AP359A - Aqueous fungicidal formulations based on prochloraz containing a crystallisation inhibitor. - Google Patents
Aqueous fungicidal formulations based on prochloraz containing a crystallisation inhibitor. Download PDFInfo
- Publication number
- AP359A AP359A APAP/P/1992/000366A AP9200366A AP359A AP 359 A AP359 A AP 359A AP 9200366 A AP9200366 A AP 9200366A AP 359 A AP359 A AP 359A
- Authority
- AP
- ARIPO
- Prior art keywords
- weight
- prochloraz
- formulation according
- surfactant
- formulation
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 69
- 238000009472 formulation Methods 0.000 title claims description 51
- 239000005820 Prochloraz Substances 0.000 title claims description 21
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 title claims description 21
- 238000002425 crystallisation Methods 0.000 title claims description 13
- 230000000855 fungicidal effect Effects 0.000 title description 5
- 239000003112 inhibitor Substances 0.000 title description 3
- 239000012669 liquid formulation Substances 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000004094 surface-active agent Substances 0.000 claims description 18
- 239000000839 emulsion Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 150000002989 phenols Chemical class 0.000 claims description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- -1 α-methylbenzyl Chemical group 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- 150000002191 fatty alcohols Chemical class 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 5
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims description 4
- 229920001400 block copolymer Polymers 0.000 claims description 4
- 239000010773 plant oil Substances 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 150000002431 hydrogen Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 150000003626 triacylglycerols Chemical class 0.000 claims description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical class O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000002904 solvent Substances 0.000 description 12
- 239000013078 crystal Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- NGFPWHGISWUQOI-UHFFFAOYSA-N 2-sec-butylphenol Chemical compound CCC(C)C1=CC=CC=C1O NGFPWHGISWUQOI-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000000417 fungicide Substances 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N isopropylmethylphenol Natural products CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 229920000847 nonoxynol Polymers 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 230000002528 anti-freeze Effects 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical group OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000004530 micro-emulsion Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 239000008096 xylene Substances 0.000 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 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical class CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- 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 description 1
- QUBBAXISAHIDNM-UHFFFAOYSA-N 1-ethyl-2,3-dimethylbenzene Chemical class CCC1=CC=CC(C)=C1C QUBBAXISAHIDNM-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical class CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical class CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000015655 Crocus sativus Nutrition 0.000 description 1
- 244000124209 Crocus sativus Species 0.000 description 1
- 239000005757 Cyproconazole Substances 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005777 Fenpropidin Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 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 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical class O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006013 carbendazim Substances 0.000 description 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000005195 diethylbenzenes Chemical class 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- BEZDDPMMPIDMGJ-UHFFFAOYSA-N pentamethylbenzene Chemical class CC1=CC(C)=C(C)C(C)=C1C BEZDDPMMPIDMGJ-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000004248 saffron Substances 0.000 description 1
