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Matthias Loffler Patents
Inventor:
Loffler; Matthias
Address:
Niedernhausen, DE
No. of patents:
40
Patents:




Patent Number Title Of Patent Date Issued
7399478 Cosmetic, pharmaceutical and dermatological products July 15, 2008
The invention provides cosmetic, pharmaceutical and dermatological compositions comprising at least one copolymer obtainable by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) if desired, one or more further olefinically unsaturated,
7393520 Decorative cosmetic and dermatological products July 1, 2008
The invention provides decorative cosmetic and dermatological compositions comprising at least one copolymer obtained by free-radical copolymerization of A) acryloyld imethyltaurine and/or acryloyld imethyltaurates, B) optionally, one or more further olefinically unsaturated, noncati
7348390 Stable dispersion concentrates March 25, 2008
The invention provides stable dispersion concentrates comprising: I) 5 to 80% by weight, preferably 10 to 80% by weight, particularly preferably 20 to 60% by weight, especially preferably 30 to 40% by weight, of a polymer which, in random distribution, consists of 90 to 99.99% by weigh
7332155 Surfactant-containing cosmetic, dermatological and pharmaceutical agents February 19, 2008
The invention provides surfactant-containing cosmetic, dermatological, and pharmaceutical agents comprising at least one water-soluble or water-swellable copolymer obtainable by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally
7323507 Stable dispersion concentrate consisting of a copolymer of acryloyldimethyltauric acid and cycli January 29, 2008
Dispersion concentrates are claimed which consist of:I) 10-80% by weight of a crosslinked copolymer obtained by polymerization of 1 to 50% by weight of a cyclic N-vinylcarboxamide and 49.99 to 98.99 by weight of acryloyldimethyltauric acid,II) 20-90% by weight of a phase selected from
7297328 Surfactant-free cosmetic, dermatological and pharmaceutical agents November 20, 2007
The invention provides a surfactant-free cosmetic, dermatological, and pharmaceutical agents comprising at least one copolymer obtainable by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more further olefinically un
7279154 Use of comb copolymers based on acryloyldimethyltaurine acid in cosmetic, pharmaceutical and der October 9, 2007
The invention relates to uses of comb polymers of acryloyldimethyltaurine and/or acryloyldimethyltaurates in cosmetic, pharmaceutical and dermatological applications as thickeners, dispersing agents, suspending agents, emulsifiers, stabilizers, solubilizers, conditioning agents, cons
7208556 Water-soluble or water-swellable crosslinked copolymers April 24, 2007
Water-soluble or water-swellable crosslinked copolymers consisting essentially of structural units of the formula 1 ##STR00001## or a mixture of the structural units of the formula 1 with structural units of the formula 2 ##STR00002## and structural units of the formula 3 ##STR0000
7186774 Silicone-modified comb polymers based on acryloyldimethyltaurine acid (2-acrylamido-2-methyl-1-p March 6, 2007
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more olefinically unsaturated, optionally crosslinking comonomers containing at least one
7186405 Deodorants and anti-perspirants March 6, 2007
The invention relates to deodorants and antiperspirants comprising at least one copolymer. The copolymer is obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, and B) optionally, one or more further olefinically unsaturated, noncat
7151137 Acryloyldimethyltaurine acid-based grafted copolymers December 19, 2006
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) if desired, one or more other olefinically unsaturated, optionally crosslinking comonomers containing at leas
7081507 Cationically modified comb polymers based on acryloyldimethyl taurine acid July 25, 2006
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more other olefinically unsaturated, noncationic, optionally crosslinking comonomers conta
7053146 Compositions containing copolymers based on acryloyldimethyl aminoethylsulfonic acid and synergi May 30, 2006
The invention relates to compositions comprising copolymers based on acryloyldimethyltaurine and also synergistic additives selected from anionic, cationic, nonionic, and betaine surfactants. The compositions exhibit a pronounced thermoassociative behavior and are outstandingly suita
7026408 Sulphonated comb polymers and preparations, in particular hair cosmetic preparations, based on s April 11, 2006
Water-soluble and/or water-dispersible comb polymers consisting of a polymer main chain and polyester side-arms which contain sulphone groups and are linked to said polymer main chain via ester groups.
