BE578415A - - Google Patents

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Publication number

BE578415A

BE578415A BE578415DA BE578415A BE 578415 A BE578415 A BE 578415A BE 578415D A BE578415D A BE 578415DA BE 578415 A BE578415 A BE 578415A

Authority

BE

Belgium

Prior art keywords

dyes

dye

materials

solution

impregnated

Prior art date

Links

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• 239000000975 dye Substances 0.000 claims description 51
• 239000000243 solution Substances 0.000 claims description 32
• 239000000463 material Substances 0.000 claims description 24
• 239000000126 substance Substances 0.000 claims description 16
• 238000000034 method Methods 0.000 claims description 13
• FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 11
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
• 230000001808 coupling Effects 0.000 claims description 10
• 238000010168 coupling process Methods 0.000 claims description 10
• 238000005859 coupling reaction Methods 0.000 claims description 10
• 239000011780 sodium chloride Substances 0.000 claims description 10
• 239000007864 aqueous solution Substances 0.000 claims description 9
• 239000000987 azo dye Substances 0.000 claims description 7
• 239000000470 constituent Substances 0.000 claims description 7
• 238000004043 dyeing Methods 0.000 claims description 5
• 150000001412 amines Chemical class 0.000 claims description 4
• 238000006243 chemical reaction Methods 0.000 claims description 4
• ZBKFYXZXZJPWNQ-UHFFFAOYSA-N isothiocyanate group Chemical group [N-]=C=S ZBKFYXZXZJPWNQ-UHFFFAOYSA-N 0.000 claims description 4
• 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
• 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
• 235000010755 mineral Nutrition 0.000 claims description 3
• 239000011707 mineral Substances 0.000 claims description 3
• 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 2
• 150000008041 alkali metal carbonates Chemical class 0.000 claims description 2
• 150000003839 salts Chemical class 0.000 claims description 2
• 239000004753 textile Substances 0.000 claims description 2
• 229910000318 alkali metal phosphate Inorganic materials 0.000 claims 1
• 239000003792 electrolyte Substances 0.000 claims 1
• 239000002253 acid Substances 0.000 description 19
• 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 19
• -1 aminoazo Chemical group 0.000 description 14
• HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
• CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 11
• 229920000742 Cotton Polymers 0.000 description 9
• 239000004744 fabric Substances 0.000 description 9
• 239000000047 product Substances 0.000 description 8
• ZWZVWGITAAIFPS-UHFFFAOYSA-N Thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 7
• XSQUKJJJFZCRTK-UHFFFAOYSA-N urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 5
• 239000011230 binding agent Substances 0.000 description 5
• 238000005470 impregnation Methods 0.000 description 5
• 239000001187 sodium carbonate Substances 0.000 description 5
• 229910000029 sodium carbonate Inorganic materials 0.000 description 5
• UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
• CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
• 150000007513 acids Chemical class 0.000 description 4
• 239000003086 colorant Substances 0.000 description 4
• 239000003599 detergent Substances 0.000 description 4
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 4
• 238000010438 heat treatment Methods 0.000 description 4
• 239000001044 red dye Substances 0.000 description 4
• 230000001034 aminogenic Effects 0.000 description 3
• 238000009835 boiling Methods 0.000 description 3
• 239000004202 carbamide Substances 0.000 description 3
• 150000001875 compounds Chemical class 0.000 description 3
• 238000001035 drying Methods 0.000 description 3
