RU2571899C2 - Содержащая пенфлуфен фунгицидная композиция, ее применение, древесина, древесные материалы или комбинированные материалы из древесины и пластика, содержащие эту композицию, и способ защиты древесины, древесных материалов из древесины и пластика - Google Patents

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Publication number

RU2571899C2

RU2571899C2 RU2013123767/13A RU2013123767A RU2571899C2 RU 2571899 C2 RU2571899 C2 RU 2571899C2 RU 2013123767/13 A RU2013123767/13 A RU 2013123767/13A RU 2013123767 A RU2013123767 A RU 2013123767A RU 2571899 C2 RU2571899 C2 RU 2571899C2

Authority

RU

Russia

Prior art keywords

wood

carbon atoms

penflufen

materials

compounds

Prior art date

2010-10-25

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• 239000002023 wood Substances 0.000 title claims abstract description 72
• 239000000463 material Substances 0.000 title claims abstract description 60
• 239000000203 mixture Substances 0.000 title claims abstract description 60
• 239000004033 plastic Substances 0.000 title claims abstract description 17
• 229920003023 plastic Polymers 0.000 title claims abstract description 17
• -1 application thereof Substances 0.000 title claims description 170
• 239000005815 Penflufen Substances 0.000 title claims description 145
• GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 title claims description 139
• 238000000034 method Methods 0.000 title claims description 13
• 230000000855 fungicidal effect Effects 0.000 title description 4
• 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 59
• LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims abstract description 43
• 150000001875 compounds Chemical class 0.000 claims abstract description 40
• 150000003839 salts Chemical class 0.000 claims abstract description 29
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 27
• 239000002253 acid Substances 0.000 claims abstract description 22
• 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 21
• 235000010292 orthophenyl phenol Nutrition 0.000 claims abstract description 21
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 17
• 244000005700 microbiome Species 0.000 claims abstract description 17
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 15
• 230000006378 damage Effects 0.000 claims abstract description 15
• 150000001639 boron compounds Chemical class 0.000 claims abstract description 12
• MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 claims abstract description 11
• 239000003513 alkali Substances 0.000 claims abstract description 10
• 125000003118 aryl group Chemical group 0.000 claims abstract description 10
• 150000001450 anions Chemical class 0.000 claims abstract description 7
• 230000000694 effects Effects 0.000 claims abstract description 5
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 24
• 229910021538 borax Inorganic materials 0.000 claims description 22
• 235000010339 sodium tetraborate Nutrition 0.000 claims description 22
• 239000004327 boric acid Substances 0.000 claims description 19
• RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 claims description 18
• JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 18
• BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 claims description 16
• 229960000686 benzalkonium chloride Drugs 0.000 claims description 15
• CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 15
• 229910052810 boron oxide Inorganic materials 0.000 claims description 14
• WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 11
• TXOJCSIIFFMREV-UHFFFAOYSA-L didecyl(dimethyl)azanium;carbonate Chemical compound [O-]C([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC TXOJCSIIFFMREV-UHFFFAOYSA-L 0.000 claims description 10
• CXIVKQSIEXBSRQ-UHFFFAOYSA-N 4,5-dichloro-2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SC(Cl)C(Cl)C1=O CXIVKQSIEXBSRQ-UHFFFAOYSA-N 0.000 claims description 9
• 229960004670 didecyldimethylammonium chloride Drugs 0.000 claims description 9
• NYNKJVPRTLBJNQ-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-dodecylpropane-1,3-diamine Chemical compound CCCCCCCCCCCCN(CCCN)CCCN NYNKJVPRTLBJNQ-UHFFFAOYSA-N 0.000 claims description 8
• BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 7
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
• 150000001342 alkaline earth metals Chemical class 0.000 claims description 7
• 125000004429 atom Chemical group 0.000 claims description 7
• 229910052799 carbon Inorganic materials 0.000 claims description 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
• 125000006286 dichlorobenzyl group Chemical group 0.000 claims description 6
• 239000004328 sodium tetraborate Substances 0.000 claims description 6
• 229940078672 didecyldimethylammonium Drugs 0.000 claims description 5
