BE432681A - - Google Patents

Info

Publication number

BE432681A

BE432681A BE432681DA BE432681A BE 432681 A BE432681 A BE 432681A BE 432681D A BE432681D A BE 432681DA BE 432681 A BE432681 A BE 432681A

Authority

BE

Belgium

Prior art keywords

sep

benzene

dyes

radical

groups

Prior art date

Links

• Espacenet
• Global Dossier
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• UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 81
• 239000000975 dye Substances 0.000 claims description 28
• 239000003960 organic solvent Substances 0.000 claims description 10
• 125000005843 halogen group Chemical group 0.000 claims description 9
• 125000001424 substituent group Chemical group 0.000 claims description 9
• -1 aralooyl Chemical group 0.000 claims description 6
• 125000003118 aryl group Chemical group 0.000 claims description 6
• 150000008049 diazo compounds Chemical class 0.000 claims description 6
• 239000004922 lacquer Substances 0.000 claims description 6
• 125000000217 alkyl group Chemical group 0.000 claims description 5
• 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 claims description 5
• 238000000034 method Methods 0.000 claims description 5
• 229920002678 cellulose Polymers 0.000 claims description 4
• 239000001913 cellulose Substances 0.000 claims description 4
• 238000002360 preparation method Methods 0.000 claims description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
• 239000000987 azo dye Substances 0.000 claims description 3
• 230000008878 coupling Effects 0.000 claims description 3
• 238000010168 coupling process Methods 0.000 claims description 3
• 238000005859 coupling reaction Methods 0.000 claims description 3
• UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 3
• 239000004033 plastic Substances 0.000 claims description 3
• 229920003023 plastic Polymers 0.000 claims description 3
• ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 claims description 2
• 150000001412 amines Chemical class 0.000 claims description 2
• 230000001034 aminogenic effect Effects 0.000 claims description 2
• 239000000470 constituent Substances 0.000 claims description 2
• 239000010408 film Substances 0.000 claims description 2
• 230000003381 solubilizing effect Effects 0.000 claims description 2
• 239000000126 substance Substances 0.000 claims description 2
• 239000002966 varnish Substances 0.000 claims description 2
• 230000001476 alcoholic effect Effects 0.000 claims 1
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
• LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
• 239000002904 solvent Substances 0.000 description 4
• ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 3
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 3
• 238000004043 dyeing Methods 0.000 description 3
• DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
• CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
• VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
• 238000001914 filtration Methods 0.000 description 2
• FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
• 239000000049 pigment Substances 0.000 description 2
• 239000001632 sodium acetate Substances 0.000 description 2
• 235000017281 sodium acetate Nutrition 0.000 description 2
• 235000011121 sodium hydroxide Nutrition 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• 239000008096 xylene Substances 0.000 description 2
• JLNGEXDJAQASHD-UHFFFAOYSA-N N,N-Diethylbenzamide Chemical compound CCN(CC)C(=O)C1=CC=CC=C1 JLNGEXDJAQASHD-UHFFFAOYSA-N 0.000 description 1
• 239000000020 Nitrocellulose Substances 0.000 description 1
• FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 150000001298 alcohols Chemical class 0.000 description 1
• 150000001408 amides Chemical class 0.000 description 1
• 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
• 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
• XDLDASNSMGOEMX-UHFFFAOYSA-N benzene benzene Chemical compound C1=CC=CC=C1.C1=CC=CC=C1 XDLDASNSMGOEMX-UHFFFAOYSA-N 0.000 description 1
• DYGUCVNENDKSND-UHFFFAOYSA-N benzene;n-phenylacetamide Chemical compound C1=CC=CC=C1.CC(=O)NC1=CC=CC=C1 DYGUCVNENDKSND-UHFFFAOYSA-N 0.000 description 1
• 229920003086 cellulose ether Polymers 0.000 description 1
• 239000003086 colorant Substances 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 150000002170 ethers Chemical class 0.000 description 1
• 230000001747 exhibiting effect Effects 0.000 description 1
• 239000003925 fat Substances 0.000 description 1
• 125000000623 heterocyclic group Chemical group 0.000 description 1
• 229930195733 hydrocarbon Natural products 0.000 description 1
• 150000002430 hydrocarbons Chemical class 0.000 description 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 150000002576 ketones Chemical class 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 235000010755 mineral Nutrition 0.000 description 1
• CNXZLZNEIYFZGU-UHFFFAOYSA-N n-(4-amino-2,5-diethoxyphenyl)benzamide Chemical compound C1=C(N)C(OCC)=CC(NC(=O)C=2C=CC=CC=2)=C1OCC CNXZLZNEIYFZGU-UHFFFAOYSA-N 0.000 description 1
• CIPHTOQKGSLCLV-UHFFFAOYSA-N n-phenylnaphthalene-1-carboxamide Chemical compound C=1C=CC2=CC=CC=C2C=1C(=O)NC1=CC=CC=C1 CIPHTOQKGSLCLV-UHFFFAOYSA-N 0.000 description 1
• 150000004780 naphthols Chemical class 0.000 description 1
• 230000007935 neutral effect Effects 0.000 description 1
• 229920001220 nitrocellulos Polymers 0.000 description 1
• 229940079938 nitrocellulose Drugs 0.000 description 1
• 150000002894 organic compounds Chemical class 0.000 description 1
• 101150032584 oxy-4 gene Proteins 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 239000001044 red dye Substances 0.000 description 1
• 239000007787 solid Substances 0.000 description 1