• 230000000694 effects Effects 0.000 description 3
• 239000007788 liquid Substances 0.000 description 3
• 150000007522 mineralic acids Chemical class 0.000 description 3
• 239000000203 mixture Substances 0.000 description 3
• 230000001264 neutralization Effects 0.000 description 3
• KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 3
• 238000003756 stirring Methods 0.000 description 3
• 238000005406 washing Methods 0.000 description 3
• 229920002456 HOTAIR Polymers 0.000 description 2
• IWDCLRJOBJJRNH-UHFFFAOYSA-N P-Cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
• 230000002378 acidificating Effects 0.000 description 2
• 239000003513 alkali Substances 0.000 description 2
• 229910052783 alkali metal Inorganic materials 0.000 description 2
• 150000001340 alkali metals Chemical class 0.000 description 2
• 150000001408 amides Chemical class 0.000 description 2
• 125000003277 amino group Chemical group 0.000 description 2
• 125000003118 aryl group Chemical group 0.000 description 2
• 239000007795 chemical reaction product Substances 0.000 description 2
• 239000003795 chemical substances by application Substances 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
• VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
• 229910052804 chromium Inorganic materials 0.000 description 2
• 239000011651 chromium Substances 0.000 description 2
• 238000001914 filtration Methods 0.000 description 2
• 229910052751 metal Chemical class 0.000 description 2
• 239000002184 metal Chemical class 0.000 description 2
• 150000004780 naphthols Chemical class 0.000 description 2
• 150000002989 phenols Chemical class 0.000 description 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
• JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
• LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2(1H)-one Chemical class C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 2
• KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
• 229910052708 sodium Inorganic materials 0.000 description 2
• 239000011734 sodium Substances 0.000 description 2
• 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
• 235000017557 sodium bicarbonate Nutrition 0.000 description 2
• 239000001488 sodium phosphate Substances 0.000 description 2
• 159000000000 sodium salts Chemical class 0.000 description 2
• 239000007787 solid Substances 0.000 description 2
• 239000002562 thickening agent Substances 0.000 description 2
• 210000001519 tissues Anatomy 0.000 description 2
• RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
• 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
• 235000019801 trisodium phosphate Nutrition 0.000 description 2
• UXBCHMIKTYBYTN-LQPTXBPRSA-N (3S,8S,9S,10R,13R,14S,17R)-3-[12-(3-iodophenyl)dodecoxy]-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene Chemical compound O([C@@H]1CC2=CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)CCCCCCCCCCCCC1=CC=CC(I)=C1 UXBCHMIKTYBYTN-LQPTXBPRSA-N 0.000 description 1
• QZYDOKBVZJLQCK-UHFFFAOYSA-N 1,2-diethoxybenzene Chemical compound CCOC1=CC=CC=C1OCC QZYDOKBVZJLQCK-UHFFFAOYSA-N 0.000 description 1
• ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical class O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 1
• QLSWIGRIBOSFMV-UHFFFAOYSA-N 1H-pyrrol-2-amine Chemical compound NC1=CC=CN1 QLSWIGRIBOSFMV-UHFFFAOYSA-N 0.000 description 1
• JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-Naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 1
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-Naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
• LDCCBULMAFILCT-UHFFFAOYSA-N 2-aminobenzene-1,4-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1S(O)(=O)=O LDCCBULMAFILCT-UHFFFAOYSA-N 0.000 description 1
