DE2020090C3 - Verwendung eines mikrobiziden Mittels im Materialschutz - Google Patents
Verwendung eines mikrobiziden Mittels im MaterialschutzInfo
- Publication number
- DE2020090C3 DE2020090C3 DE2020090A DE2020090A DE2020090C3 DE 2020090 C3 DE2020090 C3 DE 2020090C3 DE 2020090 A DE2020090 A DE 2020090A DE 2020090 A DE2020090 A DE 2020090A DE 2020090 C3 DE2020090 C3 DE 2020090C3
- Authority
- DE
- Germany
- Prior art keywords
- wood
- mixture
- active ingredient
- agar
- under
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000463 material Substances 0.000 title claims description 19
- 239000002855 microbicide agent Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims description 45
- 239000002023 wood Substances 0.000 claims description 30
- 244000005700 microbiome Species 0.000 claims description 9
- PJCQXOISTHKDDB-UHFFFAOYSA-N 2,4,5,6-tetrachloro-1h-benzimidazole Chemical compound ClC1=C(Cl)C=C2NC(Cl)=NC2=C1Cl PJCQXOISTHKDDB-UHFFFAOYSA-N 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 description 36
- 239000000243 solution Substances 0.000 description 19
- 241000233866 Fungi Species 0.000 description 13
- 229920001817 Agar Polymers 0.000 description 11
- 239000008272 agar Substances 0.000 description 10
- 235000010419 agar Nutrition 0.000 description 10
- 239000000839 emulsion Substances 0.000 description 8
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- SUQYOUJCBGMSLV-UHFFFAOYSA-N 2,5,6-trichloro-1h-benzimidazole Chemical compound ClC1=C(Cl)C=C2NC(Cl)=NC2=C1 SUQYOUJCBGMSLV-UHFFFAOYSA-N 0.000 description 7
- 241001070947 Fagus Species 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 6
- 235000010099 Fagus sylvatica Nutrition 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000006916 nutrient agar Substances 0.000 description 6
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 5
- 241000018646 Pinus brutia Species 0.000 description 5
- 235000011613 Pinus brutia Nutrition 0.000 description 5
- 239000013543 active substance Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 241000228143 Penicillium Species 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 230000003641 microbiacidal effect Effects 0.000 description 4
- -1 polyoxyethylene Polymers 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 3
- QNJDECGISPPSPD-UHFFFAOYSA-N 2,4,5,6,7-pentachloro-1h-benzimidazole Chemical compound ClC1=C(Cl)C(Cl)=C2NC(Cl)=NC2=C1Cl QNJDECGISPPSPD-UHFFFAOYSA-N 0.000 description 3
- 241000228212 Aspergillus Species 0.000 description 3
- 241000228245 Aspergillus niger Species 0.000 description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 241001626940 Coniophora cerebella Species 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 241001619461 Poria <basidiomycete fungus> Species 0.000 description 3
- 241000588767 Proteus vulgaris Species 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 244000052616 bacterial pathogen Species 0.000 description 3
- 150000001556 benzimidazoles Chemical group 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 230000000855 fungicidal effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 244000052769 pathogen Species 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229940007042 proteus vulgaris Drugs 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000001632 sodium acetate Substances 0.000 description 3
- 235000017281 sodium acetate Nutrition 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 241001112577 Acrostalagmus Species 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- 241000223602 Alternaria alternata Species 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 241000094558 Antrodia sinuosa Species 0.000 description 2