• VOENXYPDOJTAHV-UHFFFAOYSA-N 2-hydroxyethylazanium;propanoate Chemical compound NCCO.CCC(O)=O VOENXYPDOJTAHV-UHFFFAOYSA-N 0.000 claims description 4
• AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 claims description 4
• CIOQSQQVHVGYHS-UHFFFAOYSA-N 5-chloro-2-octyl-1,2-thiazolidin-4-one Chemical compound CCCCCCCCN1CC(=O)C(Cl)S1 CIOQSQQVHVGYHS-UHFFFAOYSA-N 0.000 claims description 4
• 241000221198 Basidiomycota Species 0.000 claims description 4
• 241001600093 Coniophora Species 0.000 claims description 4
• JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical compound CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 claims description 4
• MAUSFGZARPIQOD-UHFFFAOYSA-N S1NC=CC2=C1C=CC2=O Chemical compound S1NC=CC2=C1C=CC2=O MAUSFGZARPIQOD-UHFFFAOYSA-N 0.000 claims description 4
• DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 claims description 4
• BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims description 4
• 241000222356 Coriolus Species 0.000 claims description 3
• 241000123332 Gloeophyllum Species 0.000 claims description 3
• 241001619461 Poria <basidiomycete fungus> Species 0.000 claims description 3
• 241000222646 Stereum Species 0.000 claims description 3
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
• HKEBWESLPJXKAA-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-decylpropane-1,3-diamine Chemical compound CCCCCCCCCCN(CCCN)CCCN HKEBWESLPJXKAA-UHFFFAOYSA-N 0.000 claims description 3
• YNPKJCSIKJCODK-UHFFFAOYSA-N disodium boric acid hydrogen borate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].OB(O)O.OB(O)O.OB(O)O.OB([O-])[O-] YNPKJCSIKJCODK-UHFFFAOYSA-N 0.000 claims description 2
• RDMZIKMKSGCBKK-UHFFFAOYSA-N disodium;(9,11-dioxido-5-oxoboranyloxy-2,4,6,8,10,12,13-heptaoxa-1,3,5,7,9,11-hexaborabicyclo[5.5.1]tridecan-3-yl)oxy-oxoborane;tetrahydrate Chemical compound O.O.O.O.[Na+].[Na+].O1B(OB=O)OB(OB=O)OB2OB([O-])OB([O-])OB1O2 RDMZIKMKSGCBKK-UHFFFAOYSA-N 0.000 claims description 2
• FKLAQMPTKFHTBS-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-tetradecylpropane-1,3-diamine Chemical compound CCCCCCCCCCCCCCN(CCCN)CCCN FKLAQMPTKFHTBS-UHFFFAOYSA-N 0.000 claims description 2
• UUNNEBIXEUXCJL-UHFFFAOYSA-N ClC1C(N(SC1Cl)CCCCCCCC)=O.C(O)(O)=O Chemical compound ClC1C(N(SC1Cl)CCCCCCCC)=O.C(O)(O)=O UUNNEBIXEUXCJL-UHFFFAOYSA-N 0.000 claims 1
• 241000233866 Fungi Species 0.000 abstract description 5
• 239000000126 substance Substances 0.000 abstract description 5
• 229910052783 alkali metal Inorganic materials 0.000 abstract description 2
• XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 13
• PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 description 11
• 241001492489 Postia placenta Species 0.000 description 11
• 239000013543 active substance Substances 0.000 description 11
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 10
• 239000010949 copper Chemical class 0.000 description 8
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 7
• 241001492300 Gloeophyllum trabeum Species 0.000 description 7
• 241000222355 Trametes versicolor Species 0.000 description 7
• 229910052802 copper Chemical class 0.000 description 7
• CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 6
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
• NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
• 241001425746 Stereum sanguinolentum Species 0.000 description 6
• HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
• 239000000853 adhesive Substances 0.000 description 6
• 230000001070 adhesive effect Effects 0.000 description 6
• 229910052751 metal Inorganic materials 0.000 description 6
• 239000002184 metal Substances 0.000 description 6
• 150000002989 phenols Chemical class 0.000 description 6
• 230000002195 synergetic effect Effects 0.000 description 6
• JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 6
• 229910052725 zinc Inorganic materials 0.000 description 6
• 239000011701 zinc Chemical class 0.000 description 6
• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
• CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
• 150000003857 carboxamides Chemical class 0.000 description 5
• 239000002917 insecticide Substances 0.000 description 5
• 239000007788 liquid Substances 0.000 description 5
• 239000002245 particle Substances 0.000 description 5
• 238000002360 preparation method Methods 0.000 description 5
• 241000196324 Embryophyta Species 0.000 description 4
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
• LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
• URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 4
• 150000007513 acids Chemical class 0.000 description 4
• 239000000654 additive Substances 0.000 description 4
