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Salt reduction

Dehalogenating reduction Salt elimination Disproportionation Electrochemical formation Dehydrogenative catalytic coupling... [Pg.276]

Some of the current methods of increasing dissolution rates of drugs are particle size reduction, salt formation, and development of the optimized delivery systems, such as solid dispersion, soft gelatin encapsulation, etc. [Pg.31]

Use of the RP salt removal/concentration trap cartridges provides a rapid means for volume reduction, salt elimination and/or buffer exchange, since the entire procedure takes place in less than 5 minutes. With volumes... [Pg.283]

Chemical Species Percent by Weight Percent of Total Solids as Salts Volume Reduction Salt Precipitated... [Pg.44]

Water reduction Salts of sulfonated naphthalene and melamine formaldehyde condensates, lignosulfonates... [Pg.319]

Chemical skin injuries differ from thermal and electrical bums in pathophysiology. Jelenko [179] stated that chemical skin injuries are different in mechanisms from those injuries caused by exposure to heat or flames [179], These mechanisms were coagulation by protein oxidation, reduction, salt formation, corrosion, protoplasmic poisoning, metabolic competition of inhibition, desiccation, and vesicant action with resultant ischemia [179],... [Pg.131]

Azo-compounds can be obtained by reduction of nitro-compounds, or by oxidation of hydrazo-compounds. They are usually prepared, however, by reacting a phenol or amine with a diazonium salt. The coupling usually takes place in the position para to the hydroxyl or amino group, but if this position is occupied it goes to the ortho position, e.g. [Pg.49]

Ethylamine, monoethylamine, CH3CH2NH2-B.p. 19 C. Prepared by reduction of acetonitrile or by heating ethyl chloride with alcoholic ammonia under pressure. It is a strong base and will displace ammonia from ammonium salts. Forms a crystalline hydrochloride and also crystalline compounds with various metallic chlorides. [Pg.166]

Europium(TTI) salts are typical lanthanide derivatives. Europium(ll) salts are pale yellow in colour and are strong reducing agents but stable in water. EuX2 are prepared from EuX -hEu (X=C1, Br, I) or EuFa + Ca EuCl2 forms a dihydrale. EUSO4 is prepared by electrolytic reduction of Eu(III) in sulphuric acid. Eu(II) is probably the most stable +2 stale of the lanthanides... [Pg.170]

Colourless crystals m.p. 50 C, b.p. 301 C. Basic and forms sparingly soluble salts with mineral acids. Prepared by the reduction of 1-nitronaphthalene with iron and a trace of hydrochloric acid or by the action of ammonia upon l-naphlhol at a high temperature and pressure. [Pg.270]

CfiHsNjOs. Red needles m.p. 168-169°C. Soluble in dilute acids and alkalis. Prepared by reduction of picric acid with sodium hydrogen sulphide, ft is used for the preparation of azodyes, which can be after-chromed by treatment with metallic salts owing to the presence of a hydroxyl group ortho to the amino-group. [Pg.313]

NH2-C0-NH NH2,CH5N30. Colourless crystalline substance m.p. 96" C. Prepared by the electrolytic reduction of nitrourea in 20% sulphuric acid at 10 "C. Forms crystalline salts with acids. Reacts with aldehydes and ketones to give semicarbazones. Used for the isolation and identification of aldehydes and ketones. [Pg.355]

H02C(CH2)2C02H. Colourless prisms m.p. 182 C, b.p. 235°C. Occurs in amber, algae, lichens, sugar cane, beets and other plants, and is formed during the fermentation of sugar, tartrates, malates and other substances by a variety of yeasts, moulds and bacteria. Manufactured by the catalytic reduction of maleic acid or by heating 1,2-dicyanoethane with acids or alkalis. Forms an anhydride when heated at 235°C. Forms both acid and neutral salts and esters. Used in the manufacture of succinic anhydride and of polyesters with polyols. [Pg.375]

Vanadium IV) forms blue VOSO4, (0, 3 and 5H2O), vanadyl sulphate, which forms ranges of double salts, Prepared by SO, reduction of V2O5 in H2SO4. [Pg.417]

Vanadium II) forms green V2(S04)3 (electrolytic or Mg reduction of V2O5 in H2SO4). Alums and other double salts are formed. [Pg.417]

Vanadium II) forms violet VS04,7H20 (electrolytic or Na/Hg reduction). Forms double salts. [Pg.417]

One prevalent strategy for this involves tire use of a phase transfer agent, such as tetraoctyl ammonium bromide, to bring gold and silver salts into an organic phase [12, and. Reduction of tire metal salts... [Pg.2902]

Using the electron transfer definition, many more reactions can be identified as redox (reduction-oxidation) reactions. An example is the displacement of a metal from its salt by a more reactive metal. Consider the reaction between zinc and a solution of copper(If) sulphate, which can be represented by the equation... [Pg.93]

