13053-90-2 Usage
Description
(Trifluoroethoxy)pentachlorocyclotriphosphazene is a chemical compound featuring a cyclic structure composed of phosphorous and nitrogen atoms, with chlorine atoms attached to the phosphorous atoms. Each phosphorous atom is also bonded to a trifluoroethoxy group, contributing to its unique properties and applications.
Uses
Used in Flame Retardancy:
(Trifluoroethoxy)pentachlorocyclotriphosphazene is used as a flame retardant in various industries for its ability to release flame-inhibiting gases when exposed to heat. This property makes it a valuable additive for materials that require enhanced fire resistance, such as plastics, textiles, and coatings.
Used in Polymer Production:
In the polymer industry, (trifluoroethoxy)pentachlorocyclotriphosphazene is utilized as a key component in the synthesis of certain polymers. Its presence in the polymer matrix can improve the thermal stability and flame retardancy of the final product.
Used as a Chemical Stabilizer:
(Trifluoroethoxy)pentachlorocyclotriphosphazene also serves as a stabilizer for other chemicals, particularly those that are prone to decomposition or degradation under certain conditions. Its stabilizing effect can extend the shelf life and improve the performance of various chemical products.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 13053-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13053-90:
(7*1)+(6*3)+(5*0)+(4*5)+(3*3)+(2*9)+(1*0)=72
72 % 10 = 2
So 13053-90-2 is a valid CAS Registry Number.
13053-90-2Relevant articles and documents
Effects of Mass Transfer and Extraction of Quarternary Salts on a Substitution Reaction by Phase-Transfer Catalysis
Wang, Maw-Ling,Wu, Ho-Sheng
, p. 2344 - 2350 (1990)
The substitution reaction of hexachlorocyclotriphosphazene with 2,2,2-trifluoroethanol using quaternary ammonium salts as the phase-transfer catalysts in an organic solvent/alkaline solution has been investigated.The pseudo-first-order reaction rate constant of the two-phase reaction and the rate constant ratios of the sequential substitution reaction in the organic phase were obtained.The hydration number of the catalyst, QOCH2CF3, is determined from the experimental data.The reaction reactivity is influenced by the content of the acids, which include water and alcohol in the aqueous phase.For an extraction mechanism, the reactivities of all kinds of catalysts in the organic phase with the same kind of solvent are the same.The effects of mass transfer and the extraction of quaternary ammonium salts on the conversion are used to explain the experimental data.The obtained results can be used as a reference for selecting the appropriate solvent and catalyst as well as for determining the appropriate content in the aqueous phase.Meanwhile, the desired distributed products, including the intermediate and final products, can be obtained by the appropriate choice of reaction conditions.
