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Preparation compounds and

Pharmacy is the science of preparation, compounding and dispensing of drugs. It is concerned with collection, identification, purification, isolation, synthesis and standardization of medicinal /pharmaceutical substances. [Pg.3]

In CVD, solids are formed from gaseous compounds. In chemical vapour transport, a solid or solids interact with a volatile compound and a solid product is deposited in a different part of the apparatus. It is used both for preparing compounds and for growing crystals from powders or less pure crystalline material. [Pg.172]

The rheological phase reaction method offers a new and simple way to prepare compounds and materials. The prepared compounds LiCo YyMn2.x.y04 show excellent capacity and cycleability. The cathode behavior of the LiMn204 can be greatly improved by simultaneous doping of cobalt and yttrium, and our results on LiCo, YyMn2.x-y04 show that the composition with x=0.02, y=0.015 exhibits the best high current rate (IC) capacity up to 60 cycles. The compound after optimization may find potential application in practical lithium-ion cells. [Pg.129]

Orange needles very stable insoluble in water and dilute nonoxidizing acids readily soluble in ethanol, ether, acetone, benzene and other similar solvents [in contrast to Fe(CO)4Hg]. An easily prepared compound and an excellent starting material for the preparation of other cobalt carbonyl compounds. Thus, [Co(CO)4]aHg may be converted by alkali sulfides into alkali salts of Co(CO)4H, from which the hydride itself and Co(CO)4maybe obtained. [Pg.1756]

A cell of this design was employed in studies of microcrystal solids attached to a platinum flag electrode [608]. The measured ESR spectrum of electrochem-ically reduced 7,7, 8,8 -tetracyanoquinodimethane was in perfect agreement with the respective spectrum of the chemically prepared compound and the simulated spectrum. [Pg.151]

In a great number of cases, zeolites are used as auxiliary elements. They may act either as a framework to stabilize the sensor material, as filter layers (either catalytic or size restrictive) to enhance selectivity of a sensitive film, or as a preconcentrator of specific analytes from diluted solutions. For example, due to excellent chemical and thermal stability, zeolites can be used as a substrate to prepare compounds and devices with desirable fundamental physical and chemical properties (Xu et al. 2006). For example, inorganic or organic compounds, metal and metal-organic compounds, and their clusters can be assembled into the pores and cages in zeohtes. Some nanosized metal or metal oxide particles have been successfully inserted into the caves and the pores or highly dispersed on the external surface of zeohtes. [Pg.140]

Lecolley F, Tao L, Mantovani G, Durkin I, Lautru S, Haddleton DM (2004) A new approach to bioconjugates for proteins and peptides ( pegylation ) utilising living radical polymerisation. Chem Commun 2026. Electronic supplementary information (ESI) available Experimental procedures on prepared compounds and characterisation. See http //www.rsc. [Pg.66]

Place a suitable sample of the freshly prepared nitrito-complex in an oven at 150 C. At intervals say, 20, 40, 70, 110 minutes, take a small amount and run an ir spectrum and quickly prepare a 0.01 M solution and run die visible electronic spectrum between 400-750 nm. Compare these with the freshly prepared compound and with the spectra of the nitro-compound. Draw your conclusions. [Pg.208]

Both boron and aluminium chlorides can be prepared by the direct combination of the elements. Boron trichloride can also be prepared by passing chlorine gas over a strongly heated mixture of boron trioxide and carbon. Like boron trifluoride, this is a covalent compound and a gas at ordinary temperature and pressure (boiling point 285 K). It reacts vigorously with water, the mechanism probably involving initial co-ordination of a water molecule (p, 152). and hydrochloric acid is obtained ... [Pg.154]

Many of these sulphides occur naturally, for example iron(ll) sulphide, FeS (magnetic pyrites), and antimony(III) sulphide, Sb S, (stibnite). They can usually be prepared by the direct combination of the elements, effected by heating, but this rarely produces a pure stoichiometric compound and the product often contains a slight excess of the metal, or of sulphur. [Pg.288]

The student is recommended to carry out the preparation of iodo-benzene in order to gain experience in the preparation of aqueous solutions of diazonium compounds, and then to prepare a solution of benzenediazonium hydrogen sulphate with which to carry out the chief reactions that diazonium compounds undergo. [Pg.184]

The aniline and the monomethylaniline can be obtained from their respective sulphonyl derivatives by hydrolysis with 70% sulphuric acid (preparation, p. 109), the mixture of the sulphonyl compound and the acid being gently boiled under reflux to illustrate the separation of the three amines, however, this is not necessary. [Pg.251]

Zinc dust of good quality usually contains only negligible quantities of halogen and sulphur, and is nitrogen-free. A blank for these elements should, however, be made with every fresh batch of reagent prepared if perceptible traces of halogen or sulphur are present, a blank or control test must be performed side by side with that on the organic compound, and the results compared. [Pg.326]

Commercial preparations of acetyl chloride are best freed from volatile phos. phorus compounds and dissolved hydrogen chloride by redistillation from 5-10 per cent, of the volume of pure dimethylaniline. [Pg.367]