Each of these elements can be extracted by reduction of the respective oxide at high temperature, using either carbon or hydrogen or by electrolysis of an aqueous solution of a salt of the required element. [Pg.143]

This provides a method of estimating an iron(lll) salt. After reduction the iron(II) salt is titrated with manganate(VII) solution. [Pg.198]

If the acid of the ammonium salt is an oxidising agent, then on heating the salt, mutual oxidation and reduction occurs. The oxidation products can be nitrogen or one of its oxides and the reactions can be explosive, for example ... [Pg.221]

Reduction products vary depending on the reducing agent, for example dinitrogen oxide is obtained with sulphurous acid, nitrogen is obtained when the gas is passed over heated metals (e.g. copper and iron) and ammonia is produced when the gas reacts with aqueous chromiumfll) salts. [Pg.231]


See other pages where Salt reduction is mentioned: [Pg.501]    [Pg.4882]    [Pg.195]    [Pg.195]    [Pg.195]    [Pg.196]    [Pg.436]    [Pg.4881]    [Pg.446]    [Pg.436]    [Pg.501]    [Pg.4882]    [Pg.195]    [Pg.195]    [Pg.195]    [Pg.196]    [Pg.436]    [Pg.4881]    [Pg.446]    [Pg.436]    [Pg.28]    [Pg.37]    [Pg.99]    [Pg.194]    [Pg.211]    [Pg.212]    [Pg.275]    [Pg.291]    [Pg.324]    [Pg.395]    [Pg.395]    [Pg.401]    [Pg.417]    [Pg.2783]    [Pg.301]    [Pg.367]    [Pg.376]    [Pg.379]   


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1- Methylquinolinium salt, reduction with

1- Methylquinolinium salt, reduction with tributylstannyl hydride

1.2.4- Triazolium salts reduction

1.4.2- Dithiazolium salts, reduction

A-Carbolinium salts, alkyl reduction

Alkenes, reduction salts

Amidinium salts reduction

Ammonium salts electrolytic reduction

Ammonium salts reduction

Ammonium salts, alkyl reduction

Ammonium salts, alkyl tetraalkyl, reduction

Arenediazonium salt reduction

Arsonium salts, reductive cleavage

Benzenediazonium salt, reduction

Benzothiazolium salts reduction

Bisphosphonium salts reduction

Chromium salts reduction

Cobalt, bis catalyst partial reduction of pyridinium salts

Colloid salt reduction

Copper salts reduction

Copper salts reduction, aromatic nitro compounds

Copper salts, cation reductions

Cyclimmonium salts reductive

Diazonium salts aryl, reduction

Diazonium salts reduction

Diazonium salts reduction with sodium sulfite

Diazonium salts reductive cleavage

Diazonium salts, amine reactions reduction

Diazonium salts, aryl reduction, reagents

Electrochemical Reduction of Metal Salts

Electrochemical reduction chromium salt catalyst

Electrochemical reduction pyridinium salts

Enamine salts reduction

Ethanol reduction of aryl diazonium salts

Ferric salts, reduction

Formiminium salts reduction

Fuel molten salt oxidation-reduction

Halide salts reductive cleavage

Hydroxylamine salts reductants

Imidazolium salts reduction

Iminium salts cathodic reduction

Iminium salts reduction by samarium diiodide

Indazolium salts reduction

Iodonium salt reduction

Isoquinolinium salts reduction

Isoxazolium salts, reduction

Lukes reduction pyridinium salts

Metallic salts, adsorption reduction

Metals salts reduction

Molybdenum salts reduction

Optically active phosphonium salts, reduction

Oxazolinium salts reduction

Oxazolium salts reduction

Oxidation-reduction reactions molten salt extraction

Phosphonium salts reduction

Phosphonium salts, reductive cleavage

Pyridinium salts dithionite reduction

Pyridinium salts lithium aluminum hydride reduction

Pyridinium salts reduction with dithionite

Pyridinium salts, reduction

Quaternary ammonium salts, reduction

Quaternary pyridinium salts, reduction

Quinolinium salts reduction

Reactions oxidation-reduction, molten salt

Reduction Reinecke salt

Reduction aryldiazonium salt

Reduction of Phosphonium Salts

Reduction of aryl diazonium salts

Reduction of diazonium salts

Reduction of iminium salts

Reduction of metal salts

Reduction of solid silver salts

Reduction process molten salt electrolysis

Reduction with Hydrazinium Salt

Reduction, of iminium salts, with

Reductions by Electrochemically Generated Low-Valent Metal Salts and Base Metals

Reductive dealkylation of quaternary ammonium salts

Sulfite, sodium, reduction diazonium salts

Symmetry reduction salts

Tetrazolium salts electrochemical reduction

Tetrazolium salts, reduction

Titanium salts reduction

Titanium salts reductive cleavage

Tungsten salts reduction

Vanadium salts reduction

Viologen salts, reduction

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