ES263070A1 - Procedimiento para la preparaciën de nuevos colorantes - Google Patents

Procedimiento para la preparaciën de nuevos colorantes

Info

Publication number: ES263070A1
Authority: ES; Spain
Prior art keywords: formula; hydrogen; dyes; cellulose; groups
Prior art date: 1959-12-08
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

ES0263070A

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

BASF Schweiz AG

Original Assignee

Ciba Geigy AG

Ciba 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.)

1959-12-08

Filing date

1960-12-07

Publication date

1961-05-16

1960-12-07 Application filed by Ciba Geigy AG, Ciba AG filed Critical Ciba Geigy AG

1961-05-16 Publication of ES263070A1 publication Critical patent/ES263070A1/es

Status Expired legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title 1
238000000034 method Methods 0.000 title 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 4
239000000975 dye Substances 0.000 abstract 4
229910052739 hydrogen Inorganic materials 0.000 abstract 4
239000001257 hydrogen Substances 0.000 abstract 4
125000002837 carbocyclic group Chemical group 0.000 abstract 3
239000004922 lacquer Substances 0.000 abstract 3
239000000049 pigment Substances 0.000 abstract 3
-1 polyethylene Polymers 0.000 abstract 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-methoxynaphthalene Chemical group C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 abstract 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
239000004952 Polyamide Substances 0.000 abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 2
150000004056 anthraquinones Chemical group 0.000 abstract 2
125000003118 aryl group Chemical group 0.000 abstract 2
125000004432 carbon atom Chemical group C* 0.000 abstract 2
229920002678 cellulose Polymers 0.000 abstract 2
WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical group C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 abstract 2
229910052736 halogen Inorganic materials 0.000 abstract 2
150000002367 halogens Chemical class 0.000 abstract 2
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
229920002647 polyamide Polymers 0.000 abstract 2
229920000915 polyvinyl chloride Polymers 0.000 abstract 2
239000004800 polyvinyl chloride Substances 0.000 abstract 2
229920005989 resin Polymers 0.000 abstract 2
239000011347 resin Substances 0.000 abstract 2
239000004408 titanium dioxide Substances 0.000 abstract 2
RPQOZSKWYNULKS-UHFFFAOYSA-N 1,2-dicarbamoylperylene-3,4-dicarboxylic acid Chemical class C1=C(C(O)=O)C2=C(C(O)=O)C(C(=N)O)=C(C(O)=N)C(C=3C4=C5C=CC=C4C=CC=3)=C2C5=C1 RPQOZSKWYNULKS-UHFFFAOYSA-N 0.000 abstract 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 abstract 1
239000000020 Nitrocellulose Substances 0.000 abstract 1
239000004698 Polyethylene Substances 0.000 abstract 1
239000004743 Polypropylene Substances 0.000 abstract 1
239000004793 Polystyrene Substances 0.000 abstract 1
YFPSDOXLHBDCOR-UHFFFAOYSA-N Pyrene-1,6-dione Chemical compound C1=CC(C(=O)C=C2)=C3C2=CC=C2C(=O)C=CC1=C32 YFPSDOXLHBDCOR-UHFFFAOYSA-N 0.000 abstract 1
229920000297 Rayon Polymers 0.000 abstract 1
SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 abstract 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 abstract 1
NUNPDAMQSBMCIG-UHFFFAOYSA-N aceanthryleno[2,1-a]aceanthrylene-5,13-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=CC3=C4C(C=5C(=CC=CC=5)C5=O)=C6C5=CC=CC6=C4C1=C23 NUNPDAMQSBMCIG-UHFFFAOYSA-N 0.000 abstract 1
229940081735 acetylcellulose Drugs 0.000 abstract 1
239000002253 acid Substances 0.000 abstract 1
125000003277 amino group Chemical group 0.000 abstract 1
229920003180 amino resin Polymers 0.000 abstract 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Chemical group CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 1
150000004984 aromatic diamines Chemical class 0.000 abstract 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 abstract 1
125000001246 bromo group Chemical group Br* 0.000 abstract 1
239000001913 cellulose Substances 0.000 abstract 1
229920003086 cellulose ether Polymers 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
125000001309 chloro group Chemical group Cl* 0.000 abstract 1
238000004040 coloring Methods 0.000 abstract 1
230000005494 condensation Effects 0.000 abstract 1
238000009833 condensation Methods 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 abstract 1
RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical group C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 abstract 1
239000011888 foil Substances 0.000 abstract 1
150000004820 halides Chemical class 0.000 abstract 1
229920001220 nitrocellulos Polymers 0.000 abstract 1
229940079938 nitrocellulose Drugs 0.000 abstract 1
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Chemical group C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 abstract 1
229920001568 phenolic resin Polymers 0.000 abstract 1
229920000728 polyester Polymers 0.000 abstract 1
229920000573 polyethylene Polymers 0.000 abstract 1
238000006116 polymerization reaction Methods 0.000 abstract 1
229920001155 polypropylene Polymers 0.000 abstract 1
229920005990 polystyrene resin Polymers 0.000 abstract 1
229920002635 polyurethane Polymers 0.000 abstract 1
239000004814 polyurethane Substances 0.000 abstract 1
150000003254 radicals Chemical class 0.000 abstract 1
229920002050 silicone resin Polymers 0.000 abstract 1
229920002994 synthetic fiber Polymers 0.000 abstract 1
239000000984 vat dye Substances 0.000 abstract 1
210000002268 wool Anatomy 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3437—Six-membered rings condensed with carbocyclic rings
- 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
- C09B57/00—Other synthetic dyes of known constitution

