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Mixed solvent solubility

Keywords Gas solubility Mixed solvents Polymer solutions... [Pg.172]

Keywords Drug solubility Mixed solvent Thermodynamic consistency test... [Pg.232]

When the correct solvent for recrystallisation is not known a procedure similar to that given on pp. 15-16 should be followed, but on the semi-micro scale not more than 10 mg. of the solid should be placed in the tapered-end test-tube (Fig. 29(B)) and about o i ml. of the solvent should be added from the calibrated dropping-pipette (Fig. 30(B)). If the compound dissolves readily in the cold, the solvent is unsuitable, but the solution should not be discarded. [In this case recourse should be had to the use of mixed solvents (p. 18). For example if the substance is very soluble in ethanol, water should be added from a calibrated pipette with shaking to determine whether crystallisation will now take place, indicated by a cloudiness or by the separation of solid.]... [Pg.67]

If the substance is found to be far too soluble in one solvent and much too insoluble in another solvent to allow of satisfactory recrystallisation, mixed solvents or solvent pairs may frequently be used with excellent results. The two solvents must, of course, be completely miscible. Recrystallisation from mixed solvents is carried out near the boiling point of the solvent. The compound is dissolved in the solvent in which it is very soluble, and the hot solvent, in which the substance is only sparingly soluble, is added cautiously until a slight turbidity is produced. The turbidity is then just cleared by the addition of a small quantity of the first solvent and the mixture is allowed to cool to room temperature crystals will separate. Pairs of liquids which may be used include alcohol and water alcohol and benzene benzene and petroleum ether acetone and petroleum ether glacial acetic acid and water. [Pg.125]

Mixed Solvents. Where a substance is too soluble in one solvent and too insoluble in another, for either to be used for recrystallisation, it is often possible (provided they are miscible) to use them as a mixed solvent. (In general, however, it is preferable to use a single solvent if this is practicable.) Table 8 contains many of the common pairs of miscible solvents. [Pg.16]

Mixed solvents are intermediate in strength, and so provide a finely graded series. In choosing a solvent for use as an eluent it is necessary to consider the solubility of the substance in it, and the ease with which it can subsequently be removed. [Pg.19]

Supersaturation can also be achieved by adding a liquid that is miscible with the solvent and decreases the solubility of the solute in the mixed solvent. This is called precipitation. In fine chemicals manufacture, the solid is usually dissolved in an organic solvent and water is used as the desalting agent. Precipitation also occurs when a solid product, which is insoluble in the reaction mixture, is formed by chemical reaction. For instance, a phenolic product can be purified by three possible routes ... [Pg.240]

The solubihty parameter theory can be also used for the mixed-solvent systems. The total-solubility parameter 8, is given by the sum of the individual solubihty parameters in terms of the volume fractions (pj in the mixture, according to Equation 4.6 ... [Pg.73]

If the compound is virtually insoluble (solubility mixed solvent approach can be tried [2, 28-30]. For example, the pka of the antiarrhythmic amiodarone, 9.06 0.14, was estimated from water-methanol... [Pg.60]

Isohydric 385 localizing 378 mixed solvents strength 465 isoeluotropic 467 properties 460 solubility parameters 460 solvatochromic parameters 461 solvent triangle classification 463 types 458... [Pg.517]

It is advantageous with a new drug substance to be able to estimate what its solubility will be prior to carrying out dissolution experiments. There are several systems of solubility prediction, most notably those published by Amidon and Yalkowsky [14-16] in the 1970s. Their equation for solubility of p-aminobenzo-ates in polar and mixed solvents is a simplified two-dimensional analog of the Scatchard-Hildebrand equation and is based on the product of the interfacial tension and the molecular surface area of the hydrocarbon portion of a molecule. [Pg.178]

Drug solubility can be increased by the use of solubilizing agents, such as those listed in Table 2, and by nonaqueous solvents or mixed solvent systems, to be... [Pg.394]

In this study, we extend the range of inorganic materials produced from polymeric precursors to include copper composites. Soluble complexes between poly(2-vinylpyridine) (P2VPy) and cupric chloride were prepared in a mixed solvent of 95% methanol 5% water. Pyrolysis of the isolated complexes results in the formation of carbonaceous composites of copper. The decomposition mechanism of the complexes was studied by optical, infrared, x-ray photoelectron and pyrolysis mass spectroscopy as well as thermogravimetric analysis and magnetic susceptibility measurements. [Pg.430]

Special care has to be taken if the polymer is only soluble in a solvent mixture or if a certain property, e.g., a definite value of the second virial coefficient, needs to be adjusted by adding another solvent. In this case the analysis is complicated due to the different refractive indices of the solvent components [32]. In case of a binary solvent mixture we find, that formally Equation (42) is still valid. The refractive index increment needs to be replaced by an increment accounting for a complex formation of the polymer and the solvent mixture, when one of the solvents adsorbs preferentially on the polymer. Instead of measuring the true molar mass Mw the apparent molar mass Mapp is measured. How large the difference is depends on the difference between the refractive index increments ([dn/dc) — (dn/dc)A>0. (dn/dc)fl is the increment determined in the mixed solvents in osmotic equilibrium, while (dn/dc)A0 is determined for infinite dilution of the polymer in solvent A. For clarity we omitted the fixed parameters such as temperature, T, and pressure, p. [Pg.222]

The third effective approach is the preparation of ionic Pcs with large balanced ions [69-77], It is well known that ionic compounds are usually more soluble than neutral compounds in most organic solvents, especially in polar and mixing solvents. Ionic Pcs include cationic and anionic Pcs. The preparation of ionic Pcs is usually by means of electrochemistry. Sometimes they can be synthesized through oxidation reactions, ion exchange reactions or ion coordination reactions. [Pg.55]

Gas solubility in mixed solvents (and, therefore, Henry s constant) varies with solvent composition. The simplest approximation for this is given in Eq. (16) [23] ... [Pg.1525]

From this, you should get the idea that it would be good to use a mixed solvent to recrystallize compounds that are soluble in alcohol yet insoluble in water. You see, each solvent alone cannot be used. If the material is soluble in the alcohol, not many crystals come back from alcohol alone. If the material is insoluble in water, you cannot even begin to dissolve it. So, you have a mixed solvent, with the best properties of both solvents. To actually perform a mixed-solvent recrystallization you... [Pg.105]

Add more solvent. If it s a mixed-solvent system, try adding more of the solvent the solid is NOT soluble in. Or add more of the OTHER solvent. No contradiction. The point is to change the composition. Single solvent or mixed solvent, changing the composition is one way out of this mess. [Pg.106]


See other pages where Mixed solvent solubility is mentioned: [Pg.329]    [Pg.455]    [Pg.63]    [Pg.329]    [Pg.170]    [Pg.229]    [Pg.297]    [Pg.60]    [Pg.298]    [Pg.21]    [Pg.56]    [Pg.185]    [Pg.396]    [Pg.25]    [Pg.29]    [Pg.137]    [Pg.205]    [Pg.200]    [Pg.515]    [Pg.347]    [Pg.34]    [Pg.16]    [Pg.19]    [Pg.357]    [Pg.426]    [Pg.306]    [Pg.306]    [Pg.307]    [Pg.133]    [Pg.125]   


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