AP351A - Mixed agrochemical combination. - Google Patents

Mixed agrochemical combination. Download PDF

Info

Publication number: AP351A
Authority: AP; ARIPO
Prior art keywords: plant; combination; process according; active materials; fungicide
Prior art date: 1991-12-06

Application number

APAP/P/1992/000455A

Other languages

English (en)

Other versions

AP9200455A0 (en

Inventor

Pascal Caruhell

Jacques Mugnier

Original Assignee

Rhone Poulenc Agrochimie

Priority date (The priority date 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 date listed.)

1991-12-06

Filing date

1992-12-04

Publication date

1994-08-09

1992-12-04 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1993-01-31 Publication of AP9200455A0 publication Critical patent/AP9200455A0/xx

1994-08-09 Application granted granted Critical

1994-08-09 Publication of AP351A publication Critical patent/AP351A/en

Links

239000003905 agrochemical Substances 0.000 title claims abstract description 8
YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims abstract description 13
239000005906 Imidacloprid Substances 0.000 claims abstract description 12
239000000417 fungicide Substances 0.000 claims abstract description 12
229940056881 imidacloprid Drugs 0.000 claims abstract description 12
230000000855 fungicidal effect Effects 0.000 claims abstract description 11
201000010099 disease Diseases 0.000 claims abstract description 10
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 10
241000238631 Hexapoda Species 0.000 claims abstract description 9
125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 8
239000002917 insecticide Substances 0.000 claims abstract description 7
239000011149 active material Substances 0.000 claims description 27
238000000034 method Methods 0.000 claims description 12
PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical group C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 9
239000005859 Triticonazole Substances 0.000 claims description 9
239000004094 surface-active agent Substances 0.000 claims description 9
239000002689 soil Substances 0.000 claims description 4
239000012872 agrochemical composition Substances 0.000 claims 2
235000013339 cereals Nutrition 0.000 claims 1
239000003085 diluting agent Substances 0.000 claims 1
239000000203 mixture Substances 0.000 description 35
239000000843 powder Substances 0.000 description 18
241000196324 Embryophyta Species 0.000 description 16
239000000470 constituent Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
239000007788 liquid Substances 0.000 description 8
239000007787 solid Substances 0.000 description 8
239000005995 Aluminium silicate Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
235000012211 aluminium silicate Nutrition 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
241001600407 Aphis <genus> Species 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
241001123569 Puccinia recondita Species 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
235000019993 champagne Nutrition 0.000 description 4
239000000463 material Substances 0.000 description 4
230000035515 penetration Effects 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
239000000080 wetting agent Substances 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
238000010410 dusting Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
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 3
230000008635 plant growth Effects 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
206010061217 Infestation Diseases 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
ZMXDDKWLCZADIW-UHFFFAOYSA-N Vilsmeier-Haack reagent Natural products CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
239000002518 antifoaming agent Substances 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
229920005551 calcium lignosulfonate Polymers 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000000975 dye Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000008187 granular material Substances 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
230000000749 insecticidal effect Effects 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
239000011368 organic material Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
239000004550 soluble concentrate Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000004546 suspension concentrate Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000013008 thixotropic agent Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical class C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 1
UQFGXXUMKQOQPH-UHFFFAOYSA-N 2-[(4-chlorophenyl)methylidene]-1-(1,2,4-triazol-1-ylmethyl)cyclohexan-1-ol Chemical compound C1CCCC(=CC=2C=CC(Cl)=CC=2)C1(O)CN1C=NC=N1 UQFGXXUMKQOQPH-UHFFFAOYSA-N 0.000 description 1
IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 1
PPDBOQMNKNNODG-UHFFFAOYSA-N 5-[(4-chlorophenyl)methylidene]-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1=CC1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-UHFFFAOYSA-N 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
206010037888 Rash pustular Diseases 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
241000607479 Yersinia pestis Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
239000004531 microgranule Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003415 peat Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
-1 poly(acrylic acids) Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
208000029561 pustule Diseases 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical group [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
230000001018 virulence Effects 0.000 description 1
238000011179 visual inspection Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000008096 xylene 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

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)

APAP/P/1992/000455A 1991-12-06 1992-12-04 Mixed agrochemical combination. AP351A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR9115397A FR2684519B1 (fr)	1991-12-06	1991-12-06	Association d'un fongicide de la famille des triazoles et d'imidacloprid.

