Tris(2,4-di-tert-butylphenyl)phosphite

Tris(2,4-di-tert-butylphenyl)phosphite
Names
Preferred IUPAC name
Tris(2,4-di-tert-butylphenyl) phosphite
Other names
  • Plastic additive 12
  • Alkanox 240
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.046.084 Edit this at Wikidata
EC Number
  • 250-709-6
UNII
  • InChI=1S/C42H63O3P/c1-37(2,3)28-19-22-34(31(25-28)40(10,11)12)43-46(44-35-23-20-29(38(4,5)6)26-32(35)41(13,14)15)45-36-24-21-30(39(7,8)9)27-33(36)42(16,17)18/h19-27H,1-18H3
    Key: JKIJEFPNVSHHEI-UHFFFAOYSA-N
  • CC(C)(C)C1=CC(=C(C=C1)OP(OC2=C(C=C(C=C2)C(C)(C)C)C(C)(C)C)OC3=C(C=C(C=C3)C(C)(C)C)C(C)(C)C)C(C)(C)C
Properties
C42H63O3P
Molar mass 646.937 g·mol−1
Appearance white solid
Melting point 181–184 °C (358–363 °F; 454–457 K)
<0.1 g/100g
Solubility in n-hexane 14 g/100g
Solubility in ethyl acetate 5 g/100g
Solubility in chloroform 58 g/100g
Solubility in toluene 40 g/100g
Solubility in methanol <0.5 g/100g
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tris(2,4-di-tert-butylphenyl)phosphite is an organophosphorus compound with the formula [(C4H9)2C6H3O]3P. This white solid is a widely used stabilizer in polymers where it functions as a secondary antioxidant. It also reduces discoloration (yellowing) of plastics. The compound is a phosphite ester formed by the reaction of 2,4-di-tert-butylphenol with phosphorus trichloride.[1] It is an approved food contact materials in the US.[2]

See also

References

  1. ^ Rainer Wolf; Bansi Lal Kaul (2000). "Plastics, Additives". Ullmann's Encyclopedia Of Industrial Chemistry. doi:10.1002/14356007.a20_459. ISBN 3527306730.
  2. ^ Markley, Laura C.; González Bonet, Andrés M.; Ogungbesan, Adejoke; Bandele, Omari J.; Bailey, Allan B.; Patton, Geoffrey W. (August 2023). "Safety assessment for Tris(2,4-di-tert-butylphenyl) phosphite (Irgafos 168) used as an antioxidant and stabilizer in food contact applications". Food and Chemical Toxicology. 178: 113877. doi:10.1016/j.fct.2023.113877.