- 241000228193 Aspergillus clavatus Species 0.000 description 2
- 241000223678 Aureobasidium pullulans Species 0.000 description 2
- 241000194103 Bacillus pumilus Species 0.000 description 2
- 244000063299 Bacillus subtilis Species 0.000 description 2
- 235000014469 Bacillus subtilis Nutrition 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 241001503016 Ctenomyces Species 0.000 description 2
- 241000235646 Cyberlindnera jadinii Species 0.000 description 2
- 241000194032 Enterococcus faecalis Species 0.000 description 2
- 241000223221 Fusarium oxysporum Species 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- 241000222634 Lenzites Species 0.000 description 2
- 241000191938 Micrococcus luteus Species 0.000 description 2
- 241001363490 Monilia Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 241000588770 Proteus mirabilis Species 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 239000006004 Quartz sand Substances 0.000 description 2
- 241000607683 Salmonella enterica subsp. enterica serovar Pullorum Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241001279364 Stachybotrys chartarum Species 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- 240000007313 Tilia cordata Species 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- 241000223261 Trichoderma viride Species 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 235000011475 lollipops Nutrition 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XOMKZKJEJBZBJJ-UHFFFAOYSA-N 1,2-dichloro-3-phenylbenzene Chemical group ClC1=CC=CC(C=2C=CC=CC=2)=C1Cl XOMKZKJEJBZBJJ-UHFFFAOYSA-N 0.000 description 1
- LLIARSREYVCQHL-UHFFFAOYSA-N 2,6-dichloro-1h-benzimidazole Chemical compound C1=C(Cl)C=C2NC(Cl)=NC2=C1 LLIARSREYVCQHL-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- 241000228197 Aspergillus flavus Species 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- 241000186146 Brevibacterium Species 0.000 description 1
- RZZPDXZPRHQOCG-OJAKKHQRSA-O CDP-choline(1+) Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OCC[N+](C)(C)C)O[C@H]1N1C(=O)N=C(N)C=C1 RZZPDXZPRHQOCG-OJAKKHQRSA-O 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241001515917 Chaetomium globosum Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241001600093 Coniophora Species 0.000 description 1
- 241000186216 Corynebacterium Species 0.000 description 1
- 241000123284 Daedalea Species 0.000 description 1
- 241001480035 Epidermophyton Species 0.000 description 1
- 241000588722 Escherichia Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000735439 Heterobasidion annosum Species 0.000 description 1
- 241001174458 Kendrickiella phycomyces Species 0.000 description 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 1
- 241000222418 Lentinus Species 0.000 description 1
- 244000162269 Lentinus lepideus Species 0.000 description 1
- 235000017066 Lentinus lepideus Nutrition 0.000 description 1
- 241000186359 Mycobacterium Species 0.000 description 1
- 241000893976 Nannizzia gypsea Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001236817 Paecilomyces <Clavicipitaceae> Species 0.000 description 1
- 241001123663 Penicillium expansum Species 0.000 description 1
- 241000122123 Penicillium italicum Species 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 235000005205 Pinus Nutrition 0.000 description 1
- 241000218602 Pinus <genus> Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241001581437 Polystictus Species 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000588769 Proteus <enterobacteria> Species 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 241000589540 Pseudomonas fluorescens Species 0.000 description 1
