DE2837500C2 - - Google Patents
Info
- Publication number
- DE2837500C2 DE2837500C2 DE2837500A DE2837500A DE2837500C2 DE 2837500 C2 DE2837500 C2 DE 2837500C2 DE 2837500 A DE2837500 A DE 2837500A DE 2837500 A DE2837500 A DE 2837500A DE 2837500 C2 DE2837500 C2 DE 2837500C2
- Authority
- DE
- Germany
- Prior art keywords
- chlorine
- methyl
- ethyl
- parts
- bromine
- 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
- 238000000034 method Methods 0.000 claims abstract description 8
- 238000004043 dyeing Methods 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 claims abstract description 3
- 239000004753 textile Substances 0.000 claims abstract description 3
- 239000000975 dye Substances 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 239000000460 chlorine Substances 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- -1 hydroxy, methoxy, ethoxy, phenoxy, nitro, cyano, methylsulfonyl Chemical group 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 229920000742 Cotton Polymers 0.000 abstract description 5
- 239000004744 fabric Substances 0.000 abstract description 4
- 125000001931 aliphatic group Chemical group 0.000 abstract description 2
- 229920002678 cellulose Polymers 0.000 abstract description 2
- 239000001913 cellulose Substances 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 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 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 229940072056 alginate Drugs 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 150000003254 radicals Chemical group 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- ZLCUIOWQYBYEBG-UHFFFAOYSA-N 1-Amino-2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=C(N)C(C)=CC=C3C(=O)C2=C1 ZLCUIOWQYBYEBG-UHFFFAOYSA-N 0.000 description 1
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
- VQUYNUJARXBNPK-UHFFFAOYSA-N 2-chloroethoxybenzene Chemical compound ClCCOC1=CC=CC=C1 VQUYNUJARXBNPK-UHFFFAOYSA-N 0.000 description 1
- WMPPDTMATNBGJN-UHFFFAOYSA-N 2-phenylethylbromide Chemical compound BrCCC1=CC=CC=C1 WMPPDTMATNBGJN-UHFFFAOYSA-N 0.000 description 1
- FWTBRYBHCBCJEQ-UHFFFAOYSA-N 4-[(4-phenyldiazenylnaphthalen-1-yl)diazenyl]phenol Chemical compound C1=CC(O)=CC=C1N=NC(C1=CC=CC=C11)=CC=C1N=NC1=CC=CC=C1 FWTBRYBHCBCJEQ-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical compound [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/18—Preparation of azo dyes from other azo compounds by acylation of hydroxyl group or of mercapto group
- C09B43/24—Preparation of azo dyes from other azo compounds by acylation of hydroxyl group or of mercapto group with formation of —O—SO2—R or —O—SO3H 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/06—Disazo dyes from a coupling component "C" containing a directive hydroxyl group
- C09B31/062—Phenols
-
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/16—Trisazo dyes
- C09B31/20—Trisazo dyes from a coupling component"D" containing a directive hydroxyl group
-
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/35—Trisazo dyes in which the tetrazo component is a diamino-azo-aryl compound
-
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/28—Preparation of azo dyes from other azo compounds by etherification of hydroxyl groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/6033—Natural or regenerated cellulose using dispersed dyes
- D06P3/6041—Natural or regenerated cellulose using dispersed dyes using specified dyes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S534/00—Organic compounds -- part of the class 532-570 series
- Y10S534/02—Azo compounds containing chains of eight or more carbon atoms not provided for elsewhere in this class
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782837500 DE2837500A1 (de) | 1978-08-28 | 1978-08-28 | Verfahren zum faerben von cellulosehaltigem textilmaterial und neue farbstoffe |
| IT25175/79A IT1163700B (it) | 1978-08-28 | 1979-08-20 | Processo per la tintura di materiale tessile contenente cellulosa, e coloranti |
| US06/068,566 US4231746A (en) | 1978-08-28 | 1979-08-22 | Dyeing of cellulose-containing textile material and novel dyes for use therein |
| CH769079A CH651995GA3 (en, 2012) | 1978-08-28 | 1979-08-23 | |
| GB7929517A GB2034758B (en) | 1978-08-28 | 1979-08-24 | Dyeing of cellulose -containing textile material and dyes for use therein |
| FR7921435A FR2434891A1 (fr) | 1978-08-28 | 1979-08-27 | Procede de teinture pour matieres textiles cellulosiques et colorants nouveaux utilises |
| JP10873979A JPS5531899A (en) | 1978-08-28 | 1979-08-28 | Method of dying cellulose contained fiber material and novel dyestuff |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782837500 DE2837500A1 (de) | 1978-08-28 | 1978-08-28 | Verfahren zum faerben von cellulosehaltigem textilmaterial und neue farbstoffe |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2837500A1 DE2837500A1 (de) | 1980-03-20 |
