ES2199584T3 - Procedimiento para el tratamiento de madera contra el ataque por hongos dañinos para la madera. - Google Patents
Procedimiento para el tratamiento de madera contra el ataque por hongos dañinos para la madera.Info
- Publication number
- ES2199584T3 ES2199584T3 ES99934692T ES99934692T ES2199584T3 ES 2199584 T3 ES2199584 T3 ES 2199584T3 ES 99934692 T ES99934692 T ES 99934692T ES 99934692 T ES99934692 T ES 99934692T ES 2199584 T3 ES2199584 T3 ES 2199584T3
- Authority
- ES
- Spain
- Prior art keywords
- iii
- triazol
- carbon atoms
- ylmethyl
- chlorophenyl
- 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 - Lifetime
Links
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- 241000233866 Fungi Species 0.000 title description 9
- 238000000034 method Methods 0.000 title description 8
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- 150000001875 compounds Chemical class 0.000 claims abstract description 19
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 15
- 239000002245 particle Substances 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims abstract description 5
- 150000001556 benzimidazoles Chemical class 0.000 claims abstract description 4
- 239000002243 precursor Substances 0.000 claims abstract description 3
- 239000000725 suspension Substances 0.000 claims description 45
- -1 1H-1,2,4-triazol-1-ylmethyl Chemical group 0.000 claims description 28
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 13
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 5
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 claims description 5
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 5
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 229940052296 esters of benzoic acid for local anesthesia Drugs 0.000 claims description 4
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 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
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000003851 azoles Chemical class 0.000 claims description 2
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-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 class [H]* 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 abstract description 20
- 239000005778 Fenpropimorph Substances 0.000 abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 14
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000417 fungicide Substances 0.000 abstract description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract description 3
- 230000002538 fungal effect Effects 0.000 abstract description 3
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 abstract description 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 abstract description 2
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005777 Fenpropidin Substances 0.000 abstract description 2
- 239000005837 Spiroxamine Substances 0.000 abstract description 2
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract description 2
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000004548 suspo-emulsion Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 59
- 239000000047 product Substances 0.000 description 37
- 238000009472 formulation Methods 0.000 description 31
- 239000012071 phase Substances 0.000 description 17
- 239000002253 acid Substances 0.000 description 16
- 239000003795 chemical substances by application Substances 0.000 description 15
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 238000012360 testing method Methods 0.000 description 11
- 239000006013 carbendazim Substances 0.000 description 10
- 239000006071 cream Substances 0.000 description 9
- 239000005822 Propiconazole Substances 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 239000002904 solvent Substances 0.000 description 7
- 150000003852 triazoles Chemical class 0.000 description 7
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000012752 auxiliary agent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229920001983 poloxamer Polymers 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 description 4
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 4
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 4
- 239000005767 Epoxiconazole Substances 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-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
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 239000005839 Tebuconazole Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229920001285 xanthan gum Polymers 0.000 description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 3
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- 239000005813 Penconazole Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 2
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- 239000012265 solid product Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- HXJNZPXGMGELDP-UHFFFAOYSA-J tin(4+);tetrabenzoate Chemical compound [Sn+4].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 HXJNZPXGMGELDP-UHFFFAOYSA-J 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- DYWSVUBJGFTOQC-UHFFFAOYSA-N xi-2-Ethylheptanoic acid Chemical compound CCCCCC(CC)C(O)=O DYWSVUBJGFTOQC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/249925—Fiber-containing wood product [e.g., hardboard, lumber, or wood board, etc.]
