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Beate Strecker

Alfred Oftring

Dieter Hertel

Richard Baur

Johannes Perner

Volker Schwendemann

Oral Aydin

Wolfgang Reif

Gerhard Bauer

Gerhard Wolf

Richard R Schmidt

Martin Aus Dem Kahmen

Helmut Wolf

Hans-Heinrich Bechtolsheimer

Georg Schuh

Wolfgang Klotz

Hendrik Wulff

Preparation of N-acylamino carboxylic acids and N-acylamino sulfonic

Use of endgroup-capped fatty amide alkoxylates

1-(2'-hydroxy and 2'-sulfatoalkyl) glycoside

Process for the preparation of N-alkanoyl-polyhydroxyalkylamines

A compound of the formula ##STR1## where R.sup.1 and R.sup.2, independently of one another, are each C.sub.1 -C.sub.10 -alkyl, C.sub.1 -C.sub.10 -alkoxy, C.sub.5 -C.sub.10 --cycloalkyl or C.sub.5 -C.sub.10 -aryl, each of which may furthermore contain from 1 to 3 non-adjacent nitrogen, oxygen or sulfur atoms as hetero atoms in the carbon chain or carbon ring and may be substituted by 1 to 3 C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy groups, R.sup.1 or R.sup.2 may be hydrogen or R.sup.1 and R.sup.2 together form a bridge of 2 to 14 carbon atoms, where some of the carbon atoms may furthermore be part of an aromatic ring system, A is an n-valent organic radical and n is an integer equal to or greater than 2.

.beta.-hydroxyoxime ethers and solutions or dispersions crosslinkable at

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Ludwigshafen, Germany

Beate Strecker