BE386697A - - Google Patents

Info

Publication number

BE386697A

BE386697A BE386697DA BE386697A BE 386697 A BE386697 A BE 386697A BE 386697D A BE386697D A BE 386697DA BE 386697 A BE386697 A BE 386697A

Authority

BE

Belgium

Prior art keywords

rubber

molecules

diazotized

compositions

dye

Prior art date

Links

• Espacenet
• Global Dossier
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• 239000000203 mixture Substances 0.000 claims description 17
• 239000000987 azo dye Substances 0.000 claims description 5
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
• 239000004033 plastic Substances 0.000 claims description 4
• 229920003023 plastic Polymers 0.000 claims description 4
• GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical compound CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 claims description 3
• 238000000034 method Methods 0.000 claims description 3
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 229910052757 nitrogen Inorganic materials 0.000 claims description 2
• 239000000975 dye Substances 0.000 description 16
• 238000004073 vulcanization Methods 0.000 description 9
• KADRARSMBUXHLL-UHFFFAOYSA-N 2-methylaniline;3-oxobutanoic acid Chemical compound CC(=O)CC(O)=O.CC1=CC=CC=C1N KADRARSMBUXHLL-UHFFFAOYSA-N 0.000 description 6
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
• 239000000126 substance Substances 0.000 description 4
• 229910052717 sulfur Inorganic materials 0.000 description 4
• 239000011593 sulfur Substances 0.000 description 4
• HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical class C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 3
• 238000009833 condensation Methods 0.000 description 3
• 230000005494 condensation Effects 0.000 description 3
• 239000000945 filler Substances 0.000 description 3
• 238000005096 rolling process Methods 0.000 description 3
• -1 xylidine acetylacetate Chemical compound 0.000 description 3
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
• WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic anhydride Substances CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 2
• 239000005018 casein Substances 0.000 description 2
• BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
• 235000021240 caseins Nutrition 0.000 description 2
• 239000011248 coating agent Substances 0.000 description 2
• 238000000576 coating method Methods 0.000 description 2
• 210000003298 dental enamel Anatomy 0.000 description 2
• PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 2
• WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
• LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
• XCIPTTJFZCOUCG-UHFFFAOYSA-N 2-chloroaniline;3-oxobutanoic acid Chemical compound CC(=O)CC(O)=O.NC1=CC=CC=C1Cl XCIPTTJFZCOUCG-UHFFFAOYSA-N 0.000 description 1
• HUWXDEQWWKGHRV-UHFFFAOYSA-N 3,3'-Dichlorobenzidine Chemical compound C1=C(Cl)C(N)=CC=C1C1=CC=C(N)C(Cl)=C1 HUWXDEQWWKGHRV-UHFFFAOYSA-N 0.000 description 1
• YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
• XKXPBJBODVHDAW-UHFFFAOYSA-N 4-(4-amino-2-chlorophenyl)-3-chloroaniline Chemical compound ClC1=CC(N)=CC=C1C1=CC=C(N)C=C1Cl XKXPBJBODVHDAW-UHFFFAOYSA-N 0.000 description 1
• GDIIPKWHAQGCJF-UHFFFAOYSA-N 4-Amino-2-nitrotoluene Chemical compound CC1=CC=C(N)C=C1[N+]([O-])=O GDIIPKWHAQGCJF-UHFFFAOYSA-N 0.000 description 1
• 229920002160 Celluloid Polymers 0.000 description 1
• 239000000020 Nitrocellulose Substances 0.000 description 1
• WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
• 125000000217 alkyl group Chemical group 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 150000003931 anilides Chemical class 0.000 description 1
• 125000003710 aryl alkyl group Chemical group 0.000 description 1
• RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 150000008049 diazo compounds Chemical class 0.000 description 1
• 238000006253 efflorescence Methods 0.000 description 1
• 238000005562 fading Methods 0.000 description 1
• 125000005843 halogen group Chemical group 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 238000007654 immersion Methods 0.000 description 1
• 238000004898 kneading Methods 0.000 description 1
• 229920001220 nitrocellulos Polymers 0.000 description 1
• 239000004014 plasticizer Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 206010037844 rash Diseases 0.000 description 1
• 239000008149 soap solution Substances 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 238000003860 storage Methods 0.000 description 1
• 239000004636 vulcanized rubber Substances 0.000 description 1