6266-48-4 Usage
Uses
Used in Plastics Industry:
2,4,6-tris(diphenylmethyl)phenol is used as a flame retardant for plastics to enhance their fire resistance and safety in various applications, including electrical and electronic devices, automotive parts, and construction materials.
Used in Rubber Industry:
In the rubber industry, 2,4,6-tris(diphenylmethyl)phenol is used as a flame retardant to improve the fire safety of rubber products, such as cables, hoses, and seals, which are used in various industrial and consumer applications.
Used in Textile Industry:
2,4,6-tris(diphenylmethyl)phenol is used as a flame retardant in textiles to provide fire resistance to fabrics used in clothing, upholstery, and other textile products, thereby enhancing their safety and durability.
However, there is growing concern about the potential negative effects of TDTBPP on human health and the environment. Studies have suggested that it may be toxic to aquatic organisms and could have adverse health effects in humans, including potential carcinogenic and mutagenic properties. As a result, there is a growing interest in finding alternative flame retardants that are safer for both humans and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6266-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6266-48:
(6*6)+(5*2)+(4*6)+(3*6)+(2*4)+(1*8)=104
104 % 10 = 4
So 6266-48-4 is a valid CAS Registry Number.
6266-48-4Relevant articles and documents
BENZHYDRYLATED AROMATIC SURFACTANTS
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Paragraph 0076, (2020/07/14)
The present disclosure provides an alkoxylate compound containing aromatic groups in the hydrophobe allowing the compound to exhibit unique functionality, high performance and low cost, but without the toxicity and/or skin and eye irritation problems asso
Electron transfer in the peroxytrifluoroacetic acid-assisted sulfoxidation and oxidative destruction of benzhydryl sulfides
Akopova,Morkovnik,Khrustalev,Bicherov
, p. 1164 - 1175 (2014/03/21)
The reactions of benzhydryl sulfides Ph2CHSCH2R (R = H, CONH2, COOH, CN) with peroxytrifluoroacetic acid in CF 3COOH were studied experimentally and by the quantum chemical density functional theory (DFT) method and exhibited an unusual dependence on the substituent R. When R≠H, a complicated oxidative destruction of the substrates occurs to form 2,4,6-tribenzhydrylphenol as one of the products, while in the case of R = H, the starting benzhydryl sulfide is smoothly sulfoxidated. This fact is due to the common electron transfer from the substrate to reagent at the initial step and the difference in subsequent transformations of the species formed.
