| Patent Number |
Title Of Patent |
Date Issued |
| 6828275 |
Synergistic insecticide mixtures |
December 7, 2004 |
| The invention relates to insecticidal mixtures of fipronil and agonists or antagonists of nicotinic acetylcholine receptors for the protection of industrial materials and plants. |
| 6534529 |
Synergistic insecticide mixtures |
March 18, 2003 |
| The invention relates to insecticidal mixtures of fipronil and agonists or antagonists of nicotinic acetylcholine receptors for the protection of industrial materials and plants. |
| 6521653 |
Microbicidal benzotriazoles |
February 18, 2003 |
| Novel benzotriazoles of the formula ##STR1##in which R, X.sup.1, X.sup.2, X.sup.3, X.sup.4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes,a process for the preparation of these substances and their use as microbicides in cro |
| 6380225 |
Microbicidal benzotriazoles |
April 30, 2002 |
| Novel benzotriazoles of the formula ##STR1##in whichR, X.sup.1, X.sup.2, X.sup.3, X.sup.4 and Y have the meanings given in the description,and their acid addition salts and metal salt complexes,a process for the preparation of these substances and their use as microbicides in crop protec |
| 6217642 |
Benzothiophene-2-carboxamide s,s-dioxides for use in anti-fouling applications |
April 17, 2001 |
| A method and composition for protection against fouling of objects which come into contact with sea water or brackish water comprising a benzothiophene-2-carbomide S,S-dioxide as the essential component are described. |
| 6197799 |
Dithiazoldioxides and the use thereof as microbicides |
March 6, 2001 |
| The invention relates to novel dithiazole dioxides, to processes for their preparation and to their use in crop protection and in the protection of materials. |
| 6172092 |
Microbicidal benzotriazoles |
January 9, 2001 |
| Novel benzotriazoles of the formula ##STR1##in whichR, X.sup.1, X.sup.2, X.sup.3, X.sup.4 and Y have the meanings given in the description,and their acid addition salts and metal salt complexes,a process for the preparation of these substances and their use as microbicides in crop protec |
| 6107336 |
Dihydrofuran carboxamides |
August 22, 2000 |
| The invention concerns novel dihydrofuran carboxamides of formula (I), ##STR1## in which R stands for groups of formulae (a), (b) or (c), ##STR2## in which R.sup.1, R.sup.2, R.sup.3, X, m, n and p have the meanings given in the description. The invention also concerns a process f |
| 5990043 |
Anti-fouling compositions |
November 23, 1999 |
| An anti-fouling composition comprising a carrier, and a binder, the improvement which comprises an effective amount of at least one insecticide. The composition is applied to the surfaces of articles which come into contact with seawater or brackish water, especially wood. Other conv |
| 5985903 |
Microbicidal benzotriazoles |
November 16, 1999 |
| Novel benzotriazoles of the formula ##STR1## in which R, X.sup.1, X.sup.2, X.sup.3, X.sup.4 and Y have the meanings given in the description,and their acid addition salts and metal salt complexes,a process for the preparation of these substances and their use as microbicides in crop |
| 5972971 |
Fungicidal active compound combinations |
October 26, 1999 |
| The present application relates to new active compound combinations composed, on the one hand, of prior art compounds metaconazole, 5-[(4-chlorophenyl)methyl]-2,2-dimethyl-1-(1H-1,2,4-triazol-1-yl-methyl)cy clopentanol and imidacloprid, 1-[(6-chloro-3-pyridinyl)-methyl]-4,5-dihydro-N- |
| 5925675 |
N-sulfonyliminodithio compounds useful for in plant and material protection |
July 20, 1999 |
| N-sulfonyliminodithio compounds have the formula (I), in which R.sup.1 and R.sup.2 stand for optionally substituted alkyl, alkenyl or alkinyl, and Ar stands for optionally substituted aryl; also disclosed are processes for preparing these compounds and their use for plant and material pr |
| 5712304 |
Carboxylic acid amide benzothiophenecarboxamide s-oxides |
January 27, 1998 |
| New benzothiophenecarboxamide S-oxides of the formula (I) ##STR1## in which R.sup.1 represents optionally substituted alkyl, or represents alkenyl or alkinyl, or represents in each case optionally substituted cycloalkyl or cycloalkylalkyl, or represents in each case optionally su |
