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Molecule amphoteric

Purines absorb only ultraviolet light and they contribute to structural colors (white and silver) in animals. Pterines are generally yellow, orange, or red pigments. Because they are amphoteric molecules, the absorption spectra depend on the pH and present three or two absorption maxima, usually one in the visible region. Sepiapterin has an absorption maximum at 340 nm in O.IM NaOH and at 410 nm in O.IM HCl." Leucopterin has three maxima 240, 285, and 340 nm. Xanthopterin has two 255 and 391 nm. Because they are conjugated with proteins, pterins show bathochromic shifts in vivo. They also present fluorescence when excited with UV light. [Pg.110]

Takacs-Novak, K. Jozan, M. Szasz, G., Lipophilicity of amphoteric molecules expressed by the true partition coefficient, Int. J. Pharm. 113, 47 (1995). [Pg.263]

Amphoteric molecules of this type, where the acidic and basic sites are relatively close to each other but cannot interact directly, can heterolytically cleave H-X and C-X bonds where X is a halide, alkoxide, amide, alcohol, thiol, trimethylsilyl, or alkyl group.18,18a The ability to effect changes in the reactivity of borollide complexes by adjusting metal oxidation states and ligands allows fine-tuning of catalytic and other properties, which in turn advances the application of these compounds in synthesis. [Pg.6]

In many respects the chlorine oxyfluorides resemble the chlorine fluorides. For example, they exhibit little or no self-ionization, but are amphoteric. With strong Lewis acids or bases they can form stable adducts. The tendency to form adducts was found (64) not to be so much a function of the relative acidity of the parent chlorine oxyfluoride but rather to depend on the structure of the amphoteric molecule and of that of the anion or the cation formed. The preferred structures are the energetically favored tetrahedron and octahedron. Consequently, a trigonal bipyramidal molecule, such as CIF3O (64), exhibits a pronounced tendency to form either a stable pseudotetrahedral cation or a pseudo-octahedral anion ... [Pg.327]

This type of interaction is not restricted to one dimension, as indicated in the formulation. The bonds between AsCls and SeOa would be much weaker if the amphoteric properties of the molecules were less well developed. This is analogous to bulk effects in solutions and solvate structures involving amphoteric molecules. [Pg.156]

In principle, amphoteric molecules should bind to both anionic and cationic exchangers. However, when one is dealing with large biomolecules, the pH range of stability must also be evaluated. The range of stability refers to the pH range in which the biomolecule is not denatured. Figure 3.8... [Pg.76]

An L-B film is formed by the dispersion of amphoteric molecules at an air-water surface (Figure 8.20). These molecules have a polar group at one end, something like a carboxy substituent (in this respect they resemble the surfactant molecules which make micelles), and a long non-polar aliphatic chain. The polar group stays in the polar water phase, and the aliphatic chain stays in the non-polar air environment. The L-B film at the water surface is then made by the controlled compression of these molecules by means of a floating barrier. The molecules then line up to form a mono-molecular layer on the water surface. [Pg.271]

The proposed reaction schemes (Figures 4-17 and 4-18) show the molecular breakdown commencing at the extremities of both molecules to leave a polar core that eventually separates from the liquid reaction medium. In the case of the decomposition of the amphoteric molecule, thermal degradation could just as easily commence at the aliphatic carbon sulfur bonds followed by thermal scission of the alkyl moieties from the aromatic systems. If the removal of the... [Pg.173]

Takacs-Novak, K., M. Jozan, and G. Szasz. 1995. Lipophilicity of Amphoteric Molecules Expressed by the True Partition Coefficient. Intern. J. Pharmaceut. 113, 47-55. [Pg.133]

Isoelectric An electrophoretic method for separating amphoteric molecules in pH gradients. [Pg.137]

Isoelectric focusing is performed in a pH gradient where amphoteric molecules like proteins move to the position in the gradient where the pH corresponds to that of the isoelectric point (pi) where their net charge is zero (Figure 4-20). [Pg.108]

Figure 4-31. Migration of amphoteric molecules in isoelectric focusing. The diagram illustrates the migration of an amphoteric molecule (pi = 8) in an IEF gel with a pH range 3-11. Figure 4-31. Migration of amphoteric molecules in isoelectric focusing. The diagram illustrates the migration of an amphoteric molecule (pi = 8) in an IEF gel with a pH range 3-11.
From equilibrium (28) it is seen that Ki and K2 constants determine the value of the isoelectric point of amphoteric molecules. In a general form the isoelectric point is equal to ... [Pg.721]

Amphoteric molecules such as/j-aminobenzoic acid (H2NC6H4COOH, where. H2... [Pg.219]

Each protein is composed of building blocks called amino acids. Amino acids are amphoteric molecules that is, they can act as either an acid or a base. In addition to their primary function as components of proteins, amino acids have several important biological roles. [Pg.113]

Specific Component of the Surface Free Energy of Heat-Treated Silicas. Specific interaction capacities of heat-treated silicas, that is, their ability to interact with polar molecules, were examined with chloroform (Lewis acid probe) and toluene and benzene (amphoteric molecules). Figure 2 provides examples of the evolution of the specific interaction parameter Zsp of the different silicas with chloroform as a probe. [Pg.248]


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See also in sourсe #XX -- [ Pg.110 ]

See also in sourсe #XX -- [ Pg.286 ]




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