n.1.(Chem.) A salt of xylic acid.
Webster's Revised Unabridged Dictionary, published 1913 by G. & C. Merriam Co.
References in periodicals archive ?
2001: Yeast estrogen screen assay--effective concentration inducing 20% of maximum response observed with [E.sub.2] Estradiol-17[beta] (reference chemical) 0.022000 E[C.sub.20] (ng/mL) Ethinylestradiol- 17[alpha] 0.059 E[C.sub.20] (ng/mL) Estrone 0.166 E[C.sub.20] (ng/mL) Estriol 0.627 E[C.sub.20] (ng/mL) Nonylphenol 246.7 E[C.sub.20] (ng/mL) Nonylphenol monoethoxylate 10,985.4 E[C.sub.20] (ng/mL) Nonylphenol monoethoxylate/ nonylphenol diethoxylate 9,627.6 E[C.sub.20] (ng/mL) Nonylphenol monoethoxycarbo- xylate 0.0 E[C.sub.20] (ng/mL) Nonylphenol monoethoxycarbo- xylate/nonyl- phenol diethoxy- carboxylate 0.0 E[C.sub.20] (ng/mL) Bisphenol A 597.3 E[C.sub.20] (ng/mL) Diethylhexyl phthalate 0.0 E[C.sub.20] (ng/mL) Madigou et al.
A simple one-step mechanism, similar to ionomer neutralization, is proposed in which carbo xylate anions displace anionic chloride ligands in the 1st-shell coordination sphere of [Eu.sup.3+];
For chlorodiorganotin(IV) dithiocarbo- xylates, fragmentation also commence either by loss of R+ or the organic part of the anion.