Decorative Jeweled Wheel Cover
An improved wheel is provided wherein decorative items such as gem stones are embedded in either the wheel surface, a special mounting section attached to the wheel surface, or to a spoke strap that wraps around each spoke and positions embedded gem stones on the outside surface of the spoke.
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| Number | Title | Issue Date |
| 5371060 | Selective herbicidal composition comprising 1,5-diphenylpyrazole-3-carboxylic acid safeners and sulfonylurea herbicides A selective herbicidal composition for controlling grasses and weeds in crops of useful plants is composed of a) a herbicidally effective amount of a sulfonylurea of the formula I ##STR1## in which ##STR2## R0 is hydrogen, halogen, me... | 12/06/1994 |
| 5243033 | Fiber-reactive disazo and tetrakisazo halotriazinyl dyes Reactive dyes of the formula ##STR1## in which R1, R2 and R3, independently of one another, are C1 -C4 alkyl, C1 -C4 alkoxy, halogen, ureido, C1 -C4 ac... | 09/07/1993 |
| 5230820 | Storage-stable bleaching detergents containing bis-benzofuranyl fluoescent whitening agents Detergents which, in addition to inorganic and/or organic peracids, contain specific bis-benzofuranyl compounds as fluorescent whitening agents. These detergents are stable for several months and already show the customary cleaning properties at washing t... | 07/27/1993 |
| 5229502 | Preparation of 1:2 chromium complexes one sulfo substituted and one sulfonamido or the like substituted azo dyes A process is described for the preparation of pure, asymmetric 1:2 chromium complex dyes containing at least two groups which impart solubility in water, which process comprises reacting a mixture of two dyes of the formulae F1 --(SO3 | 07/20/1993 |
| 5229426 | Ethers useful for controlling pests There are disclosed 1-[4-(halophenoxy)phenoxy]-4-pentines of formula ##STR1## wherein R1 and R2 are each independently of the other chloro or fluoro and one of R1 and R2 is also hydrogen, a process for thei... | 07/20/1993 |
| 5225545 | Disazo dyes containing a 1-hydroxy-3-sulfo-acylaminophenyl-amino-naphthalene coupling component The compounds of the formula (1) indicated in claim 1 are suitable for use as direct dyes for dyeing and printing a wide range of materials, in particular cellulose-containing fibre materials, producing dyeings and prints having good fastness properties.... | 07/06/1993 |
| 5218095 | Phthalimidylazo dyes The novel dispersion dyes of the formula ##STR1## in which R1 is a C2 -C8 alkyl radical which is substituted by hydroxyl, halogen, a radical --X--C1 -C8 alkyl or --X--phenyl, in which X is a brid... | 06/08/1993 |
| 5211719 | Concentrated acqueous solutions of anionic disazo dyes with polyglycol-amine Concentrated aqueous solutions are described comprising specific anionic disazo dyes and polyglycol amines, which are highly suitable as commercial forms.... | 05/18/1993 |
| 5209832 | Process for the preparation of metal complex dyes The invention relates to a process for the preparation of a metal complex dye under production conditions, which comprises reacting at least one dye with a metal donor, adding said metal donor or said dye discontinuously before the end point of the metall... | 05/11/1993 |
| 5207801 | Reactive dye mixtures, processes for their preparation and their use: reactive sulfonated tri-phenol-dioxazine dye mixture for cellulose fibers The invention relates to reactive dye mixtures comprising the reactive dyes of the formulae ##STR1## in which X1, X2 and X3 are reactive radicals bonded via a diaminoalkylene bridge and the other substituents are as d... | 05/04/1993 |
| 5207799 | Process for dyeing wool and blends thereof with other fibres using reactive dyes and colorless fiber-reactive dyeing assistant A process is described for fibre- and surface-level dyeing of wool and blends thereof with other fibers using a compound of formula (1) ##STR1## in which n is 0 or 1, and if n is 1, A is a radical of the formula ##STR2## and B is an alkylene or ... | 05/04/1993 |
| 5204453 | Process for the preparation of 1:2 metal complex azo compounds by carrying out diazotization and coupling in the presence of a metal donor The invention relates to a process for the preparation of 1:2 chromium, 1:2 cobalt, 1:2 nickel or 1:2 iron complex azo dyes diazotisation, coupling and metallizing, without isolation of the coupling product, which process comprises diazotizing at least on... | 04/20/1993 |