- 235000013974 saffron Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005201 tetramethylbenzenes Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000005199 trimethylbenzenes Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4108871A DE4108871A1 (de) | 1991-03-19 | 1991-03-19 | Waessrige formulierung von prochloraz, ihre herstellung und ihre verwendung |
| IL10141692A IL101416A (en) | 1991-03-19 | 1992-03-30 | Fungicides containing problorase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP9200366A0 AP9200366A0 (en) | 1992-04-30 |
| AP359A true AP359A (en) | 1994-09-07 |
Family
ID=25902020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1992/000366A AP359A (en) | 1991-03-19 | 1992-03-18 | Aqueous fungicidal formulations based on prochloraz containing a crystallisation inhibitor. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US5389665A (cg-RX-API-DMAC7.html) |
| EP (2) | EP0505053A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP3049368B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR100210630B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1054024C (cg-RX-API-DMAC7.html) |
| AP (1) | AP359A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE143567T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU659137B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR9205749A (cg-RX-API-DMAC7.html) |
| DE (2) | DE4108871A1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK0576484T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2092676T3 (cg-RX-API-DMAC7.html) |
| IE (1) | IE920849A1 (cg-RX-API-DMAC7.html) |
| IL (1) | IL101416A (cg-RX-API-DMAC7.html) |
| MA (1) | MA22470A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MX9201182A (cg-RX-API-DMAC7.html) |
| NZ (1) | NZ242036A (cg-RX-API-DMAC7.html) |
| TR (1) | TR25992A (cg-RX-API-DMAC7.html) |
| WO (1) | WO1992016105A1 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA921980B (cg-RX-API-DMAC7.html) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9203429D0 (en) * | 1992-02-18 | 1992-04-01 | Schering Agrochemicals Ltd | Pesticidal compositions |
| EP0592880B1 (de) * | 1992-10-13 | 1997-04-09 | Hoechst Schering AgrEvo GmbH | Wässriges Dispersionskonzentrat, enthaltend Linuron als Wirkstoff |
| JP3331679B2 (ja) | 1993-07-02 | 2002-10-07 | 住友化学工業株式会社 | 農薬組成物 |
| US6319949B1 (en) | 1996-07-11 | 2001-11-20 | Syngenta Limited | Pesticidal sprays |
| CN1092485C (zh) * | 1996-09-20 | 2002-10-16 | 英国阿格里沃有限公司 | 农用杀菌剂组合物 |
| CN1332605C (zh) * | 2005-12-27 | 2007-08-22 | 云南农业大学 | 含有咪鲜胺的高脂膜植物杀菌剂 |
| TW200915984A (en) | 2007-08-08 | 2009-04-16 | Basf Se | Aqueous microemulsions containing organic insecticide compounds |
| EA017661B1 (ru) * | 2008-04-08 | 2013-02-28 | Басф Се | Эмульгируемый концентрат |
| TW201018400A (en) * | 2008-10-10 | 2010-05-16 | Basf Se | Liquid aqueous plant protection formulations |
| UA106213C2 (ru) | 2008-10-10 | 2014-08-11 | Басф Се | Жидкие препараты для защиты растений, содержащие пираклостробин |
| DE102009004368A1 (de) | 2009-01-08 | 2010-07-15 | Heraeus Kulzer Gmbh | Dentalmaterialien enthaltend antimikrobielle Wirkstoffe zur Verhinderung von Plaque-Anlagerungen |
| EP3348143B1 (en) | 2017-01-17 | 2020-04-08 | Evergreen Animal Health LLC | Novel spot-on active substance formulation |
| CN108552168A (zh) * | 2018-06-02 | 2018-09-21 | 允发化工（上海）有限公司 | 一种高稳定性吡虫啉液剂 |
| BR112021009434A2 (pt) * | 2018-12-18 | 2021-08-17 | Indorama Ventures Oxides Llc | alcoxilato benzidrilado, método para preparação do alcoxilato benzidrilado, composição, produto embalado, composição de concentrado, formulação química de desempenho, formulação para cuidados pessoais, concentrado emulsificável agroquímico, concentrado de suspensão agroquímica, concentrado líquido solúvel em agroquímico, e, pó molhável agroquímico |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2059773A (en) * | 1979-10-12 | 1981-04-29 | Boots Co Ltd | Fungicidal compositions |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1469772A (en) * | 1973-06-21 | 1977-04-06 | Boots Co Ltd | Fungicidal imidazole derivatives |
