CH484316A - Verfahren zum Färben oder Bedrucken von synthetischen textilen Materialien mit Anthrachinonfarbstoffen - Google Patents

Verfahren zum Färben oder Bedrucken von synthetischen textilen Materialien mit Anthrachinonfarbstoffen

Info

Publication number: CH484316A
Authority: CH; Switzerland
Prior art keywords: sep; dye; anthraquinonylamino; formula; amino
Prior art date: 1966-05-03

Application number

CH1362167A

Other languages

German (de)

English (en)

Other versions

CH1362167A4 (2

Inventor

Ruetger Dr Neeff

Original Assignee

Bayer 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.)

1966-05-03

Filing date

1967-04-14

Publication date

1970-02-27

1967-04-14 Application filed by Bayer Ag filed Critical Bayer Ag

1969-06-30 Publication of CH1362167A4 publication Critical patent/CH1362167A4/xx

1970-02-27 Publication of CH484316A publication Critical patent/CH484316A/de

Links

238000000034 method Methods 0.000 title claims description 18
238000004043 dyeing Methods 0.000 title claims description 12
239000000463 material Substances 0.000 title claims description 10
229920002994 synthetic fiber Polymers 0.000 title claims description 9
239000004758 synthetic textile Substances 0.000 title claims description 9
239000001000 anthraquinone dye Substances 0.000 title description 3
239000000975 dye Substances 0.000 claims description 66
239000004952 Polyamide Substances 0.000 claims description 25
229920002647 polyamide Polymers 0.000 claims description 25
229920000728 polyester Polymers 0.000 claims description 13
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
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 claims description 3
229920002678 cellulose Polymers 0.000 claims description 3
KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims description 2
150000001733 carboxylic acid esters Chemical group 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
229920002635 polyurethane Polymers 0.000 claims description 2
239000004814 polyurethane Substances 0.000 claims description 2
-1 hydrocarbon radical Chemical class 0.000 description 145
239000000835 fiber Substances 0.000 description 49
229920000139 polyethylene terephthalate Polymers 0.000 description 32
239000005020 polyethylene terephthalate Substances 0.000 description 32
229920002284 Cellulose triacetate Polymers 0.000 description 23
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 23
238000005406 washing Methods 0.000 description 15
239000002253 acid Substances 0.000 description 11
235000005811 Viola adunca Nutrition 0.000 description 10
240000009038 Viola odorata Species 0.000 description 10
235000013487 Viola odorata Nutrition 0.000 description 10
235000002254 Viola papilionacea Nutrition 0.000 description 10
238000009998 heat setting Methods 0.000 description 10
MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 9
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
150000002825 nitriles Chemical class 0.000 description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 6
239000004744 fabric Substances 0.000 description 6
238000010409 ironing Methods 0.000 description 6
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
HGUMYMRHRBCLIU-UHFFFAOYSA-N N1=CC=CC2=C(C=C3C(CC(C=C3)=O)=C3)C3=CC=C21 Chemical compound N1=CC=CC2=C(C=C3C(CC(C=C3)=O)=C3)C3=CC=C21 HGUMYMRHRBCLIU-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
VJMAITQRABEEKP-UHFFFAOYSA-N [6-(phenylmethoxymethyl)-1,4-dioxan-2-yl]methyl acetate Chemical compound O1C(COC(=O)C)COCC1COCC1=CC=CC=C1 VJMAITQRABEEKP-UHFFFAOYSA-N 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
150000001805 chlorine compounds Chemical class 0.000 description 3
238000004040 coloring Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000003973 paint Substances 0.000 description 3
229920003002 synthetic resin Polymers 0.000 description 3
239000000057 synthetic resin Substances 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 2
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 2
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 2
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
150000004056 anthraquinones Chemical class 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
150000005840 aryl radicals Chemical class 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
239000013078 crystal Substances 0.000 description 2
229960001577 dantron Drugs 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
229960001156 mitoxantrone Drugs 0.000 description 2
229920006149 polyester-amide block copolymer Polymers 0.000 description 2
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000344 soap Substances 0.000 description 2
238000000859 sublimation Methods 0.000 description 2
230000008022 sublimation Effects 0.000 description 2
229920001187 thermosetting polymer Polymers 0.000 description 2
230000008719 thickening Effects 0.000 description 2
239000001052 yellow pigment Substances 0.000 description 2
XHTBQEDDFNUDSX-UHFFFAOYSA-N 1-amino-4,5-dihydroxy-8-nitroanthracene-9,10-dione Chemical compound O=C1C2=C(O)C=CC([N+]([O-])=O)=C2C(=O)C2=C1C(O)=CC=C2N XHTBQEDDFNUDSX-UHFFFAOYSA-N 0.000 description 1
MLIREBYILWEBDM-UHFFFAOYSA-M 2-cyanoacetate Chemical compound [O-]C(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-M 0.000 description 1
IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical class OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 description 1
JXPDNDHCMMOJPC-UHFFFAOYSA-N 2-hydroxybutanedinitrile Chemical compound N#CC(O)CC#N JXPDNDHCMMOJPC-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
229920001651 Cyanoacrylate Polymers 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
229920006221 acetate fiber Polymers 0.000 description 1
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
229940072056 alginate Drugs 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000001450 anions Chemical group 0.000 description 1
125000001769 aryl amino group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000003086 colorant Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
125000006310 cycloalkyl amino group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
239000003599 detergent Substances 0.000 description 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000004898 kneading Methods 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
SUHLUMKZPUMAFP-UHFFFAOYSA-N methyl 2-hydroxy-3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1O SUHLUMKZPUMAFP-UHFFFAOYSA-N 0.000 description 1
ANGDWNBGPBMQHW-UHFFFAOYSA-N methyl cyanoacetate Chemical compound COC(=O)CC#N ANGDWNBGPBMQHW-UHFFFAOYSA-N 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
239000000203 mixture Substances 0.000 description 1
150000004767 nitrides Chemical class 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920006306 polyurethane fiber Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000001054 red pigment Substances 0.000 description 1
238000001226 reprecipitation Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000565 sulfonamide group Chemical group 0.000 description 1
239000004753 textile Substances 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/16—Benz-diazabenzanthrones, e.g. anthrapyrimidones
- 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
- C09B1/205—Dyes with an unsaturated C on the N atom attached to the nucleus
- 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
- C09B1/56—Mercapto-anthraquinones
- C09B1/58—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/10—Isothiazolanthrones; Isoxazolanthrones; Isoselenazolanthrones
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/14—Benz-azabenzanthrones (anthrapyridones)
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R4/00—Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation
- H01R4/10—Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation effected solely by twisting, wrapping, bending, crimping, or other permanent deformation
- H01R4/18—Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation effected solely by twisting, wrapping, bending, crimping, or other permanent deformation by crimping
- H01R4/20—Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation effected solely by twisting, wrapping, bending, crimping, or other permanent deformation by crimping using a crimping sleeve
- H01R4/203—Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation effected solely by twisting, wrapping, bending, crimping, or other permanent deformation by crimping using a crimping sleeve having an uneven wire-receiving surface to improve the contact