Publications (2)

Publication Number	Publication Date
AP9200455A0 AP9200455A0 (en)	1993-01-31
AP351A true AP351A (en)	1994-08-09

Family

ID=9419943

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
APAP/P/1992/000455A AP351A (en)	1991-12-06	1992-12-04	Mixed agrochemical combination.

Country Status (24)

Country	Link
EP (1)	EP0545834A1 (fr)
JP (1)	JPH05246806A (fr)
KR (1)	KR930011819A (fr)
CN (1)	CN1072817A (fr)
AP (1)	AP351A (fr)
AU (1)	AU2978992A (fr)
BR (1)	BR9204924A (fr)
CA (1)	CA2084140A1 (fr)
CZ (1)	CZ358292A3 (fr)
FI (1)	FI925532A7 (fr)
FR (1)	FR2684519B1 (fr)
HR (1)	HRP921391A2 (fr)
HU (2)	HU9203846D0 (fr)
IL (1)	IL103923A0 (fr)
MA (1)	MA22728A1 (fr)
MX (1)	MX9206976A (fr)
MY (1)	MY131280A (fr)
NO (1)	NO924677L (fr)
PL (1)	PL296848A1 (fr)
SI (1)	SI9200364A (fr)
SK (1)	SK358292A3 (fr)
TR (1)	TR26842A (fr)
YU (1)	YU104692A (fr)
ZA (1)	ZA929342B (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4853798A (en) *	1983-07-21	1989-08-01	Sony Corporation	Method and apparatus for reproducing digital or analog signals
FR2712144B1 (fr) *	1993-11-04	1997-07-18	Rhone Poulenc Agrochimie	Association d'un fongicide à groupe azole avec un insecticide à groupe pyrazole, pyrrole ou phénylimidazole.
FR2711893B1 (fr) *	1993-11-04	1996-01-12	Rhone Poulenc Agrochimie	Association d'un fongicide à groupe azole avec un insecticide à groupe pyrazole, pyrrole ou phénylimidazole.
DE4412833A1 (de) *	1994-04-14	1995-10-19	Bayer Ag	Insektizide Düngemischungen
DE4417742A1 (de) *	1994-05-20	1995-11-23	Bayer Ag	Nicht-systemische Bekämpfung von Parasiten
DE4426753A1 (de) *	1994-07-28	1996-02-01	Bayer Ag	Mittel zur Bekämpfung von Pflanzenschädlingen
EP0883345A1 (fr) *	1995-12-18	1998-12-16	Novartis AG	Composition pesticide
CN1297545C (zh)	1998-06-10	2007-01-31	拜尔公司	防治植物有害生物的组合物
DE19829113A1 (de)	1998-06-10	1999-12-16	Bayer Ag	Mittel zur Bekämpfung von Pflanzenschädlingen
BR9911348B1 (pt)	1998-06-17	2013-03-19		agentes para o combate de pragas vegetais, sua aplicaÇço e seu processo de preparaÇço, bem como processo para combater fungos e insetos.
GB9816638D0 (en) *	1998-07-30	1998-09-30	Novartis Ag	Organic compounds
UA82788C2 (uk) *	2004-06-17	2008-05-12	Басф Акцієнгезельшафт	Застосування (e)-5-(4-хлорбензиліден)-2,2-диметил-1-(1h-1,2,4-триазол-1-метил)циклопентанолу для боротьби з іржею на рослинах сої та спосіб боротьби з іржею в культурах сої
US8211828B2 (en)	2007-01-19	2012-07-03	Basf Se	Fungicidal mixtures of 1-methylpyrazol-4-ylcarboxanilides and azolopyrimidinylamines
BRPI0806766A2 (pt) *	2007-01-30	2011-09-13	Basf Se	misturas pesticidas, métodos para melhorar a saúde de plantas, para controlar ou prevenir infestação fúngica em plantas, partes de planta, sementes, ou seu local de crescimento, para controlar ou prevenir nematódeos ou insetos nocivos em plantas, partes de planta, sementes, ou seu local de crescimento, e para proteger sementes, material de propagação de planta, semente, e, composição pesticida
EP2109366A2 (fr) *	2007-02-06	2009-10-21	Basf Se	Mélanges pesticides
EA020203B1 (ru)	2007-09-20	2014-09-30	Басф Се	Композиции и агенты, содержащие фунгицидный штамм и активное соединение
AR071344A1 (es) *	2008-02-05	2010-06-16	Basf Se	Mezclas de plaguicidas
CN105685082B (zh) *	2012-03-05	2018-06-26	陕西韦尔奇作物保护有限公司	一种含灭菌唑的农药组合物
CN103416422A (zh) *	2013-08-31	2013-12-04	红河蔗保科技有限责任公司	一种甘蔗杀虫剂及其生产方法
CN113545343B (zh) *	2021-07-02	2022-09-20	中化化工科学技术研究总院有限公司	一种清除农业害虫分泌物喷雾助剂及其制备和使用方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2641277A1 (fr) *	1988-12-29	1990-07-06	Rhone Poulenc Agrochimie	Azolylmethylcyclopentane ou cyclopentene benzolidene et utilisation comme fongicide
DE4111389A1 (de) *	1991-04-09	1992-10-15	Bayer Ag	Verwendung von imidacloprid als laufkaefer-repellent in molluskizid-formulierungen
EP0511541A1 (fr) *	1991-04-27	1992-11-04	Nihon Bayer Agrochem K.K.	Agent de préservation du bois ou de matériaux à base de bois contre les insectes
WO1993000009A1 (fr) *	1991-06-26	1993-01-07	Schering Aktiengesellschaft	Compositions pesticides comportant l'amitraz et l'imidacloprid
US5246953A (en) *	1990-06-12	1993-09-21	Rhone-Poulenc Secteur Agrochimie	Process for protecting plant propagation products and the plants obtained from them

