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Dehydrating agents, organic

Perchlorates and perchloric acid. At 160° perchloric acid is an exceedingly strong oxidising acid and a strong dehydrating agent. Organic perchlorates, such as methyl and ethyl perchlorates, are unstable and are violently... [Pg.29]

A simpler nonphosgene process for the manufacture of isocyanates consists of the reaction of amines with carbon dioxide in the presence of an aprotic organic solvent and a nitrogeneous base. The corresponding ammonium carbamate is treated with a dehydrating agent. This concept has been apphed to the synthesis of aromatic and aUphatic isocyanates. The process rehes on the facile formation of amine—carbon dioxide salts using acid haUdes such as phosphoryl chloride [10025-87-3] and thionyl chloride [7719-09-7] (30). [Pg.448]

Organic Reactions. Nitric acid is used extensively ia iadustry to nitrate aHphatic and aromatic compounds (21). In many iastances nitration requires the use of sulfuric acid as a dehydrating agent or catalyst the extent of nitration achieved depends on the concentration of nitric and sulfuric acids used. This is of iadustrial importance ia the manufacture of nitrobenzene and dinitrotoluene, which are iatermediates ia the manufacture of polyurethanes. Trinitrotoluene (TNT) is an explosive. Various isomers of mononitrotoluene are used to make optical brighteners, herbicides (qv), and iasecticides. Such nitrations are generally attributed to the presence of the nitronium ion, NO2, the concentration of which iacreases with acid strength (see Nitration). [Pg.39]

The steric bulk of steroid structures prevents their use as the only organic side group present. However, mixed-substituent polymers that contain both steroidal side groups and amino acid ester or other cosubstituent units can be readily synthesized. If a saturated A ring is present in the steroid, linkage to the polymer chain is complicated by side reactions that result from dehydration of the steroid (chlorophosphazenes are powerful dehydrating agents). [Pg.176]

Because trifluoromethanesulfonic acid is a stronger acid than perchloric acid, under no circumstances should perchlorate salts be used with the neat acid, because the hot anhydrous perchloric acid so formed represents an extreme explosion hazard, especially in contact with transition metal complexes (or with organic materials). See Perchloric acid Dehydrating agents See other ORGANIC ACIDS... [Pg.152]

Both triflouroacetic acid and sulfur trioxide will cause very severe skin burns, and their vapors are extremely irritating. Sulfur trioxide is such a strong dehydrating agent that it chars organic material, and its heat of dehydration is so high that it will start a fire if spilled on wood, which could prove fatal were flammable solvents in use at the time or stored nearby. [Pg.125]

The development of the colour is carried out in the organic phase used for extraction by the addition of curcumin in glacial acetic acid and phosphoric acid as dehydrating agent. Spectrophotometric evaluation is carried out at 510nm. [Pg.312]

Sodium amide is a dehydrating agent. It is used in preparing sodium cyanide and hydrazine, and in many organic synthetic reactions such as Claisen condensations, alkylations of ketones and nitriles, and in ammonoly-sis reactions. [Pg.853]


See other pages where Dehydrating agents, organic is mentioned: [Pg.5]    [Pg.29]    [Pg.3]    [Pg.5]    [Pg.5]    [Pg.5064]    [Pg.226]    [Pg.150]    [Pg.137]    [Pg.5]    [Pg.29]    [Pg.3]    [Pg.5]    [Pg.5]    [Pg.5064]    [Pg.226]    [Pg.150]    [Pg.137]    [Pg.194]    [Pg.252]    [Pg.38]    [Pg.174]    [Pg.187]    [Pg.399]    [Pg.86]    [Pg.426]    [Pg.76]    [Pg.438]    [Pg.69]    [Pg.385]    [Pg.965]    [Pg.56]    [Pg.572]    [Pg.37]    [Pg.69]    [Pg.449]    [Pg.489]    [Pg.188]    [Pg.508]    [Pg.44]    [Pg.1594]    [Pg.419]    [Pg.455]    [Pg.145]    [Pg.213]    [Pg.43]    [Pg.198]    [Pg.157]    [Pg.899]   


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Dehydrate agent

Dehydrating agent

Dehydration organic

Organic agents

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