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Coloring (AREA)
Compositions Of Macromolecular Compounds (AREA)

ES0263070A 1959-12-08 1960-12-07 Procedimiento para la preparaciën de nuevos colorantes Expired ES263070A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH8156559A CH382345A (de)	1959-12-08	1959-12-08	Verfahren zur Herstellung neuer Farbstoffe

Publications (1)

Publication Number	Publication Date
ES263070A1 true ES263070A1 (es)	1961-05-16

Family

ID=4538925

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0263070A Expired ES263070A1 (es)	1959-12-08	1960-12-07	Procedimiento para la preparaciën de nuevos colorantes

Country Status (3)

Country	Link
CH (1)	CH382345A (de)
ES (1)	ES263070A1 (de)
GB (1)	GB902393A (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE665978A (de) *	1964-06-26

1959
- 1959-12-08 CH CH8156559A patent/CH382345A/de unknown
1960
- 1960-12-07 ES ES0263070A patent/ES263070A1/es not_active Expired
- 1960-12-08 GB GB4235260A patent/GB902393A/en not_active Expired

Also Published As

Publication number	Publication date
CH382345A (de)	1964-09-30
GB902393A (en)	1962-08-01

Publication	Publication Date	Title
GB883337A (en)	1961-11-29	New dyestuffs of the peri-dicarboxylic acid imide series capable of being fixed on the fibre and process for their manufacture
GB867571A (en)	1961-05-10	New dyestuffs of the anthraquinone series containing a halogenated triazine radical, their manufacture and use
ES263070A1 (es)	1961-05-16	Procedimiento para la preparaciën de nuevos colorantes
ES260463A1 (es)	1961-12-01	Procedimiento para la preparaciën de colorantes de dioxazina
GB844794A (en)	1960-08-17	New acid amide disazo-pigment-dyestuffs and process for their manufacture
GB924662A (en)	1963-05-01	New pigment dyestuffs of the quinacridone series
ES262662A1 (es)	1961-06-01	Procedimiento para la preparaciën de nuevos colorantes
ES262762A1 (es)	1961-06-01	Procedimiento para la preparaciën de nuevos colorantes
GB887729A (en)	1962-01-24	Process for colouring organic products such as lacquers, resins and artificial fibres with pigment dyestuffs
US3088949A (en)	1963-05-07	New dyestuffs
GB902396A (en)	1962-08-01	Dyestuffs of the 2:3-phthaloyl-pyrrocoline series and process for their manufacture
GB1085894A (en)	1967-10-04	New pigments containing more than two condensed benzene rings, their production and uses
US3579518A (en)	1971-05-18	Anthrapyrimidine-substituted anthraquinone amides
ES314634A1 (es)	1966-02-16	Procedimiento para la elaboracion de pigmentos de 3-hidroxiquinoftalona
GB1028816A (en)	1966-05-11	Water-insoluble disazo dyes, their production and use
GB1121974A (en)	1968-07-31	A process for pigmenting organic compounds of high molecular weight with anthraquinone dyestuffs
US3356693A (en)	1967-12-05	Alpha, alpha-bis (4-anilino-3-nitro-benzamido)-anthraquinones
GB1058749A (en)	1967-02-15	New disazo pigments and processes for their manufacture
GB1019579A (en)	1966-02-09	New disazo pigments and process for their manufacture
US1972094A (en)	1934-09-04	Dyes of the anthraquinonyl-amino anthraquinone-acridone series and their production
GB892092A (en)	1962-03-21	New dioxazine dyestuffs and process for their manufacture
GB972957A (en)	1964-10-21	New anthraquinone dyestuffs and process for their manufacture
GB976523A (en)	1964-11-25	New carboxylic acid amide mono azo dyestuffs and processes for their manufacture
GB878632A (en)	1961-10-04	New dyestuffs of the naphthoylene-benzimidazole series and their methods of preparation
GB860889A (en)	1961-02-15	New dyestuffs of the perylene tetracarboxylic acid series and process for their manufacture