BE545737A - - Google Patents

Info

Publication number

BE545737A

BE545737A BE545737DA BE545737A BE 545737 A BE545737 A BE 545737A BE 545737D A BE545737D A BE 545737DA BE 545737 A BE545737 A BE 545737A

Authority

BE

Belgium

Prior art keywords

hydroxy

azobenzene

chloro

methyl

methoxy

Prior art date

Links

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• 125000000217 alkyl group Chemical group 0.000 claims description 6
• 229910052801 chlorine Inorganic materials 0.000 claims description 6
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
• 238000000034 method Methods 0.000 claims description 5
• -1 3'-methoxy-5-chloro-2-hydroxy-1.1'-azobenzene Chemical compound 0.000 claims description 4
• 125000003545 alkoxy group Chemical group 0.000 claims description 4
• FYIBGDKNYYMMAG-UHFFFAOYSA-N ethane-1,2-diol;terephthalic acid Chemical compound OCCO.OC(=O)C1=CC=C(C(O)=O)C=C1 FYIBGDKNYYMMAG-UHFFFAOYSA-N 0.000 claims description 4
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
• 229920000642 polymer Polymers 0.000 claims description 4
• 125000003172 aldehyde group Chemical group 0.000 claims description 3
• 125000003118 aryl group Chemical group 0.000 claims description 2
• DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 claims description 2
• 229920000728 polyester Polymers 0.000 claims description 2
• YZBLFDRWSHBLSP-UHFFFAOYSA-N 1-phenyldiazenylcyclohexa-2,4-dien-1-ol Chemical class OC1(CC=CC=C1)N=NC1=CC=CC=C1 YZBLFDRWSHBLSP-UHFFFAOYSA-N 0.000 claims 1
• DRUBUDNRVKAQSU-UHFFFAOYSA-N 2-[(2-chlorophenyl)diazenyl]-4-methylphenol Chemical compound OC1=C(C=C(C=C1)C)N=NC1=C(C=CC=C1)Cl DRUBUDNRVKAQSU-UHFFFAOYSA-N 0.000 claims 1
• PEXGTUZWTLMFID-UHFFFAOYSA-N 2-phenyldiazenylphenol Chemical class OC1=CC=CC=C1N=NC1=CC=CC=C1 PEXGTUZWTLMFID-UHFFFAOYSA-N 0.000 claims 1
• CIZVQWNPBGYCGK-UHFFFAOYSA-N benzenediazonium Chemical group N#[N+]C1=CC=CC=C1 CIZVQWNPBGYCGK-UHFFFAOYSA-N 0.000 claims 1
• 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
• 238000002844 melting Methods 0.000 description 9
• 230000008018 melting Effects 0.000 description 9
• 239000000975 dye Substances 0.000 description 6
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• 239000002253 acid Substances 0.000 description 2
• HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
• 239000003086 colorant Substances 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• 229910000029 sodium carbonate Inorganic materials 0.000 description 2
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
• DZKFWJMJNUTVQL-UHFFFAOYSA-N COC1=C(C=CC=C1)N=NC1=C(C=CC(=C1)Cl)O Chemical compound COC1=C(C=CC=C1)N=NC1=C(C=CC(=C1)Cl)O DZKFWJMJNUTVQL-UHFFFAOYSA-N 0.000 description 1
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
• SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 1
• 230000002378 acidificating effect Effects 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 239000007900 aqueous suspension Substances 0.000 description 1
• 125000004429 atom Chemical group 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 239000007859 condensation product Substances 0.000 description 1
• 230000008878 coupling Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 238000005859 coupling reaction Methods 0.000 description 1
• 235000014113 dietary fatty acids Nutrition 0.000 description 1
• 229930195729 fatty acid Natural products 0.000 description 1
• 239000000194 fatty acid Substances 0.000 description 1
• 150000004665 fatty acids Chemical class 0.000 description 1
• 230000004927 fusion Effects 0.000 description 1
• 239000001257 hydrogen Substances 0.000 description 1
• 229910052739 hydrogen Inorganic materials 0.000 description 1
• 150000002440 hydroxy compounds Chemical class 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 239000000463 material Substances 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
• 150000003141 primary amines Chemical class 0.000 description 1
• 239000007787 solid Substances 0.000 description 1
• UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
• 239000001043 yellow dye Substances 0.000 description 1