleasure, is an annual plant that belongs to the Brassicaceae family. Camelina was an important CTop in Europe until it was replaced with rapeseed. There was no commercial production of camelina in the United States until 2004. A rapid increase in production has been observed since 2004 reaching approximately 30000ha in 2009 (Berti et al, 2011). [Pg.20]

Ghamkhar K, Croser J, Aryamanesh N, Campbell M, Kon kova N, Francis C. 2010. CameUna (Camelina Sativa (L.) Crantz) as an Alternative Oilseed Molecular and Ecogeographic Analyses. Genome 53(7) 558-567. [Pg.29]

Pdgeram AL, Sand DC, Boss D, et al. 2007. Camelina Sativa, a Montana Omega-3 Fatty Acid and Fuel Crop. In Janick, J Whipkey A (editors). Issues in New Crops and New Uses. Alexandria, VA ASHS Press, pp. 129-131. [Pg.33]

The reported order of activity of alkaline earth oxide catalysts was observed to be BaO>SrO>CaO>MgO. Among them, MgO was more active than CaO in the transesterifieation of rapeseed oil, but was also responsible for soap formation. In the transesterifieation of Camelina sativa oil, BaO and SrO were found to be effective catalysts for the synthesis of biodiesel at 100° C compared to CaO and MgO [20]. The authors suggested that SrO can be preferred over BaO due to the noxious nature of BaO. Similar results were also observed for the transesterifieation of palm oil using CaO, SrO and BaO as heterogeneous base catalyst imder ultra sonic assisted preparation of biodiesel. BaO and SrO were found to be efficient catalysts than CaO for production biodiesel with a yield of 95%. With BaO, there was a drop in catalytic activity due to the dissolution of BaO catalyst in methanol [21]. [Pg.443]

Na jCa gTiOj nanorods were used as heterogeneous base catalysts for the transesterification of Camelina sativa oil to biodiesel. With oil to MeOH ratio of 1 36 at 60° C with 6% catalyst, a biodiesel yield of 93% was achieved in 8 h [87]. [Pg.458]


See other pages where Camelina sativa is mentioned: [Pg.202]    [Pg.148]    [Pg.71]    [Pg.159]    [Pg.368]    [Pg.280]    [Pg.297]    [Pg.934]    [Pg.128]    [Pg.253]    [Pg.1945]    [Pg.31]    [Pg.91]    [Pg.109]    [Pg.533]    [Pg.444]    [Pg.129]    [Pg.10]    [Pg.207]    [Pg.209]    [Pg.211]    [Pg.219]   
See also in sourсe #XX -- [ Pg.144 , Pg.148 ]

See also in sourсe #XX -- [ Pg.51 ]




SEARCH



Camelina

© 2024 chempedia.info