NO772758L - Ftalocyanidsalter og steriliserte oppl¦sninger derav - Google Patents

Ftalocyanidsalter og steriliserte oppl¦sninger derav

Info

Publication number: NO772758L
Authority: NO; Norway
Prior art keywords: approx; substituents; hydrochloric acid; methanesulfonic acid; water
Prior art date: 1976-08-06

Application number

NO772758A

Other languages

English (en)

Norwegian (no)

Inventor

Patrick Joseph Jefferies

Original Assignee

Sterling Drug Inc

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.)

1976-08-06

Filing date

1977-08-05

Publication date

1978-02-07

1977-08-05 Application filed by Sterling Drug Inc filed Critical Sterling Drug Inc

1978-02-07 Publication of NO772758L publication Critical patent/NO772758L/no

Links

AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 98
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 64
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 64
150000003839 salts Chemical class 0.000 claims description 63
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
229940098779 methanesulfonic acid Drugs 0.000 claims description 46
238000002360 preparation method Methods 0.000 claims description 39
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 28
239000000203 mixture Substances 0.000 claims description 26
238000000034 method Methods 0.000 claims description 25
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 24
XOPUORAQCYGJPT-UHFFFAOYSA-N methanesulfonic acid;hydrochloride Chemical compound Cl.CS(O)(=O)=O XOPUORAQCYGJPT-UHFFFAOYSA-N 0.000 claims description 24
125000001424 substituent group Chemical group 0.000 claims description 24
125000000542 sulfonic acid group Chemical group 0.000 claims description 24
229910052751 metal Inorganic materials 0.000 claims description 22
239000002184 metal Substances 0.000 claims description 22
239000007864 aqueous solution Substances 0.000 claims description 20
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 18
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 10
229910052725 zinc Inorganic materials 0.000 claims description 10
239000011701 zinc Substances 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 9
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
229910052802 copper Inorganic materials 0.000 claims description 8
239000010949 copper Substances 0.000 claims description 8
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 8
229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims description 8
MPMSMUBQXQALQI-UHFFFAOYSA-N cobalt phthalocyanine Chemical compound [Co+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 MPMSMUBQXQALQI-UHFFFAOYSA-N 0.000 claims description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 2
239000000243 solution Substances 0.000 description 63
239000000123 paper Substances 0.000 description 58
239000000975 dye Substances 0.000 description 37
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 27
235000011167 hydrochloric acid Nutrition 0.000 description 27
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
238000012360 testing method Methods 0.000 description 24
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 18
238000003756 stirring Methods 0.000 description 18
239000002253 acid Substances 0.000 description 16
238000004042 decolorization Methods 0.000 description 14
239000000047 product Substances 0.000 description 14
239000007787 solid Substances 0.000 description 13
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 12
239000002002 slurry Substances 0.000 description 9
239000000344 soap Substances 0.000 description 9
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
238000003860 storage Methods 0.000 description 8
239000012141 concentrate Substances 0.000 description 7
239000000835 fiber Substances 0.000 description 7
239000010981 turquoise Substances 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
238000004043 dyeing Methods 0.000 description 6
238000001914 filtration Methods 0.000 description 6
239000000463 material Substances 0.000 description 6
238000010992 reflux Methods 0.000 description 6
238000000862 absorption spectrum Methods 0.000 description 5
238000004061 bleaching Methods 0.000 description 5
238000001704 evaporation Methods 0.000 description 5
230000008020 evaporation Effects 0.000 description 5
238000012546 transfer Methods 0.000 description 5
239000012670 alkaline solution Substances 0.000 description 4
239000007844 bleaching agent Substances 0.000 description 4
239000001913 cellulose Substances 0.000 description 4
229920002678 cellulose Polymers 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
FCJRNRNWMSLWNE-UHFFFAOYSA-N C1(C=2C(C(N1C[Cu](CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)CN1C(C=3C(C1=O)=CC=CC=3)=O)=O)=CC=CC=2)=O Chemical compound C1(C=2C(C(N1C[Cu](CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)CN1C(C=3C(C1=O)=CC=CC=3)=O)=O)=CC=CC=2)=O FCJRNRNWMSLWNE-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
229930040373 Paraformaldehyde Natural products 0.000 description 3
