"Telephone, n. An invention of the devil which abrogates some of the advantages of making a disagreeable person keep his distance. "
|7655805||Method for synthesizing benzotriazole|
A method for synthesizing benzotriazole comprises acts of: preparing a first solvent comprising 2-(2-hydroxy-5-methylphenyl) benzotriazole, a basic agent and molecular sieves and a second solvent comprising 3-chloro-2-alkyl propylene; mixing the solvents; and heatin...
The present invention relates to non-steroidal progestins of the general formula (I) wherein R1 and R2 are independently of each other —H or —F, R3 is —CH
|7381762||Ultraviolet light (UV) absorbing compounds and compositions containing UV absorbing compounds|
Hydroxybenzotriazole-based compounds are useful for ultraviolet light absorbing additives for a variety of applications. Such compounds have particular usefulness in various applications, including plastics, automotive, coatings, and food packaging applications. Suc...
The invention relates to α-sulfonylamino-acetonitrile derivatives of the general formula (I) including the optical isomers thereof and mixtures of such isomers, wherein Ar1, and Ar2 independently of each other stand for an optionally substitut...
|7368489||Additive for inhibiting photolytic degradation reactions in aminoplasts|
The invention relates to a UV additive for aminoplast resins, to a method for producing a UV additive as well as to uses thereof. Said UV additive contains soluble sterically-hindered nitroxyl compounds in an aqueous aminoplast precondensate. A UV additive for amino...
|7361449||Specific dye compound, optical information recording medium comprising specific dye, and information recording method using this optical information recording medium|
The present invention provides an optical information recording medium comprising a substrate having disposed thereon a recording layer, wherein the recording layer includes a recording dye represented by the following formula (I) or (II):
|7326744||Low dusting crystal transformations of 2,2′-methylenebis[4-(1,1,3,3-tetramethylbutyl)-6-benzotriazolylphenol] and mixture thereof, method for preparing them, and ultraviolet light absorber using them|
The present invention relates to a low dusting crystalline 2,2′-methylenebis[4-(1,1,3,3-tetramethylbutyl)-6-benzotriazolylphenol] type I crystal transformation which exhibits diffraction peaks at diffraction angles (2θ±0.1°) of 7.1°, 8.6°, 14.3°, 16.1°, 18....
|7288583||Method of content protection with durable UV absorbers|
The contents of clear or lightly colored plastic containers or films are protected from ultraviolet radiation by the incorporation of certain UV absorbers of the class of durable benzotriazoles and tris-aryl-s-triazines in the container or film. Contents to be prote...
|7276265||Method of making a surface covering having gloss-in-register|
Surface covering components that include a topcoat layer with different gloss levels in various regions on the top coat layer, and methods of manufacturing such surface covering components, are disclosed. The surface covering components include a coating layer that ...
|7276990||Single-pole multi-throw switch having low parasitic reactance, and an antenna incorporating the same|
A switch arrangement comprises a plurality of MEMS switches arranged on a substrate about, and close to, a central point, each MEMS switch being disposed on a common imaginary circle centered on the central point. Additionally, and each MEMS switch is preferably spa...
|7229988||Dialkylhydroxybenzoic acid derivatives containing metal chelating groups and their therapeutic uses|
The present invention provides novel dialkylhydroxybenzoic acid derivatives containing metal chelating groups and the use of the novel compounds as therapeutics for treating and/or preventing various medical dysfunctions and diseases arising from reactive oxygen spe...
|7211675||Antiozonant based on functionalized benzotriazole UV absorbers and the process thereof|
A process for the preparation of a novel antiozonant and antioxidant, based on functionalized benzotriazole UV absorbers, and the process for the preparation thereof having a general Formula I: wherein R1
|7179924||Use of benzotriazole UV absorbers|
The use of benzotriazole UV absorbers of formula wherein A is a radical of formula B is a radical of formula
|7166659||Substituted 5-aryl-2-(2-hydroxyphenyl)-2H-benzotriazole UV absorbers, compositions stabilized therewith and process for preparation thereof|
Compounds of formula I or II where R is an aryl moiety, such as phenyl, naphthyl or biphenylyl, or is phenyl substituted by one or more trifluoromethyl, bromo or cyano, and E1 and E2 are ind...
