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Quaternary dependence

Amines and amides are classified as primary, secondary, tertiary, or quaternary depending on the number of bonds from nitrogen to carbon(Following fig.). Note that a quaternary amine is positively charged and is therefore known as a quaternary ammonium ion. It is not possible to get a quaternary amide. [Pg.75]

Figure 3.3 A schematic of the core of a high-pressure mixing (two-pump) system. The pumps are called binary, ternary or quaternary depending upon the number of solvents that can be mixed together (here binary). The mixing chamber, which controls the mobile phase composition, is at the output of the two high-pressure pumps on the downstream side of the pumps. Figure 3.3 A schematic of the core of a high-pressure mixing (two-pump) system. The pumps are called binary, ternary or quaternary depending upon the number of solvents that can be mixed together (here binary). The mixing chamber, which controls the mobile phase composition, is at the output of the two high-pressure pumps on the downstream side of the pumps.
The specific sequence of amino acids in a protein determines its structure, conformation, and physicochemical properties. The structure of protein is categorized as primary, secondary, tertiary, or quaternary, depending on the progressive state of spatial arrangement of polypeptide chains of the protein (1,2). Although the primary structures of almost all major food proteins are known, the exact conformation of only a few native proteins e.g. 9-lactoglobulin has been elucidated (3-5). [Pg.629]

Temary and quaternary semiconductors are theoretically described by the virtual crystal approximation (VGA) [7], Within the VGA, ternary alloys with the composition AB are considered to contain two sublattices. One of them is occupied only by atoms A, the other is occupied by atoms B or G. The second sublattice consists of virtual atoms, represented by a weighted average of atoms B and G. Many physical properties of ternary alloys are then expressed as weighted linear combinations of the corresponding properties of the two binary compounds. For example, the lattice constant d dependence on composition is written as ... [Pg.2880]

A sufficient concentration of base B is necessary for the removal of a proton of the CH, group. In a first step, the equilibrium in Scheme 20 results, in which the monomeric anhydrobase Bi constitutes the conjugated base of the quaternary salt A,. As has been shown for other rings (24). the equilibrium depends upon the concentration of the different species and the relative strength of the bases B and Bj, and depends also upon the nature of X. [Pg.37]

Oral Cleansing Products. Toothpastes and mouthwashes are considered cosmetic oral cleansers as long as claims about them are restricted to cleaning or deodorization. Because deodorization may depend on reduction of microbiota in the mouth, several antimicrobial agents, either quaternaries, such as benzethonium chloride [121 -54-0] or phenoHcs, such as triclosan [3380-35-5] are permitted. Products that include anticaries or antigingivitis agents or claim to provide such treatment are considered dmgs. [Pg.299]

The sorbent of fibrous stmcture has the best kinetic characteristics in relation to noble metals, for which reaching soi ption balance does not exceed 20 minutes. The rate of soi ption balance establishment depends on the form of nitrogen in functional groups of sorbents used and decreases in a line tertiary nitrogen (linear group) > tertiary nitrogen (heterocycle) > quaternary nitrogen. [Pg.262]

High tendency of ZnfSCN) ion to extraction into organic phase is widely used for zinc determination by extraction photometry method. Recently it was shown that when single-chai ged anions ai e exchanged for double-chai ged ones, the selectivity of this process depends on the number of methyl substitutients in quaternary ammonium salt (QAS) cation. [Pg.275]

Protein molecules that have only one chain are called monomeric proteins. But a fairly large number of proteins have a quaternary structure, which consists of several identical polypeptide chains (subunits) that associate into a multimeric molecule in a specific way. These subunits can function either independently of each other or cooperatively so that the function of one subunit is dependent on the functional state of other subunits. Other protein molecules are assembled from several different subunits with different functions for example, RNA polymerase from E. coli contains five different polypeptide chains. [Pg.29]

The change in the quaternary structure and the structural change in the 6-F helix as the molecule moves from one state to the other are intimately related. The dimer interactions in the T state are not compatible with the presence of the 6-F helix, which would, if present, clash with the neighbouring dimer. The quaternary structure of the T state requires that the 6-F helix be unwound. Conversely the R state quaternary structure depends on the presence of the 6-F helix. [Pg.117]