| 5703103 |
Thiazolylpyrazolinones and their use for protecting technical materials |
December 30, 1997 |
| The present invention relates to novel thiazolylpyrazolinones, a process for their preparation and their use for the protection of technical materials. |
| 5672617 |
Medicaments containing 1-thiocarbamoyl-5-hydroxy-pyrazoles and their use as agents for combating |
September 30, 1997 |
| This application relates to new thiocarbamoyl compounds of the formula (I) ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4 have the meanings given in the description. |
| 5622546 |
Mould-resistant emulsion paints |
April 22, 1997 |
| The application relates to emulsion paints which are protected against fungal infestation by the use of N-alkyl-benzothiophene-2-carboxamide S,S-dioxides. |
| 5315049 |
Process for the nuclear chlorination of aromatic hydrocarbons |
May 24, 1994 |
| Alkylaromatics are subjected to nuclear chlorination in the liquid phase in the presence of Friedel-Crafts catalyst mixtures comprising compounds of iron and antimony and cocatalysts of the formula (II) ##STR1## wherein the substituents have the meaning given in the description. |
| 5314986 |
Phenolic resins from bisphenol a residual resins and mixtures of chloro-substituted hydrocarbons |
May 24, 1994 |
| Rubber components of a vulcanizable rubber composition are homogenized by adding to the composition, prior to vulcanization, a phenolic resin formed by reacting a bisphenol A residual resin with chlorinated C.sub.4 to C.sub.8 hydrocarbons in the presence of a Friedel-Crafts alkylation |
| 5292975 |
Process for decreasing the halogen content of polyhalogenated aromatics |
March 8, 1994 |
| When the halogen content of polyhalogenated aromatics is decreased by reaction with monohalogenated and/or non-halogenated aromatics in the gas phase, good yields and significantly improved catalyst service lives are achieved if the reaction is carried out in the presence of a catalyst a |
| 5292712 |
Thermoreactive recording material having particular stability |
March 8, 1994 |
| New thermoreactive recording materials contain at least one salt of a specially modified bisphenolcarboxylic acid and are distinguished by good stabilisation of the ink, even upon extended storage time, good light stabilities and excellent stabilities to water, plasticisers, fats and |
| 5221718 |
Process for the preparation of copolymers containing nitrile groups based on ethylenically unsat |
June 22, 1993 |
| Copolymers containing nitrile groups based on ethylenically unsaturated monomers are prepared by reacting the copolymers on which they are based with ammonia at temperatures of from 150.degree. to 270.degree. C. and pressures from 30 to 350 bar in the presence of an aliphatic nitrile |
| 5219976 |
Process for the preparation of phenol resins using by-products of the chlorination of butadiene |
June 15, 1993 |
| By-products from the chlorination of butadiene may be reacted with phenols in the presence of iron catalysts to form Novolak type phenol resins. |
| 5214100 |
Use of certain phenolic resins for reinforcing rubber vulcanizates |
May 25, 1993 |
| Phenolic resins obtainable by Friedel-Crafts alkylation of phenols with polyfunctional compounds are eminently suitable as a reinforcing resin for rubber vulcanizates. |
| 5126429 |
Flexible polyamide from dimer acid and bis-secondary diamine |
June 30, 1992 |
| This invention relates to amorphous, flexible elastomeric polyamides based on dimer fatty acids and special disecondary diamines which have a glass transition temperature below 10.degree. C., to the production of these elastomeric polyamides and to their use as rubbers, plasticizers and, |
| 5071943 |
Process for the isolation of tetrachlorobutane and for the production of phenolic resins from mi |
December 10, 1991 |
| Secondary products formed in the chlorination of butadiene can be reacted with phenols in the absence of iron catalysts to form novolak-like phenolic resins in such a way that the tetrachlorobutane present in the secondary products does not react. It can be distilled off with the excess |
