DE222930C - - Google Patents
Info
- Publication number
- DE222930C DE222930C DENDAT222930D DE222930DA DE222930C DE 222930 C DE222930 C DE 222930C DE NDAT222930 D DENDAT222930 D DE NDAT222930D DE 222930D A DE222930D A DE 222930DA DE 222930 C DE222930 C DE 222930C
- Authority
- DE
- Germany
- Prior art keywords
- naphthol
- parts
- acid
- red
- dye
- 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.)
- Active
Links
- 239000000975 dye Substances 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 5
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 3
- 150000004679 hydroxides Chemical class 0.000 claims description 3
- 150000008049 diazo compounds Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- 229950011260 betanaphthol Drugs 0.000 claims 1
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 239000000920 calcium hydroxide Substances 0.000 description 4
- 235000011116 calcium hydroxide Nutrition 0.000 description 4
- HUYJTJXLNBOVFO-UHFFFAOYSA-N 7-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(O)=CC=C21 HUYJTJXLNBOVFO-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 238000007747 plating Methods 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- -1 naphthol sulfonic acids Chemical class 0.000 description 2
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- AACMNEWXGKOJJK-UHFFFAOYSA-N 2-amino-6-nitrophenol Chemical compound NC1=CC=CC([N+]([O-])=O)=C1O AACMNEWXGKOJJK-UHFFFAOYSA-N 0.000 description 1
- ULUIMLJNTCECJU-UHFFFAOYSA-N 3-amino-4-hydroxybenzenesulfonate;hydron Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1O ULUIMLJNTCECJU-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HLVXFWDLRHCZEI-UHFFFAOYSA-N chromotropic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(O)=CC(S(O)(=O)=O)=CC2=C1 HLVXFWDLRHCZEI-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Coloring (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE222930C true DE222930C (en:Method) |
Family
ID=483785
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT222930D Active DE222930C (en:Method) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE222930C (en:Method) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5069179A (en) * | 1989-10-25 | 1991-12-03 | Mercedes-Benz Ag | Internal combustion engine |
US6877473B2 (en) | 2000-06-16 | 2005-04-12 | Mahle Gmbh | Diesel engine piston |
-
0
- DE DENDAT222930D patent/DE222930C/de active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5069179A (en) * | 1989-10-25 | 1991-12-03 | Mercedes-Benz Ag | Internal combustion engine |
US6877473B2 (en) | 2000-06-16 | 2005-04-12 | Mahle Gmbh | Diesel engine piston |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE222930C (en:Method) | ||
DE35615C (de) | Verfahren zur Darstellung von Azofarbstoffe^ durch Kombination von Tetrazoditolyl mit et- und ^9-Naphtylamin oder deren Mono- und Disulfosäuren | |
DE844768C (de) | Verfahren zur Herstellung esterartiger Derivate von o, o'-Dioxymonoazofarbstoffen | |
DE636358C (de) | Verfahren zur Herstellung von kupferhaltigen Azofarbstoffen | |
CH273301A (de) | Verfahren zur Herstellung eines metallhaltigen Monoazofarbstoffes. | |
DE119662C (en:Method) | ||
DE280505C (en:Method) | ||
DE620257C (de) | Verfahren zur Herstellung von chromhaltigen Azofarbstoffen | |
DE221620C (en:Method) | ||
DE146655C (en:Method) | ||
DE256899C (en:Method) | ||
DE165743C (en:Method) | ||
DE144475C (en:Method) | ||
DE659840C (de) | Verfahren zur Herstellung von Azofarbstoffen | |
DE79165C (de) | Verfahren zur Darstellung rother bis violetter Azofarbstoffe aus a, aj-Dioxynaphtalinäj-mono- und -a2 /Ji-disulfosäure | |
DE196923C (en:Method) | ||
DE99575C (en:Method) | ||
DE457388C (de) | Verfahren zur Herstellung von o-Oxyazofarbstoffen | |
DE224024C (en:Method) | ||
AT101004B (de) | Verfahren zur Herstellung von Säurefarbstoffen. | |
AT141138B (de) | Verfahren zur Herstellung neuer chromhaltiger Farbstoffe. | |
DE201377C (en:Method) | ||
DE69722C (de) | Verfahren zur Darstellung von α 1 α 4 - AmidonaphtoI - β 2 β 3 - disulfosäure. | |
DE234805C (en:Method) | ||
DE925904C (de) | Verfahren zur Herstellung von Azofarbstoffen |