7025973 Acid cosmetic, dermatological and pharmaceutical agents April 11, 2006
The invention provides acidic cosmetic, dermatological, and pharmaceutical agents comprising at least one copolymer obtainable by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more further olefinically unsaturated,
7022791 Cosmetic, pharmaceutical and dermatological products containing an electrolyte April 4, 2006
The invention relates to cosmetic, dermatological, and pharmaceutical products containing an electrolyte. The products are obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, and B) optionally, one or more further olefinically un
6964995 Grafted comb polymers based on acryloyldimethyltaurine acid November 15, 2005
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more other olefinically unsaturated, noncationic, optionally crosslinking comonomers contain
6891011 Comb-shaped copolymers based on acryloyldimethyltaurine acid May 10, 2005
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more other olefinically unsaturated, nopcationic comonomers, C) optionally, one or more o
6891009 Water-soluble or water-swellable crosslinked copolymers May 10, 2005
Water-soluble or water-swellable crosslinked copolymers consisting essentially of structural units of the formula 1 ##STR1##or a mixture of the structural units of the formula 1 with structural units of the formula 2 ##STR2##and structural units of the formula 3 ##STR3##where R,
6833419 Fluorine-modified comb polymers based on acryloydimethyltaurine acid December 21, 2004
The invention provides water-soluble or water-swellable copolymers obtained by free-radical copolymerization of A) acryloyldimethyltaurine and/or acryloyldimethyltaurates, B) optionally, one or more other olefinically unsaturated, optionally crosslinking, comonomers containing at least
6833129 Aqueous or aqueous-alcoholic body-cleansing compositions comprising oligoesters December 21, 2004
Body-cleansing compositions are claimed which comprise oligoesters obtained by condensation of one or more dicarboxylic acids or esters thereof and one or more polyhydric alcohols.
6803478 Process for the preparation of alk(en)ylphosphoric ester salts October 12, 2004
The invention relates to a process for the preparation of alk(en)ylphosphoric ester salts which comprises reacting the alk(en)ylphosphoric esters in the form of their melts with a base. Advantageously, the alk(en)ylphosphoric esters do not need to be dissolved in a solvent prior to n
6696517 Use of copolymers based on acrylamidoalkylsulfonic acids as thickeners in preparations comprisin February 24, 2004
The invention relates to the use of copolymers consisting essentially of a1) 1 to 50% by weight of the repeat structural unit of the formula (1): ##STR1## where n is an integer from 2 to 9 or a2) 1 to 50% by weight of a mixture of the repeat structural unit of the formula (1) and o
6683144 Water-soluble or water-swellable crosslinked copolymers January 27, 2004
Water-soluble or water-swellable crosslinked copolymers consisting essentially of structural units of the formula 1 ##STR1##or a mixture of the structural units of the formula 1 with structural units of the formula 2 ##STR2##and structural units of the formula 3 ##STR3##where R,
6682750 Surfactant-free cosmetic, dermatological and pharmaceutical compositions January 27, 2004
The invention relates to surfactant-free cosmetic, dermatological and pharmaceutical compositions, comprising at least one copolymer consisting essentially of a1) 1 to 50% by weight of the repeat structural unit of the formula (1) ##STR1## where n is an integer from 2 to 9, or
6645476 Water-soluble polymers and their use in cosmetic and pharmaceutical compositions November 11, 2003
The invention provides water-soluble polymers preparable by free-radical copolymerization of A) one or more macromonomers containing an end-group capable of polymerization, a hydrophilic moiety based on polyalkylene oxides, and a hydrophobic moiety which comprises hydrogen or a saturated
6541016 Mixtures of alkylphosphoric esters and use thereof as cosmetic and pharmaceutical emulsifiers April 1, 2003
This invention relates to monoalkyl phosphoric esters, dialkyl phosphoric esters, and, in small amounts, trialkyl phosphoric esters or salts thereof, which are preferably based on .beta.-branched fatty alcohols, particularly Guerbet alcohol, which are effective in lowering the surface
6489395 Emulsions December 3, 2002
Emulsions are claimed which comprise oligoesters as emulsifiers. These oligoesters have hitherto only been used as soil release polymers.
