ZA200309214B - Novel formazan reactive dyes. - Google Patents

Novel formazan reactive dyes. Download PDF

Info

Publication number: ZA200309214B
Authority: ZA; South Africa
Prior art keywords: formula; compounds; parts; independently; dyeing
Prior art date: 2001-07-31

Application number

ZA200309214A

Other languages

English (en)

Inventor

Markus Gisler

Original Assignee

Clariant Finance Bvi Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-07-31

Filing date

2003-11-26

Publication date

2004-11-26

2003-11-26 Application filed by Clariant Finance Bvi Ltd filed Critical Clariant Finance Bvi Ltd

2004-11-26 Publication of ZA200309214B publication Critical patent/ZA200309214B/en

Links

239000000985 reactive dye Substances 0.000 title description 6
VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 title description 3
BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims description 25
238000004043 dyeing Methods 0.000 claims description 19
238000007639 printing Methods 0.000 claims description 11
239000000758 substrate Substances 0.000 claims description 11
239000000203 mixture Substances 0.000 claims description 10
150000003839 salts Chemical class 0.000 claims description 7
239000004952 Polyamide Substances 0.000 claims description 6
229920002647 polyamide Polymers 0.000 claims description 6
229920002678 cellulose Polymers 0.000 claims description 5
239000001913 cellulose Substances 0.000 claims description 5
239000000976 ink Substances 0.000 claims description 4
238000007641 inkjet printing Methods 0.000 claims description 4
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
-1 amino compound Chemical class 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
229910052802 copper Inorganic materials 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
229910052698 phosphorus Inorganic materials 0.000 claims 2
229910052739 hydrogen Inorganic materials 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
239000000975 dye Substances 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
229920000742 Cotton Polymers 0.000 description 11
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
239000000463 material Substances 0.000 description 8
239000010949 copper Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 4
229910000029 sodium carbonate Inorganic materials 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
AOLYLEFSPFALGJ-UHFFFAOYSA-N copper formazan Chemical compound [Cu].NN=CN=N AOLYLEFSPFALGJ-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
229920000297 Rayon Polymers 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000004744 fabric Substances 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
239000010446 mirabilite Substances 0.000 description 2
230000001590 oxidative effect Effects 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000005185 salting out Methods 0.000 description 2
HBENZIXOGRCSQN-VQWWACLZSA-N (1S,2S,6R,14R,15R,16R)-5-(cyclopropylmethyl)-16-[(2S)-2-hydroxy-3,3-dimethylpentan-2-yl]-15-methoxy-13-oxa-5-azahexacyclo[13.2.2.12,8.01,6.02,14.012,20]icosa-8(20),9,11-trien-11-ol Chemical compound N1([C@@H]2CC=3C4=C(C(=CC=3)O)O[C@H]3[C@@]5(OC)CC[C@@]2([C@@]43CC1)C[C@@H]5[C@](C)(O)C(C)(C)CC)CC1CC1 HBENZIXOGRCSQN-VQWWACLZSA-N 0.000 description 1
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
NTSYSQNAPGMSIH-UHFFFAOYSA-N 2,4,6-trifluoropyrimidine Chemical compound FC1=CC(F)=NC(F)=N1 NTSYSQNAPGMSIH-UHFFFAOYSA-N 0.000 description 1
SIXYIEWSUKAOEN-UHFFFAOYSA-N 3-aminobenzaldehyde Chemical compound NC1=CC=CC(C=O)=C1 SIXYIEWSUKAOEN-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
JZCCFEFSEZPSOG-UHFFFAOYSA-L copper(II) sulfate pentahydrate Chemical compound O.O.O.O.O.[Cu+2].[O-]S([O-])(=O)=O JZCCFEFSEZPSOG-UHFFFAOYSA-L 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
239000000835 fiber Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000010985 leather Substances 0.000 description 1
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
RLGHWJVBICGXRA-UHFFFAOYSA-N n'-amino-n-hydrazinylidenemethanimidamide Chemical compound NN=CN=NN RLGHWJVBICGXRA-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
239000013535 sea water Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/20—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a pyrimidine ring
- C09B62/24—Azo dyes
- C09B62/242—Dyes containing in the molecule at least one azo group and at least one other chromophore group
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/04—Nickel compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Coloring (AREA)
Plural Heterocyclic Compounds (AREA)

ZA200309214A 2001-07-31 2003-11-26 Novel formazan reactive dyes. ZA200309214B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH14232001		2001-07-31

Publications (1)

Publication Number	Publication Date
ZA200309214B true ZA200309214B (en)	2004-11-26

Family

ID=4565465

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200309214A ZA200309214B (en)	2001-07-31	2003-11-26	Novel formazan reactive dyes.