239000000908 ammonium hydroxide Substances 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000002845 discoloration Methods 0.000 description 3
229920002866 paraformaldehyde Polymers 0.000 description 3
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 3
239000001007 phthalocyanine dye Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
229920001131 Pulp (paper) Polymers 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
239000002250 absorbent Substances 0.000 description 2
230000002745 absorbent Effects 0.000 description 2
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
238000009826 distribution Methods 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
-1 filaments Substances 0.000 description 2
239000012065 filter cake Substances 0.000 description 2
230000014509 gene expression Effects 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
239000002243 precursor Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000004064 recycling Methods 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
238000005185 salting out Methods 0.000 description 2
238000010186 staining Methods 0.000 description 2
239000012258 stirred mixture Substances 0.000 description 2
229920002994 synthetic fiber Polymers 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
239000004753 textile Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 1
LQVYCDPEZPBOMT-UHFFFAOYSA-N 4-[4-(diethylamino)benzenecarboximidoyl]-n,n-diethylaniline;hydrochloride Chemical compound Cl.C1=CC(N(CC)CC)=CC=C1C(=N)C1=CC=C(N(CC)CC)C=C1 LQVYCDPEZPBOMT-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NVOVCNZYNSEKFB-UHFFFAOYSA-N C(=O)(O)C1=C(C(=O)NC[Co](CNC(C2=C(C=CC=C2)C(=O)O)=O)(CNC(C2=C(C=CC=C2)C(=O)O)=O)CNC(C2=C(C=CC=C2)C(=O)O)=O)C=CC=C1 Chemical compound C(=O)(O)C1=C(C(=O)NC[Co](CNC(C2=C(C=CC=C2)C(=O)O)=O)(CNC(C2=C(C=CC=C2)C(=O)O)=O)CNC(C2=C(C=CC=C2)C(=O)O)=O)C=CC=C1 NVOVCNZYNSEKFB-UHFFFAOYSA-N 0.000 description 1
CFWDHXHTCRDDOB-UHFFFAOYSA-N C1(C=2C(C(N1C[Zn](CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)CN1C(C=3C(C1=O)=CC=CC=3)=O)=O)=CC=CC=2)=O Chemical compound C1(C=2C(C(N1C[Zn](CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)(CN1C(C=3C(C1=O)=CC=CC=3)=O)CN1C(C=3C(C1=O)=CC=CC=3)=O)=O)=CC=CC=2)=O CFWDHXHTCRDDOB-UHFFFAOYSA-N 0.000 description 1
229920003043 Cellulose fiber Polymers 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
229920004934 Dacron® Polymers 0.000 description 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 description 1
239000004677 Nylon Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
239000004133 Sodium thiosulphate Substances 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229940037003 alum Drugs 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
239000000981 basic dye Substances 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000014171 carbonated beverage Nutrition 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
238000010494 dissociation reaction Methods 0.000 description 1
230000005593 dissociations Effects 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000005357 flat glass Substances 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000002655 kraft paper Substances 0.000 description 1
239000008267 milk Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
NINOYJQVULROET-UHFFFAOYSA-N n,n-dimethylethenamine Chemical compound CN(C)C=C NINOYJQVULROET-UHFFFAOYSA-N 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
239000010893 paper waste Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000002985 plastic film Substances 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 1
238000005956 quaternization reaction Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000008149 soap solution Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
238000007655 standard test method Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003751 zinc Chemical class 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
- 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
- C09B67/0032—Treatment of phthalocyanine 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/02—Dyestuff salts, e.g. salts of acid dyes with basic dyes
- C09B69/06—Dyestuff salts, e.g. salts of acid dyes with basic dyes of cationic dyes with organic acids or with inorganic complex acids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Coloring (AREA)
Paper (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

NO772758A 1976-08-06 1977-08-05 Ftalocyanidsalter og steriliserte oppl¦sninger derav NO772758L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/712,175 US4081239A (en)	1976-08-06	1976-08-06	Storage stable concentrated aqueous solutions of aminomethylated phthalocyanines

Publications (1)

Publication Number	Publication Date
NO772758L true NO772758L (no)	1978-02-07

Family

ID=24861052

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO772758A NO772758L (no)	1976-08-06	1977-08-05	Ftalocyanidsalter og steriliserte oppl¦sninger derav

Country Status (11)

