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Materials alcohols

The chemical resistance of PCTFE is good but not as good as that of PTFE. Under certain circumstances substances such as chlorosulphonic acid, molten caustic alkalis and molten alkali metal will adversely affect the material. Alcohols, acids, phenols and aliphatic hydrocarbons have little effect but certain aromatic hydrocarbons, esters, halogenated hydrocarbons and ethers may cause swelling at elevated temperatures. [Pg.375]

There is a risk of acute renal failure when iodi-nated contrast material that is used for radiological studies is administered with metformin. Metformin therapy is stopped for 48 hours before and after radiological studies using iodinated material. Alcohol, amiloride, digoxin, morphine, procainamide, quini-dine, quinine ranitidine, triamterene, trimethoprim, vancomycin, cimetidine, and furosemide all increase the risk of hypoglycemia. There is an increased risk of lactic acidosis when metformin is administered with the glucocorticoids. [Pg.504]

To check the completion of the reaction depicted in Scheme 12.9, single bead FTIR seemed quite conclusive because the IR band from the starting material (alcohol) has converted to the product carbonate band (Fig. 12.13). The hydroxyl stretch disappeared completely in the FTIR data. However, the possible presence of a trace amount of hydroxyl groups might not be evident in the IR spectrum. The fluorescent dye 9-anthroylnitrile reacted with resin-bound alcohol and it was very sensitive in detecting trace amount of hydroxyl groups [19]. It was used to detect the residual resin-bound alcohol and to confirm the reaction completion. [Pg.511]

Caution. l,3-Diaza-2-boracycloalkanes are moisture-sensitive and react readily with protonic materials. Alcohols, in particular, may occasionally cause an explosive solvolysis reaction on contact with these heterocycles. The compounds should be handled under dry inert gas (nitrogen or argon) to avoid their contamination. The possible toxicity of boron compounds has not yet been explored. [Pg.165]

After completion of the reaction, the resultant NO gas, the unreacted starting materials, alcohol, the desired intermediate (i.e., l-phenyl-2,2-dialkoxypropanes), the optional amines and copper compounds are distilled under a reduced pressure and recovered. [Pg.55]

CHLORINE FLUORIDE OXIDE (7616-94-6) Noncombustible, but many chemical reactions can cause fire and explosions. A powerful oxidizer. Reacts violently with reducing materials, alcohols, alkalis, amines, anilines, benzene, butyl-amine, calcium hydride, calcium acetylide, charcoal, combustible materials, ethers, hydrazine, hydrogen sulfide, finely divided metals, nitric oxide, olefins, orgtinic substances, potassium cyanide, potassium thiocyanate, sodium, strontium hydride, sulfur, sulfur dichloride, sulfuric acid. Incompatible with hydrogen sulfide, potassium thiocyanate, vinylidene chloride. Forms heat-, friction-, and shock-sensitive explosives with calcium hydride, nitrogenous bases, isopropylamine. Attacks some plastics, rubber, and coatings. [Pg.283]

Materials Alcohols and normal octane were supplied by Fisher Scientific Company and Phillips Petroleum Company, respectively, and were 99+ mole % purity. One surfactant used was a synthetic sodium dodecyl orthoxylene sulfonate provided by Exxon Chemical Company. After deoiling, the product is a light beige crystal. [Pg.118]

The effect of surface active agents, caustic materials, alcohols, etc., can be explained through wettability alteration, molecular interaction, mutual adsorption, and changes in the coil and the solution structure. No general explanation exists and all special systems must be treated individually. [Pg.840]

Oxyethylation is a moderately fast gas-liquid reaction in which mass transfer and reaction are consecutive, often rate-determining processes. A kinetic model [34,40-42] was proposed for oxyethylation of various starting materials (alcohols, alkylphenols, and fatty acids), carried ont in the presence of a typical alkaline catalyst. Oxyethylation of nonylphenol carried out in an autoclave under common conditions and vigorous mixing (up to 3000 rpm) is controlled by diffusion. [Pg.277]

Strict specificity toward a coenzyme regardless of the source material. Alcohol dehydrogenase isolated from yeast and horse liver reacts with DPN but not at all with TPN. Triosephosphate dehydrogenase might have been cited as another example of strict DPN specificity except that current... [Pg.292]

The high hydrogen bonding character of alcoholic solvents makes these substances valuable solvents for dissolving many polymeric and resin-like materials. Alcoholic fianctionai groups are also valuable reaction sites for a large number of synthetic reactions of commercial importance. [Pg.32]

ABSOLUTES. Entirely alcohol-soluble extracts prepared by alcohol extraction of concretes or related fat-soluble or waxy materials, alcohol-insoluble substances being removed before evaporation of the solvent ABTS. 2,2 -Azino-bis-(3-ethyl-1,2-dihydro-benzothiazoline 6-sulfonate)... [Pg.695]


See other pages where Materials alcohols is mentioned: [Pg.21]    [Pg.95]    [Pg.80]    [Pg.16]    [Pg.68]    [Pg.69]    [Pg.133]    [Pg.133]    [Pg.266]    [Pg.266]    [Pg.270]    [Pg.339]    [Pg.339]    [Pg.340]    [Pg.414]    [Pg.636]    [Pg.637]    [Pg.678]    [Pg.889]    [Pg.890]    [Pg.951]    [Pg.954]    [Pg.955]    [Pg.1091]    [Pg.1092]    [Pg.410]    [Pg.762]    [Pg.763]    [Pg.1063]    [Pg.167]    [Pg.89]    [Pg.73]    [Pg.409]    [Pg.52]   
See also in sourсe #XX -- [ Pg.132 , Pg.133 ]




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Alcohol reaction with active materials

Alcohols as starting materials

Amino alcohols as starting materials

Embolic materials polyvinyl alcohol particles

Phosphate esters alcohol starting material

Polymeric materials polyvinyl alcohol

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