6448297 Alkyl phosphate and aqueous emulsions thereof September 10, 2002
The invention relates to alkyl phosphates, in particular their mixtures, of the formula ##STR1##in which R is C.sub.12 -C.sub.22 -alkyl, preferably C.sub.14 -C.sub.18 -alkyl, X is a group of the formulae NH.sub.3 R.sup.1, NH.sub.2 R.sup.2 R.sup.3 or NHR.sup.4 R.sup.5 R.sup.6, Y is as
6437068 Water-soluble or water-swellable crosslinked copolymers August 20, 2002
Water-soluble or water-swellable crosslinked copolymers consisting essentially of structural units of the formula 1 ##STR1##or a mixture of the structural units of the formula 1 with structural units of the formula 2 ##STR2##and structural units of the formula 3 ##STR3##where R,
6355752 Neutralized crosslinked polymers of acrylamidoalkylsulfonic acids and N-vinylamides March 12, 2002
Water-soluble or water-swellable polymers, preferably having a particle size no greater than 10 .mu.m, which, in addition to from 0.01 to 5% by weight of crosslinking structures originating from monomers having at least two olefinic double bonds, comprise, in random distribution, from 1
6291422 Surfactant-containing formulations September 18, 2001
The invention relates to surfactant-containing formulations which comprise, as surfactant, an N-(3-dialkylamino)propyl-N-polyhydroxyalkylcarboxamide of the formula ##STR1##where R is an aliphatic radical having from 8 to 24 carbon atoms, R.sup.1 and R.sup.2, which are identical or di
6180591 Use of N-(3-dialkylamino) propyl-N-polyhydroxyalkylcarboxamides and their acid adducts as thicke January 30, 2001
The invention relates to the use of compounds of the formula 1 as thickeners for liquid, aqueous surfactant systems ##STR1##where R is an aliphatic radical having from 8 to 24 carbon atoms, R.sub.1 and R.sup.2, which are identical or different, are alkyl groups having from 1 to 4 car
6133216 Coated ammonium nitrile bleach activator granules October 17, 2000
The invention relates to coated bleach activator granules of ammonium nitriles, which have been obtained by coating ammonium nitrile base granules with a water-soluble coating substance. The base granules are preferably thermally conditioned during or after the coating with the coati
6066753 Mixtures of long-chain alkyl phosphates May 23, 2000
The invention relates to mixtures of long-chain alkyl phosphates of the formula ##STR1## in which R is a mixture of C.sub.12 -C.sub.22, preferably C.sub.14 -C.sub.20, straight-chain alkyl radicals and C.sub.12 -C.sub.22, preferably C.sub.14 -C.sub.20, .beta.-branched alkyl radica
6063750 Bleach activator granules May 16, 2000
The invention relates to bleach activator granules of ammonium nitrile and phyllosilicate, obtained by mixing the two components, compressing them and comminuting the resulting agglomerates to the desired particle size.
5952283 Quaternary ammonium compounds as bleach activators and their preparation September 14, 1999
Quaternary ammonium compounds, their preparation and use Compounds of the formula I ##STR1## are claimed, as are their preparation and use, in which the radicals R.sub.1, R.sub.2 and R.sub.3 are organic substituents, L is either a lactam or a cyclic amidine and X is an appropriat
5952282 Sulfonylimine derivatives as bleach catalysts September 14, 1999
The use is claimed of compounds of the general formula ##STR1## in which the radicals A and R are as defined in the description. The novel compounds are employed as bleach catalysts in bleaching detergents and cleaning products.
5877325 Quaternary ammonium compounds as bleach activators and their preparation March 2, 1999
Compounds of the formula I ##STR1## are claimed, as are their preparation and use, in which the radicals R.sub.1, R.sub.2 and R.sub.3 are organic substituents, L is either a lactam or a cyclic amidine and X is an appropriate anion. The novel compounds are employed as bleach activ
5648521 Process for the preparation of amidoperoxycarboxylic acids July 15, 1997
Process for the preparation of amidoperoxycarboxylic acids, comprising the process steps: ring opening of the N-acyllactam to give the corresponding amidocarboxylic acid and, subsequently, oxidation of the resulting amidocarboxylic acid to the corresponding amidoperoxycarboxylic acid.


 
 
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