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Conjugates availability

The absence of coplanarity in both 1-phenyl- and 4-phenyldibenzo-thiophene degenerates their UV spectra to that of dibenzothiophene. In contrast, the main absorption bands of the 2- and 3-phenyl derivatives exhibit the expected bathochromic shift, indicating enhanced conjugation. Available data for the UV absorption of 1,2,3,4-tetraphenyl-dibenzothiophene is insufficient to correlate with these deductions. ... [Pg.201]

The tautomer (78) is the most stable form of 2-hydroxy thiophene (76). The conjugation available between the double bond stabilizes this form over (77). The position of equilibrium can, of course, be affected by other substituents on the thiophene ring. Likewise 3-hydroxythiophene (79) occurs chiefly as its tautomer (80). [Pg.727]

Table 1.1 Polymer-protein conjugates available commercially, or in clinical development... Table 1.1 Polymer-protein conjugates available commercially, or in clinical development...
Antidigoxigenin antibody/alkaline phosphatase conjugate (available from Boehringer) A1/5000 dilution in Buffer 1 should be made immediately before use (Section 3.2., step 4). 30 mL are required for one 10 x 18 cm filter, 70 mL for 10 filters. [Pg.122]

Antifluorescein antibody/horseradish peroxidase conjugate. Available from Amersham International (RPN 3022). [Pg.136]

The BFC needs to be attached to a biomolecule. There are many functional groups for conjugation available some will be discussed later in this chapter. The conditions to perform the reaction between biomolecule and BFC have to be compatible with the properties of the two molecules. Undesired modifications of the biomolecule might lead to a loss of binding affinity of the radiopharmaceutical. To introduce a conjugation site to the BFC, the backbone of the chelator may be modified as follows ... [Pg.2148]

Some of pastes/putties based on granular ceramic-polymer conjugation available on the market are listed in Table 9.2. [Pg.246]

The subroutine is well suited to the typical problems of liquid-liquid separation calculations wehre good estimates of equilibrium phase compositions are not available. However, if very good initial estimates of conjugate-phase compositions are available h. priori, more effective procedures, with second-order convergence, can probably be developed for special applications such as tracing the entire boundary of a two-phase region. [Pg.128]

Let us consider RRS that contams both of the available additional resonances, as is nomially the case (though carefiil choices of colours and their time sequence can isolate one or the other of these). First, we seek out the doorway events that contain not only the usual Raman resonance after the two fields, 1 and 2, have acted conjugately, but also the new resonance that appears after the first field has acted. The appropriate doorway generators remain S and e ei, in order to retain the Raman resonance. There are now two fully resonant... [Pg.1201]

Tbis tecbnic ne is available only for the MM-i- force field. As is true for the conjugate gradient methods, yon should noi use this algorithm when the initial interatomic forces are very large (meaning, the molecular structure is far from a inmiimim). [Pg.60]

The most used EIA reagents conjugate a fluotophote such as fluorescein-isothiocyanate (EITC) or thodarnine—isothiocyanate to antibody (or antigen) free amino groups. Examples of other commonly used fluotophotes for EIA and their spectral characteristics ate presented in Table 3. EIA assays ate available in sandwich and competitive formats similar to EIAs. Unlike EIA kits which can be used directly with visual color deterrnination, EIAs require a fluorometer, and thus ate primarily laboratory-based. [Pg.26]

Isomerization. Maleic acid is isomerized to fumaric acid by thermal treatment and a variety of catalytic species. Isomerization occurs above the 130 to 140°C melting point range for maleic acid but below 230°C, at which point fumaric acid is dehydrated to maleic anhydride. Derivatives of maleic acid can also be isomerized. Kinetic data are available for both the uncatalyzed (73) and thiourea catalyzed (74) isomerizations of the cis to trans diacids. These data suggest that neither carbonium ion nor succinate intermediates are involved in the isomerization. Rather, conjugate addition imparts sufficient single bond character to afford rotation about the central C—C bond of the diacid (75). [Pg.452]

The primary disadvantage of the conjugate addition approach is the necessity of performing two chiral operations (resolution or asymmetric synthesis) ia order to obtain exclusively the stereochemicaHy desired end product. However, the advent of enzymatic resolutions and stereoselective reduciag agents has resulted ia new methods to efficiently produce chiral enones and CO-chain synthons, respectively (see Enzymes, industrial Enzymes in ORGANIC synthesis). Eor example, treatment of the racemic hydroxy enone (70) with commercially available porciae pancreatic Hpase (PPL) ia vinyl acetate gave a separable mixture of (5)-hydroxyenone (71) and (R)-acetate (72) with enantiomeric excess (ee) of 90% or better (204). [Pg.162]

Data collected on the uv spectra of steroids are available in several books, spectmm adases, and review articles (263). The most characteristic absorptions in steroid hormones include a,P-unsaturated ketones, conjugated dienes, and phenoHc A-rings (264). [Pg.448]

Another group of conjugated thiophene molecules for future appHcations are those being developed as nonlinear optical (NLO) devices (75). Replacement of benzene rings with thiophene has an enormous effect on the molecular nonlinearity of such molecules. These NLO molecules are able to switch, route, and modulate light. Technology using such materials should become available by the turn of the twenty-first century. [Pg.24]

Among the appHcations of lower valent titanium, the McMurry reaction, which involves the reductive coupling of carbonyl compounds to produce alkenes, is the most weU known. An excellent review of lower valent titanium reactions is available (195). Titanium(II)-based technology is less well known. A titanium(II)-based complex has been used to mediate a stetio- and regio-specific reduction of isolated conjugated triple bonds to the corresponding polyenes (196). [Pg.153]

The apphcation of a high electric field across a thin conjugated polymer film has shown the materials to be electroluminescent (216—218). Until recentiy the development of electroluminescent displays has been confined to the use of inorganic semiconductors and a limited number of small molecule dyes as the emitter materials. Expansion to the broad array of conjugated polymers available gives advantages in control of emission frequency (color) and facihty in device fabrication as a result of the ease of processibiUty of soluble polymers (see Chromogenic materials,electrochromic). [Pg.45]

Lipoxygenase-Catalyzed Oxidations. Lipoxygenase-1 catalyzes the incorporation of dioxygen into polyunsaturated fatty acids possessing a l(Z),4(Z)-pentadienyi moiety to yield ( ),(Z)-conjugated hydroperoxides. A highly active preparation of the enzyme from soybean is commercially available in purified form. From a practical standpoint it is important to mention that the substrate does not need to be in solution to undergo the oxidation. Indeed, the treatment of 28 g/L of linoleic acid [60-33-3] with 2 mg of the enzyme results in (135)-hydroperoxide of linoleic acid in 80% yield... [Pg.349]


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See also in sourсe #XX -- [ Pg.68 ]




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Conjugated linoleic acid commercial availability

Hydrogen availability selective, conjugated dienes

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