Hydrophobic compound

Sorption of nonionic, nonpolar hydrophobic compounds occurs by weak attractive interactions such as van der Waals forces. Net attraction is the result of dispersion forces the strength of these weak forces is about 4 to 8 kj/mol ( 1 2 kcal/mol). Electrostatic interactions can also be important, especially when a molecule is polar in nature. Attraction potential can develop between polar molecules and the heterogeneous sod surface that has ionic and polar sites, resulting in stronger sorption. 

Water Repellency and Water Resistance. Water repeUency is defined as the abihty of a textile fiber, yam, or fabric to resist wetting, whereas water resistance is a general term appHed to a fabric s abiUty to resist wetting and penetration by water (2). A third term, waterproof, is appHed to those fabrics that do not allow any water penetration at all. Waterproof fabrics are generally coated with an impermeable surface layer that does not allow air permeabihty. Water-repellent finishes are hydrophobic compounds that are appHed to fabrics to inhibit water penetration while still allowing air permeabihty. 

Retention and stereoselectivity on the BSA columns can be changed by the use of additives to the aqueous mobile phase (30). Hydrophobic compounds generally are highly retained on the BSA, and a mobile-phase modifier such as 1-propanol can be added to obtain reasonable retention times. The retention and optical resolution of charged solutes such as carboxyUc acids or amines can be controlled by pH and ionic strength of the mobile phase. 

If the column is contaminated with hydrophobic compounds, clean it with water-miscible organic solvents such as MeOH, CHjCN, or EtOH. Concentrations of 10-20% organic in water should be sufficient for cleaning. 

In order to broaden the field of biocatalysis in ionic liquids, other enzyme classes have also been screened. Of special interest are oxidoreductases for the enan-tioselective reduction of prochiral ketones [40]. Formate dehydrogenase from Candida boidinii was found to be stable and active in mixtures of [MMIM][MeS04] with buffer (Entry 12) [41]. So far, however, we have not been able to find an alcohol dehydrogenase that is active in the presence of ionic liquids in order to make use of another advantage of ionic liquids that they increase the solubility of hydrophobic compounds in aqueous systems. On addition of 40 % v/v of [MMIM][MeS04] to water, for example, the solubility of acetophenone is increased from 20 mmol to 200 mmol L ... 

One particular feature of ionic liquids lies in their solvation properties, not only for hydrophobic compounds but also for hydrophilic compounds such as carbohydrates. Park and Kazlauskas reported the regioselective acylation of glucose in 99 % yield and with 93 % selectivity in [MOEMIM][BF4] (MOE = CH3OCH2CH2), values much higher than those obtained in the organic solvents commonly used for this purpose (Entry 18) [22] (Scheme 8.3-4). 

Compounds with high values are of low polarity and are described as being lipophilic and hydrophobic. Compounds with high values are of high polarity and are hydrophilic. Although the partition coefficient between octanol and water is... 

In marked contrast to hydrophobic compounds, more polar ones tend to be less adsorbed and to reach relatively high concentrations in soil water. Phenoxyalkanoic acids such as 2,4-D and MCPA are good examples (Figure 4.3). Their half-lives in soil are measured in weeks rather than years, and they are more mobile than OC insecticides in soils. When first applied they are lost only slowly. After a lag period of a... 

Dietary fats, libers, and other carotenoids have been reported to interfere with carotenoid bioaccessibility. It is clear that by their presence in the gut, lipids create an environment in favor of hydrophobic compounds such as carotenoids. When arriving in the small intestinal lumen, dietary fats stimulate bile flow from the gallbladder and therefore enhance the micelle formation, which in turn could facilitate the emulsification of carotenoids into lipid micelles. Without micelle formation, carotenoids are poorly absorbed a minimum of 3 g of fat in meal is necessary for an efficient absorption of carotenoids, except for lutein esters that require higher amounts of fat. ... 

C-18 Sep Pak cartridges have become popular because of their ease of use and high efficiency for fractionating anthocyanins. In an aqueous phase, anthocyanins and other hydrophobic compounds are bound while more hydrophilic compounds such as acids and sugars can be washed away with water. The water can be slightly acidified with 0.01% HCl to stabilize the anthocyanins on the C18 resin. ... 

Chapter 7 describes nondestructive (reversible) detection of snbstances by using iodine or water. Iodine can detect a wide variety of chemical classes as brown to yellow-brown zones on a preparative layer after exposnre to its vapor or dipping into a 1% iodine in chloroform solution. Another general, nondestmctive technique for detection of hydrophobic compounds in PLC nses water as a spray reagent [12-14]. 

B., Carrupt, P. A. The lipophihdty of cyclosporine A revisited using a RP-HPLC approach suitable to handle highly hydrophobic compounds. Unpublished results. 

A multi-residue method for 25 selected pesticides including propanil using an SPE disk has also been developed as a rapid screening method for organic contaminants in river, lake and seawater samples. Cig SPE disks are conditioned with 10 mL of acetone for 3 h. Water samples (1L) are allowed to percolate through the disks in order to trap the residues at a fiow rate of 50 mL min under vacuum. Residues trapped in the disks are extracted twice by eluting with 5 mL of dichloromethane-ethyl acetate (1 1, v/v). The more hydrophobic compounds (log/fow>3) seem to show no... 

Reversed-phase extraction of nonpolar compounds. Provides less retention of hydrophobic compounds. Normal phase extraction of polar compounds. Adsorption of polar coeqsounds. 

Superheated water at 100°-240 °C, with its obvious benefits of low cost and low toxicity, was proposed as a solvent for reversed-phase chromatography.59 Hydrophobic compounds such as parabens, sulfonamides, and barbiturates were separated rapidly on poly(styrene-divinyl benzene) and graphitic phases. Elution of simple aromatic compounds with acetonitrile-water heated at 30°-130 °C was studied on coupled colums of zirconia coated with polybutadiene and carbon.60 The retention order on the polybutadiene phase is essentially uncorrelated to that on the carbon phase, so adjusting the temperature of one of the columns allows the resolution of critical pairs of... 

Water with Hydrophobic compounds Aqueous solutions of... 

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