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19834028A DE19834028A1 (de) | 1998-07-28 | 1998-07-28 | Verfahren zur Behandlung von Holz gegen den Befall durch holzschädigende Pilze |
| DE19834028 | 1998-07-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2199584T3 true ES2199584T3 (es) | 2004-02-16 |
Family
ID=7875627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99934692T Expired - Lifetime ES2199584T3 (es) | 1998-07-28 | 1999-07-14 | Procedimiento para el tratamiento de madera contra el ataque por hongos dañinos para la madera. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6558685B1 (enExample) |
| EP (1) | EP1102534B1 (enExample) |
| JP (1) | JP2002521400A (enExample) |
| AT (1) | ATE238659T1 (enExample) |
| AU (1) | AU5037699A (enExample) |
| CA (1) | CA2338569C (enExample) |
| DE (2) | DE19834028A1 (enExample) |
| ES (1) | ES2199584T3 (enExample) |
| NZ (1) | NZ509361A (enExample) |
| PL (1) | PL200239B1 (enExample) |
| PT (1) | PT1102534E (enExample) |
| WO (1) | WO2000005955A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9808755D0 (en) * | 1998-04-25 | 1998-06-24 | Agrevo Uk Ltd | Fungicidal use |
| WO2001044215A2 (de) * | 1999-12-13 | 2001-06-21 | Bayer Aktiengesellschaft | Fungizide wirkstoffkombinationen |
| US7294189B2 (en) * | 2002-10-09 | 2007-11-13 | Hexion Specialty Chemicals, Inc. | Wax emulsion preservative compositions and method of manufacture |
| US20060257578A1 (en) * | 2003-04-09 | 2006-11-16 | Jun Zhang | Micronized wood preservative formulations comprising boron compounds |
| US20050249812A1 (en) * | 2004-04-27 | 2005-11-10 | Leach Robert M | Micronized organic preservative formulations |
| US8637089B2 (en) * | 2003-04-09 | 2014-01-28 | Osmose, Inc. | Micronized wood preservative formulations |
| EP2345329B1 (en) | 2003-04-09 | 2019-09-18 | Koppers Performance Chemicals Inc. | Micronized wood preservative formulations |
| US8747908B2 (en) * | 2003-04-09 | 2014-06-10 | Osmose, Inc. | Micronized wood preservative formulations |
| MXPA05013850A (es) * | 2003-06-17 | 2006-05-17 | Phibro Tech Inc | Conservador particulado para madera y metodo para producir el mismo. |
| US20060147632A1 (en) * | 2004-04-27 | 2006-07-06 | Jun Zhang | Composition and process for coloring and preserving wood |
| WO2005114078A2 (en) | 2004-05-13 | 2005-12-01 | Osmose, Inc. | Compositions and methods for treating cellulose-based materials with micronized additives |
| US20050252408A1 (en) | 2004-05-17 | 2005-11-17 | Richardson H W | Particulate wood preservative and method for producing same |
| WO2006031743A2 (en) * | 2004-09-10 | 2006-03-23 | Chemical Specialties, Inc. | Emulsion composition for wood protection |
| CA2576761C (en) * | 2004-09-15 | 2011-07-05 | Lg Chem, Ltd. | Films or structural exterior materials using coating composition having self-cleaning property and preparation method thereof |
| JP2008514599A (ja) * | 2004-09-27 | 2008-05-08 | ヘキソン スペシャルティ ケミカルズ インコーポレーテッド | ワックス乳剤防腐剤組成物および製造方法 |
| NZ554680A (en) | 2004-10-14 | 2010-10-29 | Osmose Inc | Micronized wood preservative formulations in organic carriers |
| AU2006262258A1 (en) * | 2005-06-21 | 2007-01-04 | Osmose, Inc. | Improved micronized wood preservative compositions |
| JP5085041B2 (ja) * | 2006-01-19 | 2012-11-28 | 日本曹達株式会社 | 防腐・防カビ性薬剤組成物および防腐・防カビ性乾燥木材の製造方法 |
| US7632567B1 (en) | 2006-08-31 | 2009-12-15 | Osmose, Inc. | Micronized wood preservative formulations comprising copper and zinc |
| FR2939068A1 (fr) * | 2008-12-01 | 2010-06-04 | Intace Internat Sarl | Procede pour lutter contre le bleuissement du bois |
| GB201010439D0 (en) | 2010-06-21 | 2010-08-04 | Arch Timber Protection Ltd | A method |
| CN102067861A (zh) * | 2011-01-20 | 2011-05-25 | 陕西美邦农药有限公司 | 一种含有腈苯唑的杀菌组合物 |
| US8968466B2 (en) | 2011-08-22 | 2015-03-03 | Momentive Specialty Chemicals Inc. | Sizing and rheology agents for gypsum stucco systems for water resistant panel production |
| US8932401B2 (en) | 2011-08-22 | 2015-01-13 | Momentive Specialty Chemicals Inc. | Sizing and rheology agents for gypsum stucco systems for water resistant panel production |
