Verfahren zur Herstellung von bei Zimmertemperatur flüssigen 2-Hydroxy-4-alkoxybenzophenonen

Verfahren zur Herstellung von bei Zimmertemperatur flüssigen 2-Hydroxy-4-alkoxybenzophenonen

1291536 Stabilizing polymers CINCINNATI MILACRON CHEMICALS Inc 19 April 1971 [11 Feb 1970] 21546/71 Heading C3P [Also in Division C2] PVC and polypropylene contain as u/v light stabilizer a 2-hydroxy-4-isoalkoxybenzophenone of formula C 6 H 5 .CO.C 6 H 3 (OH)(OR) in which R is a C 6-10 isoalkyl grou...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
1. Verfasser: HECHENBLEIKNER,INGENUIN
Format: Patent
Sprache:ger
Schlagworte:
ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
COMPOSITIONS BASED THEREON
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:1291536 Stabilizing polymers CINCINNATI MILACRON CHEMICALS Inc 19 April 1971 [11 Feb 1970] 21546/71 Heading C3P [Also in Division C2] PVC and polypropylene contain as u/v light stabilizer a 2-hydroxy-4-isoalkoxybenzophenone of formula C 6 H 5 .CO.C 6 H 3 (OH)(OR) in which R is a C 6-10 isoalkyl group. Exemplified PVC compositions also contain distearyl azelate and dibutyltin isooctyl thioglycolate, and in some cases TiO 2 and/or acrylic impact modifiers. Exemplified polypropylene compositions also contain distearyl thiodipropionate and the tetrakis ester of pentaerythritol with 4-hydroxy- 2,6-ditertbutylphenyl propionic acid, and in one case also 2,2 - thiobis - (4 - tertoctylphenolate)- n-butylamine nickel (II).