DE1959777A1 - Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien - Google Patents
Verfahren zum kontinuierlichen Faerben synthetischer FasermaterialienInfo
- Publication number
- DE1959777A1 DE1959777A1 DE19691959777 DE1959777A DE1959777A1 DE 1959777 A1 DE1959777 A1 DE 1959777A1 DE 19691959777 DE19691959777 DE 19691959777 DE 1959777 A DE1959777 A DE 1959777A DE 1959777 A1 DE1959777 A1 DE 1959777A1
- Authority
- DE
- Germany
- Prior art keywords
- aniline
- radical
- nitro
- alkyl
- formula
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 15
- 239000000463 material Substances 0.000 title claims description 8
- 229920002994 synthetic fiber Polymers 0.000 title claims description 8
- 239000012209 synthetic fiber Substances 0.000 title claims description 8
- 238000010014 continuous dyeing Methods 0.000 title claims description 4
- -1 trifluoromethyl- Chemical group 0.000 claims description 102
- 239000000975 dye Substances 0.000 claims description 41
- 239000000987 azo dye Substances 0.000 claims description 17
- 238000010438 heat treatment Methods 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 7
- 239000002657 fibrous material Substances 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000003557 thiazoles Chemical class 0.000 claims description 2
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 23
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- 229950011008 tetrachloroethylene Drugs 0.000 description 14
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- 240000009038 Viola odorata Species 0.000 description 13
- 235000013487 Viola odorata Nutrition 0.000 description 13
- 235000002254 Viola papilionacea Nutrition 0.000 description 13
- 238000004043 dyeing Methods 0.000 description 13
- 239000002904 solvent Substances 0.000 description 9
- 230000008878 coupling Effects 0.000 description 8
- 238000010168 coupling process Methods 0.000 description 8
- 238000005859 coupling reaction Methods 0.000 description 8
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- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
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- 238000009998 heat setting Methods 0.000 description 6
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- IVJDJEYBDMAWSA-UHFFFAOYSA-N C(COCCOCCOCCOCCOCCOCCO)O.C(CCCCCCCC)C1=C(C=CC=C1)O Chemical compound C(COCCOCCOCCOCCOCCOCCO)O.C(CCCCCCCC)C1=C(C=CC=C1)O IVJDJEYBDMAWSA-UHFFFAOYSA-N 0.000 description 5
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 5
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- 239000005020 polyethylene terephthalate Substances 0.000 description 5
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- 239000011737 fluorine Substances 0.000 description 4
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- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- AVGQTJUPLKNPQP-UHFFFAOYSA-N 1,1,1-trichloropropane Chemical compound CCC(Cl)(Cl)Cl AVGQTJUPLKNPQP-UHFFFAOYSA-N 0.000 description 3
- QYRDWARBHMCOAG-UHFFFAOYSA-N 2-amino-5-chlorobenzonitrile Chemical compound NC1=CC=C(Cl)C=C1C#N QYRDWARBHMCOAG-UHFFFAOYSA-N 0.000 description 3
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- PBGKNXWGYQPUJK-UHFFFAOYSA-N 4-chloro-2-nitroaniline Chemical compound NC1=CC=C(Cl)C=C1[N+]([O-])=O PBGKNXWGYQPUJK-UHFFFAOYSA-N 0.000 description 3
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- 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 3
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 3
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- SEQRDAAUNCRFIT-UHFFFAOYSA-N 1,1-dichlorobutane Chemical compound CCCC(Cl)Cl SEQRDAAUNCRFIT-UHFFFAOYSA-N 0.000 description 2
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 2
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- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 description 2
- SDYWXFYBZPNOFX-UHFFFAOYSA-N 3,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C(Cl)=C1 SDYWXFYBZPNOFX-UHFFFAOYSA-N 0.000 description 2
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- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 2
