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Fatty acids compounds

In addition, a fluid loss additive for oil-based drilling fluids, which consists of fatty acid compounds and lignite or humic acid, an oil-soluble or oil-dispersible amine or amine salt with phosphorie acid, or an aliphatic amide or hydroxyamide [392], has been described. [Pg.48]

Figure 1.7 Typical zero-order and corresponding second-derivative electronic absorption spectra of ethanol-reconstituted lipid/chloroform extracts of autoxidized model polyunsaturated fatty-acid compounds and inflammatory synovial fluid obtained after (1) reduction with NaBH4 and (2) dehydration with alcoholic H2S04- (a) Methyl linoleate subsequent to autoxidation in air at ambient temperature for a period of 72 h (—), or exposure to a Fenton reaction system containing EDTA (5.75 x 10 mol/dm ), H2O2 (1.14 X 10 mol/dm ) and Fe(ll) (5.75 x IO mol/dm ) as an aqueous suspension (—) (b) as (a) but with methyl linolenate (c) untreated rheumatoid knee-joint synovial fluid. Figure 1.7 Typical zero-order and corresponding second-derivative electronic absorption spectra of ethanol-reconstituted lipid/chloroform extracts of autoxidized model polyunsaturated fatty-acid compounds and inflammatory synovial fluid obtained after (1) reduction with NaBH4 and (2) dehydration with alcoholic H2S04- (a) Methyl linoleate subsequent to autoxidation in air at ambient temperature for a period of 72 h (—), or exposure to a Fenton reaction system containing EDTA (5.75 x 10 mol/dm ), H2O2 (1.14 X 10 mol/dm ) and Fe(ll) (5.75 x IO mol/dm ) as an aqueous suspension (—) (b) as (a) but with methyl linolenate (c) untreated rheumatoid knee-joint synovial fluid.
Linoleic acid is a polyunsaturated fatty acid (compound containing two or more double bonds) occurs as an ester in polyunsaturated fats. [Pg.396]

Low susceptibility to reef fishes in Florida and produces secondary metabolites (Paul and Hay 1986). A fatty acid compound from Guam specimens inhibits the fish Z. flavescens (Wylie and Paul 1988)... [Pg.38]

Jacobs, P.A., Maes, P., Paulussen, S.J., Tielen, M., Van Steenkiste, D.F.E., and Van Looveren, L.K. (2001) Elimination of trans-unsaturated fatty acid compounds by selective adsorption with zeolites. U.S. Patent 6,229,032. [Pg.199]

Figure 1.6 Selected small molecule inhibitors of HDACs. Compounds 7 and 8 are short-chain fatty acids, compounds 9 and 10 are hydroxamic acids, compounds 11 and 12 are cyclic tetrapeptides, compound 13 is cyclic tetrapeptide analog and compound 14 is a benzamide. Figure 1.6 Selected small molecule inhibitors of HDACs. Compounds 7 and 8 are short-chain fatty acids, compounds 9 and 10 are hydroxamic acids, compounds 11 and 12 are cyclic tetrapeptides, compound 13 is cyclic tetrapeptide analog and compound 14 is a benzamide.
Leukotriene One of the 20-carbon fatty acid compounds (eicosanoids) formed from arachidonic acid by the lipoxygenase enzyme. Leukotrienes are important in mediating certain allergic and inflammatory responses, especially in respiratory tissues. [Pg.628]

Solubility of fatty acid compounds in n-butane are higher than in SC C02 Therefore test reactions at 150 bar and 40°C were performed in n-butane. The flow of the gas was 0.5 and 1 L per min. The results showed that Lipozyme loses its activity in this media. The conversion continuously decreases from 50% at the beginning to 22% after 300 min of the reaction operation (Figure 5). [Pg.90]

CO type carbon should not be present in pure fatty acid compound. This is indicative of surface impurity. [Pg.384]

Sucrose Esters. Sucrose has eight free hydroxyl groups, which are potential sites for esterification to fatty acids. Compounds containing six or more fatty acids per sucrose molecule have been proposed for use as noncaloric fat substitutes under the name Olestra this material acts like a triglyceride fat and has no surfactant properties. Compounds containing one to three fatty acid esters, on the other hand, do act as emulsifiers and are approved for food use in that capacity. They are manufactured by the following steps ... [Pg.2227]

Liquids, soft solids, solids or flakes. Solubility properties depend on length of polyoxyethylene (POE) segment added lo a specific fatty acid. Compounds are insol in water. Sol is oil and hydrocarbon solvents when ethylene oxide units are added. Soly in water begins when 12-IS ethylene oxide units are added. Specific gravity and viscosity increase with increasing ethylene oxide content. [Pg.1207]

P-20 - Selective adsorption of trans unsaturated fatty acid compounds in MFI type zeolites... [Pg.234]

The bulk of the nonvolatile matter in the product consists of an alkali salt of fatty acids and the product s detergent properties are due to the alkali-fatty acid compounds, and... [Pg.42]

The major biosynthetic pathway leading to alkanes is by enzyme-catalyzed decarboxylation (loss of CO2) of fatty acids, compounds of the type CH3(CH2) C02H in which n is an even number and the chain has 14 or more carbons. [Pg.99]