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH1362167A 1966-05-03 1967-04-14 Verfahren zum Färben oder Bedrucken von synthetischen textilen Materialien mit Anthrachinonfarbstoffen CH484316A (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DEF0049089		1966-05-03
CH526967A CH479673A (de)	1966-05-03	1967-04-14	Verfahren zur Herstellung von Anthrachinonfarbstoffen

Publications (2)

Publication Number	Publication Date
CH1362167A4 CH1362167A4 (2)	1969-06-30
CH484316A true CH484316A (de)	1970-02-27

Family

ID=7102721

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CH1362167A CH484316A (de)	1966-05-03	1967-04-14	Verfahren zum Färben oder Bedrucken von synthetischen textilen Materialien mit Anthrachinonfarbstoffen
CH526967A CH479673A (de)	1966-05-03	1967-04-14	Verfahren zur Herstellung von Anthrachinonfarbstoffen

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CH526967A CH479673A (de)	1966-05-03	1967-04-14	Verfahren zur Herstellung von Anthrachinonfarbstoffen

Country Status (6)

Country	Link
US (1)	US3654319A (2)
BE (1)	BE697972A (2)
CH (2)	CH484316A (2)
FR (1)	FR1521906A (2)
GB (1)	GB1131005A (2)
NL (1)	NL6706234A (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE102011079114A1 (de) *	2011-07-14	2013-01-17	Tesa Se	Klebeband mit textilem Träger für die Kabelbandagierung

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3978095A (en) *	1973-07-31	1976-08-31	Ciba-Geigy Ag	Process for the manufacture of 1,4-diamino-5-nitroanthraquinone
US4141992A (en) *	1975-08-22	1979-02-27	American Cyanamid Company	Cycloalkylcarboxyamidines and halobenzamidines as anti-amebic agents
US4131676A (en) *	1977-02-25	1978-12-26	American Cyanamid Company	2,6-Bis(1-morpholinoalkylideneamino)anthraquinones as anti-amebic agents
DE10140107B4 (de) *	2001-08-16	2006-07-06	Lanxess Deutschland Gmbh	Verfahren zur Herstellung von 1-Amino-4-hydroxyanthrachinonen