• UBXYXCRCOKCZIT-UHFFFAOYSA-N biphenyl-3-ol Chemical compound OC1=CC=CC(C=2C=CC=CC=2)=C1 UBXYXCRCOKCZIT-UHFFFAOYSA-N 0.000 description 4
• YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 4
• 239000000417 fungicide Substances 0.000 description 4
• 239000008187 granular material Substances 0.000 description 4
• BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
• 239000011135 tin Substances 0.000 description 4
• 229910052718 tin Inorganic materials 0.000 description 4
• RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 3
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
• NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 3
• 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
• PMUNIMVZCACZBB-UHFFFAOYSA-N 2-hydroxyethylazanium;chloride Chemical compound Cl.NCCO PMUNIMVZCACZBB-UHFFFAOYSA-N 0.000 description 3
• 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 description 3
• VCZBJOFUOSWNHV-UHFFFAOYSA-N 4-(2,4-dimethylphenoxy)phenol Chemical compound CC1=CC(C)=CC=C1OC1=CC=C(O)C=C1 VCZBJOFUOSWNHV-UHFFFAOYSA-N 0.000 description 3
• LBVXWKKDBJEXGQ-UHFFFAOYSA-N 4-(2-tert-butyl-4-methylphenoxy)phenol Chemical compound CC(C)(C)C1=CC(C)=CC=C1OC1=CC=C(O)C=C1 LBVXWKKDBJEXGQ-UHFFFAOYSA-N 0.000 description 3
• UPZADSOVFPZTBF-UHFFFAOYSA-N 4-(4-methyl-2-propan-2-ylphenoxy)phenol Chemical compound CC(C)C1=CC(C)=CC=C1OC1=CC=C(O)C=C1 UPZADSOVFPZTBF-UHFFFAOYSA-N 0.000 description 3
• OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 3
• 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 3
• 150000005168 4-hydroxybenzoic acids Chemical class 0.000 description 3
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
• MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 3
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
• ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
• WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 3
• XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 3
• 239000004480 active ingredient Substances 0.000 description 3
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
• 235000019270 ammonium chloride Nutrition 0.000 description 3
• 230000000844 anti-bacterial effect Effects 0.000 description 3
• 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 3
• 239000003899 bactericide agent Substances 0.000 description 3
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
• 229960003887 dichlorophen Drugs 0.000 description 3
• BYNQFCJOHGOKSS-UHFFFAOYSA-N diclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1 BYNQFCJOHGOKSS-UHFFFAOYSA-N 0.000 description 3
• 239000003085 diluting agent Substances 0.000 description 3
• 239000003995 emulsifying agent Substances 0.000 description 3
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
• NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
• 239000000945 filler Substances 0.000 description 3
• 235000013312 flour Nutrition 0.000 description 3
• 230000012010 growth Effects 0.000 description 3
• ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 3
• 229960004068 hexachlorophene Drugs 0.000 description 3
• 230000002401 inhibitory effect Effects 0.000 description 3
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
• IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 3
• 238000002156 mixing Methods 0.000 description 3
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
• 150000003856 quaternary ammonium compounds Chemical class 0.000 description 3
• 150000003254 radicals Chemical class 0.000 description 3
• 239000002904 solvent Substances 0.000 description 3
• 229960003500 triclosan Drugs 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
• OUCSIUCEQVCDEL-UHFFFAOYSA-N 2,3,4-tribromophenol Chemical compound OC1=CC=C(Br)C(Br)=C1Br OUCSIUCEQVCDEL-UHFFFAOYSA-N 0.000 description 2
• YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 2
• 239000002794 2,4-DB Substances 0.000 description 2
• LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
• 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
• OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
• BQMRHYBXRAYYQS-UHFFFAOYSA-N 4-dihydroxyphosphinothioyloxy-n,n-diethyl-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(O)(O)=S)=N1 BQMRHYBXRAYYQS-UHFFFAOYSA-N 0.000 description 2
• 239000005660 Abamectin Substances 0.000 description 2
• HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
• NYQDCVLCJXRDSK-UHFFFAOYSA-N Bromofos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl NYQDCVLCJXRDSK-UHFFFAOYSA-N 0.000 description 2
• LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 2
• JMHWNJGXUIJPKG-UHFFFAOYSA-N CC(=O)O[SiH](CC=C)OC(C)=O Chemical compound CC(=O)O[SiH](CC=C)OC(C)=O JMHWNJGXUIJPKG-UHFFFAOYSA-N 0.000 description 2
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