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
MA21706A1 (fr) *	1988-12-29	1990-07-01	Rhone Poulenc Agrochimie	Benzolidene azolylmethylcycloalcane et utilisation comme fongicide.
JPH03261704A (ja) *	1990-03-12	1991-11-21	Nissan Chem Ind Ltd	有害生物防除用粒剤

1991
- 1991-12-06 FR FR9115397A patent/FR2684519B1/fr not_active Expired - Fee Related
1992
- 1992-11-30 CA CA002084140A patent/CA2084140A1/fr not_active Abandoned
- 1992-11-30 IL IL103923A patent/IL103923A0/xx unknown
- 1992-12-02 AU AU29789/92A patent/AU2978992A/en not_active Abandoned
- 1992-12-02 MA MA23018A patent/MA22728A1/fr unknown
- 1992-12-02 EP EP92420444A patent/EP0545834A1/fr not_active Withdrawn
- 1992-12-02 BR BR9204924A patent/BR9204924A/pt not_active Application Discontinuation
- 1992-12-02 ZA ZA929342A patent/ZA929342B/xx unknown
- 1992-12-03 HR HR921391A patent/HRP921391A2/xx not_active Application Discontinuation
- 1992-12-03 MX MX9206976A patent/MX9206976A/es unknown
- 1992-12-03 JP JP4324304A patent/JPH05246806A/ja active Pending
- 1992-12-04 NO NO92924677A patent/NO924677L/no unknown
- 1992-12-04 SI SI19929200364A patent/SI9200364A/sl unknown
- 1992-12-04 SK SK3582-92A patent/SK358292A3/sk unknown
- 1992-12-04 AP APAP/P/1992/000455A patent/AP351A/en active
- 1992-12-04 FI FI925532A patent/FI925532A7/fi not_active Application Discontinuation
- 1992-12-04 YU YU104692A patent/YU104692A/sh unknown
- 1992-12-04 HU HU9203846A patent/HU9203846D0/hu unknown
- 1992-12-04 CZ CS923582A patent/CZ358292A3/cs unknown
- 1992-12-04 MY MYPI92002234A patent/MY131280A/en unknown
- 1992-12-04 PL PL29684892A patent/PL296848A1/xx unknown
- 1992-12-04 CN CN92114180A patent/CN1072817A/zh active Pending
- 1992-12-04 TR TR01195/92A patent/TR26842A/xx unknown
- 1992-12-04 HU HU9203846A patent/HUT62756A/hu unknown
- 1992-12-05 KR KR1019920023419A patent/KR930011819A/ko not_active Withdrawn

