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4- Phenoxybenzoic acid

Chemical Name 3-(aminosulfonyl)-5-(butylamino)-4-phenoxybenzoic acid Common Name —... [Pg.200]

Office of Prevention, Protection and Toxic Substances Phosphinothricin acetyltransferase Phenoxybenzoic acid Polychlorinated biphenyl Polymerase chain reaction Polygalacturonase Acid dissociation constant... [Pg.12]

Figure 10 Structure of the target analyte phenoxybenzoic acid (PBA). The arrows point to the ideal sites for conjugation of the molecule to proteins for optimum recognition. Use of site 2 for conjugation to protein resulted in antibodies that recognized free PBA poorly... Figure 10 Structure of the target analyte phenoxybenzoic acid (PBA). The arrows point to the ideal sites for conjugation of the molecule to proteins for optimum recognition. Use of site 2 for conjugation to protein resulted in antibodies that recognized free PBA poorly...
Figure 11 Structure of the phenoxybenzoic acid (PBA) immunogen hapten. Conjugation to the protein through the aldehyde resulted in an immunogen that generated antibodies selective and sensitive for PBA... Figure 11 Structure of the phenoxybenzoic acid (PBA) immunogen hapten. Conjugation to the protein through the aldehyde resulted in an immunogen that generated antibodies selective and sensitive for PBA...
Metabolism of the 2,S -isomers proceeds sequentially hydroxylation at the phenoxy group, hydrolysis of the cyano group, and cleavage of the ester linkage (Coats et al. 1989). Fenvalerate and the IS-isomers yield two ester metabolites in feces from hydroxylation at the 4 - and 2 -phenoxy positions. Other significant metabolites were 3-phenoxybenzoic acid and its hydroxy derivatives from the alcohol moiety, 3-(4-chlorophenyl) isovaleric acid and its hydroxy derivatives from the acid moiety, and thiocyanate and carbon dioxide from the cyano moiety (Ohkawa et al. 1979). A slow elimination rate characterizes fenvalerate and other a-cyano pyrethroids when compared with... [Pg.1101]

Huckle KR, Hutson DH, Millbum P (1981) Species differences in the metabolism of 3-phenoxybenzoic acid. Dmg Metab Dispos 9 352-359... [Pg.133]

Moorhouse KG, Logan CJ, Hutson DH, Dodds PF (1990) The incorporation of 3-phenoxybenzoic acid and other xenobiotics acids into xenobiotic lipids by enzymes of the monoacylglycerol pathway in microsomes from adult and neonatal tissues. Biochem Pharmacol 39 1529-1536... [Pg.133]

Chuang JC, Van Emon JM, Trejo RM, Dumford J (2011) Biological monitoring of 3-phenoxybenzoic acid in urine by an enzyme-linked immunosorbent assay. Talanta 83 (5) 1317—1323... [Pg.134]

Riederer AM, Bartell SM, Barr DB, Ryan PB (2008) Diet and nondiet predictors of urinary 3-phenoxybenzoic acid in NHANES 1999-2002. Environ Health Perspect 116 1015-1022... [Pg.134]

Kimata A, Kondo T, Ueyama J, Yamamoto K, Kamijima M, Inoue T, Ito Y, Hamajima N (2009) Relationship between dietary habits and urinary concentrations of 3-phenoxybenzoic acid in a middle-aged and elderly general population in Japan. Environ Health Prev Med 14 173-179... [Pg.134]

Halden RU, Tepp SM, Halden BG, Dwyer DF (1999) Degradation of 3-phenoxybenzoic acid in soil by Pseudomonas pseudoalcaligenes POB310(pPOB) and two modified Pseudomonas strains. Appl Environ Microbiol 65 3354-3359... [Pg.199]

Phenoxybenzoic acid, see Cvpermethrin. Permethrin Phenoxybenzyl alcohol, see Permethrin 3-Phenoxybenzyl alcohol, see Permethrin... [Pg.1538]

CASRN 52315-07-8 molecular formula C22H19CI2NO3 FW 416.30 Soil. The major soil metabolite was 3-phenoxybenzoic acid (Hartley and Kidd, 1987). Chemical/Physical. The hydrolysis half-lives of cypermethrin in a sterile 1% ethanol/water solution at 25 °C and pH values of 4.5, 6.0, 7.0, and 8.0, were 99, 69, 63, and 50 wk, respectively (Chapman and Cole, 1982). [Pg.1567]

Photolytic. Photolysis of permethrin in aqueous solutions containing various solvents (acetone, hexane, and methanol) under UV light (1 >290 nm) or on soil in natural sunlight initially resulted in the isomerization of the cyclopropane moiety and ester cleavage. Photolysis products identified were 3-phenoxybenzyldimethyl acrylate, 3-phenoxybenzaldehyde, 3-phenoxybenzoic acid, mono-chlorovinyl acids, cis- and fra/is-dichlorovinyl acids, benzoic acid, 3-hydroxybenzoic acid, 3-hydroxybenzyl alcohol, benzyl alcohol, benzaldehyde, 3-hydroxybenzaldehyde, and 3-hydroxybenzoic acid (Holmstead et ah, 1978). [Pg.1603]

More recently [79], a carboxy-terminated PBZT ([r ] = 4.8 dL/g) was reacted with m-phenoxybenzoic acid via a Friedel Craft procedure in a meth-anesulfonic acid/P2Os mixture. This provided an ABA block copolymer in which the outer blocks (A) are composed of flexible coil polyetherketone (PEK) and a center block (B) which contains the rigid-rod PBZT. Thermomechanical analysis showed that 20 PBZT/80 PEK and 10 PBZT/90 PEK compositions exhibited glass transition temperatures of 157 °C and 135°C respectively. Consolidation studies have not been investigated to date. [Pg.288]

See other pages where 4- Phenoxybenzoic acid is mentioned: [Pg.891]    [Pg.891]    [Pg.891]    [Pg.326]    [Pg.326]    [Pg.393]    [Pg.138]    [Pg.286]    [Pg.287]    [Pg.2298]    [Pg.2442]    [Pg.634]    [Pg.635]    [Pg.673]    [Pg.1160]    [Pg.1160]    [Pg.1160]    [Pg.1118]    [Pg.116]    [Pg.119]    [Pg.149]    [Pg.179]    [Pg.186]    [Pg.187]    [Pg.188]    [Pg.412]    [Pg.287]    [Pg.1118]    [Pg.515]    [Pg.225]    [Pg.289]   
See also in sourсe #XX -- [ Pg.634 ]



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M-Phenoxybenzoic acid

O-Phenoxybenzoic acid

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