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Dokument EP000001681923A1 (Seiten: 1)

Bibliografische Daten Dokument EP000001681923A1 (Seiten: 1)
INID Kriterium Feld Inhalt
54 Titel TI [DE] WIRKSTOFFFORMULIERUNGEN ENTHALTEND COPOLYMERE MIT SULFONSÄURE UND PHENOXYETHYLACRYLAT
[EN] FORMULATIONS CONTAINING COPOLYMERS OF SULFONIC ACID AND PHENOXYETHYL ACETATE
[FR] FORMULATIONS CONTENANT DES COPOLYMÈRES D'ACIDE SULFONIQUE ET D'ACÉTATE DE PHENOXYÉTHYLE
71/73 Anmelder/Inhaber PA BASF AG, DE
72 Erfinder IN BRATZ MATTHIAS, DE ; GOEDEL WERNER A, DE ; HADELER JOACHIM, DE ; KOLTZENBURG SEBASTIAN, DE ; LEHMANN STEPHAN, DE ; MAYER WINFRIED, DE ; SCHROF WOLFGANG, DE ; STEINMETZ BERNHARD, DE
22/96 Anmeldedatum AD 19.10.2004
21 Anmeldenummer AN 04790621
Anmeldeland AC EP
Veröffentlichungsdatum PUB 26.07.2006
33
31
32
Priorität PRC
PRN
PRD
DE
10351004
30.10.2003
33
31
32
PRC
PRN
PRD
EP
2004011797
19.10.2004
51 IPC-Hauptklasse ICM A01N 25/04 (2006.01)
51 IPC-Nebenklasse ICS A01N 25/30 (2006.01)
A01N 47/24 (2006.01)
IPC-Zusatzklasse ICA
IPC-Indexklasse ICI
Gemeinsame Patentklassifikation CPC A01N 25/04
A01N 25/10
A01N 25/30
A01N 47/10
A01N 47/24
C08F 220/1804
C08F 220/301
C08F 220/585
MCD-Hauptklasse MCM A01N 25/10 (2006.01)
MCD-Nebenklasse MCS A01N 25/04 (2006.01)
A01N 25/30 (2006.01)
A01N 47/24 (2006.01)
MCD-Zusatzklasse MCA
57 Zusammenfassung AB [EN] New active agent formulations contain active agent(s) (A); random radical copolymer(s) (B), derived from sulfoalkyl (meth)acrylate or N-sulfoalkyl-(meth)acrylamide monomer(s) (I) (and/or their salts), (meth)acrylate ester or N-substituted (meth)acrylamide monomer(s) (II) and optionally further monomers; and optionally further additives (C). New active agent formulations contain active agent(s) (A); random radical copolymer(s) (B), derived from olefinically unsaturated sulfonic acid(s) of formula (I) (and/or their salts), monomer(s) of formula H 2C=C(R 4>)-CO-YR 6> (II) and optionally further monomers; and optionally further additives (C). n : 0-10; X, Y : O or NR 5>; R 1>, R 4>H or Me; R 2>, R 3>H or 1-6C alkyl; R 5>, R 6>H, alkyl, aryl, alkylaryl, alkoxyalkyl, aryloxyalkyl, alkoxyaryl, hydroxyalkyl, (di)alkylaminoalkyl, (di)arylaminoalkyl, alkylarylaminoalkyl or alkylarylaminoaryl (where aryl groups are optionally substituted). Independent claims are included for: (1) the preparation of aqueous dispersions, by contacting the formulations with aqueous systems (optionally in presence of additives) and dispersion conventionally; (2) the preparation of the formulations, by dissolving (A) - (C) and optionally further additives in an organic solvent (or dissolving the components separately in organic solvents then mixing the solutions), then conventionally removing the solvent; and (3) an alternative preparation of the formulations, by forming an aqueous solution of (B); dissolving (A), (C) (if present) and optionally further additives in water-miscible organic solvent(s); mixing the solutions; applying energy to form a dispersion; and conventionally removing the solvent. [Image].
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