ES272566A1 - Procedimiento para la preparaciën de colorantes reactivos - Google Patents

Procedimiento para la preparaciën de colorantes reactivos

Info

Publication number: ES272566A1
Authority: ES; Spain
Prior art keywords: radical; specified; bromo; chloro; substituent
Prior art date: 1960-11-30
Legal status (The legal status 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 status listed.): Expired

Application number

ES0272566A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

Original Assignee

JR Geigy AG

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.)

1960-11-30

Filing date

1961-11-29

Publication date

1962-07-01

1961-11-29 Application filed by JR Geigy AG filed Critical JR Geigy AG

1962-07-01 Publication of ES272566A1 publication Critical patent/ES272566A1/es

Status Expired legal-status Critical Current

Links

229910052751 metal Inorganic materials 0.000 title abstract 2
239000002184 metal Substances 0.000 title abstract 2
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 title 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
239000000975 dye Substances 0.000 abstract 5
125000001424 substituent group Chemical group 0.000 abstract 5
-1 1,3,5-triazine compound Chemical class 0.000 abstract 4
239000000460 chlorine Substances 0.000 abstract 4
229910052801 chlorine Inorganic materials 0.000 abstract 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
238000000034 method Methods 0.000 abstract 3
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 abstract 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 2
239000002253 acid Substances 0.000 abstract 2
125000003545 alkoxy group Chemical group 0.000 abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 2
125000003118 aryl group Chemical group 0.000 abstract 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
125000001246 bromo group Chemical group Br* 0.000 abstract 2
125000004432 carbon atom Chemical group C* 0.000 abstract 2
229910052804 chromium Inorganic materials 0.000 abstract 2
239000011651 chromium Substances 0.000 abstract 2
229910017052 cobalt Inorganic materials 0.000 abstract 2
239000010941 cobalt Substances 0.000 abstract 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 2
238000004043 dyeing Methods 0.000 abstract 2
239000000194 fatty acid Substances 0.000 abstract 2
229910001385 heavy metal Inorganic materials 0.000 abstract 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
229910052760 oxygen Inorganic materials 0.000 abstract 2
239000001301 oxygen Substances 0.000 abstract 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
229920006395 saturated elastomer Polymers 0.000 abstract 2
VHYBUUMUUNCHCK-UHFFFAOYSA-N 2,4,6-tribromo-1,3,5-triazine Chemical class BrC1=NC(Br)=NC(Br)=N1 VHYBUUMUUNCHCK-UHFFFAOYSA-N 0.000 abstract 1
AOEHEEBFRCAFGC-UHFFFAOYSA-N 2,4-dibromopyrimidine Chemical class BrC1=CC=NC(Br)=N1 AOEHEEBFRCAFGC-UHFFFAOYSA-N 0.000 abstract 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract 1
229920003043 Cellulose fiber Polymers 0.000 abstract 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
239000004952 Polyamide Substances 0.000 abstract 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
150000007513 acids Chemical class 0.000 abstract 1
125000002252 acyl group Chemical group 0.000 abstract 1
125000004442 acylamino group Chemical group 0.000 abstract 1
150000001298 alcohols Chemical class 0.000 abstract 1
125000003282 alkyl amino group Chemical group 0.000 abstract 1
125000003277 amino group Chemical group 0.000 abstract 1
229910021529 ammonia Inorganic materials 0.000 abstract 1
150000001555 benzenes Chemical class 0.000 abstract 1
239000011230 binding agent Substances 0.000 abstract 1
125000002843 carboxylic acid group Chemical group 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
239000007859 condensation product Substances 0.000 abstract 1
229910052802 copper Inorganic materials 0.000 abstract 1
239000010949 copper Substances 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
150000004820 halides Chemical class 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
239000010985 leather Substances 0.000 abstract 1
150000002689 maleic acids Chemical class 0.000 abstract 1
239000000463 material Substances 0.000 abstract 1
238000001465 metallisation Methods 0.000 abstract 1
150000002739 metals Chemical class 0.000 abstract 1
230000004048 modification Effects 0.000 abstract 1
238000012986 modification Methods 0.000 abstract 1
150000002790 naphthalenes Chemical class 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
229920002647 polyamide Polymers 0.000 abstract 1
235000011181 potassium carbonates Nutrition 0.000 abstract 1
238000002360 preparation method Methods 0.000 abstract 1
125000002924 primary amino group Chemical class [H]N([H])* 0.000 abstract 1
239000004627 regenerated cellulose Substances 0.000 abstract 1
125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 1
229910052708 sodium Inorganic materials 0.000 abstract 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
235000011182 sodium carbonates Nutrition 0.000 abstract 1
235000011121 sodium hydroxide Nutrition 0.000 abstract 1
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 abstract 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
239000001226 triphosphate Substances 0.000 abstract 1
235000011178 triphosphate Nutrition 0.000 abstract 1
125000002264 triphosphate group Chemical group [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 abstract 1
210000002268 wool Anatomy 0.000 abstract 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
- C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
- C09B62/006—Azodyes
- C09B62/012—Metal complex azo dyes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

