1,3,5-tris- 2-Hydroxyethyl cyanuric

Tris (2-hydroxyethyl) ammonium trihydrogen ethylenediaminetetraacetate. See TEA-EDTA Tris (hydroxyethyl) cyanurate 1,3,5-Tris (2-hydroxyethyl) cyanurate 1,3,5-Tris (2-hydroxyethyl) cyanuric acid. See Trishydroxyethyl triazine trione... 

Tris (2-hydroxyethyl) cyanurate 1,3,5-Trls (2-hydroxyethyl) cyanuric acid Tris (hydroxyethyl) isocyanurate 1,3,5-Tris (2-hydroxyethyl) isocyanurate Tris (2-hydroxyethyl) isocyanurate Tris (P-hydroxyethyl) isocyanurate N,N, N"-Tris (2-hydroxyethyl) isocyanurate 1,3,5-Tris (2-hydroxyethyl) isocyanuric acid 1,3,5-Tris (2-hydroxyethyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione 1,3,5-Tris (2-hydroxyethyl) triazine-2,4,6-trione... 

Ethoquad T/13-27W [Akzo Nobel Surf. Chem. http //www.surface.akzonobelusa.com] Trishydroxyethyl triazine trione CAS 839-90-7 EINECS/ELINCS 212-660-9 Synonyms Isocyanuric acid tris (2-hydroxyethyl) ester THEIC 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris (2-hydroxyethyl)- s-Triazine-2,4,6(1 H,3H,5H)-trione, 1,3,5-tris (2-hydroxyethyl)- Tris (hydroxyethyl) cyanurate... 

Virtually all of the organo derivatives of CA are produced by reactions characteristic of a cycHc imide, wherein isocyanurate nitrogen (frequendy as the anion) nucleophilically attacks a positively polarized carbon of the second reactant. Cyanuric acid and ethylene oxide react neady quantitatively at 100°C to form tris(2-hydroxyethyl)isocyanurate [839-90-7] (THEIC) (48—52). Substitution of propylene oxide yields the hydroxypropyl analogue (48,49). At elevated temperatures (- 200° C). CA and alkylene oxides react in inert solvent to give A/-hydroxyalkyloxazohdones in approximately 70% yield (53). Alternatively, THEIC can be prepared by reaction of CA and 2-chloroethanol in aqueous caustic (52). THEIC can react further via its hydroxyl fiinctionahty to form esters, ethers, urethanes, phosphites, etc (54). Reaction of CA with epichlorohydrin in alkaline dioxane solution gives... 

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