- 241000235546 Rhizopus stolonifer Species 0.000 description 1
- 241000192023 Sarcina Species 0.000 description 1
- 241000825258 Scopulariopsis brevicaulis Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 241000186652 Sporosarcina ureae Species 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000514831 Stemphylium botryosum Species 0.000 description 1
- 241000907897 Tilia Species 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- WERKSKAQRVDLDW-ANOHMWSOSA-N [(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO WERKSKAQRVDLDW-ANOHMWSOSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229940074323 antara Drugs 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- YMTINGFKWWXKFG-UHFFFAOYSA-N fenofibrate Chemical compound C1=CC(OC(C)(C)C(=O)OC(C)C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMTINGFKWWXKFG-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- VAOCPAMSLUNLGC-UHFFFAOYSA-N metronidazole Chemical compound CC1=NC=C([N+]([O-])=O)N1CCO VAOCPAMSLUNLGC-UHFFFAOYSA-N 0.000 description 1
- 229960000282 metronidazole Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- BFPJYWDBBLZXOM-UHFFFAOYSA-L potassium tellurite Chemical compound [K+].[K+].[O-][Te]([O-])=O BFPJYWDBBLZXOM-UHFFFAOYSA-L 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
- B27K3/40—Aromatic compounds halogenated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Paints Or Removers (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH631869 | 1969-04-25 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2020090A1 DE2020090A1 (de) | 1970-11-05 |
| DE2020090B2 DE2020090B2 (de) | 1979-01-11 |
| DE2020090C3 true DE2020090C3 (de) | 1979-09-13 |
Family
ID=4307650
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2020090A Expired DE2020090C3 (de) | 1969-04-25 | 1970-04-24 | Verwendung eines mikrobiziden Mittels im Materialschutz |
Country Status (16)
| Country | Link |
|---|---|
| JP (1) | JPS4814927B1 (enExample) |
| AT (1) | AT308287B (enExample) |
| BE (1) | BE749512A (enExample) |
| CA (1) | CA945895A (enExample) |
| CH (1) | CH494533A (enExample) |
| CS (1) | CS152356B2 (enExample) |
| DE (1) | DE2020090C3 (enExample) |
| DK (1) | DK127625B (enExample) |
| ES (1) | ES379017A1 (enExample) |
| FR (1) | FR2040228B1 (enExample) |
| GB (1) | GB1306098A (enExample) |
| IL (1) | IL34378A (enExample) |
| NL (1) | NL149379B (enExample) |
| PL (1) | PL80654B1 (enExample) |
| RO (1) | RO61088A (enExample) |
| SE (1) | SE367943B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5030423A (enExample) * | 1973-07-17 | 1975-03-26 | ||
| JPS5031736A (enExample) * | 1973-07-20 | 1975-03-28 | ||
| JPS5061926A (enExample) * | 1973-09-29 | 1975-05-27 | ||
| JPS5525959A (en) * | 1978-08-15 | 1980-02-25 | Matsushita Electronics Corp | Reinforced color picture tube |
| JPS5528242A (en) * | 1978-08-17 | 1980-02-28 | Matsushita Electronics Corp | Reinforced color picture tube |
| US5248672A (en) * | 1990-11-01 | 1993-09-28 | The Regents Of The University Of Michigan | Polysubstituted benzimidazole nucleosides as antiviral agents |
| JPH11514969A (ja) | 1995-08-10 | 1999-12-21 | バイエル・アクチエンゲゼルシヤフト | ハロベンゾイミダゾール類および殺微生物剤としてのそれらの使用 |
| EP1141453A1 (en) * | 1998-10-29 | 2001-10-10 | Ciba SC Holding AG | Incorporation of organic anti-microbials into fibres during a fibre spinning process |
| JP5103871B2 (ja) * | 2006-01-27 | 2012-12-19 | マックス株式会社 | ガスカートリッジ |
-
1969
- 1969-04-25 CH CH979570A patent/CH494533A/de not_active IP Right Cessation
-
1970
- 1970-04-20 SE SE05374/70A patent/SE367943B/xx unknown
- 1970-04-20 DK DK197870AA patent/DK127625B/da unknown