| GB201119139D0 (en) | 2011-11-04 | 2011-12-21 | Arch Timber Protection Ltd | Additives for use in wood preservation |
| MX2016014195A (es) | 2014-05-02 | 2017-02-13 | Arch Wood Protection Inc | Composicion conservante de la madera. |
| CA2852530A1 (en) | 2014-05-21 | 2015-11-21 | The Sansin Corporation | Antimicrobial composition for protecting wood |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4079062A (en) | 1974-11-18 | 1978-03-14 | Janssen Pharmaceutica N.V. | Triazole derivatives |
| DE2656747C2 (de) | 1976-12-15 | 1984-07-05 | Basf Ag, 6700 Ludwigshafen | Morpholinderivate |
| AU542623B2 (en) | 1980-05-16 | 1985-02-28 | Bayer Aktiengesellschaft | 1-hydroxyethyl-azole derivatives |
| ATE81852T1 (de) | 1980-08-18 | 1992-11-15 | Ici Plc | Triazol-verbindungen, verfahren zu ihrer herstellung und ihre verwendung als fungizide und pflanzenwachstumsregulatoren. |
| DE3175673D1 (en) | 1980-11-19 | 1987-01-15 | Ici Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| EP0072156B1 (en) | 1981-07-31 | 1984-11-28 | Fbc Limited | Fungicidal composition containing prochloraz |
| DE3631558A1 (de) | 1986-09-17 | 1988-03-31 | Hoechst Ag | Neue suspoemulsionen von pflanzenschutz-wirkstoffen |
| HU198825B (en) | 1987-03-09 | 1989-12-28 | Chinoin Gyogyszer Es Vegyeszet | Synergic fungicides |
| GB8710105D0 (en) * | 1987-04-29 | 1987-06-03 | Ici Plc | Pesticidal formulations |
| FR2626740B1 (fr) | 1988-02-08 | 1990-10-19 | Xylochimie | Concentres emulsionnables de matieres biocides, les microemulsions aqueuses obtenues et l'application de ces microemulsions au traitement du bois |
| FR2644672B1 (fr) | 1989-03-21 | 1991-05-31 | Saint Gobain Isover | Substrat pour la culture hors sol |
| GB8908794D0 (en) | 1989-04-19 | 1989-06-07 | Janssen Pharmaceutica Nv | Synergistic compositions containing propiconazole and tebuconazole |
| DE3935113A1 (de) | 1989-10-21 | 1991-04-25 | Basf Ag | Fungizide mischung |
| GB9202378D0 (en) | 1992-02-05 | 1992-03-18 | Sandoz Ltd | Inventions relating to fungicidal compositions |
| DE4322211A1 (de) | 1993-07-03 | 1995-01-12 | Basf Ag | Wäßrige, mehrphasige, stabile Fertigformulierung für Pflanzenschutz-Wirkstoffe und Verfahren zu ihrer Herstellung |
| GB9319129D0 (en) * | 1993-09-15 | 1993-11-03 | Dowelanco Ltd | Storage and dilution of stable aqueous dispersions |
| DE4343176A1 (de) | 1993-12-17 | 1995-06-22 | Basf Ag | Fungizide Mischung |
| JPH08126223A (ja) | 1994-10-26 | 1996-05-17 | Mitsubishi Electric Corp | 交流発電機の制御装置 |
| EP0898506A1 (de) | 1996-04-19 | 1999-03-03 | Dr. Wolman GmbH | Verfahren zur behandlung von holz gegen den befall durch holzschädigende pilze |
-
1998
- 1998-07-28 DE DE19834028A patent/DE19834028A1/de not_active Withdrawn
-
1999
- 1999-07-14 AT AT99934692T patent/ATE238659T1/de active
- 1999-07-14 CA CA002338569A patent/CA2338569C/en not_active Expired - Fee Related
- 1999-07-14 US US09/743,928 patent/US6558685B1/en not_active Expired - Fee Related
- 1999-07-14 PL PL345800A patent/PL200239B1/pl unknown
- 1999-07-14 AU AU50376/99A patent/AU5037699A/en not_active Abandoned
- 1999-07-14 NZ NZ509361A patent/NZ509361A/en not_active IP Right Cessation
- 1999-07-14 PT PT99934692T patent/PT1102534E/pt unknown
- 1999-07-14 DE DE59905340T patent/DE59905340D1/de not_active Expired - Lifetime
- 1999-07-14 WO PCT/EP1999/004968 patent/WO2000005955A1/de not_active Ceased
- 1999-07-14 ES ES99934692T patent/ES2199584T3/es not_active Expired - Lifetime
- 1999-07-14 EP EP99934692A patent/EP1102534B1/de not_active Expired - Lifetime
- 1999-07-14 JP JP2000561822A patent/JP2002521400A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| PL345800A1 (en) | 2002-01-02 |
| EP1102534B1 (de) | 2003-05-02 |
| NZ509361A (en) | 2003-08-29 |
| CA2338569A1 (en) | 2000-02-10 |
| EP1102534A1 (de) | 2001-05-30 |
| PT1102534E (pt) | 2003-09-30 |
| AU5037699A (en) | 2000-02-21 |
| ATE238659T1 (de) | 2003-05-15 |
| PL200239B1 (pl) | 2008-12-31 |
| DE59905340D1 (de) | 2003-06-05 |
| DE19834028A1 (de) | 2000-02-03 |
| JP2002521400A (ja) | 2002-07-16 |
| US6558685B1 (en) | 2003-05-06 |
| WO2000005955A1 (de) | 2000-02-10 |
| CA2338569C (en) | 2009-05-12 |
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