GB877402A - Coloured polymers - Google Patents
Coloured polymersInfo
- Publication number
- GB877402A GB877402A GB1509960A GB1509960A GB877402A GB 877402 A GB877402 A GB 877402A GB 1509960 A GB1509960 A GB 1509960A GB 1509960 A GB1509960 A GB 1509960A GB 877402 A GB877402 A GB 877402A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- dyestuffs
- hydrogen
- coupling diazotized
- vinyl
- Prior art date
- 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
Links
- 229920000642 polymer Polymers 0.000 title abstract 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- 230000008878 coupling Effects 0.000 abstract 6
- 238000010168 coupling process Methods 0.000 abstract 6
- 238000005859 coupling reaction Methods 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 238000006116 polymerization reaction Methods 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 abstract 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 abstract 2
- LBSXSAXOLABXMF-UHFFFAOYSA-N 4-Vinylaniline Chemical compound NC1=CC=C(C=C)C=C1 LBSXSAXOLABXMF-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 abstract 2
- -1 alkyl aryl sulphonate Chemical compound 0.000 abstract 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 2
- 150000004056 anthraquinones Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- WNVPACYPJUPHON-UHFFFAOYSA-N n-(4-aminophenyl)prop-2-enamide Chemical compound NC1=CC=C(NC(=O)C=C)C=C1 WNVPACYPJUPHON-UHFFFAOYSA-N 0.000 abstract 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical class ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 abstract 1
- HJLVRXSDMXSKMK-UHFFFAOYSA-N 1-butyl-7-methyl-3,4-dihydro-2h-quinolin-3-ol Chemical compound C1=C(C)C=C2N(CCCC)CC(O)CC2=C1 HJLVRXSDMXSKMK-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- GUUWHMTVVVFXIF-UHFFFAOYSA-N 2-acetyl-1,4-diaminoanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(N)C(C(=O)C)=CC(N)=C3C(=O)C2=C1 GUUWHMTVVVFXIF-UHFFFAOYSA-N 0.000 abstract 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical class OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 abstract 1
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- VPMAWSAODAKKSI-UHFFFAOYSA-N 3-chloroprop-2-enoyl chloride Chemical compound ClC=CC(Cl)=O VPMAWSAODAKKSI-UHFFFAOYSA-N 0.000 abstract 1
- HGWQOFDAUWCQDA-UHFFFAOYSA-N 4-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(O)=CC=C(S(O)(=O)=O)C2=C1 HGWQOFDAUWCQDA-UHFFFAOYSA-N 0.000 abstract 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004159 Potassium persulphate Substances 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- 229930188620 butyrolactone Natural products 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 abstract 1
- RRKWPXMDCPJEHS-UHFFFAOYSA-N n-(3-aminophenyl)prop-2-enamide Chemical compound NC1=CC=CC(NC(=O)C=C)=C1 RRKWPXMDCPJEHS-UHFFFAOYSA-N 0.000 abstract 1
- FWEQPMZEKHHFTB-UHFFFAOYSA-N n-(5-amino-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C1=CC=C2C(=O)C=3C(N)=CC=CC=3C(=O)C2=C1NC(=O)C1=CC=CC=C1 FWEQPMZEKHHFTB-UHFFFAOYSA-N 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 abstract 1
- 235000019394 potassium persulphate Nutrition 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 abstract 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- C09B69/101—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing an anthracene dye
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/52—Amides or imides
- C08F20/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F20/60—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F26/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F28/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
-
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
-
- 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Developing Agents For Electrophotography (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB53096A DE1142211B (de) | 1959-05-02 | 1959-05-02 | Verfahren zur Herstellung von Pigmentfarbstoffen |
Publications (1)
Publication Number | Publication Date |
---|---|
GB877402A true GB877402A (en) | 1961-09-13 |
Family
ID=6970157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1509960A Expired GB877402A (en) | 1959-05-02 | 1960-04-29 | Coloured polymers |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE590317A (enrdf_load_stackoverflow) |
CH (1) | CH391142A (enrdf_load_stackoverflow) |
DE (1) | DE1142211B (enrdf_load_stackoverflow) |
GB (1) | GB877402A (enrdf_load_stackoverflow) |
NL (4) | NL299516A (enrdf_load_stackoverflow) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3536440A (en) * | 1966-06-03 | 1970-10-27 | Bayer Ag | Process for the dyeing and printing of fibre substrates |
US3549304A (en) * | 1963-03-21 | 1970-12-22 | Basf Ag | Leather dyeing and coating with a resin dye copolymer of an n-methylolacrylamide and an alkyl acrylate |
