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Triphenyl phosphate (TPhP) is the chemical compound with the formula OP(OC 6 H 5) 3. It is the simplest aromatic organophosphate. This colourless solid is the ester (triester) of phosphoric acid and phenol. It is used as a plasticizer and a fire retardant in a wide variety of settings and products. [3]
Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C 6 H 5) 3, also written as Ph 3 PO or PPh 3 O (Ph = C 6 H 5).It is one of the more common phosphine oxides.
Phosphites are oxidized to phosphate esters: P(OR) 3 + [O] → OP(OR) 3. This reaction underpins the commercial use of some phosphite esters as stabilizers in polymers. [6] Alkyl phosphite esters are used in the Perkow reaction for the formation of vinyl phosphonates, and in the Michaelis–Arbuzov reaction to form phosphonates.
According to The Washington Post, phosphorus keeps "minerals from interfering with the cleaning process and prevent food particles from depositing again on dishes." [ 16 ] According to Time magazine, "One reason detergent makers have been using large amounts of phosphorus is that it binds with dirt and keeps it suspended in water, allowing the ...
The phosphorus-containing product is triphenylphosphine sulfide, Ph 3 PS. This reaction can be employed to assay the "labile" S 0 content of a sample, say vulcanized rubber. Triphenylphosphine selenide, Ph 3 PSe, may be easily prepared via treatment of PPh 3 with red (alpha-monoclinic) Se. Salts of selenocyanate, SeCN −, are used as the Se 0 ...
Additives are used for many purposes but the main uses are: Acids Food acids are added to make flavors "sharper", and also act as preservatives and antioxidants. Common food acids include vinegar, citric acid, tartaric acid, malic acid, folic acid, fumaric acid, and lactic acid. Acidity regulators
Triphenyl phosphite ozonide (TPPO) is a chemical compound with the formula PO 3 (C 6 H 5 O) 3 that is used to generate singlet oxygen. [ 1 ] [ 2 ] When TPPO is mixed with amines , the ozonide breaks down into singlet oxygen and leaves behind triphenyl phosphite . [ 2 ]
Triphenylphosphite is a notable example of polyamorphism in organic compounds, namely it exists in two different amorphous forms at temperatures about 200 K. [5] One polymorphic modification of triphenyl phosphite was obtained by means of crystallization in ionic liquids. [6]