BE413736A - - Google Patents

Info

Publication number

BE413736A

BE413736A BE413736DA BE413736A BE 413736 A BE413736 A BE 413736A BE 413736D A BE413736D A BE 413736DA BE 413736 A BE413736 A BE 413736A

Authority

BE

Belgium

Prior art keywords

aminophenol

ether

parts

dioxypropyl

desc

Prior art date

Links

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• 239000000975 dye Substances 0.000 claims description 13
• 238000000034 method Methods 0.000 claims description 7
• DOPJTDJKZNWLRB-UHFFFAOYSA-N 2-Amino-5-nitrophenol Chemical compound NC1=CC=C([N+]([O-])=O)C=C1O DOPJTDJKZNWLRB-UHFFFAOYSA-N 0.000 claims description 3
• 239000004922 lacquer Substances 0.000 claims description 3
• 125000005429 oxyalkyl group Chemical group 0.000 claims description 3
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims description 2
• 238000004043 dyeing Methods 0.000 claims description 2
• 229910052739 hydrogen Inorganic materials 0.000 claims description 2
• 239000001257 hydrogen Substances 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 230000008878 coupling Effects 0.000 claims 1
• 238000010168 coupling process Methods 0.000 claims 1
• 238000005859 coupling reaction Methods 0.000 claims 1
• 239000000463 material Substances 0.000 claims 1
• 150000007530 organic bases Chemical class 0.000 claims 1
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 5
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 238000004040 coloring Methods 0.000 description 3
• 239000002270 dispersing agent Substances 0.000 description 3
• -1 oxypropyl Chemical group 0.000 description 3
• CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
• 125000000664 diazo group Chemical class [N-]=[N+]=[*] 0.000 description 2
• 238000001035 drying Methods 0.000 description 2
• 229940035423 ethyl ether Drugs 0.000 description 2
• 239000000344 soap Substances 0.000 description 2
• LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
• 239000000725 suspension Substances 0.000 description 2
• DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
• 229940018563 3-aminophenol Drugs 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
• 239000002253 acid Substances 0.000 description 1
• 125000003545 alkoxy group Chemical group 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 229920003086 cellulose ether Polymers 0.000 description 1
• 239000003795 chemical substances by application Substances 0.000 description 1
• 239000006185 dispersion Substances 0.000 description 1
• 150000002170 ethers Chemical class 0.000 description 1
• 150000002191 fatty alcohols Chemical class 0.000 description 1
• 239000000835 fiber Substances 0.000 description 1
• 238000000227 grinding Methods 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 239000005457 ice water Substances 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 239000011734 sodium Substances 0.000 description 1
• 229910052708 sodium Inorganic materials 0.000 description 1
• 235000010288 sodium nitrite Nutrition 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• 238000000967 suction filtration Methods 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
• 239000002699 waste material Chemical class 0.000 description 1