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
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- 239000000460 chlorine Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- 125000003438 dodecyl 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 description 1
- MFDTVONVIRHHBR-UHFFFAOYSA-N ethyl 4-amino-3-chlorobenzoate Chemical compound CCOC(=O)C1=CC=C(N)C(Cl)=C1 MFDTVONVIRHHBR-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- XSGIZRABGIXRLA-UHFFFAOYSA-N ethyl n-phenylsulfamate Chemical compound CCOS(=O)(=O)NC1=CC=CC=C1 XSGIZRABGIXRLA-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- OMRRUNXAWXNVFW-UHFFFAOYSA-N fluoridochlorine Chemical compound ClF OMRRUNXAWXNVFW-UHFFFAOYSA-N 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- IGHVUURTQGBABT-UHFFFAOYSA-N methyl 2-amino-5-chlorobenzoate Chemical compound COC(=O)C1=CC(Cl)=CC=C1N IGHVUURTQGBABT-UHFFFAOYSA-N 0.000 description 1
- VOQBLPBLKSXCDB-UHFFFAOYSA-N methyl 2-amino-5-nitrobenzoate Chemical compound COC(=O)C1=CC([N+]([O-])=O)=CC=C1N VOQBLPBLKSXCDB-UHFFFAOYSA-N 0.000 description 1
- LZXXNPOYQCLXRS-UHFFFAOYSA-N methyl 4-aminobenzoate Chemical compound COC(=O)C1=CC=C(N)C=C1 LZXXNPOYQCLXRS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([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])C([H])([H])[H] 0.000 description 1
- ISGXOWLMGOPVPB-UHFFFAOYSA-N n,n-dibenzylaniline Chemical compound C=1C=CC=CC=1CN(C=1C=CC=CC=1)CC1=CC=CC=C1 ISGXOWLMGOPVPB-UHFFFAOYSA-N 0.000 description 1
- FZPXKEPZZOEPGX-UHFFFAOYSA-N n,n-dibutylaniline Chemical compound CCCCN(CCCC)C1=CC=CC=C1 FZPXKEPZZOEPGX-UHFFFAOYSA-N 0.000 description 1
- HXKYNBCJKDAHOJ-UHFFFAOYSA-N n-(3-methylbutyl)aniline Chemical compound CC(C)CCNC1=CC=CC=C1 HXKYNBCJKDAHOJ-UHFFFAOYSA-N 0.000 description 1
- GTWJETSWSUWSEJ-UHFFFAOYSA-N n-benzylaniline Chemical compound C=1C=CC=CC=1CNC1=CC=CC=C1 GTWJETSWSUWSEJ-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- MDLWEBWGXACWGE-UHFFFAOYSA-N octadecane Chemical compound [CH2]CCCCCCCCCCCCCCCCC MDLWEBWGXACWGE-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical group O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- JLXXLCJERIYMQG-UHFFFAOYSA-N phenylcyanamide Chemical compound N#CNC1=CC=CC=C1 JLXXLCJERIYMQG-UHFFFAOYSA-N 0.000 description 1
- RZGQJANKGMICOP-UHFFFAOYSA-N phenyldiazene Chemical compound N=NC1=CC=CC=C1 RZGQJANKGMICOP-UHFFFAOYSA-N 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- STZCRXQWRGQSJD-UHFFFAOYSA-N sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonic acid Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S(O)(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Classifications
-
- 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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/90—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using dyes dissolved in organic solvents or aqueous emulsions thereof
- D06P1/908—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using dyes dissolved in organic solvents or aqueous emulsions thereof using specified dyes
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE759527D BE759527A (fr) | 1969-11-28 | Procede de teinture en continu de matieres fibreuses synthetiques | |
| DE19691959777 DE1959777A1 (de) | 1969-11-28 | 1969-11-28 | Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien |
| CH1656670A CH556942A (enrdf_load_html_response) | 1969-11-28 | 1970-11-09 | |
| CH1656670D CH1656670A4 (enrdf_load_html_response) | 1969-11-28 | 1970-11-09 | |
| CA098059A CA935954A (en) | 1969-11-28 | 1970-11-13 | Process for the continuous dyeing of synthetic fibre materials |
| AT1032470A AT304436B (de) | 1969-11-28 | 1970-11-17 | Verfahren zum kontinuierlichen Färben synthetischer Fasermaterialien |
| NL7016903A NL7016903A (enrdf_load_html_response) | 1969-11-28 | 1970-11-18 | |
| GB5640570A GB1283278A (en) | 1969-11-28 | 1970-11-27 | Process for the impregnation dyeing of synthetic fibre materials |
| JP45104152A JPS4823518B1 (enrdf_load_html_response) | 1969-11-28 | 1970-11-27 | |
