Facilisis, 565;AO 565;ADNOX 565 polymerorum

Nomen chemicum:2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol.
Synonyma: Irganox 565, Songnox 5650;Facilisis, 565;AO 565
CAS No.:991-84-4
Chemcial Structure:

Sarcina:25KG Carton

Applicationem

ADNOX® 565 altum hypotheticum pondus est;non-maculans, multifunctionalis antioxidant elaborata ad stabiliendum elastomorum insaturatum (BR, IR, SBR, SIS, SBS, etc.), adhaesiones calidae liquefaciunt, et resina estensaria resina taciificans.

Background

565 Antioxidant polymerus multifunctionalis impeditus phenolicum antioxidant, maxime idoneum ad stabilizationem post-processus iuvantis insaturati, ad elastomorum efficacissimum, materiam tueri potest, ne in productione, processu et usu finali fiat.Donec adipiscing scelerisque oxidative.Praeclarum est antioxidantis et photothermalis stabilior propter resinas varietates.Notas habet parvae additionis, humilis LEVITAS, summus color fastigium, formationem gel impedire potest.Plurimum in sequentibus elastomoribus: Flexilis cis-butadiene isoprene (IR) Flexilis styrene-butadiene (SBR) Flexilis nitrile-butadiene (NBR) carboxylated styrene-butadiene latex emulsio polystyrene-butadiene Flexilis (ESBR) solutio polymerization Styrene- butadiene rubber (SSBR) thermoplastic styrene-butadiene rubber SBS thermoplastic styrene-butadiene rubber SIS, adhiberi potest etiam ad resinas, resinas naturales et syntheticas, ut EPDM, ABS, plasticum, polyamideum (nylon, PA), altum Impact polystyrenum (HIPS) et polyolefins.Plastica ABS est plastic polystyrene modificata composita ex tribus componentibus, quae ex acrylonitrile (A), butadiene (B) et styrene (S).ABS plasticae adhiberi possunt ad ornandas tabulas plasticas cum exemplaribus impressis, etc.

Synthesis Antioxidant 565 in hac dissertatione investigatur.2,6-di-tert-butylphenolum, substratum initiale, nitratum ad 2,6-di-tert-butyl-4-nitrophenolum 95% cedit.2,6-di-tert-butyl-4-nitrophenol reducitur ad 4-amion -2,6-di-tert-butylphenolum cum hydrogenio coram Raney Ni vel Pd/C.Ne compositione 4-amionis -2,6-di-tert-butylphenoli cum aeri expositae, 4-amion -2,6-di-tert-butylphenol permittitur agere cum chloride Cyanurico absque separatione ad formam 6-(3. ,5-di-tert-butyl-4-hydroxy) laniline-2,4-dichloro-1,3,5-triazin in 95% cede pro 2 gradibus.

Reactio 6-(3,5-di-tenti-butylis-4-hydroxis) anilini-2,4-dichloro-1,3,5-triazini cum 2 aequivalentia ipsius n-Octylthioli productum finale dedit 6-(3; 5-di-tert-butyl-4- aniline-hydroxia 2,4-bis (octylthio) -1,3,5-triazin in 94% cedit.