| US4044118A (en) * | 1974-05-16 | 1977-08-23 | Texaco Inc. | Solubilizing process for oil insoluble pesticides |
| JPS5675409A (en) * | 1979-11-26 | 1981-06-22 | Sumitomo Chem Co Ltd | Emulsion composition for herbicidal use |
| DE3319796A1 (de) * | 1983-06-01 | 1984-12-06 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von fluessigen pflanzenschutzmittelkombinationen |
| GB8715500D0 (en) * | 1987-07-01 | 1987-08-05 | Schering Agrochemicals Ltd | Fungicides |
| WO1989003176A1 (en) * | 1987-10-14 | 1989-04-20 | Dow Chemical Company Limited | Latex-based agricultural compositions |
| DE58908525D1 (de) * | 1988-09-02 | 1994-11-24 | Hoechst Ag | Wässrige Formulierungen und deren Verwendung. |
| FR2655276B1 (fr) * | 1989-12-04 | 1992-11-27 | Rhone Poulenc Chimie | Microemulsions concentrees de matieres organiques diluables sous forme d'emulsions stables et leur procede de preparation. |
| FR2655238A1 (fr) * | 1989-12-04 | 1991-06-07 | Rhone Poulenc Chimie | Emulsions aqueuses concentrees de matieres actives phytosanitaires a bas point de fusion et leur application dans les formulations phytosanitaires. |
-
1991
- 1991-03-19 DE DE4108871A patent/DE4108871A1/de not_active Withdrawn
-
1992
- 1992-03-03 EP EP92301791A patent/EP0505053A1/en active Pending
- 1992-03-03 WO PCT/GB1992/000375 patent/WO1992016105A1/en not_active Ceased
- 1992-03-03 ES ES92906511T patent/ES2092676T3/es not_active Expired - Lifetime
- 1992-03-03 KR KR1019930702802A patent/KR100210630B1/ko not_active Expired - Lifetime
- 1992-03-03 JP JP4505824A patent/JP3049368B2/ja not_active Expired - Lifetime
- 1992-03-03 US US08/119,085 patent/US5389665A/en not_active Expired - Fee Related
- 1992-03-03 AT AT92906511T patent/ATE143567T1/de not_active IP Right Cessation
- 1992-03-03 AU AU13680/92A patent/AU659137B2/en not_active Ceased
- 1992-03-03 DE DE69214278T patent/DE69214278T2/de not_active Expired - Lifetime
- 1992-03-03 BR BR9205749A patent/BR9205749A/pt not_active IP Right Cessation
- 1992-03-03 EP EP92906511A patent/EP0576484B1/en not_active Expired - Lifetime
- 1992-03-03 DK DK92906511.8T patent/DK0576484T3/da active
- 1992-03-16 TR TR92/0215A patent/TR25992A/xx unknown
- 1992-03-18 MX MX9201182A patent/MX9201182A/es unknown
- 1992-03-18 IE IE084992A patent/IE920849A1/en not_active IP Right Cessation
- 1992-03-18 ZA ZA921980A patent/ZA921980B/xx unknown
- 1992-03-18 NZ NZ242036A patent/NZ242036A/xx unknown
- 1992-03-18 AP APAP/P/1992/000366A patent/AP359A/en active
- 1992-03-19 MA MA22759A patent/MA22470A1/fr unknown
- 1992-03-19 CN CN92102480A patent/CN1054024C/zh not_active Expired - Lifetime
- 1992-03-30 IL IL10141692A patent/IL101416A/en not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2059773A (en) * | 1979-10-12 | 1981-04-29 | Boots Co Ltd | Fungicidal compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| TR25992A (tr) | 1993-11-01 |
| DE69214278D1 (de) | 1996-11-07 |
| AU659137B2 (en) | 1995-05-11 |
| IL101416A0 (en) | 1992-11-15 |
| AP9200366A0 (en) | 1992-04-30 |
| US5389665A (en) | 1995-02-14 |
| CN1066760A (zh) | 1992-12-09 |
| AU1368092A (en) | 1992-10-21 |
| JP3049368B2 (ja) | 2000-06-05 |
| DE69214278T2 (de) | 1997-04-24 |
| EP0576484B1 (en) | 1996-10-02 |
| ZA921980B (en) | 1992-11-25 |
| ATE143567T1 (de) | 1996-10-15 |
| BR9205749A (pt) | 1994-08-23 |
| MX9201182A (es) | 1994-06-30 |
| CN1054024C (zh) | 2000-07-05 |
| WO1992016105A1 (en) | 1992-10-01 |
| IE920849A1 (en) | 1992-09-23 |
| EP0576484A1 (en) | 1994-01-05 |
| KR100210630B1 (ko) | 1999-07-15 |
| ES2092676T3 (es) | 1996-12-01 |
| MA22470A1 (fr) | 1992-10-01 |
| DK0576484T3 (cg-RX-API-DMAC7.html) | 1997-03-10 |
| EP0505053A1 (en) | 1992-09-23 |
| DE4108871A1 (de) | 1992-09-24 |
| NZ242036A (en) | 1993-04-28 |
| JPH06505971A (ja) | 1994-07-07 |
| IL101416A (en) | 1996-03-31 |
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