DE101805C - - Google Patents

Info

Publication number

DE101805C

DE101805C DENDAT101805D DE101805DA DE101805C DE 101805 C DE101805 C DE 101805C DE NDAT101805 D DENDAT101805 D DE NDAT101805D DE 101805D A DE101805D A DE 101805DA DE 101805 C DE101805 C DE 101805C

Authority

DE

Germany

Prior art keywords

blue

dyes

acid

green

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

• Espacenet
• Global Dossier
• DPMA
• Discuss

• 239000002253 acid Substances 0.000 claims description 6
• 238000000034 method Methods 0.000 claims description 2
• 150000001412 amines Chemical class 0.000 claims 1
• 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 239000000126 substance Substances 0.000 claims 1
• 239000000975 dye Substances 0.000 description 12
• 210000002268 wool Anatomy 0.000 description 5
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 239000000047 product Substances 0.000 description 3
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
• WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
• 239000013078 crystal Substances 0.000 description 2
• 239000012452 mother liquor Substances 0.000 description 2
• CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 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
• VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• 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 1
• 229960000583 acetic acid Drugs 0.000 description 1
• 239000001045 blue dye Substances 0.000 description 1
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
• 239000004327 boric acid Substances 0.000 description 1
• 239000007795 chemical reaction product Substances 0.000 description 1
• 238000004040 coloring Methods 0.000 description 1
• 238000004043 dyeing Methods 0.000 description 1
• 239000012362 glacial acetic acid Substances 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 239000001103 potassium chloride Substances 0.000 description 1
• 235000011164 potassium chloride Nutrition 0.000 description 1
• 150000003142 primary aromatic amines Chemical class 0.000 description 1
• 238000005185 salting out Methods 0.000 description 1
• 229910052708 sodium Inorganic materials 0.000 description 1
• 239000011734 sodium Substances 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
• 210000003462 vein Anatomy 0.000 description 1