Country	Link
US (1)	US4081239A (fr)
JP (1)	JPS5325645A (fr)
BE (1)	BE857508A (fr)
CA (1)	CA1082176A (fr)
DE (1)	DE2735485A1 (fr)
ES (1)	ES461389A1 (fr)
FR (1)	FR2360638A1 (fr)
GB (1)	GB1550497A (fr)
IT (1)	IT1085256B (fr)
NO (1)	NO772758L (fr)
SE (1)	SE7708943L (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2387658A1 (fr) *	1977-03-25	1978-11-17	Ciba Geigy Ag	Procede pour combattre les microorganismes
US4340386A (en) *	1978-05-04	1982-07-20	Scott Paper Company	Cationic dyestuff printing inks
DE3012327A1 (de) *	1979-05-30	1981-10-08	Robert Bosch Gmbh, 7000 Stuttgart	System zur fernsehmaessigen abtastung von filmen
US4379710A (en) *	1979-05-31	1983-04-12	Sterling Drug Inc.	Novel compositions and processes
US4432900A (en) *	1980-11-14	1984-02-21	Scott Paper Company	Cationic dyestuff printing inks
US4448722A (en) *	1981-02-19	1984-05-15	The Hilton-Davis Chemical Co.	Phthalocyanines
JP4743530B2 (ja) *	2006-07-04	2011-08-10	東京理化器械株式会社	軸連結構造
EP3237465B1 (fr) *	2014-12-22	2020-11-11	Lanxess Deutschland GmbH	Procédé de fabrication de polymères en perles aminométhylés

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB717137A (en) *	1950-11-15	1954-10-20	Bayer Ag	New phthalocyanine dyestuffs
US2761868A (en) *	1953-05-13	1956-09-04	American Cyanamid Co	Sulfonated and unsulfonated imidomethyl, carboxyamidomethyl and aminomethyl phthalocyanines
FR1144249A (fr) *	1954-12-30	1957-10-10	Gen Aniline & Film Corp	Compositions colorantes du type phtalocyanine, leur procédé de préparation et cuves obtenues avec lesdites compositions
FR1377024A (fr) *	1962-12-07	1964-10-31	Basf Ag	Solutions concentrées de colorants de la série de l'auramine
DE1815420A1 (de) *	1968-12-18	1970-09-03	Bayer Ag	Loesungen basischer Farbstoffe
CH550236A (de) *	1971-01-07	1974-06-14	Sandoz Ag	Stabiles, fluessiges farbstoffpraeparat.
CH594719A5 (fr) *	1973-07-19	1978-01-31	Ciba Geigy Ag

1976
- 1976-08-06 US US05/712,175 patent/US4081239A/en not_active Expired - Lifetime
1977
- 1977-07-27 GB GB31604/77A patent/GB1550497A/en not_active Expired
- 1977-08-03 CA CA283,980A patent/CA1082176A/fr not_active Expired
- 1977-08-05 BE BE1008320A patent/BE857508A/fr unknown
- 1977-08-05 SE SE7708943A patent/SE7708943L/xx unknown
- 1977-08-05 ES ES461389A patent/ES461389A1/es not_active Expired
- 1977-08-05 NO NO772758A patent/NO772758L/no unknown
- 1977-08-05 FR FR7724289A patent/FR2360638A1/fr not_active Withdrawn
- 1977-08-05 IT IT26566/77A patent/IT1085256B/it active
- 1977-08-05 DE DE19772735485 patent/DE2735485A1/de not_active Withdrawn
- 1977-08-06 JP JP9457077A patent/JPS5325645A/ja active Pending

Also Published As

Publication number	Publication date
GB1550497A (en)	1979-08-15
SE7708943L (sv)	1978-02-07
BE857508A (fr)	1978-02-06
ES461389A1 (es)	1978-05-16
JPS5325645A (en)	1978-03-09
CA1082176A (fr)	1980-07-22
IT1085256B (it)	1985-05-28
FR2360638A1 (fr)	1978-03-03
DE2735485A1 (de)	1978-02-09
US4081239A (en)	1978-03-28

Publication	Publication Date	Title
CA1166632A (fr)	1984-05-01	Agents de conditionnement de tissus
JP2770912B2 (ja)	1998-07-02	アニオン型トリアジニルアミノジスアゾ染料
US4379710A (en)	1983-04-12	Novel compositions and processes
JPH07119367B2 (ja)	1995-12-20	カチオン性染料
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