Projet

1 2 3 4 5 6 7 8 9 1011

4582 Reaction product of di-tert-butyl- 0119345-01-6 83595 A 18 Composition:

phosphonite with biphenyl, - 4,4′-biphénylène-bis[0,0-bis(2,4-di-tert-butylphényl) phosphonite] [38613-77- obtained by condensation of 2,4-di- 3] [36-46 % m/m (*)],

tert-butylphenol with Friedel Craft - 4,3′-biphénylène-bis[0,0-bis(2,4-di-tert-butylphényl) phosphonite] [118421- reaction product of phosphorous 00-4] [17-23 % m/m (*)],

trichloride and biphenyl - 3,3′-biphénylène-bis[0,0-bis (2,4-di-tert-butylphényl)phosphonite] [118421-

01-5] [1-5 % m/m (*)],

- 4-biphénylène-0,0-bis(2,4-di-tert-butylphényl) phosphonite [91362-37-7] [11- 19 % m/m (*)],

- tris(2,4-di-tert-butylphényl)phosphite [31570-04-4)] [9-18 % m/m (*)],

- 4,4′-biphénylène-0,0-bis(2,4-di-tert-butylphényl)phosphonate-0,0-bis(2,4-ditert-butylphényl) phosphonite [112949-97-0] [< 5 % m/m (*)].

Quantité de substance utilisée/quantité de formulation.

Autres spécifications:

- Teneur en phosphore de minimum 5,4 % à maximum 5,9 %,

- Acidité maximale de 10 mg de KOH/g,

- Intervalle de fusion de 85 à 110 °C.

4588 Thiodiethanolbis(5-methoxy- 0120218-34-0 92930 A6

dihydropyridine-3-carboxylate)

carbonyl-2-6-dimethyl-1,4- 4600 Acrylic acid, 2,4-di-tert-pentyl-6-[1- 0123968-25-2 31530 A X5

(3,5-di-tert-pentyl-2-hydroxyphenyl)ethyl]phenyl ester 4601 N,N'-Bis(2,2,6,6-tetramethyl-4- 0124172-53-8 40155 A 0,052

piperidyl)-N,N'-diformyl-12

hexamethylenediamine 4623 3,3-Bis(methoxymethyl)-2,5- 0129228-21-3 39925 A X 0,05 dimethylhexane 4642 2,4-Dimethyl-6-(1-methyl- 0134701-20-5 49485 A X1

pentadecyl)phenol 4645 Bis(3,4-dimethylbenzylidene)- 0135861-56-2 38879 A sorbitol 4648 1,2-Bis(3-aminopropyl)ethylene- 0136504-96-6 38510 A5

diamine, polymer with N-butyl-

2,2,6,6-tetramethyl-4-piperidin-

amine and 2,4,6-trichloro-1,3,5-

triazine