• UJWDQHYEQXGSKW-UHFFFAOYSA-N 3-acetamido-5-aminobenzenesulfonic acid Chemical compound CC(=O)NC1=CC(N)=CC(S(O)(=O)=O)=C1 UJWDQHYEQXGSKW-UHFFFAOYSA-N 0.000 description 1
• ZLTOYIGWKLTQBJ-UHFFFAOYSA-N 3-amino-2-hydroxy-5-sulfobenzoic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC(C(O)=O)=C1O ZLTOYIGWKLTQBJ-UHFFFAOYSA-N 0.000 description 1
• ULUIMLJNTCECJU-UHFFFAOYSA-N 3-amino-4-hydroxybenzenesulfonate;hydron Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1O ULUIMLJNTCECJU-UHFFFAOYSA-N 0.000 description 1
• FLIOATBXVNLPLK-UHFFFAOYSA-N 3-amino-4-methoxybenzenesulfonic acid Chemical compound COC1=CC=C(S(O)(=O)=O)C=C1N FLIOATBXVNLPLK-UHFFFAOYSA-N 0.000 description 1
• NVLVJHQJUHUFAC-UHFFFAOYSA-N 3-aminobenzene-1,2-disulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1S(O)(=O)=O NVLVJHQJUHUFAC-UHFFFAOYSA-N 0.000 description 1
• JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 1
• 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 1
• GAVPOWTXUZVFML-UHFFFAOYSA-M 4-nitrobenzenediazonium;chloride Chemical compound [Cl-].[O-][N+](=O)C1=CC=C([N+]#N)C=C1 GAVPOWTXUZVFML-UHFFFAOYSA-M 0.000 description 1
• TWLMSPNQBKSXOP-UHFFFAOYSA-N 6358-09-4 Chemical compound NC1=CC([N+]([O-])=O)=CC(Cl)=C1O TWLMSPNQBKSXOP-UHFFFAOYSA-N 0.000 description 1
• MCJGNVYPOGVAJF-UHFFFAOYSA-N 8-Hydroxyquinoline Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
• 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
• DYRDKSSFIWVSNM-UHFFFAOYSA-N Acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
• RWZYAGGXGHYGMB-UHFFFAOYSA-N Anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
• DMLAVOWQYNRWNQ-BUHFOSPRSA-N Azobenzene Chemical compound C1=CC=CC=C1\N=N\C1=CC=CC=C1 DMLAVOWQYNRWNQ-BUHFOSPRSA-N 0.000 description 1
• 125000006519 CCH3 Chemical group 0.000 description 1
• HLVXFWDLRHCZEI-UHFFFAOYSA-N Chromotropic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(O)=CC(S(O)(=O)=O)=CC2=C1 HLVXFWDLRHCZEI-UHFFFAOYSA-N 0.000 description 1
• 229940093912 Gynecological Sulfonamides Drugs 0.000 description 1
• 150000008575 L-amino acids Chemical class 0.000 description 1
• NCBZRJODKRCREW-UHFFFAOYSA-N M-Anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 1
• MWQPFYRCFDXJMP-UHFFFAOYSA-N N(=C=S)C1=CC2=CC(=CC(=C2C=C1)O)S(=O)(=O)O Chemical compound N(=C=S)C1=CC2=CC(=CC(=C2C=C1)O)S(=O)(=O)O MWQPFYRCFDXJMP-UHFFFAOYSA-N 0.000 description 1
• DSEQJUPGRWESKP-UHFFFAOYSA-N N-(2-hydroxy-5-methylphenyl)acetamide Chemical compound CC(=O)NC1=CC(C)=CC=C1O DSEQJUPGRWESKP-UHFFFAOYSA-N 0.000 description 1
• VMPITZXILSNTON-UHFFFAOYSA-N O-Anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
• GKKCIDNWFBPDBW-UHFFFAOYSA-M Potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
• YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
• 229940005550 Sodium alginate Drugs 0.000 description 1
• IIACRCGMVDHOTQ-UHFFFAOYSA-N Sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
• 125000002252 acyl group Chemical group 0.000 description 1
• 125000004442 acylamino group Chemical group 0.000 description 1
• 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
• 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
• 150000001342 alkaline earth metals Chemical class 0.000 description 1
• 229940051880 analgesics and antipyretics Pyrazolones Drugs 0.000 description 1
• 150000004984 aromatic diamines Chemical class 0.000 description 1
• 150000007656 barbituric acids Chemical class 0.000 description 1
• 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
• UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
• SOYBJIUDKRLQTA-UHFFFAOYSA-N benzene;dinaphthalen-1-yldiazene Chemical compound C1=CC=CC=C1.C1=CC=C2C(N=NC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 SOYBJIUDKRLQTA-UHFFFAOYSA-N 0.000 description 1
• 150000001555 benzenes Chemical class 0.000 description 1
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
