DE125579C - - Google Patents
Info
- Publication number
- DE125579C DE125579C DENDAT125579D DE125579DA DE125579C DE 125579 C DE125579 C DE 125579C DE NDAT125579 D DENDAT125579 D DE NDAT125579D DE 125579D A DE125579D A DE 125579DA DE 125579 C DE125579 C DE 125579C
- Authority
- DE
- Germany
- Prior art keywords
- red
- acid
- blue
- hydroxyl
- violet
- 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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
- KGBXLFKZBHKPEV-UHFFFAOYSA-N Boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 10
- 239000004327 boric acid Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000002253 acid Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000001228 spectrum Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- BBNQQADTFFCFGB-UHFFFAOYSA-N 1,2,4-Trihydroxyanthraquinone Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC(O)=C3C(=O)C2=C1 BBNQQADTFFCFGB-UHFFFAOYSA-N 0.000 description 4
- UANTZMGIULSSNZ-UHFFFAOYSA-N [N+](=O)([O-])OOOC1=C(C(=C2C(C3=CC=CC=C3C(C2=C1)=O)=O)S(=O)(=O)O)S(=O)(=O)O Chemical compound [N+](=O)([O-])OOOC1=C(C(=C2C(C3=CC=CC=C3C(C2=C1)=O)=O)S(=O)(=O)O)S(=O)(=O)O UANTZMGIULSSNZ-UHFFFAOYSA-N 0.000 description 4
- 210000002268 Wool Anatomy 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- GUEIZVNYDFNHJU-UHFFFAOYSA-N 1,4-Dihydroxyanthraquinone Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 2
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 2
- 240000005505 Ribes rubrum Species 0.000 description 2
- 235000002355 Ribes spicatum Nutrition 0.000 description 2
- AYNUDFKSZLCYEV-UHFFFAOYSA-N [N+](=O)([O-])C1=CC=CC2=C3C(=C4C=5C=CC=CC5C(C(C4=C12)[N+](=O)[O-])=O)C1=CC2=CC=CC=C2C=C1C=C3 Chemical compound [N+](=O)([O-])C1=CC=CC2=C3C(=C4C=5C=CC=CC5C(C(C4=C12)[N+](=O)[O-])=O)C1=CC2=CC=CC=C2C=C1C=C3 AYNUDFKSZLCYEV-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-N nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 210000004369 Blood Anatomy 0.000 description 1
- NWCVEHKBLWQPKB-UHFFFAOYSA-N C12=C(S(O)(=O)=O)C([N+]([O-])=O)=C([N+]([O-])=O)C=C2C2=CC=C3C=C4C=CC=CC4=CC3=C2C2=C1C(S(=O)(=O)O)C(=O)C1=CC=CC=C12 Chemical compound C12=C(S(O)(=O)=O)C([N+]([O-])=O)=C([N+]([O-])=O)C=C2C2=CC=C3C=C4C=CC=CC4=CC3=C2C2=C1C(S(=O)(=O)O)C(=O)C1=CC=CC=C12 NWCVEHKBLWQPKB-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 235000016911 Ribes sativum Nutrition 0.000 description 1
- 235000016897 Ribes triste Nutrition 0.000 description 1
- QUDZIKKHBMBJKK-UHFFFAOYSA-N [N+](=O)([O-])OC1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O Chemical compound [N+](=O)([O-])OC1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O QUDZIKKHBMBJKK-UHFFFAOYSA-N 0.000 description 1
- KFEUJEKXCLAYIP-UHFFFAOYSA-N [N+](=O)([O-])OOOC1=CC=CC=2C(C3=CC=CC=C3C(C1=2)=O)=O Chemical compound [N+](=O)([O-])OOOC1=CC=CC=2C(C3=CC=CC=C3C(C1=2)=O)=O KFEUJEKXCLAYIP-UHFFFAOYSA-N 0.000 description 1
- QTRNDORTMVTOEG-UHFFFAOYSA-N [O-][N+](=O)OS(=O)(=O)[N+]([O-])=O Chemical compound [O-][N+](=O)OS(=O)(=O)[N+]([O-])=O QTRNDORTMVTOEG-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000005712 crystallization Effects 0.000 description 1
- 235000001535 currant Nutrition 0.000 description 1
- 235000001537 currant Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 230000000640 hydroxylating Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000001681 protective Effects 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/02—Hydroxy-anthraquinones; Ethers or esters thereof
- C09B1/06—Preparation from starting materials already containing the anthracene nucleus
- C09B1/12—Dyes containing sulfonic acid groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE125579C true DE125579C (ja) |
Family
ID=394296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT125579D Active DE125579C (ja) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE125579C (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2500749A1 (fr) * | 1981-02-27 | 1982-09-03 | Oreal | Utilisation d'hydroxyanthraquinones pour la coloration des fibres keratiniques humaines, procede et composition les mettant en oeuvre |
-
0
- DE DENDAT125579D patent/DE125579C/de active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2500749A1 (fr) * | 1981-02-27 | 1982-09-03 | Oreal | Utilisation d'hydroxyanthraquinones pour la coloration des fibres keratiniques humaines, procede et composition les mettant en oeuvre |
| DE3207036A1 (de) * | 1981-02-27 | 1982-09-16 | L'Oreal, 75008 Paris | Haarfaerbemittel, die hydroxyanthrachinonverbindungen enthalten und ein verfahren zum faerben von menschlichem haar |
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