Thermal decomposition In order to control shape and size more precisely, the method of thermal decomposition is developed. This is a method similar to the synthesis of semiconductors with high-quality nanocrystals. The smaller magnetic nanocrystals can be formed from organometallic compounds in organic solvents. By adding precursor in zerovalent, thermal decomposition will have metal formed in the end. When the decomposition happens, cationic metal will lead the electrons to the oxides and the reaction solution will have metal acid salts in nonaqueous solution. With the metal fatty acid compound in the solution, the metal will reach saturation and the metal magnetic... [Pg.6]

Fatty acids which are present as fatty acid compounds (soaps). These can be recorded following extraction with n-hexane and acidification of the aqueous solution to a pH range of pH 1 to pH 2 by means of an additional extraction process. [Pg.519]

If the fatty acids present as fatty acid compounds (soaps) in water are also to be recorded by this method, then the water samples extracted with... [Pg.522]

If the fatty acid compounds have been recorded as well following extraction... [Pg.522]

Fatty acid derivates of calcium, zinc and magnesium Barium fatty acid compounds Lead cadmium derivates... [Pg.255]

Inhibitor peptides low molecular mass oligopeptide-fatty acid compounds of microbial origin which irreversibly inactivate plant and animal proteases. The inhibition is stoichiometric, i.e. 1 molecule I.p. inhibits 1 molecule enzyme. Examples are Leupeptin [acetyl-(or propionyl-)L-Leu-L-Leu-arginal the L-leu-cine can also be replaced by L-isovaline or L-valine], from Streptomyces species, inhibits cathepsin B, papain, trypsin, plasmin and cathepsin D, the effectiveness of the inhibition decreasing in that order. Pepsta-tin (isovaleryl-L-Val-L-Val-P-hydroxy-Y-NH2- -CH3-heptanoyl-L-Ala-P-hydroxy-Y-NHj-e-heptanoic acid), from actinomycetes, inhibits pepsin and cathepsin D. Chymostatin inhibits all known chymotrypsin types, cathepsin A, B, and D and papain. Antipain inhibits papain trypsin and plasmin. [Pg.320]

Retention-aid chemicals may be added, as well as defoamers (e.g. fatty-acid compounds), pitch-control agents, optical brighteners (usually stilbene derivatives) and, in some cases, fibre deflocculants. Different slimicides are also added to the stock for microbe control. A number of chemicals can be used for this purpose, such as 1,5-pentanediol, 2,2-dibromo-3-nit-rile propionamide, 2,2-dibromo-2-cyanoacetamide, 5-chloro-2-methyl-4-isothiazolin-3-one + 2-methyl-4-iso-thiazolin-3-one (Kathon CG) or glutaraldehyde. [Pg.1034]

Fatty Acid Compounds of Human Colostrum and of Mature Milk Fats from Mothers on Diets Taken Ad Libitum and Their Changes During the Course of Lactation... [Pg.281]

Fatty acid compounds usually contain single or multiple double bonds with varying E/Z geometries. Under hydroformylation conditions, they can be hydrogenated before hydroformylation takes place [21]. A special problem is Z/ isomerization or the migration of double bonds, since most hydroformylation catalysts are also active isomerization catalysts. Isomerization may take place before, during, or after (multiple double bonds ) the reaction with syngas. [Pg.591]

After a long period of neglect of hydroformylation of fatty acid compounds derived from renewable resources, it is once again in the focus of research. In comparison to the pioneering time, smoother reaction conditions have been identified. Also, related methods such as palladium-catalyzed alkoxycarbonylation of fatty acid esters are attracting more and more attention [64]. This methodology mainly produces a,m-diesters, which cannot be produced in good yields by hydroformylation to date. [Pg.606]

Stearic acid and oleic acid are fatty acids, compounds that contain a carboxy group (COOH) attached to the end of a long carbon chain. Stearic acid is a saturated fatty acid because each carbon atom in its long chain has the maximum number of bonds to hydrogen. Oleic acid is an unsaturated fatty acid because its carbon chain contains one (cis) double bond. The presence of a double bond greatly affects the chemical and physical properties of these fatty acids. In Chapter 10 we learn about alkenes, organic compounds that contain carbon-carbon double bonds. [Pg.358]

Common fatty acid compounds a.TWgIyceride or triacylglycerol Three... [Pg.4]

CLASSIFICATION. Lipids are often classified into three major groups (1) simple lipids (2) compound lipids and (3) derived lipids. When fatty acids are esterified with alcohols, simple lipids result. If compounds such as choline or serine are esterified to alcohols in addition to fatty acids, compound lipids result. The third type of lipid, derived lipids, results from the hydrolysis or enzymatic breakdown of simple and compound lipids. [Pg.331]


See other pages where Fatty acids compounds is mentioned: [Pg.589]    [Pg.55]    [Pg.417]    [Pg.151]    [Pg.1276]    [Pg.113]    [Pg.644]    [Pg.7]    [Pg.10]    [Pg.1038]    [Pg.234]    [Pg.4]    [Pg.416]    [Pg.151]    [Pg.59]    [Pg.147]    [Pg.588]    [Pg.9]   


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Aroma Compounds from Fatty Acid Metabolism

Compounds Formed by Degradation of Fatty Acids

Fatty Acids and Derived Compounds

Fatty Acids and Related Compounds

Fatty compounds

Unsaturated fatty acid compounds

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