• 229950011260 betanaphthol Drugs 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
• 229910052803 cobalt Inorganic materials 0.000 description 1
• 239000010941 cobalt Substances 0.000 description 1
• 229910052802 copper Inorganic materials 0.000 description 1
• RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
• 239000010949 copper Substances 0.000 description 1
• 230000027326 copulation Effects 0.000 description 1
• 230000000875 corresponding Effects 0.000 description 1
• 150000001989 diazonium salts Chemical class 0.000 description 1
• 150000005575 dimethoxybenzenes Chemical class 0.000 description 1
• WSEFXLKPOBQART-UHFFFAOYSA-N dinaphthalen-1-yldiazene;naphthalene Chemical class C1=CC=CC2=CC=CC=C21.C1=CC=C2C(N=NC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 WSEFXLKPOBQART-UHFFFAOYSA-N 0.000 description 1
• 235000013601 eggs Nutrition 0.000 description 1
• 239000000835 fiber Substances 0.000 description 1
• 239000012065 filter cake Substances 0.000 description 1
• 238000005755 formation reaction Methods 0.000 description 1
• 150000002391 heterocyclic compounds Chemical class 0.000 description 1
• 238000006460 hydrolysis reaction Methods 0.000 description 1
• 150000004679 hydroxides Chemical class 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxyl anion Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
• 229940079867 intestinal antiinfectives Sulfonamides Drugs 0.000 description 1
• 125000001810 isothiocyanato group Chemical group *N=C=S 0.000 description 1
• 125000000468 ketone group Chemical group 0.000 description 1
• 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 description 1
• AFVFQIVMOAPDHO-UHFFFAOYSA-N methanesulfonic acid Substances CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
• PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
• 229940005938 ophthalmologic antiinfectives Sulfonamides Drugs 0.000 description 1
• 229960003540 oxyquinoline Drugs 0.000 description 1
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
• 239000011591 potassium Substances 0.000 description 1
• 229910052700 potassium Inorganic materials 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 230000002035 prolonged Effects 0.000 description 1
• KAESVJOAVNADME-UHFFFAOYSA-N pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
• 239000012429 reaction media Substances 0.000 description 1
• 239000011541 reaction mixture Substances 0.000 description 1
• 239000004627 regenerated cellulose Substances 0.000 description 1
• 238000007127 saponification reaction Methods 0.000 description 1
• MSXHSNHNTORCAW-UHFFFAOYSA-M sodium 3,4,5,6-tetrahydroxyoxane-2-carboxylate Chemical compound [Na+].OC1OC(C([O-])=O)C(O)C(O)C1O MSXHSNHNTORCAW-UHFFFAOYSA-M 0.000 description 1
• 239000000661 sodium alginate Substances 0.000 description 1
• 235000010413 sodium alginate Nutrition 0.000 description 1
• 229910052938 sodium sulfate Inorganic materials 0.000 description 1
• 235000011152 sodium sulphate Nutrition 0.000 description 1
• 230000003381 solubilizing Effects 0.000 description 1
• 150000003456 sulfonamides Chemical class 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
• UPKAWFACSJWKND-ZXFFUEEESA-J tetrasodium;(6E)-4-amino-6-[[4-[4-[(2Z)-2-(8-amino-1-oxo-5,7-disulfonatonaphthalen-2-ylidene)hydrazinyl]-3-methoxyphenyl]-2-methoxyphenyl]hydrazinylidene]-5-oxonaphthalene-1,3-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C\1=CC2=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C(N)=C2C(=O)C/1=N/NC(C(OC)=C1)=CC=C1C1=CC=C(N\N=C\2C(C3=C(N)C(=CC(=C3C=C/2)S([O-])(=O)=O)S([O-])(=O)=O)=O)C(OC)=C1 UPKAWFACSJWKND-ZXFFUEEESA-J 0.000 description 1
• 229940026752 topical Sulfonamides Drugs 0.000 description 1
• 238000009834 vaporization Methods 0.000 description 1
• 239000000080 wetting agent Substances 0.000 description 1