The yield of this reaction is directly dependent on the purity of the quaternary salt employed. If the salt is prepared from redistilled N,N-dimethylaminomethylferrocene, the yield of alcohol may be as high as 90%. ... [Pg.53]

Palmatine and Associated Alkaloids. Palmatine, jatrorrhizine (jateorhizine) and columbamine were first isolated from ealumba root (Jateorhiza palmata Lam., Miers) as a result of the work of Giinzel followed by that of Feist, but all three have sinee been found in other genera. All three are quaternary bases, soluble in water, and methods for their isolation have been deseribed by Giinzel, Feist, and Spath and Polgar, usually dependent upon their preeipitation as iodides, or their reduetion to the tertiary tetrahydro-bases. The latter oeeur naturally in the Rhceadales and have been deseribed already (p. 284). A method for the separate estimation of the alkaloids of ealumba root has been described by Neugebauer and Brunner. " ... [Pg.342]

In the case of 7a-quaternary salts (118), the course of elimination depends very much on the conditions employed thus, in neutral ethanol the process has Ey character and produces cholest-7-ene (119), whereas under alkaline conditions cholest-6-ene (120) is the nearly exclusive product. [Pg.337]

Epoxides are regio- and stereoselectively transformed into fluorohydrins by silicon tetrafluoride m the presence of a Lewis base, such as diisopropyleth-ylamme and, m certain instances, water or tetrabutylammonium fluoride The reactions proceed under very mild conditions (0 to 20 C in 1,2-diohloroethane or diethyl ether) and are highly chemoselective alkenes, ethers, long-chain internal oxiranes, and carbon-silicon bonds remain intact The stereochemical outcome of the epoxide ring opening with silicon tetrafluoride depends on an additive used, without addition of water or a quaternary ammonium fluoride, as fluorohydrins are formed, whereas m the presence of these additives, only anti opening leading to trans isomers is observed [17, 18] (Table 2)... [Pg.204]

Quaternary ammonium salts of pyrrolines 106) can be prepared only indirectly 197). Addition of bromine to l-dimethylamino-4-pentene followed by removal of hydrogen bromide afforded, depending upon the dehydrohalogenation conditions, quaternary bromides derived from either l,2-dimethyl-/f -pyrroline (107) or l-methyl-2-methylenepyrrolidine (108) (Scheme 7). [Pg.278]

The first step of this reaction, decarboxylation of pyruvate and transfer of the acetyl group to lipoic acid, depends on accumulation of negative charge on the carbonyl carbon of pyruvate. This is facilitated by the quaternary nitrogen on the thiazolium group of thiamine pyrophosphate. As shown in (c), this cationic... [Pg.646]

Alkylation of 3,4-dihydro-j8-carboline methiodide (371 R = H) and of 1-methyl-3,4-dihydrO jS-carboline methiodide (371 R = CH3) in alkaline solution is accompanied by ring cleavage, and gives quaternary 3-acyltryptamine derivatives (372) or their acetals (373) depending on reaction conditions. [Pg.174]

The ultraviolet absorption spectra of 3,4-dihydro-jS-carboline derivatives exhibit a dependence on pH similar to that shown by the speetra of the fully aromatie compounds. 3,4-Dihydro-/S-carboline and 1-methyl- and 7-methoxy-l-methyl-3,4-dihydro-jS-carbo-line serve as examples. The quaternary 3,4-dihydro-jS-earbolin-ium salts obtained on p /r-A-alkylation of these dihydro-j3-earbo-lines show a bathoehromic shift of 5 mp, eompared to the... [Pg.203]


See other pages where Quaternary dependence is mentioned: [Pg.279]    [Pg.279]    [Pg.1255]    [Pg.279]    [Pg.279]    [Pg.1255]    [Pg.60]    [Pg.7]    [Pg.65]    [Pg.208]    [Pg.556]    [Pg.320]    [Pg.182]    [Pg.184]    [Pg.258]    [Pg.256]    [Pg.383]    [Pg.166]    [Pg.187]    [Pg.99]    [Pg.22]    [Pg.501]    [Pg.232]    [Pg.54]    [Pg.81]    [Pg.69]    [Pg.337]    [Pg.644]    [Pg.108]    [Pg.277]    [Pg.466]    [Pg.480]    [Pg.176]    [Pg.366]    [Pg.34]   
See also in sourсe #XX -- [ Pg.148 ]




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