NO330409B1 - Anvendelse av triazolopyrimidinderivater som mikrobiocider for beskyttelse av materialer, fremgangsmate for beskyttelse av tekniske materialer samt tekniske materialer inneholdende de nevnte derivatene. - Google Patents

Info

Publication number

NO330409B1

NO330409B1 NO20035012A NO20035012A NO330409B1 NO 330409 B1 NO330409 B1 NO 330409B1 NO 20035012 A NO20035012 A NO 20035012A NO 20035012 A NO20035012 A NO 20035012A NO 330409 B1 NO330409 B1 NO 330409B1

Authority

NO

Norway

Prior art keywords

protection

technical materials

wood

methyl

materials

Prior art date

2001-05-18

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• 239000000463 material Substances 0.000 title claims abstract description 39
• 230000003641 microbiacidal effect Effects 0.000 title claims abstract description 11
• 238000000034 method Methods 0.000 title claims abstract description 9
• YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 title abstract description 9
• 150000001875 compounds Chemical class 0.000 claims abstract description 24
• 150000003839 salts Chemical class 0.000 claims abstract description 21
• 239000002253 acid Substances 0.000 claims abstract description 17
• 229910052751 metal Inorganic materials 0.000 claims abstract description 15
• 239000002184 metal Substances 0.000 claims abstract description 15
• 244000005700 microbiome Species 0.000 claims abstract description 15
• 230000006378 damage Effects 0.000 claims abstract description 6
• 150000001204 N-oxides Chemical class 0.000 claims abstract description 5
• -1 trimethylcyclopentyl Chemical group 0.000 claims description 105
• 239000002023 wood Substances 0.000 claims description 17
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
• 239000003973 paint Substances 0.000 claims description 12
• 241000233866 Fungi Species 0.000 claims description 10
• 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 claims description 8
• 239000006185 dispersion Substances 0.000 claims description 7
• 239000004744 fabric Substances 0.000 claims description 7
• 239000000835 fiber Substances 0.000 claims description 7
• 239000000123 paper Substances 0.000 claims description 7
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
• 239000003795 chemical substances by application Substances 0.000 claims description 5
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
• 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
• 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 2
• 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 claims description 2
• 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
• 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 2
• 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 2
• 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 2
• 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 2
• 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims description 2
• 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 2
• 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
• 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 2
• 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 2
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
• 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
• 125000002785 azepinyl group Chemical group 0.000 claims description 2
• 239000000460 chlorine Substances 0.000 claims description 2
• 229910052801 chlorine Inorganic materials 0.000 claims description 2
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
• 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
• 239000001257 hydrogen Substances 0.000 claims description 2
• 229910052739 hydrogen Inorganic materials 0.000 claims description 2
• 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 2
• 229910052757 nitrogen Inorganic materials 0.000 claims description 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
• 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
• 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
• 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 claims description 2
• 125000005936 piperidyl group Chemical group 0.000 claims description 2
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
• 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 2
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
• 239000011505 plaster Substances 0.000 claims 1
• 239000004557 technical material Substances 0.000 claims 1
• 239000000203 mixture Substances 0.000 abstract description 15
• 239000002904 solvent Substances 0.000 abstract description 4
• 229940124561 microbicide Drugs 0.000 abstract description 3
• 125000003342 alkenyl group Chemical group 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 125000000304 alkynyl group Chemical group 0.000 abstract 1
• 230000000845 anti-microbial effect Effects 0.000 abstract 1
• 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
• 239000003085 diluting agent Substances 0.000 abstract 1
• 125000001475 halogen functional group Chemical group 0.000 abstract 1
• 125000000623 heterocyclic group Chemical group 0.000 abstract 1
• 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
• 125000003107 substituted aryl group Chemical group 0.000 abstract 1
• 239000013543 active substance Substances 0.000 description 12
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• 238000009472 formulation Methods 0.000 description 8
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• 239000010949 copper Substances 0.000 description 6
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• 239000008187 granular material Substances 0.000 description 5
• 239000000126 substance Substances 0.000 description 5
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
• 239000000969 carrier Substances 0.000 description 4
• 229910052742 iron Inorganic materials 0.000 description 4
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• 239000011701 zinc Substances 0.000 description 4
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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