Clariant International Ltd

Clariant Finance (Bvi) Limited

Clariant Produkte (Deutschland) Gmbh

Franz-Xaver Scherl

Peter Klug

Joerg Peter Grohmann

Waltraud Simsch

Adelgunde Oberhauser

Martin Glos

Dirk Leinweber

Peter Baur

Achim Stankowiak

Jonathan James Wylde

Maurice Frederic Pilz

Klaus Raab

Klaus-Dieter Vorlop

Ute Back

Ulf Pruesse

Oliver Franke

Nadine Decker

Andreas Gallas

Olaf Wachsen

Beate Siefer

Martin Knoebl

Sonja Gehm

Guiseppina Kluth

Jan Gauczinski

Carina Mildner

Matthias Loeffler

Elisabeth Wasmund

Nihal U Obeyesekere

Heidi Rausch

Ulf Prüsse

Thenuka Ariyaratna

Dirk Buehring

Roland Arnold

Nirupam Purkayastha

Eva-Maria Keitzl

Jörg Grohmann

Giuseppina Kluth

Amir Mahmoudkhani

George Italo Pitombeira Nunes

The present invention relates to a composition for inhibiting micro-organisms, as well as related processes, formulations, concentrates and uses. The composition comprises at least 30 wt.-% compound X, wherein compound X is according to Formula (I): wherein R is a saturated or unsaturated hydrocarbon chain having seven or nine carbon atoms, or a mixture thereof.

Composition for inhibiting micro-organisms

Compositions comprising isosorbide monoesters and alcohols comprising at least one aromatic group What are described are compositions comprising  The compositions are distinguished in particular by an advantageous antimicrobial activity.

Compositions containing isosorbide monoester and alcohols that contain at least one aromatic group

What are described are compositions comprising in which In an advantageous manner, the compositions are suitable for producing cosmetic, dermatological or pharmaceutical compositions, crop protection formulations, washing or cleaning compositions or paints or coatings.

Composition comprising isosorbide monoesters and isosorbide diesters

The use of one or more compounds of the formula (I)  The use is preferably in cosmetic, dermatological or pharmaceutical compositions, in crop protection formulations, in washing or cleaning compositions or in paints or coatings.

Use of isosorbide monoesters as antimicrobial active substances

A process for preparing acylglycinates of the formula (I) wherein Ris a linear or branched, saturated alkanoyl group having 6 to 30 carbon atoms, or is a linear or branched, singly or multiply unsaturated alkenoyl group having 6 to 30 carbon atoms, and Qis a cation, wherein glycine is reacted with fatty acid chloride RCl, in water and in the presence of a basic alkali metal compound which yields cations Q, but in the absence of organic solvents, at 25-50&#xb0; C. Also described are compositions comprising acylglycinates of the formula (I). 

Process for preparing acylglycinates and compositions comprising such compounds

The invention relates to liquid compositions which contain a) from 5 to 95% by weight of sorbitan monocaprylate and b) from 5 to 95% by weight of one or more alcohols of formula (1)R&#x2014;OH&#x2003;&#x2003;(1),wherein R is a group consisting of carbon, hydrogen and optionally oxygen atoms with 5 to 12, preferably 6 to 11, carbon atoms, and the carbon atoms can be interlinked in a linear, branched and/or cyclic fashion via saturated, unsaturated and/or aromatic carbon-carbon bonds and the groups can also contain ether units and hydrogen atoms and/or hydroxyl groups can be bound to the individual carbon atoms. The liquid compositions are suitable for the production of cosmetic, dermatological or pharmaceutical products.

Composition containing sorbitan monocaprylate and alcohol

Use of isosorbide monoesters as thickeners

The invention relates to a surfactant solution containing: (a) 28 to 65 wt.-% of a mixture of (a1) 5 to 20 wt.-% of N-methyl-N-oleylglucamine, (a2) 50 to 93 wt.-% of N-methyl-N&#x2014;C-C-acylglucamines, (a3) 0 to 30 wt.-% of other N-methyl-N-acylglucamines, components (a1), (a2) and (a3) adding up to 100 wt.-%, (b) 0 to 20 wt.-% of one or more alcohols, (c) 20 to 72 wt.-% of water, and (d) 0 to 5 wt.-% of additives, components (a), (b), (c) and (d) adding up to 100 wt.-%.

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What are described are compositions comprising  In an advantageous manner, the compositions are suitable for producing cosmetic, dermatological or pharmaceutical compositions, crop protection formulations, washing or cleaning compositions or paints or coatings.

Composition containing isosorbide monoester and isosorbide diester

Use of isosorbide diesters as thickeners

What are described are compositions comprising  The compositions are distinguished in particular by an advantageous antimicrobial activity.

Compositions comprising isosorbide monoester and N-hydroxypyridones

The invention relates to liquid compositions which contain a) from 40 to 99.9% by weight of sorbitan monocaprylate and b) from 0.1 to 60% by weight of one or more antimicrobial substances selected from the group consisting of the components b1) to b5): b1) specific organic acids and the salts thereof, b2) specific formaldehyde donors, b3) specific isothiazolinones, b4) specific paraben esters and the salts thereof, and b5) specific pyridones and the salts thereof. The liquid compositions are suitable for the production of cosmetic, dermatological or pharmaceutical products.

Composition containing sorbitan monocaprylate and antimicrobial substances

The invention relates to a method for producing phosphoric acid triesters of formula (I). According to said method, phosphoric acid or a phosphoric acid derivative selected from orthophosphoric acid, tetraphosphoric decaoxide and polyphosphoric acid is reacted with alkoxylated alcohols of formulae (II) R&#x2014;(OA)&#x2014;OH, (III) R&#x2014;(OA)&#x2014;OH, and (IV) R&#x2014;(OA)&#x2014;OH, in the molar ratio phosphoric acid or phosphoric acid derivative to alkoxylated alcohol of 1:2.5 to 1:3.3, at between 200 and 240&#xb0; C. 

Method for producing alkoxylated phosphoric acid triesters

Phosphoric esters comprise The phosphoric esters of the invention are very useful in the manufacture of cosmetic, pharmaceutical and dermatological compositions.

Phosphoric acid esters containing phosphorus atoms bridged by diol units

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Burgkirchen, Germany

Franz-Xaver Scherl