78902-17-7 Usage
Uses
Used in Plastics Industry:
Phosphorous acid, 2,6-bis(1,1-dimethylethyl)-4-methylphenyl dioctyl ester is used as a flame retardant and plasticizer for enhancing the flexibility, durability, and reducing the flammability of materials. It is particularly useful in the production of polyvinyl chloride (PVC) products, such as cables, flooring, and packaging materials.
Used in Cable Industry:
In the cable industry, Phosphorous acid, 2,6-bis(1,1-dimethylethyl)-4-methylphenyl dioctyl ester is used as a flame retardant to improve the safety and performance of cables by reducing their flammability.
Used in Flooring Industry:
Phosphorous acid, 2,6-bis(1,1-dimethylethyl)-4-methylphenyl dioctyl ester is used as a plasticizer in the flooring industry to enhance the flexibility and durability of flooring materials, making them more resistant to wear and tear.
Used in Packaging Materials Industry:
In the packaging materials industry, Phosphorous acid, 2,6-bis(1,1-dimethylethyl)-4-methylphenyl dioctyl ester is used as a flame retardant and plasticizer to improve the safety and flexibility of packaging materials, reducing their flammability and increasing their durability.
However, due to its potential environmental and health hazards, proper handling and disposal of this chemical are necessary to minimize negative impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 78902-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,0 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78902-17:
(7*7)+(6*8)+(5*9)+(4*0)+(3*2)+(2*1)+(1*7)=157
157 % 10 = 7
So 78902-17-7 is a valid CAS Registry Number.
78902-17-7Relevant academic research and scientific papers
Syntheses und NMR-Spektren phosphororganischer Antioxidantien und verwandter Verbindungen
Koenig, T.,Habicher, W.D.,Haehner, U.,Pionteck, J.,Rueger, C.,Schwetlick, K.
, p. 333 - 349 (2007/10/02)
The syntheses of various aliphatic, aromatic, sterically hindered, and cyclic organophosphorus compounds (phosphorous acid esters, esters chlorides and ester amides, hydrogen phosphites, phosphinates and phosphates) are reported, and general procedures for preparation are given.The compounds synthesized were investigated by means of 31P-, 1H- and 13C-n.m.r. spectroscopy, and the chemical shifts measured are listed.
