Phosphoric acid diphenyl ester

Phosphonic acid, (phthalimidomethyl)-, diethyl ester, 65, 119 Phosphorazidic acid, diphenyl ester (26386-88-9), 68,1 Phosphoric triamide, hexamethyl- (680-31-9), 66, 51, 94 Phosphorodichloridic acid, 2-chloroethyl ester, 65, 68 Phosphorous acid, triethyl ester, 65, 108.119 Phosphorus oxychloride, 66,173, 176 67,1 68, 41,162 Phosphorus tribromide (7789-60-8), 67, 210 Phthalimide, N-(bromoethyl)-, 65, 119 Phthalimide, N-(hydroxymethyl)-, 65,119 Pig liver esterase, 69, 20... 

Phosphoric acid isooctyl ester. See Isooctyl acid phosphate Phosphoric acid methylphenyl diphenyl ester. See Diphenylcresyl phosphate... 

Phosphoric acid methylphenyl diphenyl ester. See Diphenylcresyl phosphate Phosphoric acid, monodecyl ester, potassium salt. See Potassium decyl phosphate Phosphoric acid, mono- and di-C9-15-alkyl esters. See C9-15 alkyl phosphate Phosphoric acid, monohexyl ester. See Hexyl phosphate... 

Name PHOSPHORIC ACID, DIPHENYL 2-ETHYLHEXYL ESTER... 

C20H19O4P phosphoric acid diphenyl dimethylphenyl ester... 

Considerable efforts have centered on carrying out the synthesis of polybenzimidazoles at more moderate temperatures. Polymerization of the isophthalic acid or its diphenyl ester have been successfully carried out in polyphosphoric acid or methanesulfonic acid-phosphorous pentoxide at 140-180°C, but the reaction is limited by the very low solubilities (<5%) of the reactants in that solvent. The lower reaction temperature is a consequence of activation of the carboxyl reactant via phosphorylation. Lower reaction temperatures are also achieved in hot molten nonsolvents such as sulfolane and diphenyl sulfone, but the need to remove such solvents by a filtration or solvent extraction is a disadvantage. 

The methodology of the catalytic asymmetric aldol reaction has been further extended to the aldol-type condensation of (isocyanomethyl)phosphonates (12) with aldehydes, providing a useful method for the synthesis of optically active (l-aminoalkyl)phosphonic acids, which are a class of biologically interesting phosphorous analogs of a-amino acids (Scheme 8B1.6) [21,22], Higher enantioselectivity and reactivity are obtained with diphenyl ester 12b than with diethyl ester 12a (Table 8B1.6). 

SYNS 2-ETHYL-l-HEXANOL ESTER with DIPHENYL PHOSPHATE 2-ETHYLHEXYL DIPHENYL ESTER PHOSPHORIC ACID 2-ETHYLHEXYL DIPHENYLPHOSPHATE SANTICIZER 141 (MONSANTO)... 

The third most commonly used class of flame-retardants is phosphorus-containing compounds such as phosphoric acid esters, diphenyl cre-sylphosphate, dimethyl methylphosphonate, and dibutyl dihydroxyethyl diphosphate. They have good flame-retarding performance and are effective in small amounts. They are, however, expensive and have low hydrolysis stability. 

Phosphoric Acid Phosphorus Photoallergens Photochemical Oxidants Phthalate Ester Plasticizers Physical Hazards Picloram Picric Acid Piperazine Piperonyl Butoxide "Plants, Poisonous" Platinum (Pt) Plutonium (Pu) Poinsettia Poisoning Emergencies in Humans Pokeweed Pollutant Release and Transfer Registries (PRTRs) Pollution Prevention Act "Pollution, Air" "Pollution, Air Indoor" "Pollution, Soil" "Pollution, Water" Polybrominated Biphenyls (PBBs) Polybrominated Diphenyl Ethers (PBDEs) Polychlorinated Biphenyls (PCBs)... 

In these reactions, hydrolysis of diphenyl and triaryl phosphites to monoaryl phosphites and phenol was coupled by dehydration between carboxylic acids and amines or alcohols to the corresponding amides and esters. Therefore, the reaction can be generalized as a hydrolysis-dehydration reaction (Scheme 2). The concept of the hydrolysis-dehydration reaction using phosphites has been drown to be applicable also to reactions with other phosphorus compounds such as phosphinites, phos-phonites and phosphorates s Aryl esters of these phosphorus compounds are effective as condensing agents in the production of carboxylic amides and esters (from carboxylic acids and amines or alcohols, respectively) whereas alkyl esters are ineffective (Eqs. (1-3)) ... 

Phosphoric acid, (1,1-dimethylethyl)phenyl diphenyl ester. t-Butylphenyl diphenyl phosphate tert-Butylphenyl diphenyl phosphate CCRIS 4761 EINECS 260-391-0 HSDB 6102 Phosphate, tert-butylphenyl diphenyl Phosphoric acid, (1,1-dimethylethyl)phenyl diphenyl ester Syn-O-Ad 8478 Syn-O-Ad ... 

Beilstein Handbook Reference) AI3-16360 BRN 2568983 CCRIS 6199 Diphenyl-2-ethylhexyl phosphate EINECS 214-987-2 2-Ethylhexyldiphenylphosphate HSDB 370 Ooticizer Phosphoric acid, 2-ethylhexyl diphenyl ester Santicizer 141. Flame retardant plasticizer for type PVC applications, dip, rotationally, extruded and injection molded parts, mechanical foam. Liquid bps = 232° d = 1.090 LDsO (mus ip) = 930 mg/kg. Akzo Nobel Ashland Bayer AG Marwick Miles Inc. Monsanto Co. Polysar. 

Chelex MD Diphenyl isodecyl phosphite DPDP EINECS 247-777-4 Isodecyl alcohol, diphenyl phosphite Isodecyl diphenyl phosphite Mark 135A Phoselere T 26 Phosphorous acid, isodecyl diphenyl ester Weston DPDP, Chelating agent with metal carboxylates as polymer additives, especially for chlorinated polymers such as PVC and chlorinated PE Improves color, heat and light stability. Liquid bp = 190° d = 1,022-1.032 flash point = 154 . Akzo Chemie, Dover. 

CCRIS 4830 Diphenyl isodecyl phosphate EINECS 249-828-6 HSDB 6797 isodecyl diphenyl phosphate Phosflex 390 Phosphoric acid, isodecyl diphenyl ester Santicizer 148 Syn-O-Ad 8479. 

Doverphos DPIOP DPIOP EINECS 247-658-7 Isooctyl diphenyl phosphite Phosphorous acid, isooctyl diphenyl ester Weston ODPP. Color stabilizer for ABC, PC stabilizer for PVC antioxidant... 

Phosphoric acid (l-methylethyl)phenyl diphenyl ester. 

CCRIS 4661 EINECS 248-848-2 HSDB 6795 Isopropylphenyl diphenyl phosphate Kronitex 100 Phosflex 41P Phosphoric acid, (l-methylethyl)phenyl diphenyl ester Syn-O-Ad 8460, Antiwear and EP agents in non-crankcase lubricants ferrous metal passivator fluid base stock where inhibition of flame propagation is desired. Insoluble in H2O, soluble in organic solvents, Akzo Chemie. 

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