Add 4 0 g. (4 0 ml.) of pure anihne dropwise to a cold solution of ethyl magnesium bromide (or iodide) prepared from 1 Og. of magnesium, 5 0 g. (3-5 ml.) of ethyl bromide (or the equivalent quantity of ethyl iodide), and 30 ml. of pure, sodium-dried ether. When the vigorous evolution of ethane has ceased, introduce 0 02 mol of the ester in 10 ml. of anhydrous ether, and warm the mixture on a water bath for 10 minutes cool. Add dilute hydrochloric acid to dissolve the magnesium compounds and excess of aniline. Separate the ethereal layer, dry it with anhydrous magnesium sulphate and evaporate the ether. Recrystallise the residual anihde, which is obtained in almost quantitative yield, from dilute alcohol or other suitable solvent. [Pg.394]

Compounds containing two primary amino groups attached to a benzene ring can be prepared by the reduction of dinitro compounds and of nitroanilines, usually with tin or stannous chloride and hydrochloric acid or with iron and very dilute hydrochloric acid. / ara-diamines may also be obtained by the reduction of aromatic amino-azo compounds (e.g., p-aminodimethylanihne from methyl orange, see Section IV,78). p-Phenylenediamine may also be prepared from p-nitroacetanilide reduction with iron and acid yields p-amino-acetaniUde,.which may be hydrolysed to the diamine. [Pg.640]

Picric acid, the 2 4 6-trinitro derivative of phenol, cannot be prepared in good yield by the action of nitric acid upon phenol since much of the latter is destroyed by oxidation and resinous products are also formed. It is more convenient to heat the phenol with concentrated sulphuric acid whereby a mixture of o- and p-phenolsulphonic acids is obtained upon treatment of the mixture with concentrated nitric acid, nitration occurs at the two positicsis mela to the —SOjH group in each compound, and finally, since sulphonation is reversible, the acid groups are replaced by a third iiitro group yielding picric acid in both cases ... [Pg.666]

Hydroxyquinoline ( oxine ). The technique adopted in this preparation is based upon the fact that, in general, the reactants glycerol, amine, nitro compound and sulphuric acid can be mixed with temperature control, and then maintained at any convenient temperature below 120° without any appreciable chemical reaction taking place. A pre-mix of the amine, glycerol and sulphuric acid, maintained at a temperature which keeps it fluid (60-90°), is added in portions to a reaction vessel containiug the nitro compound and warmed with stirring to 140-170° at which temperature the Skraup reaction takes place. [Pg.830]

Chapters V-X deal respectively with Heterocyclic and Alicyclic Compounds Miscellaneous Reactions Organic Reagents in Inorganic and Organic Chemistry Dyestuffs, Indicators and Related Compounds Some Physiologically-Active Compounds and Synthetic Polymers. Many of these preparations are of course intended for advanced students, but a mere perusal of the experimental details of selected preparations by those whose time for experimental work is limited may assist to impress them on the memory. Attention is particularly directed to the chapter... [Pg.1193]

L. silex, silicis, flint) Davy in 1800 thought silica to be a compound and not an element later in 1811, Gay Lussac and Thenard probably prepared impure amorphous silicon by heating potassium with silicon tetrafluoride. [Pg.33]

Its natural and prepared compounds are widely used. Quicklime (CaO), which is made by heating limestone that is changed into slaked lime by carefully adding water, is the great base of chemical refinery with countless uses. [Pg.48]


See other pages where Preparation compounds and is mentioned: [Pg.97]    [Pg.110]    [Pg.4]    [Pg.481]    [Pg.193]    [Pg.129]    [Pg.347]    [Pg.78]    [Pg.71]    [Pg.72]    [Pg.399]    [Pg.406]    [Pg.72]    [Pg.34]    [Pg.97]    [Pg.110]    [Pg.4]    [Pg.481]    [Pg.193]    [Pg.129]    [Pg.347]    [Pg.78]    [Pg.71]    [Pg.72]    [Pg.399]    [Pg.406]    [Pg.72]    [Pg.34]    [Pg.48]    [Pg.94]    [Pg.215]    [Pg.226]    [Pg.261]    [Pg.319]    [Pg.362]    [Pg.2513]    [Pg.248]    [Pg.108]    [Pg.586]    [Pg.352]    [Pg.936]    [Pg.1193]    [Pg.48]    [Pg.59]   


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Biotransformations in the Preparation of Compounds Labeled with Carbon and Hydrogen Isotopes

Compound Preparation, Mixture Characterisation and Process Enhancement of Particulate-Filled Polymer Compounds

Compound preparation

Compounding preparations

Methods for the Preparation of Aromatic and Heteroaromatic Diazo Compounds

Preparation and Analysis of Cr(II) Compounds

Preparation and Properties of Organolithium Compounds

Preparation and Reactions of Organoboron Compounds

Preparation and Reactions of Organometallic Compounds

Preparation and Reactions of Organotin Compounds

Preparation from Halogen Compounds and Metal

Preparation of Alcohols, Ethers, and Related Compounds

Preparation of Azo and Diazoamino Compounds

Preparation of Diboron Compounds and Their Properties

Preparation of Organolithium and Organomagnesium Compounds

Preparation of Radiotracers and Their Compounds

Preparation of Thioarabinofuranosyl Compounds and Use Thereof

Preparation of metal carbonyls and organometallic compounds

Preparation of sealants and compounds

Preparation, Structure and Properties of Polyvalent Iodine Compounds

Preparation, Tests and Analysis of Mn(III) Compounds

Preparations and Reactions of Coordination Compounds

Preparative Extraction and Separation of Phenolic Compounds

Rare earth elements, and compounds preparation

Rare earth elements, and compounds thereof preparation

Synthetic Compounds Prepared and Tested

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