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INDEX alcohol oxidation

Oxidative damage to membrane polyunsaturated fatty acids leads to the formation of numerous lipid peroxidation products, some of which can be measured as index of oxidative stress, including hydrocarbons, aldehydes, alcohols, ketones, and short carboxylic acids. [Pg.275]

Polyvinyl alcohol oxidation affected by hydrogen peroxide in the presence of ferrous sulfate (II) in aqueous solutions is accompanied by chemiluminescence in the visible spectrum (Fig. 23.6). In Fig. 23.6, it is seen that luminous intensity passes through a maximum. This facts shows that luminescence emitter is an intermediate product of liquid-phase PVA oxidation. The analysis of the kinetic curve of chemiluminescence intensity showed that its initial part is well linearized (Fig. 23.6, the correlation index r = 0.998) in the equation coordinates... [Pg.275]

Methylene iodide [75-11-6], CH2I2, also known as diio dome thane, mol wt 267.87, 94.76% I, mp 6.0°C, and bp 181°C, is a very heavy colorless Hquid. It has a density of 3.325 g/mL at 20°C and a refractive index of 1.7538 at 4°C. It darkens in contact with air, moisture, and light. Its solubiHty in water is 1.42 g/100 g H2O at 20°C it is soluble in alcohol, chloroform, ben2ene, and ether. Methylene iodide is prepared by reaction of sodium arsenite and iodoform with sodium hydroxide reaction of iodine, sodium ethoxide, and hydroiodic acid on iodoform the oxidation of iodoacetic acid with potassium persulfate and by reaction of potassium iodide and methylene chloride (124,125). Diiodoform is used for determining the density and refractive index of minerals. It is also used as a starting material in the manufacture of x-ray contrast media and other synthetic pharmaceuticals (qv). [Pg.366]

The choice of which reactions to include is not an easy one. First there are the well known "Name Reactions", that have appeared in various monographs or in the old Merck index. Some of these are so obvious mechanistically to the modern organic chemistry practitioner that we have in fact omitted them for instance esterification of alcohols with acid chlorides - the Schotten-Baumann procedure. Others are so important and so well entrenched by name, like the Baeyer-Villiger ketone oxidation, that it is impossible to ignore them. In general we have kept older name reactions that are not obvious at first glance. [Pg.459]

Alkyl and aryl arenediazoates ( diazoethers ) are generally unstable and even explosive compounds. They are produced by interaction of alcohols with (explosive) bis(arenediazo) oxides, or of -blocked phenols with diazonium salts. The thio analogues are similar. Individually indexed compounds are ... [Pg.63]

Other synthetics derived from petroleum, having high viscosity index, low volatility, and low pour point, include polyoxyethylene and polyoxypropylene monohydroxy compounds (22). These can be made by an addition reaction between a monohydric alcohol and an alkylene oxide. [Pg.245]

Iodobenzene [591-50-4], C6HBI, mol wt 204.02, 62.23% I, mp —30°C, bp 188—189°C, is a colodess liquid that rapidly becomes yellow and has a characteristic odor. It is insoluble in water, but completely miscible with alcohol, chloroform, and ether. It has a density of 1.832 g/mL at 20°C and a refractive index of 1.621 at 4°C. Iodobenzene is prepared by the reaction of iodine and benzene in the presence of an oxidizing agent and from benzeneiazonium sulfate and potassium iodide (122). Iodobenzene is used as a heavy liquid for refractive index determinations, but probably its principal use is in the synthesis of iodoso compounds, RIO iodoxy compounds, RI02 and iodonium salts, R IX. [Pg.366]

Sharpless asymmetric epoxidation of allylic alcohols, asymmetric epoxidation of conjugated ketones, asymmetric sulfoxidations catalyzed, or mediated, by chiral titanium complexes, and allylic oxidations are the main classes of oxidation where asymmetric amplification effects have been discovered. The various references are listed in Table 4 with the maximum amplification index observed. [Pg.278]

Linoleic Acid occurs as a colorless to pale yellow, oily liquid that is easily oxidized by air. It is an essential fatty acid and the major constituent of many vegetable oils, including cottonseed, soybean, peanut, corn, sunflower seed, safflower, poppy seed, and linseed. Its specific gravity is about 0.901, and its refractive index is about 1.469. It has a boiling point ranging from 225° to 230° and a melting point around -5°. One milliliter dissolves in 10 mL of petroleum ether. It is freely soluble in ether soluble in absolute alcohol and in chloroform and miscible with dimethylformamide, fat solvents, and oils. It is insoluble in water. [Pg.255]

Poloxamer 331 occurs as a practically colorless liquid. It is a block copolymer condensate of ethylene oxide and propylene oxide with an average formula weight of 3800, a specific gravity of about 1.02, and a refractive index of about 1.452. It is very slightly soluble in water at 25°, but is freely soluble at 0° it is freely soluble in alcohol, but is insoluble in propylene glycol and in ethylene glycol. [Pg.334]

Properties Colorless gas or liquid sharp, pungent odor. D 1.4337, liquid at 0C, fp -76.1C, bp -10C, vap press 3.2 atm (20C), refr index (liquid) 1.410 (24C), an outstanding oxidizing and reducing agent. Soluble in water, alcohol, and ether forms sulfurous acid (H,S03). Noncombustible. [Pg.1192]

Properties Colorless liquid penetrating odor and taste. D 0.9394 (20/4C), bp 185.4C, refr index 1.4081 (20C), vap press 0.08 mm Hg (20C), fp -34C, flash p 205F (96C) (OC). Soluble in water, alcohol and ether. Undergoes reactions typical of normal monobasic organic acids. Combustible. Derivation With other C5 acids by distillation from valerian, by oxidation of n-amyl alcohol, numerous essential oils. [Pg.1310]


See other pages where INDEX alcohol oxidation is mentioned: [Pg.396]    [Pg.325]    [Pg.1624]    [Pg.792]    [Pg.220]    [Pg.299]    [Pg.793]    [Pg.402]    [Pg.1255]    [Pg.64]    [Pg.11]    [Pg.249]    [Pg.403]    [Pg.859]    [Pg.930]    [Pg.396]    [Pg.512]    [Pg.2390]    [Pg.182]    [Pg.188]    [Pg.33]    [Pg.78]    [Pg.48]    [Pg.268]    [Pg.402]    [Pg.412]    [Pg.1893]    [Pg.185]    [Pg.279]    [Pg.132]    [Pg.891]    [Pg.153]   
See also in sourсe #XX -- [ Pg.419 , Pg.426 , Pg.427 , Pg.428 , Pg.429 ]




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INDEX oxide

INDEX oxids

Oxidants INDEX

Oxidation indices

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