ES0272566A 1960-11-30 1961-11-29 Procedimiento para la preparaciën de colorantes reactivos Expired ES272566A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1341560A CH391148A (de)	1960-11-30	1960-11-30	Verfahren zur Herstellung von reaktiven Farbstoffen

Publications (1)

Publication Number	Publication Date
ES272566A1 true ES272566A1 (es)	1962-07-01

Family

ID=4392224

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0272566A Expired ES272566A1 (es)	1960-11-30	1961-11-29	Procedimiento para la preparaciën de colorantes reactivos

Country Status (4)

Country	Link
BE (1)	BE610945A (fr)
CH (1)	CH391148A (fr)
ES (1)	ES272566A1 (fr)
GB (1)	GB964258A (fr)

1960
- 1960-11-30 CH CH1341560A patent/CH391148A/de unknown
1961
- 1961-11-29 BE BE610945A patent/BE610945A/fr unknown
- 1961-11-29 ES ES0272566A patent/ES272566A1/es not_active Expired
- 1961-11-29 GB GB4264161A patent/GB964258A/en not_active Expired

Also Published As

Publication number	Publication date
GB964258A (en)	1964-07-22
CH391148A (de)	1965-04-30
BE610945A (fr)	1962-05-29

Publication	Publication Date	Title
GB955313A (en)	1964-04-15	Metal-containing reactive dyestuffs
GB864080A (en)	1961-03-29	New dis- and tris-azo dyestuffs containing a triazine nucleus
GB1112394A (en)	1968-05-01	Water-soluble mono-and disazo dyestuffs containing a thiosulphuric acid group,complex metal compounds thereof and processes for their manufacture
GB978721A (en)	1964-12-23	Improvements in or relating to reactive azo dyestuffs
ES272566A1 (es)	1962-07-01	Procedimiento para la preparaciën de colorantes reactivos
US2620331A (en)	1952-12-02	Copper-containing azo dyestuffs
GB1015789A (en)	1966-01-05	Metalliferous azo-dyestuffs and process for preparing them
GB992558A (en)	1965-05-19	New monoazo dyestuffs and processes for their manufacture and use
GB988958A (en)	1965-04-14	New metal-containing azo dyestuffs
GB760347A (en)	1956-10-31	Azo-dyestuffs, metalliferous azo-dyestuffs and process for making them
ES262432A1 (es)	1961-06-01	Procedimiento para la preparaciën de colorantes reactivos
GB1037166A (en)	1966-07-27	Reactive dyes containing ethylene imide groups and their use in dyeing
GB870985A (en)	1961-06-21	New complex metal compounds of monoazo-dyestuffs derived from cyanuric halides, their manufacture and use
GB971366A (en)	1964-09-30	New metal-containing azo dyestuffs
GB887867A (en)	1962-01-24	New metalliferous triazine monoazo-dyestuffs and their manufacture and use
GB974403A (en)	1964-11-04	Mixed chromium complexes of monoazo dyes containing sulphonic acid groups
GB927614A (en)	1963-05-29	Metal-containing azo dyestuffs
GB1019561A (en)	1966-02-09	Azo dyestuffs and process for their production
ES262431A1 (es)	1961-06-01	Procedimiento para la preparaciën de colorantes reactivos
GB988904A (en)	1965-04-14	New metallized azo dyestuffs
GB961552A (en)	1964-06-24	Improvements relating to metal-containing reactive azo dyestuffs containing pyrimidylamino groups and their use
GB930293A (en)	1963-07-03	New metallised azo dyestuffs
GB985746A (en)	1965-03-10	New metallised monoazo dyes containing chloro-and/or bromopyrimidylamino groups and their manufacture and use
ES254935A1 (es)	1960-07-01	Procedimiento para la preparaciën de colorantes de ftalocianina
GB837985A (en)	1960-06-22	New copper-containing triazine monoazo dyestuffs