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Fatty Esters (fatty + ester)
Selected AbstractsComposition of essential oil, concrete, absolute, wax and headspace volatiles of Murrarya paniculata (Linn.) Jack flowersFLAVOUR AND FRAGRANCE JOURNAL, Issue 5 2007P. K. Rout Abstract Murraya paniculata (Linn) Jack, syn. M. exotica Linn., commonly known as orange jessamine, is grown in gardens for its large clusters of fragrant flowers. Distillation of the fresh flowers in water furnished the essential oil in 0.027% yield. Extraction of the fresh flowers with pentane afforded the concrete (0.78%). Precipitating the waxes from the concrete with methanol gave absolute (0.62%). The chemical composition of essential oil, concrete, absolute and wax were analysed by GC and GC,MS. The components of essential oil in significant amounts were , -elemene (1.4%), (E)-caryophyllene (3.6%), germacrene D (2.7%), (E)-nerolidol (25.7%), benzyl benzoate (8.1%), phenyl ethyl benzoate (8.0%) and manool (18.7%). The major components in the concrete and absolute, respectively, were phenyl ethyl alcohol (2.9%, 3.0%), indole (0.8%, 1.0%), (E)-nerolidol (6.5%, 7.0%), benzyl benzoate (5.0%, 6.5%), phenyl ethyl benzoate (8.0%, 8.6%) and manool (25.2%, 27.9%). The methanol-insoluble wax contained (E)-nerolidol (2.6%), manool (9.4%) and most of the fatty acids/esters. The composition of the volatile components in the headspace emitted by flowers still on the branch (live flowers) and also by the picked flowers was determined by HS,SPME on a PDMS fibre and these results are also presented. The major components found in the headspace were linalool, indole, (E)-caryophyllene, germacrene D, bicyclogermacrene and (E,E)- , -farnesene. Copyright © 2007 John Wiley & Sons, Ltd. [source] Polymerization of linseed oil with phenolic resinsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010Gökhan Çayl Abstract In this study, linseed oil was directly polymerized with different oil soluble resoles. p- Ethyl (PEP), p-tertiary butyl (PTB), p-tertiary octyl (PTO), and p- phenyl (PPP) phenols were separately reacted with formaldehyde to give linseed oil soluble resoles. These were then reacted with linseed oil to give transparent rubbery polymers. A model reaction was performed with methyl oleate and PTB phenol resole to clarify the reaction mechanism. Reaction products were characterized with 1H-NMR and IR techniques. Spectral examination of the model reaction showed that polymerization reaction proceeded via ene reaction of the quinone methide formed at the end group of the resole with the allylic positions of the fatty ester. Rubbery polymers were obtained with linseed oil using 10 to 40% of the different resoles. Hard, load bearing and tough materials were obtained at 40% phenolic resin loading. Mechanical properties of the materials were characterized by dynamic mechanical analyzer (DMA) and stress,strain tests. The best mechanical and thermal properties were obtained with PEP resole which showed a storage modulus of 350 MPa and a tan , peak at 65°C. Storage moduli of 275, 250, and 30 were obtained for PPP, PTB, and PTO resoles-linseed oil polymers, respectively. At the same phenolic resin loading, elongation at break and swelling ratios in CH2Cl2 increased with the longer alkyl substitution on the resole resins. The highest thermal stability was observed by PEP resole,linseed oil polymer which has a 5% weight loss temperature of 340°C as determined by TGA. The lowest thermal stability was observed for PTB resole-linseed oil polymer at 220°C. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] First Transformation of Unsaturated Fatty Esters Involving Enyne Cross-MetathesisADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 7-8 2009Ravalec, Virginie Le Abstract The ruthenium-catalysed enyne cross-metathesis of several alkyne derivatives with terminal olefins was performed. These reactions were efficiently achieved under mild conditions in dimethyl carbonate, an eco-friendly solvent. A unique one-pot reaction based on an ethenolysis step followed by an enyne cross-metathesis allowed the efficient transformation of renewable unsaturated fatty esters into valuable conjugated 1,3-dienes of interest for further transformations. [source] Complementary (secondary) metabolites in a soft coral: sex-specific variability, inter-clonal variability, and competitionMARINE ECOLOGY, Issue 3 2006Beatriz Fleury Abstract Sex-specific interactions involving competition for space between the dioecious alcyonacean soft coral Sarcophyton glaucum and the scleractinian coral Acropora robusta were assessed experimentally on Bald Rock, central region of the Great Barrier Reef. To examine this, plus inter-clonal responses, one male colony of S. glaucum, known to produce sarcophytoxide as its predominant complementary (secondary) metabolite, was sectioned, producing 10 clones. The same was done for a female colony. These two sets of clones were then relocated to grids and placed in contact with Acropora clones. Relocated and non-relocated controls were also monitored. High levels of tissue necrosis were observed in the hard coral under contact conditions with both the male and female clones after 20 days. The development of a protective polysaccharide layer in the alcyonacean was also observed. Differences observed in the concentrations of complementary metabolites within the two different S. glaucum colonies were related to sex. Both under competition and non-competition conditions, females exhibited significantly higher concentrations of sarcophytoxide than males, and this increased with time. Fatty ester concentration was also higher in females than males, varying significantly through time, and falling dramatically just after spawning. Fatty ester concentrations decreased linearly through time in the male clones. When involved in competition for space, females possessed higher concentrations of fatty esters than males, both at the site of contact and in non-contact sites, again, decreasing after spawning. No significant changes in sarcophytoxide levels were noted in the parental colonies, but such changes were observed in fatty esters, with the female producing higher concentrations until after spawning. The use of these two variates in the form of a ratio (sarcophytoxide concentration:fatty ester concentration) yielded a variable Rho (,) which was a more sensitive indicator of biochemical change than either of its components alone. These two sets of compounds appeared to have a negative association through time and varied highly significantly between sexes. The diterpene sarcophytoxide may be considered an allelopathic or stress metabolite, while the lipids act as energy storage metabolites. [source] Glycerol upgrading by ketalization in a zeolite membrane reactorASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 3 2009Laura Roldán Abstract Solketal, a valuable green solvent, has been produced from glycerol and acetone in a catalytic system, using K10 montmorillonite as a heterogeneous catalyst. The use of a zeolite membrane to remove water formed during the reaction gives rise to a significant improvement in the achievable glycerol conversion with a reduction in the excess of acetone needed because of the low equilibrium constant. Several zeolite membranes are compared, showing that the quality of the membrane is a key factor for this improvement, and that water/acetone separation is more difficult to achieve than the commonly used ethanol/water separation test. This method is compatible with a mixture of glycerol and fatty esters, showing the possible future application in an integrated system of biodiesel and solketal production. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Ethenolysis of Methyl Oleate in Room-Temperature Ionic LiquidsCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 1-2 2008Cyril Thurier Abstract Unsaturated vegetable oils are an attractive renewable feedstock, and the selective cleavage of unsaturated fatty esters is an important transformation in this respect. The efficient and selective cross-metathesis of methyl oleate with ethylene was achieved under mild conditions with ruthenium-alkylidene catalysts in toluene and room-temperature ionic liquids (RTILs) to give two important chemical intermediates, 1-decene and methyl 9-decenoate, without double-bond migration. As recovery of the catalyst is an important target with respect to industrial applications, catalyst recycling studies were also carried out in RTILs with the first-generation Hoveyda catalyst. [source] | ||||||||||