| 5196520 | Azo dyes, their preparation and the use thereof The invention relates to azo dyes of formula ##STR1## wherein R1 is hydrogen or C1 -C4 alkyl, R2 is C2 -C4 alkyl, R3 is hydrogen, C1 -C4 alkyl or unsub... | 03/23/1993 |
| 5196518 | Process for the preparation of metallizable azo dyes by carrying out the coupling in the presence of a buffer mixture A process for the preparation of azo dyes of formula ##STR1## wherein K is the radical of a coupling component of the benzene or naphthalene series or of the heterocyclic series, and the hydroxy group is attached to K adjacent to the azo group, X is ... | 03/23/1993 |
| 5196260 | Process for the treatment of fibrous materials with modified organopolysiloxanes and the materials The present invention relates to a process for the treatment of fibrous materials with modified organopolysiloxanes, wherein, in an aqueous medium, an organopolysiloxane copolymer prepared in a first stage from customary cyclic siloxanes (A) and unsaturat... | 03/23/1993 |
| 5190928 | Process and a composition for immunizing plants against diseases A method and composition for the immunization of healthy useful plants against plant diseases containing as active ingredients compounds of formula ##STR1## in which: X is hydrogen, halogen, hydroxy, methyl, methoxy, HOOC or MOOC; Y is hydrogen, halo... | 03/02/1993 |
| 5181935 | Thermal and photochemical stabilization of dyeings on polyamide fibers:sterically hindered phenol and ultra-violet absorber Processes for improving the thermal and/or photochemical stability of undyed and dyed polyamide fibers by treatment with an agent from an aqueous bath containing (A) a compound of the formula (I) defined in claim 1 and (B) a UV absorber.... | 01/26/1993 |
| 5176717 | Use of sulfonated polyazo dyes for dyeing leather in brilliant fast red shades The use of compounds of the formula ##STR1## in which the symbols are as defined in claim 1, for dyeing leather is described.... | 01/05/1993 |
| 5176715 | Process for dyeing cellulosic fiber materials with vat dyes: dosing continuously over time interval There is disclosed a process for dyeing cellulosic fibre materials with vat dyes, which comprises adding to the dyebath all or some of the auxiliary chemicals required for the dyeing process, and subsequently, after a pretratment time, adding the vat dye ... | 01/05/1993 |
| 5175293 | Pesticides Compounds of the formula ##STR1## wherein: R1 is phenyl or phenyl mono- to tri-substituted by R4 ; R2 is hydrogen, C1 -C5 alkyl, C1 -C5 alkyl substituted by the radical OR | 12/29/1992 |
| 5169951 | Process for preparing nematicidal compositions Nematicidal compositions which comprise as active ingredient compounds of formula I ##STR1## wherein R is nitro or halogen, and also processes for the preparation of the compounds of formula I, novel intermediates of the preparation process and ... | 12/08/1992 |
| 5162550 | Bisphthalide lactones, their preparation and the use thereof in recording materials Bisphthalide lactones of formula ##STR1## wherein R1, R2, R3 and R4 are each independently of one another hydrogen, alkyl of at most 12 carbon atoms which is unsubstituted or substituted by halogen, hydroxy... | 11/10/1992 |
| 5160346 | Photochemical and thermal stabilization of polyamide fibre materials with tetra-methyl-piperidinyl substituted triazine There is described a process for the photochemical and thermal stabilization of polyamide fiber materials according to claim 1 and also novel water-soluble triazine derivatives according to claim 7. The novel process and compounds confer good thermal and photo... | 11/03/1992 |
| 5153200 | Pesticides Compounds of the formula ##STR1## in which: R1 and R2 independently of one anther are hydrogen, halogen, C1 -C3 alkyl, C1 -C2 haloalkyl, C1 -C3 alkoxy or C1 | 10/06/1992 |
| 5152922 | 1,4-distyrylbenzene compounds and mixtures thereof with other 1,4-distyrybenzene compounds Novel 1,4-distyrylbenzene compounds of the formula ##STR1## and mixtures thereof with compounds of the formulae ##STR2## and/or ##STR3## in which R1 is C1 -C4 -alkyl or phenyl, R2 is cyano, C... | 10/06/1992 |