|7166274||Synergistically high SPF photoprotective UV-screening compositions comprising insoluble organic sunscreen particles/diarylbutadiene compounds|
Topically applicable high SPF cosmetic/dermatological UV-screening compositions suited for the photoprotection of the skin and/or hair, comprise (a) particulates of at least one insoluble organic UV-screening agent having a particle size ranging from 10 nm to 5 μm,...
|7157586||Bloom-resistant benzotriazole UV absorbers and compositions stabilized therewith|
Benzotriazole UV absorbers substituted with a ultra long ester or amide moiety wherein the ester or amide group is a hydrocarbyl group of 25 to 100 carbon atoms or is a group of alkyl of 25 to 100 carbon atoms interrupted by 5 to 39 oxygen atoms and terminated with ...
|7153588||UV resistant naphthalate polyester articles|
Naphthalate polyester articles can be coated with polymerizable compositions containing a vinyl-functional crosslinkable film former, a large amount of benzotriazole and a copolymerizable monomer that solubilizes the benzotriazole. The cured compositions help protec...
|7148274||Substituted 5-aryl-2-(2-hydroxyphenyl)-2h-benzotriazole UV absorbers, compositions stabilized therewith and process for preparation thereof|
where R is an aryl moiety, such as phenyl, naphthyl or biphenylyl, or is phenyl substituted by one or more trifluoromethyl, bromo or cyano, and E1 and E2 are independently hydrogen, alkyl, aralkyl ...
|7129198||Use of benzotriazole UV absorbers|
The use of benzotriazole UV absorbers of formula wherein A is a radical of formula B is a radical of formula
|7119210||Dual function UV-absorbers for ophthalmic lens materials|
Disclosed are UV absorbers that contain a labile functional group capable of initiating free radical polymerization. ...
|7105479||Fabric rinse composition containing a benztriazole UV absorber|
Disclosed is a fabric rinse composition comprising a) 0.1 to 10% by weight of a UV absorber of formula (1), wherein A is a radical of formula (1a); B is a radical of formula (1c); (1d); (1e); (1f), (1g); (1b); (1i); (1k); (1l); or (1m); R1, R2,...
|7078421||Substituted phenylacetic acids|
Substituted phenylacetic acids, phenylethanols and related compounds are provided that are useful in treating or controlling a number of diseases associated with glucose metabolism, lipid metabolism and insulin secretion. ...
|7074906||Organic solvent-free process for the preparation of 2-(2-nitrophenylazo)phenols|
Provided is a novel one-pot, organic solvent-free process for the preparation of 2-(2-nitrophenylazo) substituted phenols. The 2-(2-nitrophenylazo) substituted phenols are precursors for hydroxyphenylbenzotriazole UV absorbers. ...
|7073899||Ink jet recording method|
An ink jet recording method including a step of: jetting a dye ink onto a surface of a recording medium, wherein said dye ink includes a latex capable of absorbing ultraviolet light, and said recording medium includes a substrate having thereon at least one ink abso...
|7066184||Use of benzotriazole UV absorbers|
The use of benzotriazole UV absorbers of formula (1), wherein A is a radical of formula (1a); (1b); or (1c); B is a radical of formula (1d); (1e); (1f), (1g); (1h); (1i); (1k); (1l); (1m); or (1n); R1, R2, R3, R4, R5 ...
|7018570||Ultraviolet absorber composition and resin composition stabilized therewith|
The present invention is directed to an ultraviolet absorber composition which is formed by melt-mixing a compound (A) represented by formula (I): and a resin stabilizer (B) selected from the group consisting of a pheno...
|6946468||3-mercaptopyrrolidines as farnesyl protein transferase inhibitors|
The present invention relates to inhibitors of ras farnesylation of the Formula I wherein: R1 is for example H and further values as defined in the specification; R2
|6930136||Adhesion promoters containing benzotriazoles|
Benzotriazole adducts contain a benzotriazole segment and a segment with a curable and polymerizable functionality, or an adhesion promoting functionality, particularly suitable for use on metal substrates or in adhesive, sealant or coating compositions for use in p...