| DE2837500C2 true DE2837500C2 (en, 2012) | 1989-06-01 |
Family
ID=6048087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782837500 Granted DE2837500A1 (de) | 1978-08-28 | 1978-08-28 | Verfahren zum faerben von cellulosehaltigem textilmaterial und neue farbstoffe |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4231746A (en, 2012) |
| JP (1) | JPS5531899A (en, 2012) |
| CH (1) | CH651995GA3 (en, 2012) |
| DE (1) | DE2837500A1 (en, 2012) |
| FR (1) | FR2434891A1 (en, 2012) |
| GB (1) | GB2034758B (en, 2012) |
| IT (1) | IT1163700B (en, 2012) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3049453A1 (de) * | 1980-12-30 | 1982-07-29 | Bayer Ag, 5090 Leverkusen | Farbstoffgemische und fluessigkristalline materialien enthaltend diese farbstoffgemische |
| DE3342040A1 (de) * | 1983-11-22 | 1985-05-30 | Basf Ag, 6700 Ludwigshafen | Azofarbstoffe und fluessigkristalline materialien, enthaltend diese farbstoffe |
| US4749784A (en) * | 1985-03-11 | 1988-06-07 | Crompton & Knowles Corporation | Alkanol substituted disazo orange dye for nylon |
| DE3529988A1 (de) * | 1985-08-22 | 1987-02-26 | Basf Ag | Trisazofarbstoffe und deren verwendung in fluessigkristallinen materialien |
| DE3536267A1 (de) * | 1985-10-11 | 1987-04-16 | Bayer Ag | Azofarbstoffe sowie fluessigkristallines material enthaltend azofarbstoffe |
| DE3639156A1 (de) * | 1986-11-15 | 1988-05-26 | Basf Ag | Trisazofarbstoffe |
| JPH0333462A (ja) * | 1989-06-30 | 1991-02-13 | Shinagawa Diecast Kogyo Kk | 膜式気化器 |
| JPH0731184B2 (ja) * | 1990-09-19 | 1995-04-10 | 新日本製鐵株式会社 | 油の酸価、鹸化価の自動分析方法及び装置 |
| JP2000186222A (ja) * | 1998-12-22 | 2000-07-04 | Mitsubishi Chemicals Corp | 感熱転写用ジスアゾ系色素、及びそれを用いた感熱転写用シート並びに感熱転写用インク |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1811796C3 (de) * | 1968-11-25 | 1974-01-03 | E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) | Verfahren zum Färben von Cellulosefasern oder Gemischen derselben mit synthetischen Fasern |
| CH532640A (de) * | 1969-04-17 | 1973-01-15 | Ciba Geigy Ag | Verwendung bestimmter Disazoverbindungen als Farbstoffe |
| US3667897A (en) * | 1969-11-25 | 1972-06-06 | Du Pont | Uniformly dyed yellow to navy blue water swellable cellulosic fibers |
| US3711245A (en) * | 1970-09-18 | 1973-01-16 | Du Pont | Liquid for pad-bath dyeing containing glycol compound and boric acid or borax |
| US3706525A (en) * | 1971-03-08 | 1972-12-19 | Du Pont | Water swollen cellulose dyeing with high molecular weight disperse dye in a glycol ether solution |
| GB1387811A (en) * | 1971-04-01 | 1975-03-19 | Yorkshire Chemicals Ltd | Process for the colouration of polyester fibres |
| JPS5230637B2 (en, 2012) * | 1972-03-06 | 1977-08-09 | ||
| JPS491871A (en, 2012) * | 1972-04-20 | 1974-01-09 | ||
| DE2251704A1 (de) * | 1972-10-21 | 1974-05-22 | Hoechst Ag | Verfahren zum faerben von synthetischen fasermaterialien aus organischen loesemitteln |
| JPS5218311B2 (en, 2012) * | 1973-06-08 | 1977-05-20 | ||
| JPS5753472B2 (en, 2012) * | 1973-08-02 | 1982-11-12 | ||
| DE2524243C3 (de) * | 1975-05-31 | 1980-06-04 | Basf Ag, 6700 Ludwigshafen | Verfahren zum Färben und Bedrucken von Cellulose-Fasern oder Gemischen von Cellulose-Fasern mit synthetischen Fasern |
| DE2528743C2 (de) * | 1975-06-27 | 1982-06-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zum Färben und Bedrucken von Cellulose-Fasern oder Gemischen von Cellulose-Fasern mit synthetischen Fasern |
| US4150943A (en) * | 1975-10-29 | 1979-04-24 | Basf Aktiengesellschaft | Uniformly dyed water-swellable cellulosic fibers |
| DE2715984A1 (de) * | 1977-04-09 | 1978-10-26 | Basf Ag | Farbstoffzubereitungen fuer cellulose und cellulosehaltiges textilmaterial |
| DE2716934A1 (de) * | 1977-04-16 | 1978-10-26 | Basf Ag | Farbstoffzubereitungen zum faerben von cellulose und cellulosehaltigem textilmaterial sowie neue farbstoffe |
-
1978
- 1978-08-28 DE DE19782837500 patent/DE2837500A1/de active Granted
-
1979
- 1979-08-20 IT IT25175/79A patent/IT1163700B/it active
- 1979-08-22 US US06/068,566 patent/US4231746A/en not_active Expired - Lifetime
- 1979-08-23 CH CH769079A patent/CH651995GA3/de unknown
- 1979-08-24 GB GB7929517A patent/GB2034758B/en not_active Expired
- 1979-08-27 FR FR7921435A patent/FR2434891A1/fr active Granted
- 1979-08-28 JP JP10873979A patent/JPS5531899A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE2837500A1 (de) | 1980-03-20 |
| US4231746A (en) | 1980-11-04 |
| FR2434891B1 (en, 2012) | 1983-08-19 |
| IT7925175A0 (it) | 1979-08-20 |
| JPS6344865B2 (en, 2012) | 1988-09-07 |
| GB2034758A (en) | 1980-06-11 |
| CH651995GA3 (en, 2012) | 1985-10-31 |
| GB2034758B (en) | 1983-01-19 |
| FR2434891A1 (fr) | 1980-03-28 |
| JPS5531899A (en) | 1980-03-06 |
| IT1163700B (it) | 1987-04-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8125 | Change of the main classification |
Ipc: C09B 31/06 |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8330 | Complete renunciation |