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Water Quaternary ammonium compound

From ehloromethyl or bromomethyl aromatic compounds by heating with hexamethylenetetramine (hexamine) in aqueous alcohol or aqueous acetic acid. A quaternary ammonium compound is formed, which yields the aldehyde upon treatment with water in the presence of hexamine for example... [Pg.692]

Physical Properties. Most quaternary compounds are soHd materials that have indefinite melting poiats and decompose on heating. Physical properties are determined by the chemical stmcture of the quaternary ammonium compound as well as any additives such as solvents. The simplest quaternary ammonium compound, tetramethylammonium chloride [75-57-0] is very soluble ia water (163) and iasoluble ia nonpolar solvents. As the molecular weight of the quaternary compound iacreases, solubiUty ia polar solvents decreases and solubiUty ia nonpolar solvents iacreases (164—166). For example, trimethyloctadecylammonium chloride [112-03-8] is soluble ia water up to whereas dimethyldioctadecylammonium chloride [107-64-2] has... [Pg.377]

Surface Applied Surfactants. Antistat agents can be appHed direcdy to the surface of a plastic part. Usually the antistat is diluted in water or in a solvent. The antistat solution is appHed by spraying, dipping, or wiping on the surface. The water or solvent dries leaving a thin film that attracts moisture. Since it is appHed to the surface, migration through the resin is not a factor. In practice, the quaternary ammonium compounds find the most use. They are soluble in water and effective at low concentrations. [Pg.299]

Disinfectants. Several disinfecting agents can be used in hatcheries and two are of particular interest. Because they are not considered dmg or food additive uses by FDA, povidone—iodine compounds can be used to disinfect the surface of eggs (9). Benzalkonium chloride [68424-85-1] and benzethonium chloride (quaternary ammonium compounds), are allowed at 2 mg/L by FDA to disinfect water containing fish. These compounds are also known to have therapeutic properties, especially against external bacteria (9). [Pg.322]

Cationic quaternary ammonium compounds such as distearyldimethylammonium-chloride (DSDMAC) used as a softener and as an antistatic, form hydrated particles in a dispersed phase having a similar structure to that of the multilayered liposomes or vesicles of phospholipids 77,79). This liposome-like structure could be made visible by electron microscopy using the freeze-fracture replica technique as shown by Okumura et al. 79). The concentric circles observed should be bimolecular lamellar layers with the sandwiched parts being the entrapped water. In addition, the longest spacings of the small angle X-ray diffraction pattern can be attributed to the inter-lamellar distances. These liposome structures are formed by the hydrated detergent not only in the gel state but also at relatively low concentrations. [Pg.12]

In order to avoid the necessity of adding a quaternary ammonium compound to solubilize the organotin derivative, a number of new, anionic, tributyltin salts of the type (RsR P)" (BuaSnClt) , where R = Ri = "Bu or Ph R = Ph, R = Bz, were prepared (440, 536). Although these contain discrete, trigonal, bipyrEimidal tributyldichloro-stannate anions (440), their solubility in water was found to be very low. [Pg.55]

There are a number of industrially important reactions where two liquid phases are involved and the aqueous phase contains ionic species. Here the rate may be severely limited due to low solubiblity of the reactant, located in the organic phase, in water. We would benefit from using a pha.se-transfer (PT) catalyst, which ferries the ionic species into the organic phase thus overcoming a severe limitation. Such PT catalysts are typically quaternary ammonium compounds like tetrabutylammonium halides, trioctylmethylammonium chloride, etc. (see also Section 3.8). [Pg.145]

Theory As pure adrenaline is sparingly soluble in distilled water, therefore, its solution is made in 1 M hydrochloric acid whereby the N-atom gets protonated and results into the formation of a quaternary ammonium compounds as shown in under ... [Pg.279]

Dodecyltrimethylammonium chloride is rapidly mineralized in fresh water after an acclimation period, and the rate is faster following the second rather than the first addition of the quaternary ammonium compound. [Pg.341]

Absorption of some highly ionized compounds (e.g., sulfonic acids and quaternary ammonium compounds) from the gastrointestinal tract cannot be explained in terms of the transport mechanisms discussed earUer. These compounds are known to penetrate the Upid membrane despite their low Upid-water partition coefficients. It is postulated that these highly lipophobic drugs combine reversibly with such endogenous compounds as mucin in the gastrointestinal lumen, forming neutral ion pair complexes it is this neutral complex that penetrates the Upid membrane by passive diffusion. [Pg.24]

Like most quaternary ammonium compounds, 2-PAM is distributed mainly to extracellular water, and some tissue sequestration occurs.100 2-PAM is only weakly bound to plasma proteins.100... [Pg.349]

The quaternary ammonium compounds (23) and (24) are most often used as disinfectants and sanitizers for hard surfaces. Other industrial applications are limited to slimicides for paper mills and cooling-water systems. [Pg.400]

The water-soluble resins are inexpensive, and compared with quaternary ammonium compounds relatively small quantities often suffice to achieve a marked improvement in wetfastness and fastness to perspiration. A disadvantage is a certain influence on lightfastness. This may be lowered by one to two steps on the eight-step blue scale when these resins are used on materials dyed by substantive dyes. Formaldehyde condensation resins are therefore used especially for articles in which wet fastness and fastness to perspiration are important, but light fastness is less crucial, e.g., lining fabrics. [Pg.174]

Quaternary ammonium compounds are important as osmoprotectants in times of water deficiency and cold stress, as well as being constituents of membrane phospholipids, p-Alanine and phosphoethanolamine are each methylated three times on their nitrogens to produce the products P-alanine betaine and phosphocholine, respectively (Fig. ll.l).24"27 An example of O-methylation and N-methylation occurring on the same molecule can be found in the indole alkaloid vindoline from Catharanthus roseus (Fig. 11.1) 28,29... [Pg.256]


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See also in sourсe #XX -- [ Pg.14 ]




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