2045-00-3Relevant academic research and scientific papers
Interaction of phenylarsonic acid derivatives with Group IIA metal ions
Sharma,Sud,Pannu
, p. 169 - 170 (2007/10/03)
The proton-ligand stability constants and stability constants of complexes of Group IIA metal ions with o-amino- and o-hydroxyphenylarsonic acids have been determined potentiometrically at 30° at ionic strengths of 0.05, 0.10, 0.20 M and also at 20° and 40° at an ionic strength of 0.05 M. The stability order for 1:1 complexes is CaII II II. In case of MgII and BeII complexes, precipitation occurred early during titration. The thermodynamic parameters have been evaluated.
Asymmetric dioxazine compounds and method for dyeing or printing fiber materials using the same
-
, (2008/06/13)
An asymmetric dioxazine compound represented by the following formula (I) in the free acid form: STR1 wherein A1 and A2 independently of one another are each sulfo, halo, alkyl or alkoxy, X1 and X2 independently of one another are each hydrogen, halo, alkyl, alkoxy or phenoxy, R1 is hydrogen or unsubstituted or substituted alkyl, R2 and R3 independently of one another are each hydrogen, alkyl, alkoxy, halo or unsubstituted or substituted amino, Z is a fiber-reactive group, m and n independently of one another are each 0 or 1, provided that mn, and L is 1 or 2. This compound is suitable for dyeing and printing cellulose fiber, natural and synthetic polyamide fibers, polyurethane fiber, leather and the like and mixed yarns thereof, to obtain dyed or printed products of a color fast to light, wetness and chlorine with superior build-up and level dyeing properties.
Asymmetric dioxazine compounds and method for dyeing or printing fiber materials using the same
-
, (2008/06/13)
An asymmetric dioxazine compound represented by the following formula (I) in the free acid form: STR1 wherein A1 and A2 independently of one another are each sulfo, halo, alkyl or alkoxy, W is an unsubstituted or substituted aliphatic or aromatic bridging group, X1 and X2 independently of one another are each hydrogen, halo, alkyl, alkoxy or phenoxy, R1 and R2 independently of one another are each hydrogen or unsubstituted or substituted alkyl, R3 and R4 independently of one another are each hydrogen, halo, alkyl, alkoxy or unsubstituted or substituted amino, Z is a fiber-reactive group, m and n independently of one another are each 0 or 1, provided that m≠n, and l is 1 or 2. This compound is suitable for dyeing and printing cellulose fiber, natural and synthetic polyamide fibers, polyrethane fiber, leather and the like and mixed yarns thereof, to obtain dyed or printed products of a color fast to light, wetness and chlorine with superior build-up and level dyeing properties.
Asymmetric dioxazine compounds having a triazinyl bridging group and a method of production and use thereof
-
, (2008/06/13)
An asymmetric dioxazine compound of the following formula in the free acid form, STR1 wherein R is hydrogen, halogen, sulfo or alkoxy, R1, R2 and R3 are each hydrogen or alkyl, X1 and X2 are each hydrogen, halogen, alkyl, alkoxy or phenoxy, Y is alkylene, phenylene or naphthylene, Z is --SO2 CH=CH2, --SO2 CH2 CH2 OSO3 H or the like, V is hydrogen, alkyl, acyl or substituted triazinyl, and Q is halogen, alkoxy, amino or a group similar to that of STR2 provided that R is hydrogen, and Q is amino or a group similar to that of STR3 when V is substituted triazinyl, which is useful for dyeing or printing fiber materials to give dyed or printed products of a brilliant blue color superior in fastness properties, particularly those such as chlorine fastness with superior build-up property.
Bisazo brown reactive dye
-
, (2008/06/13)
A brown reactive dye represented by a free acid of the formula, STR1 wherein R is a hydrogen atom or a C1 to C4 alkyl group, X is --SO2 CH2 CH2 Cl, --SO2 CH=CH2, --SO2 CH2 CH2 OSO3 H or --SO2 CH2 CH2 OPO3 H2, rings A, B and C are each a benzene or naphthalene ring which may have other substituent, m is 0 to 3 and n is 0 to 1. This dye is suitable for dyeing cellulose fibers brown to afford dyeings superior in fastnesses, acid stability, build-up property and level dyeing property.
Fiber-reactive disazo brown dye having vinylsulfone-type reactive group
-
, (2008/06/13)
A compound, or a salt thereof, represented by the following formula, STR1 wherein A is a substituted or unsubstituted phenylene or naphthylene group, B is STR2 in which R3 is a hydrogen atom or a lower alkyl, lower alkoxy, acylamino or ureido group, and R4 is a hydrogen atom or a lower alkyl or lower alkoxy group, R1 and R3 are independently a hydrogen atom or a substituted or unsubstituted lower alkyl group, X is a substituted or unsubstituted amino, lower alkoxy, substituted phenoxy or sulfo group, Y is --SO2 CH=CH2 or --SO2 CH2 CH2 Z, in which Z is a group capable of being split by the action of an alkali, and m is 2 or 3, which is useful for dyeing hydroxyl group- or amide group-containing fiber materials to give dyed products of a brown color having excellent fastness properties with good build-up property.
Azo dyestuffs
-
, (2008/06/13)
Azo dyestuffs, which in the acid form, are represented by the formula: wherein A is an aromatic radical, M is a 1,4-benzene radical which may be substituted, E is the residue of a coupling component which is free from azo groups, At least one of A and M containing a phosphonic acid group, and the metal complexes of those having a metallisable group are reactive dyes suitable for use in the process of German OLS No. 2324809.