| 5149791 | Chlorotriazine reactive dyes having a 4-methoxy-2-sulfoaniline diazo component and 2-amino-5-naphthol-7-sulfonic acid coupling component Novel reactive dyes of the formula ##STR1## in which Z is a radical of the formula ##STR2## in which R1 and R2 independently of one another are hydrogen or C1 -C6 alkyl, which can be substituted by C | 09/22/1992 |
| 5147410 | Process for the end-to-end dyeing of cellulosic fibres: desalted direct dye and migration inhibitor The invention relates to a process for the end-to-end dyeing of cellulosic fibres or cellulosic fibre blends with direct dyes by the pad dyeing process, which comprises padding said fibre materials with an aqueous liquor containing one or more deionized d... | 09/15/1992 |
| 5145991 | Distyrylbiphenyl compounds Distyrylbiphenyl compounds of formula ##STR1## wherein R1, R3, R6 and R7 are halogen, hydrogen, C1 -C4 alkyl or cyano, and M.sym. is a salt-forming cation, are used as fluor... | 09/08/1992 |
| 5145486 | Process for dyeing wool with reactive dyes There is disclosed a process for producing non-skittery and level dyeings on wool with reactive dyes in the presence of an auxiliary combination, which process comprises dyeing wool with an aqueous liquor consisting of at least one reactive dye and an aux... | 09/08/1992 |
| 5143519 | Concentrated acid dye solutions: storage stable aqueous dye concentrate with di-ethyl-amino-propylamine Concentrated dye solutions of dyes of the formula (1) shown in claim are described. The dye solutions are distinguished by a good storage stability and are suitable, in particular, for dyeing paper.... | 09/01/1992 |
| 5136028 | Reactive azo dyes Novel reactive dyes of formula ##STR1## wherein Z is a radical of formula ##STR2## and R1, R2, R3, (R4)2-3, (R5)1-3, R7 and (R8)1-3 are... | 08/04/1992 |
| 5135927 | Microbicidal composition A microbicidal composition contains as active ingredient 2-chloro-4-trifluoromethylthiazol-5-carboxylic acid derivatives of the formula I ##STR1## R is an organic radical with up to 40 carbon atoms, which optionally contains nitrogen, oxygen or ... | 08/04/1992 |
| 5132314 | Anthelmintics Anthelmintically active compounds of formula I are described ##STR1## in which R1 is hydrogen, halogen, C1 -C2 alkyl, C1 -C2 thioalkyl, C1 -C2 haloalkyl, nitro, C1 -C | 07/21/1992 |
| 5131919 | Blue anthraquinone dye mixture for natural and synthetic polyamides The invention relates to a dye mixture containing a dye of the formula ##STR1## and a dye of the formula ##STR2## where R is cyclohexyl or phenyl, which may each be substituted by C1 -C4 alkyl, acetylamino, N-C1 ... | 07/21/1992 |
| 5128456 | Reactive dyes Novel reactive dyes of the formula ##STR1## in which (R)0-3 is 0-3 substituents R, independent of one another, from the group comprising halogen, nitro, cyano, trifluoromethyl, sulfamoyl, carbamoyl, C1-4 alkyl, C1-4 a... | 07/07/1992 |
| 5128371 | Acylated naphthlamines as plant fungicides There are described novel acylated naphthylamines of the formula I defined herein ##STR1## which have valuable fungicidal properties. They can be used in practice on their own or in the form of compositions for the protection of cultivated plant... | 07/07/1992 |
| 5126474 | Polyadducts of alkylene oxide and styrene oxide with aryl alkanols Polyadducts of an alkylene oxide and styrene oxide with an aryl alcohol, especially polyadducts of formulae ##STR1## wherein the ring A is an unsubstituted phenyl radical or a phenyl radical which is substituted by halogen, methyl or C1 -C... | 06/30/1992 |
| 5126435 | Process for the preparation of metallisable azo dyes A process for the preparation of azo dyes of formula ##STR1## wherein K is the radical of a coupling component of the benzene or naphthalene series or of the heterocyclic series, and the hydroxy group is attached to K adjacent to the azo group, X is ... | 06/30/1992 |
| 5120872 | Compounds containing a 3-sulfoalkanoylamino or 3-sulfoalylsulfonylaminoaniline coupling component A compound of the formula ##STR1## in which R1 and R2 independently of one another are each C1 -C10 alkyl which is unsubstituted or substituted by hydroxyl, C1 -C4 alkoxy, phenyl, sulf... | 06/09/1992 |
| 5120741 | Microbicides Compounds of the formula ##STR1## in which R1 is hydrogen, halogen, methyl, methoxy or trifluoromethyl; n is 1 or 2; R2 is hydrogen, C1 -C6 alkyl, C1 -C3 alkyl which is substituted by ... | 06/09/1992 |