1967
- 1967-04-14 CH CH1362167A patent/CH484316A/de not_active IP Right Cessation
- 1967-04-14 CH CH526967A patent/CH479673A/de not_active IP Right Cessation
- 1967-05-03 US US635648A patent/US3654319A/en not_active Expired - Lifetime
- 1967-05-03 GB GB20581/67A patent/GB1131005A/en not_active Expired
- 1967-05-03 BE BE697972D patent/BE697972A/xx unknown
- 1967-05-03 FR FR105198A patent/FR1521906A/fr not_active Expired
- 1967-05-03 NL NL6706234A patent/NL6706234A/xx unknown

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE102011079114A1 (de) *	2011-07-14	2013-01-17	Tesa Se	Klebeband mit textilem Träger für die Kabelbandagierung
US9695339B2 (en)	2011-07-14	2017-07-04	Tesa Se	Adhesive tape with textile carrier for cable bandaging

Also Published As

Publication number	Publication date
CH1362167A4 (2)	1969-06-30
BE697972A (2)	1967-11-03
NL6706234A (2)	1967-11-06
DE1644604A1 (de)	1970-08-06
US3654319A (en)	1972-04-04
FR1521906A (fr)	1968-04-19
GB1131005A (en)	1968-10-16
CH479673A (de)	1969-10-15

Legal Events

Date	Code	Title	Description
1976-11-15	PL	Patent ceased

Publication	Publication Date	Title
CH654267A5 (de)	1986-02-14	Tragkarton.
DE2844299A1 (de)	1979-04-19	Neue farbstoffe, deren herstellung und verwendung
CH484316A (de)	1970-02-27	Verfahren zum Färben oder Bedrucken von synthetischen textilen Materialien mit Anthrachinonfarbstoffen
DE1263676C2 (de)	1974-08-08	Verfahren zum faerben und bedrucken von polyestermaterialien mit 1-amino-2-aralkylbzw. arylsulfonylanthrachinonfarbstoffen nach dem thermosolverfahren
CH655760A5 (en)	1986-05-15	Corner deflection for espagnolette fittings of windows or doors
CH516967A (de)	1971-12-31	Zusatzgerät an einem Schneidbrenner
DE1644605A1 (de)	1970-12-17	Anthrachinonfarbstoffe
DE1950679A1 (de)	1971-04-15	Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien
DE1644604C (de)	1973-03-15	Anthrachinonfarbstoffe sowie deren Herstellung und Verwendung
US3740185A (en)	1973-06-19	Exhaust process for the dyeing of synthetic fibre materials
DE1619480C3 (de)	1975-04-24	Anthrachinonfarbstoffe und ihre Verwendung zum Färben und Bedrucken von synthetischen Fasermaterialien
DE1644606C3 (de)	1975-01-23	Anthrachinonfarbstoffe
DE1904433A1 (de)	1969-08-28	Neue Kuepenfarbstoffe,Verfahren zu deren Herstellung und Verwendung
DE2919509A1 (de)	1979-11-22	Verfahren zur herstellung von kuepenfarbstoffen
DE1644604B (de)		Anthrachinonfarbstoffe sowie deren Herstellung und Verwendung
AT232471B (de)	1964-03-25	Verfahren zum Färben und Bedrucken von Fasern und Folien aus linearen aromatischen Polyestern
CH402066A (de)	1965-11-15	Speicheranordnung
CH477503A (de)	1969-08-31	Verfahren zur Herstellung von Anthrachinonfarbstoffen
DE2351517A1 (de)	1975-04-24	Anthrachinonfarbstoffe
CH449154A (de)	1967-12-31	Verfahren zur Herstellung neuer Küpenfarbstoffe
DE1198781B (de)	1965-08-19	Verfahren zum Faerben und Bedrucken von Fasern oder Folien aus linearen aromatischen Polyestern, insbesondere aus Polyaethylenterephthalaten
DE1936462A1 (de)	1970-03-12	Anthrachinonfarbstoffe,ihre Herstellung und ihre Verwendung
DE2044162C3 (de)	1974-05-09	Azoverbindungen und ihre Verwendung
CH524664A (de)	1972-06-30	Verfahren zur Herstellung von Anthrachinonfarbstoffen
CH327965A (de)	1958-02-15	Fahrradhalter