| FR7042783A FR2115078B1 (enrdf_load_html_response) | 1969-11-28 | 1970-11-27 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691959777 DE1959777A1 (de) | 1969-11-28 | 1969-11-28 | Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1959777A1 true DE1959777A1 (de) | 1971-06-03 |
Family
ID=5752368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691959777 Pending DE1959777A1 (de) | 1969-11-28 | 1969-11-28 | Verfahren zum kontinuierlichen Faerben synthetischer Fasermaterialien |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS4823518B1 (enrdf_load_html_response) |
| AT (1) | AT304436B (enrdf_load_html_response) |
| BE (1) | BE759527A (enrdf_load_html_response) |
| CA (1) | CA935954A (enrdf_load_html_response) |
| CH (2) | CH1656670A4 (enrdf_load_html_response) |
| DE (1) | DE1959777A1 (enrdf_load_html_response) |
| FR (1) | FR2115078B1 (enrdf_load_html_response) |
| GB (1) | GB1283278A (enrdf_load_html_response) |
| NL (1) | NL7016903A (enrdf_load_html_response) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2187987A1 (enrdf_load_html_response) * | 1972-06-07 | 1974-01-18 | Hoechst Ag | |
| FR2197049A1 (enrdf_load_html_response) * | 1972-08-23 | 1974-03-22 | Cassella Farbwerke Mainkur Ag | |
| EP0013809A1 (en) * | 1978-12-25 | 1980-08-06 | Sumitomo Chemical Company, Limited | Monoazo dyes of the benzothiazole series, their preparation and use in dyeing or printing hydrophobic fibres |
| EP0036512A3 (en) * | 1980-03-13 | 1981-10-07 | Cassella Aktiengesellschaft | Water-insoluble azo dyestuffs, their preparation and use |
| FR2602251A1 (fr) * | 1986-08-01 | 1988-02-05 | Sandoz Sa | Utilisation de composes monoazoiques comme colorants |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54168341U (enrdf_load_html_response) * | 1978-05-19 | 1979-11-27 | ||
| GB2031926A (en) * | 1978-09-08 | 1980-04-30 | Ici Ltd | Dyestuffs |
| GB2134130A (en) * | 1983-01-21 | 1984-08-08 | Yorkshire Chemicals Ltd | Disperse azo dyes |
| JPS612024U (ja) * | 1984-06-12 | 1986-01-08 | 三郎 末瀬 | 丸鋸 |
| JPS6131013A (ja) * | 1984-07-23 | 1986-02-13 | 末瀬 三郎 | 刈払機用丸鋸 |
| JPS6310840U (enrdf_load_html_response) * | 1986-07-09 | 1988-01-25 | ||
| WO2021187447A1 (ja) * | 2020-03-17 | 2021-09-23 | 紀和化学工業株式会社 | 染料組成物 |
| WO2021187446A1 (ja) * | 2020-03-17 | 2021-09-23 | 国立大学法人福井大学 | 超臨界二酸化炭素を用いて染色するための染料 |
-
0
- BE BE759527D patent/BE759527A/xx unknown
-
1969
- 1969-11-28 DE DE19691959777 patent/DE1959777A1/de active Pending
-
1970
- 1970-11-09 CH CH1656670D patent/CH1656670A4/xx unknown
- 1970-11-09 CH CH1656670A patent/CH556942A/xx unknown
- 1970-11-13 CA CA098059A patent/CA935954A/en not_active Expired
- 1970-11-17 AT AT1032470A patent/AT304436B/de not_active IP Right Cessation
- 1970-11-18 NL NL7016903A patent/NL7016903A/xx unknown
- 1970-11-27 JP JP45104152A patent/JPS4823518B1/ja active Pending
- 1970-11-27 FR FR7042783A patent/FR2115078B1/fr not_active Expired
- 1970-11-27 GB GB5640570A patent/GB1283278A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2187987A1 (enrdf_load_html_response) * | 1972-06-07 | 1974-01-18 | Hoechst Ag | |
| FR2197049A1 (enrdf_load_html_response) * | 1972-08-23 | 1974-03-22 | Cassella Farbwerke Mainkur Ag | |
| EP0013809A1 (en) * | 1978-12-25 | 1980-08-06 | Sumitomo Chemical Company, Limited | Monoazo dyes of the benzothiazole series, their preparation and use in dyeing or printing hydrophobic fibres |
| EP0036512A3 (en) * | 1980-03-13 | 1981-10-07 | Cassella Aktiengesellschaft | Water-insoluble azo dyestuffs, their preparation and use |
| FR2602251A1 (fr) * | 1986-08-01 | 1988-02-05 | Sandoz Sa | Utilisation de composes monoazoiques comme colorants |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1283278A (en) | 1972-07-26 |
| FR2115078B1 (enrdf_load_html_response) | 1976-05-28 |
| BE759527A (fr) | 1971-04-30 |
| CH1656670A4 (enrdf_load_html_response) | 1974-06-14 |
| CH556942A (enrdf_load_html_response) | 1974-12-13 |
| FR2115078A1 (enrdf_load_html_response) | 1972-07-07 |
| AT304436B (de) | 1973-01-10 |
| NL7016903A (enrdf_load_html_response) | 1971-06-02 |
| JPS4823518B1 (enrdf_load_html_response) | 1973-07-13 |
| CA935954A (en) | 1973-10-30 |
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