BE420332A - - Google Patents

Info

Publication number

BE420332A

BE420332A BE420332DA BE420332A BE 420332 A BE420332 A BE 420332A BE 420332D A BE420332D A BE 420332DA BE 420332 A BE420332 A BE 420332A

Authority

BE

Belgium

Prior art keywords

sep

benzoylaminobenzene

group

amino

purple

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• 239000000975 dye Substances 0.000 claims description 13
• 229920001971 elastomer Polymers 0.000 claims description 10
• UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 10
• 239000004033 plastic Substances 0.000 claims description 6
• 229920003023 plastic Polymers 0.000 claims description 6
• 239000000463 material Substances 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 4
• 125000001424 substituent group Chemical group 0.000 claims description 4
• 125000000217 alkyl group Chemical group 0.000 claims description 2
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
• 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 2
• 229910052736 halogen Inorganic materials 0.000 claims description 2
• 150000002367 halogens Chemical class 0.000 claims description 2
• 229910052739 hydrogen Inorganic materials 0.000 claims description 2
• 239000001257 hydrogen Substances 0.000 claims description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
• 125000001624 naphthyl group Chemical group 0.000 claims description 2
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
• 239000000126 substance Substances 0.000 claims 2
• 125000003118 aryl group Chemical group 0.000 claims 1
• ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 17
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 13
• 239000000047 product Substances 0.000 description 9
• 238000004073 vulcanization Methods 0.000 description 6
• 239000000203 mixture Substances 0.000 description 5
• KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
• -1 benzene radical Chemical class 0.000 description 4
• 239000003086 colorant Substances 0.000 description 3
• 244000043261 Hevea brasiliensis Species 0.000 description 2
• RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
• 238000004040 coloring Methods 0.000 description 2
• 230000008878 coupling Effects 0.000 description 2
• 238000010168 coupling process Methods 0.000 description 2
• 238000005859 coupling reaction Methods 0.000 description 2
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
• 239000004615 ingredient Substances 0.000 description 2
• 229920003052 natural elastomer Polymers 0.000 description 2
• 229920001194 natural rubber Polymers 0.000 description 2
• 239000007787 solid Substances 0.000 description 2
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
• 150000005840 aryl radicals Chemical class 0.000 description 1
• 239000005018 casein Substances 0.000 description 1
• 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 1
• 235000021240 caseins Nutrition 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 239000007859 condensation product Substances 0.000 description 1
• 150000008049 diazo compounds Chemical class 0.000 description 1
• PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
• 229930195733 hydrocarbon Natural products 0.000 description 1
• 150000002430 hydrocarbons Chemical class 0.000 description 1
• WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
• CLXWSQCXMNVBQP-UHFFFAOYSA-N n-(3,4-diethoxyphenyl)benzamide Chemical compound C1=C(OCC)C(OCC)=CC=C1NC(=O)C1=CC=CC=C1 CLXWSQCXMNVBQP-UHFFFAOYSA-N 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
• FRZFJTUTPKVROY-UHFFFAOYSA-N n-phenylbenzamide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1.C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 FRZFJTUTPKVROY-UHFFFAOYSA-N 0.000 description 1
• AZTGEJBZSFKULT-UHFFFAOYSA-N n-phenylcyclohexanecarboxamide Chemical compound C1CCCCC1C(=O)NC1=CC=CC=C1 AZTGEJBZSFKULT-UHFFFAOYSA-N 0.000 description 1
• 238000006116 polymerization reaction Methods 0.000 description 1
• 239000011593 sulfur Substances 0.000 description 1
• 229910052717 sulfur Inorganic materials 0.000 description 1