|6908936||Substituted benzimidazole antiviral agents|
The present invention concerns antiviral compounds, their compositions, and use in the treatment of viral infections. More particularly, the invention provides benzimidazole derivatives for the treatment of respiratory syncytial virus infection. ...
|6908608||Stabilization of body-care and household products|
A description is given of the use of light stabilizers of formulae (1) and/or (2) for protecting body-care and household products from photolytic degradation. ...
|6864254||Inhibitor for 20-hete-yielding enzyme|
An inhibitor for 20-hydroxyeicosatetraenoic acid production which comprises as the active ingredient a specific hydroxyformamidine derivative or a pharmacologically acceptable salt thereof. It is useful especially as a remedy for kidney diseases, cerebrovascular dis...
|6858607||7,8-fused 4H-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof|
The present invention is directed to substituted 4H-chromene and analogs thereof, represented by the general Formula I: or pharmaceutically acceptable salts or prodrugs thereof, wherein: wherein A, R1
|6818206||USE OF AMPHIPHILIC COPOLYMERS TO STABILIZE DISPERSIONS OF INSOLUBLE ORGANIC COMPOUNDS FOR SCREENING OUT UV RADIATION, DISPERSIONS STABILIZED WITH THESE COPOLYMERS AND COSMETIC COMPOSITIONS CONTAINING THEM|
The invention relates to the use of at least one amphiphilic copolymer comprising at least one hydrophilic block and at least one hydrophobic block to stabilize dispersions of insoluble organic compounds comprising at least one group that absorbs UV radiation, which...
|6815550||Processes for the preparation of benzotriazole UV absorbers|
Provided is a process for preparing 2H-benzotriazole UV absorbers containing a perfluoroalkyl moiety at the 5-position of the benzoic ring, for example a trifluoromethyl group, which involves digitizing the perfluoroalkyl substituted o-nitroaniline using concentrate...
|6800676||Benzotriazoles containing phenyl groups substituted by heteroatoms and compositions stabilized therewith|
2H-Benzotriazole UV absorbers substituted at the 3-position and/or the 5-position of the phenyl ring by a phenyl moiety which is substituted by a heteroatom are particularly photostable in automotive coatings, and are of low color and exhibit low volatility in therm...
|6777433||Protein tyrosine phosphatase 1B (PTP-1B) inhibitors containing two ortho-substituted aromatic phosphonates|
The invention encompasses the novel class of compounds represented by formula I, which are inhibitors of the PTP-1B enzyme. The invention also encompasses pharmaceutical compositions and methods of treating or preventing...
|6774238||Substituted 5-aryl-2-(2-hydroxyphenyl)-2H-benzotriazole UV absorbers, compositions stabilized therewith and process for preparation thereof|
Compounds of formula I or II where R is an aryl moiety, such as phenyl, naphthyl or biphenylyl, or is phenyl substituted by one or more trifluoromethyl, bromo or cyano, and E1 and E2 are independent...
|6756499||Process for the preparation of novel diol-functionalized UV absorbers|
The invention pertains to a process for the preparation of a novel UV absorbing diol of the general formula: wherein R1 is hydrogen, tert-butyl; X1 is selected the group consisting of hydrogen, halo...
|6703510||Substituted 5-aryl-2-(2-hydroxyphenyl)-2H-benzotriazole UV absorbers, compositions stabilized therewith and process for preparation thereof|
Compounds of formula I or II ##STR1## where R is an aryl moiety, such as phenyl, naphthyl or biphenylyl, or is phenyl substituted by one or more trifluoromethyl, bromo or cyano, and E1 and E2 are independently hydrogen, alkyl, aralky...
|6677392||Photostable, silylated benzotriazole UV absorbers and compositions stabilized therewith|
Photostable, silylated benzotriazole compounds of formula (I) or (II) ##STR1## where at least one of E1, E2, E5, E8, E9, G2 and G7 is a silylated group; and G2 and/or G