Abstract:
The instant invention pertains to a process and to an oral composition which when applied onto the surface of teeth acts to whiten teeth. More particularly, it relates to a process and an oral composition with an improved teeth whitening effect comprising a safe and effective amount of peroxy compounds, terpyridine transition metal complexes as catalysts and in addition, optionally further adjuvants.
Abstract:
The present invention relates to the use of novel nitrification inhibitors of formula (I), which are N-functionalized alkoxy pyrazole compounds. Moreover, the invention relates to the use of compounds of formula (I) as nitrification inhibitors, i.e. for reducing nitrification, as well as agrochemical mixtures and compositions comprising the nitrification inhibitors of formula (I).
Abstract:
The present invention relates to novel nitrification inhibitors of formula (I), which are pyrazole propargyl ether compounds. Moreover, the invention relates to the use of compounds of formula (I) as nitrification inhibitors, i.e. for reducing nitrification, as well as agrochemical mixtures and compositions comprising the nitrification inhibitors of formula (I).
Abstract:
Disclosed is the use of benzylidene malonates of formula (1), wherein R 1 is methyl; ethyl; propyl; or n-butyl; if R 1 is methyl, then R is tert. butyl; formula (A); a radical of formula (1a); or a radical of formula (1b); wherein R 2 and R 3 , independently from each other are hydrogen; or methyl; R 4 is methyl; ethyl; or n-propyl; R 5 and R 6 independently from each other are hydrogen; or C 1 -C 3 alkyl; if R 1 is ethyl; propyl; or n-butyl, then R is isopropyl; for the protection of human and animal hair and skin against UV radiation.
Abstract:
Monoazoquilolone pigments which, in one of the tautomeric forms thereof, correspond to formula (1), wherein Ar is a radical of formula (2a), (2b), (2c), (2d), 2(e) or (2f) wherein R1 is C1-C4alkyl, R2 and R3 are each independently of the other hydrogen, halogen, C1-C4alkyl, carboxy, sulfo, cyano, C1-C4alkoxycarbonal, C1-C4alkylcarbonyl,, C1-C4alkanoylamino, benzoylamino that is unsubstituted or substituted in the phenyl ring by halogen, nitro, C1-C4alkyl or by C1-C¿4alkoxy; carbamoyl, N-C1-C4alkylaminocarbonyl, N-arylaminocarbonyl that is unsubstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or by C1-C4alkoxy; N,N-di-C1-C4alkylaminocarbonyl, C1-C4alkoxysulfonyl, C1-C4alkylsulfonyl, sulfamoyl, N-C1-C4alkylaminosulfonyl, N-arylaminosulfonyl that is unsubstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or by C1-C¿4alkoxy; or N,N-di-C1-C4alklaminosulfonyl, wherein carboxy and sulfo are in the form of the free aci or in salt form, R8 and R9 are each independently of the other hydrogen, halogen, C1-C4alkyl, C1-C4alkoxy, carboxy, sulfo, cyano, C1-C4alkoxycarbonyl, C1-C4alkylcarbonyl, C1 -C4alkanoylamino, benzoylamino that is unsubstituted or substituted in the phenyl ring by halogen, nitro, C1-C4alkyl or by C1-C4alkoxy; carbamoyl, N-C1-C4alkylaminocarbonyl, N-arylaminocarbonyl that is unsubstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or C1-C4alkoxy, N,N-di-C1-C4alkylaminocarbonyl, C1-C4alkoxysulfonyl, C1-C4alkylsulfonyl, sulfamoyl, N-C1-C4alkylaminosulfonyl, N-arylaminosulfonyl that is unsusbstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or by C1-C4alkoxy; or N,N-di-C1-C4alkylaminosulfonyl, wherein carboxy and sulfo are in the form of the free acid or in salt form, Ar1 is an aryl radical, p is a number 0, 1 or 2, and r is a number 0, 1 or 2, wherein (R8)r in formula (2f) denodes r identical or different radicals R8, are suitable for the colouring of high molecular weight material and are distinguished by good fastness properties of the resulting colourations.
Abstract:
Disclosed are olymeric dye of formula (1a), (1b), (1c), A and B, independently from each other represent a polymer backbone; X1 and X2 independently from each other are a linkage group selected from -C1-C30alkylene- or -C2-C12alkenylene-, which is interrupted and/or terminated at one or both ends by one or more than one -S-, -N-, -N=-, -N(R5)-, -S(O)-, -SO2-, -(CH2CH2-O)1-5-, -(CH2CH2CH2-O)1-5-, -C(O)-, -C(O)O-, -OCO-, (II), -CON(R1)-, -C(NR1R2)2-, -(R1)NC(O)-, -C(S)R1-; or an optionally substituted, saturated or unsaturated, fused or non-fused aromatic or nonaromatic (heterocyclic) bivalent radical optionally comprising at least one heteroatom; a saturated or unsaturated, fused or non-fused aromatic or nonaromatic bivalent radical comprising at least one heteroatom, which is optionally substituted by C1-C30alkyl, C1-C30alkoxy, C2-C12alkenyl, C5-C10aryl, C5-C10cycloalkyl, C1-C10alkyl(C5-C10arylene), hydroxy or halogen; R1 and R2 independently from each other are hydrogen; unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1- C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alkyl(C5-C10aryl); Y1 and Y2 independently from each other are a residue of an organic dye; or hydrogen; wherein at least one of Y1 and Y2 is a residue of an organic dye; An1, An2 and An3, independently from each other are an anion; a and b independently from each other are a number from 1 to 3; m is a
Abstract:
Disclosed are cationic polymeric dye with a hue value of h=210° to 330° comprising: a) a polymer backbone, b) a residue of an organic dye, and c) optionally colorless organic groups, wherein (b) and (c) are covalently bound to the polymer backbone (a), and wherein the cationic charges can independently be part of the dye or the colorless organic groups. The dyes are distinguished by their depth of shade and their good fastness properties to washing, such as, for example, fastness to light, shampooing and rubbing.