70146-21-3 Usage
Uses
Used in Plastics Industry:
Bis(2,4-di-tert-butylphenyl)phenyl phosphonite is used as a stabilizer and antioxidant for [application reason] to prevent the degradation of polymers caused by heat, light, and oxygen exposure. This extends the lifespan and improves the performance of plastic products.
Used in Rubber Industry:
In the rubber industry, Bis(2,4-di-tert-butylphenyl)phenyl phosphonite is used as a stabilizer and antioxidant for [application reason] to enhance the durability and resistance of rubber products against environmental factors.
Used in Adhesives Production:
Bis(2,4-di-tert-butylphenyl)phenyl phosphonite is used as a stabilizer and antioxidant in the production of adhesives for [application reason] to ensure the long-term stability and performance of the adhesives, even under harsh conditions.
Used in Coatings Production:
In the coatings industry, Bis(2,4-di-tert-butylphenyl)phenyl phosphonite is used as a stabilizer and antioxidant for [application reason] to protect the coatings from degradation, ensuring their longevity and maintaining their appearance.
Used in Sealants Production:
Bis(2,4-di-tert-butylphenyl)phenyl phosphonite is used as a stabilizer and antioxidant in the production of sealants for [application reason] to improve their resistance to environmental factors, such as heat, light, and oxygen, thus prolonging their service life.
Check Digit Verification of cas no
The CAS Registry Mumber 70146-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,4 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70146-21:
(7*7)+(6*0)+(5*1)+(4*4)+(3*6)+(2*2)+(1*1)=93
93 % 10 = 3
So 70146-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C68H91O2P/c1-61(2,3)43-31-35-47(53(39-43)65(13,14)15)49-27-25-29-57(59(49)51-37-33-45(63(7,8)9)41-55(51)67(19,20)21)69-71-70-58-30-26-28-50(48-36-32-44(62(4,5)6)40-54(48)66(16,17)18)60(58)52-38-34-46(64(10,11)12)42-56(52)68(22,23)24/h25-42,71H,1-24H3
70146-21-3Relevant academic research and scientific papers
STERICALLY HINDERED PHOSPHONITES
Pastor, Stephen D.,Spivack, John D.,Steinhuebel, Leander P.
, p. 169 - 176 (2007/10/02)
Phosphonochloridous and phosphonous esters were prepared from the reaction of phenylphosphonous dichloride with 2,4-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, and 2,4,6-tri-tert-butylphenol.Various synthetic methodologies, including phase-transfer catalysis, are described and compared.Phosphonous diesters containing two different substituted-phenyl moieties were prepared from phosphonochloridous monoesters.The reaction of O-(2,6-di-tert-butyl-4-methylphenyl)-phenylphosphonochloridite with N-methyldiethanolamine, n-octyl mercaptan, and water was studied and found to give a biphosphonite, phosphonothioite and phosphinate, respectively.
