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Acid anhydride regulation

Many compounds contain more than one functional group Prostaglandin Ei a hormone that regulates the relaxation of smooth muscles con tains two different kinds of carbonyl groups Classify each one (aldehyde ketone carboxylic acid ester amide acyl chloride or acid anhydride) Identify the most acidic proton in prostaglandin Ei and use Table 1 7 to estimate its pK ... [Pg.144]

Environmental Protection. Since alkali dichromates or chromic acid anhydride are used as starting materials for the production of chromium(III) oxides, occupational health requirements for the handling of hexavalent chromium compounds must be observed [3.59]. The sulfur dioxide formed on reduction with excess sulfur must be removed from the flue gases according to national regulations, e.g., by oxidation to... [Pg.97]

The role of the APS sulfohydrolases in sulfate metabolism is not understood precisely. The lysosomal APS sulfohydrolase can hydrolyze bis(4-nitro-phenyl) phosphate and 4-nitrophenyl 5 -phosphothymidine (Roger et al., 1978). Thus the lysosomal APS sulfohydrolase is less specific than its cytosolic counterpart, which does not hydrolyze these nitrophenyl derivatives. The apparent role of the lysosomal enzyme is to hydrolyze the acid anhydrides of such compounds as FAD, ATP, and ADP in secondary lysosomes. Thus lysosomal APS sulfohydrolase is an acid anhydride hydrolase that helps the cell in the recovery of nucleoside monophosphates from acid anhydrides. The APS sulfohydrolase in the cytosolic fraction probably regulates the concentrations of PAPS and therefore plays an important role in the control of sulfate conjugation. [Pg.174]

DISPOSAL AND STORAGE METHODS dissolve or mix the material with a combustible solvent and bum in a chemical incinerator equipped with an afterburner and scrubber dispose of in accordance with federal, state and local environmental regulations store in a cool, dry location use only with adequate ventilation keep container tightly closed separate fi om strong oxidizing agents, strong acids, acid chlorides, and acid anhydrides. [Pg.818]

From the chemical point of view, succinic acid and its anhydride are characterized by the reactivity of the two carboxyUc functions and of the two methylene groups. Uses range from pharmaceuticals to food, detergents, cosmetics, plastics and resins, plant growth regulators, textiles, photography, and gas and water treatment. [Pg.534]

Aconitic acid has been prepared from citric acid by the action of sulfuric acid or hydrogen chloride, or by heating. It has been prepared also from methyl acetylcitrate and from acetylcitric anhydride. The method described is essentially that of Hentschel. Phosphoric acid (85 per cent) can be used in place of sulfuric acid, but much closer regulation of the conditions seems necessary and the yield is not greatly improved. [Pg.3]

Conversion of p-benzoquinone into 1,2,4-triacetoxybenzene (Thiele acetylation). Add 11 g (0.1 mol) of p-benzoquinone in small portions to a mechanically stirred mixture of 33 g (0.32 mol) of acetic anhydride and 0.25 ml of concentrated sulphuric acid. The temperature of the mixture rises to 40-50 °C and is kept within this range by regulating the rate of addition of the quinone. When the addition is complete allow the solution to cool to about 25 °C and pour into 150ml of cold water. Collect the precipitated triacetate and recrystallise it from about 50 ml of rectified spirit the yield is 22 g (86%), m.p. 97 °C. [Pg.1026]

The copolymerization between trioxane and suitable comonomers (ethylene oxide, 1,3-dioxolane, diethylene glycol formal, 1,4-butane diol formal in amounts of 2-5% by weight) is performed using cationic initiators. The cationic initiators could be Lewis acids, such as BF3 or its etherate BF3Bu20 which was used, for example by Celanese (the mechanism of this reaction was studied in detail [163,164]) or protic acids such as perchloric acid, perfluoroalkane sulfonic acids and their esters and anhydrides. Heteropoly acids were used and also a series of carbenium, oxocarbenium salts, onium compounds, and metal chelates. To regulate the molecular weight chain-transfer agents, such as methylal and butylal, are added. [Pg.728]


See other pages where Acid anhydride regulation is mentioned: [Pg.205]    [Pg.116]    [Pg.146]    [Pg.425]    [Pg.425]    [Pg.290]    [Pg.538]    [Pg.463]    [Pg.90]    [Pg.30]    [Pg.85]    [Pg.186]    [Pg.11]    [Pg.374]    [Pg.570]    [Pg.105]    [Pg.160]    [Pg.88]    [Pg.425]    [Pg.425]    [Pg.6]    [Pg.310]    [Pg.758]    [Pg.46]    [Pg.463]    [Pg.635]    [Pg.206]    [Pg.538]    [Pg.88]    [Pg.109]    [Pg.635]    [Pg.50]    [Pg.259]    [Pg.52]   
See also in sourсe #XX -- [ Pg.369 ]




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Acidity regulators

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