- 1970-04-21 RO RO63149A patent/RO61088A/ro unknown
- 1970-04-24 ES ES379017A patent/ES379017A1/es not_active Expired
- 1970-04-24 IL IL34378A patent/IL34378A/en unknown
- 1970-04-24 CA CA081,017A patent/CA945895A/en not_active Expired
- 1970-04-24 BE BE749512D patent/BE749512A/xx unknown
- 1970-04-24 DE DE2020090A patent/DE2020090C3/de not_active Expired
- 1970-04-24 NL NL707006028A patent/NL149379B/xx not_active IP Right Cessation
- 1970-04-24 GB GB1940770A patent/GB1306098A/en not_active Expired
- 1970-04-24 FR FR707015046A patent/FR2040228B1/fr not_active Expired
- 1970-04-24 PL PL1970140246A patent/PL80654B1/pl unknown
- 1970-04-24 JP JP45035081A patent/JPS4814927B1/ja active Pending
- 1970-04-24 AT AT376270A patent/AT308287B/de active
- 1970-04-24 CS CS2880A patent/CS152356B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2040228A1 (enExample) | 1971-01-22 |
| DE2020090A1 (de) | 1970-11-05 |
| DK127625B (da) | 1973-12-10 |
| FR2040228B1 (enExample) | 1973-08-10 |
| BE749512A (fr) | 1970-10-26 |
| IL34378A (en) | 1973-06-29 |
| ES379017A1 (es) | 1972-08-01 |
| AT308287B (de) | 1973-06-25 |
| DE2020090B2 (de) | 1979-01-11 |
| SE367943B (enExample) | 1974-06-17 |
| NL149379B (nl) | 1976-05-17 |
| RO61088A (enExample) | 1976-11-15 |
| PL80654B1 (enExample) | 1975-08-30 |
| CA945895A (en) | 1974-04-23 |
| GB1306098A (enExample) | 1973-02-07 |
| IL34378A0 (en) | 1970-06-17 |
| NL7006028A (enExample) | 1970-10-27 |
| CS152356B2 (enExample) | 1973-12-19 |
| CH494533A (de) | 1970-08-15 |
| JPS4814927B1 (enExample) | 1973-05-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1147007B (de) | Fungizide Mittel | |
| DE2931838A1 (de) | Verfahren zum schuetzen von organischen oder anorganischen materialien vor dem befall durch mikroorganismen | |
| DE2020090B2 (de) | Verwendung eines mikrobiziden Mittels im Materialschutz | |
| DE1568744A1 (de) | Verfahren zur Herstellung von Propinylaethern | |
| CA2852530A1 (en) | Antimicrobial composition for protecting wood | |
| EP0254857B1 (de) | Verwendung von 1-Aryl-3-hydroxy-3-alkyl-4-(1,2,4-triazol-1-yl)-butan-derivaten als Mikrobizide für den Materialschutz | |
| JPS5826805A (ja) | 殺菌作用及び駆かび作用を有する水で希釈し得る薬品及び木材の保護法 | |
| DE2242187A1 (de) | Heterocyclische verbindungen | |
| EP0135112A1 (de) | Wässriges Holzschutzmittel | |
| DE4230956A1 (de) | Verwendung von Thiadiazolen als Biozide für den Materialschutz | |
| DE2633452A1 (de) | Triorganozinnverbindungen von hydroxydiazeniumoxiden | |
| SU346834A1 (enExample) | ||
| US4514225A (en) | Triorganotin acetylsalicylates and biocides containing the same | |
| DE3824807A1 (de) | Diorganozinnverbindungen und diese enthaltende mittel mit bakterizider und fungizider wirkung | |
| DE1953435A1 (de) | Fungicide und bakterizide Mittel | |
| DE2600800C2 (de) | Verfahren zur Bekämpfung von Pilzen im Haushaltssektor | |
| DE2438853A1 (de) | Mittel zur bekaempfung von schaedlichen mikroorganismen | |
| EP0016857B1 (de) | Mikrobizides Mittel und seine Verwendung | |
| US3536815A (en) | 1,2-dinitro-tetrachlorobenzene as a microbicidal wood preservative | |
| DE3428163A1 (de) | N,n-diethyl-n'-aryl-n'-(dichlorfluormethylthio)-sulfamide, ein verfahren zu ihrer herstellung und ihre verwendung | |
| CH524312A (de) | Verwendung von Organozinnazoliden zur Bekämpfung von Fungi und Mikroben | |
| NO130713B (enExample) | ||
| EP0291800B1 (de) | Neue Cyanhydrin-Iodpropargylether, Verfahren zu ihrer Herstellung und ihre Verwendung als Mikrobizide | |
| DE2625391A1 (de) | Mikrobizides mittel | |
| AT215085B (de) | Verfahren zur Herstellung einer keimtötenden Mischung |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |