DE127140C - - Google Patents

Info

Publication number

DE127140C

DE127140C DENDAT127140D DE127140DA DE127140C DE 127140 C DE127140 C DE 127140C DE NDAT127140 D DENDAT127140 D DE NDAT127140D DE 127140D A DE127140D A DE 127140DA DE 127140 C DE127140 C DE 127140C

Authority

DE

Germany

Prior art keywords

bordeaux

precipitation

red

bluish

acid

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.)

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• 238000001556 precipitation Methods 0.000 claims description 21
• 239000000975 dye Substances 0.000 claims description 13
• 239000000843 powder Substances 0.000 claims description 12
• YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 10
• 239000002253 acid Substances 0.000 claims description 8
• UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
• HFACYLZERDEVSX-UHFFFAOYSA-N Benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 5
• 235000020127 ayran Nutrition 0.000 claims description 5
• 229960004889 salicylic acid Drugs 0.000 claims description 5
• JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 claims description 4
• NUIURNJTPRWVAP-UHFFFAOYSA-N Tolidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 claims description 4
• 239000004744 fabric Substances 0.000 claims description 4
• 150000003839 salts Chemical class 0.000 claims description 4
• 239000011780 sodium chloride Substances 0.000 claims description 4
• CBCKQZAAMUWICA-UHFFFAOYSA-N P-Phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 3
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
• 210000002268 Wool Anatomy 0.000 claims description 3
• 239000003086 colorant Substances 0.000 claims description 3
• 235000017557 sodium bicarbonate Nutrition 0.000 claims description 3
• 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 3
• 235000011121 sodium hydroxide Nutrition 0.000 claims description 3
• WHSXTWFYRGOBGO-UHFFFAOYSA-N 3-methylsalicylic acid Chemical compound CC1=CC=CC(C(O)=O)=C1O WHSXTWFYRGOBGO-UHFFFAOYSA-N 0.000 claims 1
• NJESAXZANHETJV-UHFFFAOYSA-N 4-Methylsalicylic acid Chemical compound CC1=CC=C(C(O)=O)C(O)=C1 NJESAXZANHETJV-UHFFFAOYSA-N 0.000 claims 1
• 125000003368 amide group Chemical group 0.000 claims 1
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 1
• 239000000543 intermediate Substances 0.000 claims 1
• 150000007513 acids Chemical class 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• 229920000742 Cotton Polymers 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• LPXPTNMVRIOKMN-UHFFFAOYSA-M Sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
• UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
• 230000000875 corresponding Effects 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 238000010186 staining Methods 0.000 description 2
• KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-Naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
• UEUGTXFKMNWFRE-UHFFFAOYSA-L Scarlet GN Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC(C)=C1N=NC1=CC=C(C(=CC=C2)S([O-])(=O)=O)C2=C1O UEUGTXFKMNWFRE-UHFFFAOYSA-L 0.000 description 1
• LIPOUNRJVLNBCD-UHFFFAOYSA-N acetyl dihydrogen phosphate Chemical compound CC(=O)OP(O)(O)=O LIPOUNRJVLNBCD-UHFFFAOYSA-N 0.000 description 1
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
• 239000000987 azo dye Substances 0.000 description 1
• 150000001555 benzenes Chemical class 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 150000004985 diamines Chemical class 0.000 description 1
• MRVNLKITQIBNKU-UKOJIYRKSA-L disodium;(4E)-4-(naphthalen-1-ylhydrazinylidene)-3-oxonaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].C1=CC=C2C(N\N=C3/C4=CC=C(C=C4C=C(C3=O)S(=O)(=O)[O-])S([O-])(=O)=O)=CC=CC2=C1 MRVNLKITQIBNKU-UKOJIYRKSA-L 0.000 description 1
• 230000000694 effects Effects 0.000 description 1
• PLYDMIIYRWUYBP-UHFFFAOYSA-N ethyl 4-[[2-chloro-4-[3-chloro-4-[(3-ethoxycarbonyl-5-oxo-1-phenyl-4H-pyrazol-4-yl)diazenyl]phenyl]phenyl]diazenyl]-5-oxo-1-phenyl-4H-pyrazole-3-carboxylate Chemical compound CCOC(=O)C1=NN(C=2C=CC=CC=2)C(=O)C1N=NC(C(=C1)Cl)=CC=C1C(C=C1Cl)=CC=C1N=NC(C(=N1)C(=O)OCC)C(=O)N1C1=CC=CC=C1 PLYDMIIYRWUYBP-UHFFFAOYSA-N 0.000 description 1
• 238000005755 formation reaction Methods 0.000 description 1
• -1 oxyazo Chemical group 0.000 description 1
• 239000001044 red dye Substances 0.000 description 1
• 235000010288 sodium nitrite Nutrition 0.000 description 1
• 238000001228 spectrum Methods 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
• 150000003460 sulfonic acids Chemical class 0.000 description 1