NO135586B - - Google Patents
Download PDFInfo
- Publication number
- NO135586B NO135586B NO357973A NO357973A NO135586B NO 135586 B NO135586 B NO 135586B NO 357973 A NO357973 A NO 357973A NO 357973 A NO357973 A NO 357973A NO 135586 B NO135586 B NO 135586B
- Authority
- NO
- Norway
- Prior art keywords
- dye
- water
- diazotized
- compound
- amino
- Prior art date
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- -1 amino-azo compound Chemical class 0.000 claims description 4
- 239000000987 azo dye Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- QQBPIHBUCMDKFG-UHFFFAOYSA-N phenazopyridine hydrochloride Chemical group Cl.NC1=NC(N)=CC=C1N=NC1=CC=CC=C1 QQBPIHBUCMDKFG-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000000975 dye Substances 0.000 description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000010298 pulverizing process Methods 0.000 description 6
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- IVUQHXKKRQEFBU-UHFFFAOYSA-N 3-methyl-4-[(3-methylphenyl)diazenyl]aniline Chemical compound CC1=CC=CC(N=NC=2C(=CC(N)=CC=2)C)=C1 IVUQHXKKRQEFBU-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- VOWZNBNDMFLQGM-UHFFFAOYSA-N 2,5-dimethylaniline Chemical compound CC1=CC=C(C)C(N)=C1 VOWZNBNDMFLQGM-UHFFFAOYSA-N 0.000 description 2
- HXDOZKJGKXYMEW-UHFFFAOYSA-N 4-ethylphenol Chemical compound CCC1=CC=C(O)C=C1 HXDOZKJGKXYMEW-UHFFFAOYSA-N 0.000 description 2
- YQUQWHNMBPIWGK-UHFFFAOYSA-N 4-isopropylphenol Chemical compound CC(C)C1=CC=C(O)C=C1 YQUQWHNMBPIWGK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- FKTXSJWQORNULK-UHFFFAOYSA-N 2-methyl-4-[(3-methylphenyl)diazenyl]aniline Chemical compound CC1=CC=CC(N=NC=2C=C(C)C(N)=CC=2)=C1 FKTXSJWQORNULK-UHFFFAOYSA-N 0.000 description 1
- YSNKZJBCZRIRQO-UHFFFAOYSA-N 4-Isopentylphenol Chemical compound CC(C)CCC1=CC=C(O)C=C1 YSNKZJBCZRIRQO-UHFFFAOYSA-N 0.000 description 1
- GJEHZBACLUVNHJ-UHFFFAOYSA-N 4-[(2,5-dimethylphenyl)diazenyl]-2,5-dimethylaniline Chemical compound CC1=CC=C(C)C(N=NC=2C(=CC(N)=C(C)C=2)C)=C1 GJEHZBACLUVNHJ-UHFFFAOYSA-N 0.000 description 1
- MZVVWYZHNTVDHX-UHFFFAOYSA-N 4-[(2,5-dimethylphenyl)diazenyl]-2-methylaniline Chemical compound CC1=CC=C(C)C(N=NC=2C=C(C)C(N)=CC=2)=C1 MZVVWYZHNTVDHX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000004816 paper chromatography Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/20—Uniting glass pieces by fusing without substantial reshaping
- C03B23/24—Making hollow glass sheets or bricks
- C03B23/245—Hollow glass sheets
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Paper (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Joining Of Glass To Other Materials (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO751821A NO138942C (no) | 1972-10-07 | 1975-05-23 | Anordning for innstilling av ensartet avstand mellom enkeltrutene i dobbeltglassruter ved sammensveising av de vertikale lengdekanter |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE7233864 | 1972-09-14 | ||
| DE2314715A DE2314715C3 (de) | 1973-03-24 | 1973-03-24 | Vorrichtung zur Herstellung von Ganzglasdoppelscheiben wechselnder Höhe durch Verschweißender Kanten innerhalb eines Tunnelofens |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO135586B true NO135586B (enExample) | 1977-01-17 |
| NO135586C NO135586C (enExample) | 1977-04-27 |
Family
ID=25764867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO357973A NO135586C (enExample) | 1972-09-14 | 1973-09-13 |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB1417298A (enExample) |
| NO (1) | NO135586C (enExample) |
-
1973
- 1973-09-13 NO NO357973A patent/NO135586C/no unknown
- 1973-09-14 GB GB4327773A patent/GB1417298A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1417298A (en) | 1975-12-10 |
| NO135586C (enExample) | 1977-04-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO135589B (enExample) | ||
| NO135587B (enExample) | ||
| NO135588B (enExample) | ||
| US2864813A (en) | Water soluble colour salts | |
| US2864812A (en) | Water soluble dye salts | |
| US4296028A (en) | Pyrazolonyl substituted disazo pigments | |
| US2155001A (en) | Azo dyestuffs | |
| US3726851A (en) | Water-soluble benzothiazolylphenylazo-barbituric acid dyestuffs | |
| NO135586B (enExample) | ||
| US4354969A (en) | Dye mixtures | |
| US2746955A (en) | Manufacture of azo dyestuffs | |
| US3045004A (en) | Disazo dyes | |
| US2195784A (en) | Azo dyestuffs | |
| US3528961A (en) | Monoazo dyes from e-caprolactam | |
| US2864815A (en) | Method of preparing formazane dyestuffs | |
| US2195788A (en) | Complex metal compoijnds of azo | |
| US2217693A (en) | Azo compound and process for coloring therewith | |
| US2659721A (en) | Trisazo dyestuffs | |
| US2054489A (en) | Azodyestuffs containing chromium | |
| US4115380A (en) | Process for the preparation of dihydroxyphenylazophenylazophenyl dyestuffs | |
| US2554443A (en) | Azo safranine leather dyestuffs | |
| US3478010A (en) | Azo dyestuffs of the acridone series | |
| US2125625A (en) | Azo dyestuffs | |
| US2153627A (en) | New monoazo dyestuffs | |
| US1656233A (en) | Production of oil soluble azo coloring matters |