Country Status (10)

Country	Link
US (1)	US7015314B2 (zh)
EP (1)	EP1414911A1 (zh)
JP (1)	JP2005523341A (zh)
KR (1)	KR20040019083A (zh)
CN (1)	CN1289610C (zh)
BR (1)	BR0211487B1 (zh)
MX (1)	MXPA04000878A (zh)
TW (1)	TW593566B (zh)
WO (1)	WO2003011979A1 (zh)
ZA (1)	ZA200309214B (zh)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN100482248C (zh) *	2004-02-11	2009-04-29	吴芳	肾康注射液在制备治疗糖尿病肾病的药物中的应用
CN100482249C (zh) *	2004-02-11	2009-04-29	吴芳	肾康注射液在制备治疗肾病综合征的药物中的应用
WO2020139953A1 (en)	2018-12-26	2020-07-02	Rebound Technologies, Inc	Solid production systems, devices, and methods utilizing oleophilic surfaces

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH499604A (de) *	1966-04-22	1970-11-30	Ciba Geigy Ag	Verfahren zur Herstellung von faserreaktiven schwermetallhaltigen Formazanazofarbstoffen
DE4125754A1 (de)	1991-08-03	1993-02-04	Bayer Ag	Fluorpyrimidin-reaktivfarbstoffe
DE4241918A1 (zh)	1991-12-20	1993-06-24	Sandoz Ag
CH690649A5 (de)	1995-06-07	2000-11-30	Clariant Finance Bvi Ltd	Phthalocyanin-Reaktivfarbstoffe für Fasern.

2002
- 2002-07-29 JP JP2003517159A patent/JP2005523341A/ja active Pending
- 2002-07-29 EP EP02749227A patent/EP1414911A1/en not_active Withdrawn
- 2002-07-29 US US10/484,564 patent/US7015314B2/en not_active Expired - Fee Related
- 2002-07-29 MX MXPA04000878A patent/MXPA04000878A/es active IP Right Grant
- 2002-07-29 KR KR10-2004-7001374A patent/KR20040019083A/ko not_active Application Discontinuation
- 2002-07-29 CN CNB028150023A patent/CN1289610C/zh not_active Expired - Fee Related
- 2002-07-29 TW TW091116879A patent/TW593566B/zh not_active IP Right Cessation
- 2002-07-29 BR BRPI0211487-9A patent/BR0211487B1/pt not_active IP Right Cessation
- 2002-07-29 WO PCT/IB2002/002986 patent/WO2003011979A1/en active Application Filing
2003
- 2003-11-26 ZA ZA200309214A patent/ZA200309214B/en unknown

Also Published As

Publication number	Publication date
KR20040019083A (ko)	2004-03-04
US7015314B2 (en)	2006-03-21
US20040167321A1 (en)	2004-08-26
WO2003011979A1 (en)	2003-02-13
TW593566B (en)	2004-06-21
JP2005523341A (ja)	2005-08-04
MXPA04000878A (es)	2004-06-03
BR0211487B1 (pt)	2012-11-27
CN1537148A (zh)	2004-10-13
BR0211487A (pt)	2004-08-17
CN1289610C (zh)	2006-12-13
EP1414911A1 (en)	2004-05-06

Publication	Publication Date	Title
US6458936B2 (en)	2002-10-01	Fiber-reactive disazo compounds
CA2448867C (en)	2010-06-01	Fibre-reactive trisazo dyes
EP1230304B1 (en)	2010-03-31	Azo dyestuffs
ZA200309214B (en)	2004-11-26	Novel formazan reactive dyes.
AU712094B2 (en)	1999-10-28	Fibre-reactive dyestuffs
EP0983321B1 (en)	2003-01-15	Fiber-reactive disazo dyestuffs
WO2002031057A2 (en)	2002-04-18	Fiber-reactive copper complexes of monoazo dyes
WO2000036025A1 (en)	2000-06-22	Fiber-reactive disazo dyestuffs
US6084077A (en)	2000-07-04	Disazo dyestuffs
EP0409778A1 (en)	1991-01-23	Fibre reactive disazo dyes
MXPA02012736A (es)	2003-05-14	Compuestos organicos.
US5216136A (en)	1993-06-01	Fiber-reactive disazo dyes containing piperazino linking radicals and processes of dyeing therewith
WO2000049092A1 (en)	2000-08-24	Fiber-reactive disazo dyestuffs
GB2221471A (en)	1990-02-07	Fibre-reactive disazo dyestuffs containing two chlorotriazine rings linked by piperazine
MXPA96001653A (en)	1999-09-20	New dis colorants