DE1492063B2 (de) * | 1961-10-05 | 1973-02-01 | Oreal | Verwendung von faerbenden Polymerisaten,in deren Molekuelgeruesten das die Faerbung bewirkende Molekuel selbst eingefuehrt worden ist,als faerbender Bestandteil in Haarfaerbemitteln |
WO1986005505A1 (en) * | 1985-03-11 | 1986-09-25 | Minnesota Mining And Manufacturing Company | Polymeric dyes |
EP0342052A3 (en) * | 1988-05-13 | 1990-06-13 | S.A. Vilmax | Novel monomers for producing coloured polymers; coloured polymers; process for preparing said polymers and for separating substances biologically active trough the use of said polymers |
EP0339393A3 (de) * | 1988-04-27 | 1991-01-02 | Bayer Ag | Polymerisierbare Aryldiazosulfonate und Polymere enthaltend wiederkehrende Einheiten mit Aryldiazosulfonatgruppen |
US5637637A (en) * | 1995-06-30 | 1997-06-10 | Eastman Chemical Company | Waterborne copolymeric colorants |
US5900445A (en) * | 1994-12-20 | 1999-05-04 | Bic Corporation | Erasable ink composition containing a polymer dye obtained from ethylenic monomers and marking instrument containing same |
US6252025B1 (en) | 1998-08-11 | 2001-06-26 | Eastman Kodak Company | Vinyl hyperbranched polymer with photographically useful end groups |
WO2004024801A1 (en) * | 2002-09-12 | 2004-03-25 | 3M Innovative Properties Company | Oligomeric dyes and use thereof |
US8399661B2 (en) | 2007-08-30 | 2013-03-19 | National Sun Yat-Sen University | Sulfur-containing compound, method of preparation and pharmaceutical uses thereof |
WO2015177062A1 (en) * | 2014-05-21 | 2015-11-26 | Rolic Ag | Polymerizable dichroic dyes |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1282978B (de) * | 1961-10-27 | 1968-11-14 | Basf Ag | Herstellen von transparenten farbigen Formteilen |
NL287281A (enrdf_load_stackoverflow) * | 1961-12-29 |
-
0
- NL NL110673D patent/NL110673C/xx active
- NL NL126037D patent/NL126037C/xx active
- NL NL251042D patent/NL251042A/xx unknown
- NL NL299516D patent/NL299516A/xx unknown
-
1959
- 1959-05-02 DE DEB53096A patent/DE1142211B/de active Pending
-
1960
- 1960-04-13 CH CH420960A patent/CH391142A/de unknown
- 1960-04-29 BE BE590317A patent/BE590317A/fr unknown
- 1960-04-29 GB GB1509960A patent/GB877402A/en not_active Expired
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1492063B2 (de) * | 1961-10-05 | 1973-02-01 | Oreal | Verwendung von faerbenden Polymerisaten,in deren Molekuelgeruesten das die Faerbung bewirkende Molekuel selbst eingefuehrt worden ist,als faerbender Bestandteil in Haarfaerbemitteln |
US3549304A (en) * | 1963-03-21 | 1970-12-22 | Basf Ag | Leather dyeing and coating with a resin dye copolymer of an n-methylolacrylamide and an alkyl acrylate |
US3536440A (en) * | 1966-06-03 | 1970-10-27 | Bayer Ag | Process for the dyeing and printing of fibre substrates |
WO1986005505A1 (en) * | 1985-03-11 | 1986-09-25 | Minnesota Mining And Manufacturing Company | Polymeric dyes |
EP0339393A3 (de) * | 1988-04-27 | 1991-01-02 | Bayer Ag | Polymerisierbare Aryldiazosulfonate und Polymere enthaltend wiederkehrende Einheiten mit Aryldiazosulfonatgruppen |
US5037961A (en) * | 1988-04-27 | 1991-08-06 | Oskar Nuyken | Polymerizable aryldiazosulphonates diazosulphonate groups and ethylenically unsaturated groups bound to aromatic radicals |
EP0342052A3 (en) * | 1988-05-13 | 1990-06-13 | S.A. Vilmax | Novel monomers for producing coloured polymers; coloured polymers; process for preparing said polymers and for separating substances biologically active trough the use of said polymers |
US5900445A (en) * | 1994-12-20 | 1999-05-04 | Bic Corporation | Erasable ink composition containing a polymer dye obtained from ethylenic monomers and marking instrument containing same |
US5637637A (en) * | 1995-06-30 | 1997-06-10 | Eastman Chemical Company | Waterborne copolymeric colorants |
US6252025B1 (en) | 1998-08-11 | 2001-06-26 | Eastman Kodak Company | Vinyl hyperbranched polymer with photographically useful end groups |
WO2004024801A1 (en) * | 2002-09-12 | 2004-03-25 | 3M Innovative Properties Company | Oligomeric dyes and use thereof |
US8399661B2 (en) | 2007-08-30 | 2013-03-19 | National Sun Yat-Sen University | Sulfur-containing compound, method of preparation and pharmaceutical uses thereof |
WO2015177062A1 (en) * | 2014-05-21 | 2015-11-26 | Rolic Ag | Polymerizable dichroic dyes |
CN106414617A (zh) * | 2014-05-21 | 2017-02-15 | 罗利克有限公司 | 可聚合的二色性染料 |
JP2017518413A (ja) * | 2014-05-21 | 2017-07-06 | ロリク アーゲーRolic Ag | 重合性二色性染料 |
US10385215B2 (en) | 2014-05-21 | 2019-08-20 | Rolic Ag | Polymerizable dichroic dyes |
JP2020019974A (ja) * | 2014-05-21 | 2020-02-06 | ロリク アーゲーRolic Ag | 重合性二色性染料 |
Also Published As
Publication number | Publication date |
---|---|
DE1142211B (de) | 1963-01-10 |
CH391142A (de) | 1965-04-30 |
NL299516A (enrdf_load_stackoverflow) | |
NL110673C (enrdf_load_stackoverflow) | |
BE590317A (fr) | 1960-08-16 |
NL251042A (enrdf_load_stackoverflow) | |
NL126037C (enrdf_load_stackoverflow) |
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