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Also Published As

Publication number	Publication date
SI9200364A (en)	1993-06-30
HU9203846D0 (en)	1993-03-29
BR9204924A (pt)	1993-06-08
PL296848A1 (en)	1993-08-23
JPH05246806A (ja)	1993-09-24
IL103923A0 (en)	1993-04-04
FI925532A0 (fi)	1992-12-04
HRP921391A2 (en)	1995-12-31
KR930011819A (ko)	1993-07-20
FI925532L (fi)	1993-06-07
MA22728A1 (fr)	1993-07-01
MY131280A (en)	2007-07-31
CZ358292A3 (en)	1993-09-15
FI925532A7 (fi)	1993-06-07
AP9200455A0 (en)	1993-01-31
EP0545834A1 (fr)	1993-06-09
CN1072817A (zh)	1993-06-09
CA2084140A1 (fr)	1993-06-07
FR2684519B1 (fr)	1994-01-28
SK358292A3 (en)	1995-03-08
NO924677D0 (no)	1992-12-04
ZA929342B (en)	1993-06-04
TR26842A (tr)	1994-08-19
YU104692A (sh)	1995-10-03
MX9206976A (es)	1993-06-01
NO924677L (no)	1993-06-07
FR2684519A1 (fr)	1993-06-11
HUT62756A (en)	1993-06-28
AU2978992A (en)	1993-06-10

Publication	Publication Date	Title
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CA2211105C (fr)	2008-01-08	Associations insecticides comprenant un insecticide de la famille des chloronicotinyls et un insecticide a groupe pyrazole, pyrrole ou phenylimidazole
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JP5502854B2 (ja)	2014-05-28	菌類感染から大豆を保護する方法
EP3664614B1 (fr)	2024-01-03	Procédé de contrôle ou de prévention de l'infestation de plantes de soja par fusarium virguliforme
KR100353181B1 (ko)	2004-12-23	아인산 또는 그의 염증의 하나를 사용한 종자처리, 및 이와같이 처리된 종자
US5877194A (en)	1999-03-02	Combinations of a fungicide containing an azole group with an insecticide containing a pyrazole, pyrrole or phenylimidazole group
FI93600C (fi)	1995-05-10	Rikkakasvien torjuntamenetelmä, jossa käytetään diflufenikaania, ja herbisidikoostumus
JPS6333307A (ja)	1988-02-13	ジフルフエニカンを使用する除草方法
JP3714692B2 (ja)	2005-11-09	殺菌剤組成物
JPH01146807A (ja)	1989-06-08	ジフルフェニカンを使用する除草方法
EP0001328A1 (fr)	1979-04-04	Procédé et composition pour la lutte contre les mauvaises herbes
SK284515B6 (sk)	2005-05-05	Synergická fungicídna kompozícia na báze bromuconazolu a triazolovej zlúčeniny a spôsob kuratívneho alebo preventívneho ošetrenia kultúrnych plodín proti fungálnemu napadnutiu
US5866582A (en)	1999-02-02	Fungicidal combination of a dicarboximide compound and cyprodinil
US6043267A (en)	2000-03-28	Fungicidal compositions and the use thereof
GB2095114A (en)	1982-09-29	Antifungal compositions based on phosphorous acid derivatives, and their application to the protection of plants
JPS6117803B2 (fr)	1986-05-09
EP0127945B1 (fr)	1990-01-17	Composition pour régler la croissance des plantes
WO2025068980A1 (fr)	2025-04-03	Composition synergique comprenant un fongicide triazolinthione et son procédé de préparation
EP0106558A2 (fr)	1984-04-25	Mélanges fongicides
MXPA97005721A (en)	1998-07-03	Insecticides combinations that include an insecticide of the class of clinical scientific einsecticida that has a pirazol group, pirrol ofenilimida
JPS62155274A (ja)	1987-07-10	トリアゾ−ル基およびオリゴエ−テル基を有する殺菌剤並びにその組合せ物
HU194699B (en)	1988-03-28	Sinergetic herbicid mixture containing as active substance benzamisole, diuron and/or linuron
HU176859B (en)	1981-05-28	Fungicide preparation containing 1,3,4-oxadiazolin-2-one derivatives as active material