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US4634448A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for dyeing of natural leathers using reactive dyes

Assignee: Nippon Kayaku Co Ltd
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Filing: 1985-08-08
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Granted: 1987-01-06
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Expires: 2005-08-08
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Abstract

Abstract Disclosed herein is a method for dyeing of natural leathers by using a reactive dyestuff having at least one S-triazinyl group to which a substituent group having a quaternary nitrogen atom is bonded via the quaternary nitrogen atom without using any acid-binder, any substance releasing the acid-binder or any inorganic electrolyte, thereby obtaining the dyed natural leathers excellent in light fastness, alkaline-sweat and wet fastness.

Inventors

  • 👤 Syohei Ajioka
  • 👤 Toshio Tanaka

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 18:11
CPC Classifications
C; C09; C09B; C09B62/00; C09B62/02; C09B62/04; C09B62/043; D; D06; D06P; D06P3/00; D06P3/02; D06P3/04; D06P3/32; D06P3/3286

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 142 words
A method for dyeing natural leather by an exhaustion of a reactive dyestuff represented by the formulae (III) to (VI): ##STR153## wherein Y represents a group ##STR154## Y 1 and Y 2 are a group ##STR155## or one of Y 1 and Y 2 is a group ##STR156## and the other represents a chlorine atom, a fluorine atom or a bromine atom; D represents a chromophore having at least one water-soluble group, and D is bonded to the triazinyl group via a group ##STR157## wherein R is a hydrogen atom or an alkyl (C 1 ˜C 3 ) group; A represents an unsubstituted or substituted amino group, an alkoxy (C 1 ˜C 4 ) group or a phenoxy group which does not react with the chromophore; and X represents a diamino residual group bonded to the triazinyl group via two amino groups.
Claim 2
Independent Claim 142 words
A method for dyeing natural leather by an exhaustion of a reactive dyestuff represented by the formulae (III) to (VI): ##STR153## wherein Y represents a group ##STR154## Y 1 and Y 2 are a group ##STR155## or one of Y 1 and Y 2 is a group ##STR156## and the other represents a chlorine atom, a fluorine atom or a bromine atom; D represents a chromophore having at least one water-soluble group, and D is bonded to the triazinyl group via a group ##STR157## wherein R is a hydrogen atom or an alkyl (C 1 ˜C 3 ) group; A represents an unsubstituted or substituted amino group, an alkoxy (C 1 ˜C 4 ) group or a phenoxy group which does not react with the chromophore; and X represents a diamino residual group bonded to the triazinyl group via two amino groups.
Claim 3
Dependent Claim 312 words
A method according to claim 1, wherein Y and at least one of Y 1 and Y 2 represent a quaternary pyridinium group represented by the formula: ##STR158## wherein R 1 and R 2 represent independently a hydrogen atom, a chlorine atom, a bromine atom, a methyl group, a sulfo group, a carboxyl group, a carbamoyl group, a lower alkoxy (C 1 ˜C 4 ) carbonyl group and a cyano group, or a quaternary ammonium group represented by the formula: ##STR159## wherein R 3 , R 4 and R 5 independently represent an alkyl (C 1 ˜C 4 ) group, a hydroxyalkyl (C 1 ˜C 4 ) group, a benzyl group, a sulfoalkyl (C 1 ˜C 4 ) group, a carboxyalkyl (C 1 ˜C 4 ) group and an alkoxy (C 1 ˜C 4 ) alkyl (C 1 ˜C 4 ) group; D represents a chromophore of non-metal containing azo dyestuffs, metal-containing azo dyestuffs, formazane dyestuffs, phlhalocyanine dyestuffs or anthraquinone dyestuffs; A represents an amino group, an alkyl (C 1 ˜C 4 ) amino group, a hydroxyalkyl (C 1 ˜C 4 ) amino group, a cyanoalkyl (C 1 ˜C 4 ) amino group, a β-sulfoethylamino group, --NHC 2 H 4 SO 3 H, --NHCH 2 COOH, an anilino group, anilino groups substituted by a chlorine atom, a sulfo group, an alkyl (C 1 ˜C 4 ) group, an alkoxy (C 1 ˜C 4 ) group, a nitro group or a carboxyl group, an N-methylanilino group, an N-ethyl-4-chloroanilino group, an alkoxy (C 1 ˜C 4 ) groups, an alkoxy (C 1 ˜C 4 ) alkoxy (C 1 ˜C 4 ) groups, a phenoxy group, phenoxy groups substituted by a chlorine atom, a nitro group, a methyl group, a sulfo group or a carboxyl group, a morpholino group, a piperidino group or a piperadino group; X represents an alkylenediamino group or an arylenediamino group.
Claim 4
Dependent Claim 244 words
A method according to claim 2, wherein Y and one of Y 1 and Y 2 represent ##STR160## A represents an amino group, a methylamino group, an ethylamino group, a propylamino group, a butylamino group, a dimethylamino group, a diethylamino group, an N-methyl, N-ethyl amino, an octylamino group, a cyclohexylamino group, a monoethanolamino group, a diethanolamino group, a β-cyanoethylamino group, a di-β-cyanoethylamino group, a β-sulfoethylamino group, --NHC 2 H 4 SO 3 H, --NHCH 2 COOH, an anilino group, o-, m- or p-sulfoanilino group, 2,5-disulfoanilino group, o-, m- or p-toluidino group, o-, m- or p-methoxyanilino group, o-, m- or p-chloroanilino group, 2-methyl-4-sulfoanilino group, 2-methoxy-4-sulfoanilino group, p-nitroanilino group, 2-sulfo-4-methylanilino group, 4-chloro-2-sulfoanilino group, o-, m- or p-carboxyanilino group, 2-carboxy-4-sulfoanilino group, an N-methylanilino group, an N-ethyl-4-chloroanilino group, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a methoxyethoxy group, an ethoxyethoxy group, a methoxypropoxy group, a phenoxy group, o-, m- or p-chlorophenoxy group, o-, m- or p-nitrophenoxy group, o-, m- or p-sulfophenoxy group, o-, m- or p-carboxyphenoxy group, a morpholino group, a piperidino group or a piperadino group; X represents an ethylenediamino group, a 1,3-propylenediamino group, a 1,6-hexylenediamino group, a 2-hydroxy-1,3-propylenediamino group, --NHCH 2 CH 2 OCH 2 CH 2 NH--, a 1,4-phenylenediamino group, a 1-methyl-2,6-phenylenediamino group, a 1,3-phenylenediamino group, a 4-sulfo-1,3-phenylenediamino group, a 4,6-disulfo-1,3-phenylenediamino group, a 2-sulfo-1,4-phenylenediamino group, a 2,5-disulfo-1,4-phenylenediamino group, a 5-carboxyl-1,3-phenylenediamino group, a 2,5-dimethoxy-1,4-phenylenediamino group, a 1-N-methylaminoanilino group, a 1,2-phenylenediamino group, a 2,4,6-trimethyl-5-sulfo-1,4-phenylenediamino group, ##STR161## a 2-methyl-5-sulfo-1,3-phenylenediamino group, 4-methyl-1,2-phenylenediamino group, ##STR162##

References Cited (Backward Citations)

US3211513A Cited
US3347617A Cited
US3519614A Cited
US3556708A Cited
US4453945A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-01-05 1990-07-07 1991-01-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-01-05 1994-07-07 1995-01-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-01-05 1998-07-07 1999-01-06 $7700.00 Window Closed / Lapsed

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