SE540536C2 - Liquid agrochemical - Google Patents

Liquid agrochemical

Info

Publication number: SE540536C2
Authority: SE; Sweden
Prior art keywords: weight; manufactured; benzyl alcohol; aromatic hydrocarbon; present
Prior art date: 2016-03-04

Application number

SE1750195A

Other languages

English (en)

Other versions

SE1750195A1 (en

Inventor

Watanabe Atsushi

Abe Toru

Kawanaka Hideo

Teramoto Takeshi

Nakagawa Kota

Original Assignee

Sumitomo Chemical Co

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.)

2016-03-04

Filing date

2017-02-23

Publication date

2018-09-25

2017-02-23 Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co

2017-09-05 Publication of SE1750195A1 publication Critical patent/SE1750195A1/sv

2018-09-25 Publication of SE540536C2 publication Critical patent/SE540536C2/en

Links

239000003905 agrochemical Substances 0.000 title claims abstract description 69
239000007788 liquid Substances 0.000 title claims abstract description 44
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims abstract description 99
150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 95
-1 pyridazine compound Chemical class 0.000 claims abstract description 84
235000019445 benzyl alcohol Nutrition 0.000 claims abstract description 33
239000004094 surface-active agent Substances 0.000 claims abstract description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 9
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 9
125000001246 bromo group Chemical group Br* 0.000 claims abstract description 8
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 8
150000005215 alkyl ethers Chemical class 0.000 claims description 12
150000004996 alkyl benzenes Chemical class 0.000 claims description 8
229920000090 poly(aryl ether) Polymers 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
239000002736 nonionic surfactant Substances 0.000 claims description 6
239000003945 anionic surfactant Substances 0.000 claims description 5
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 claims description 4
229940071161 dodecylbenzenesulfonate Drugs 0.000 claims description 4
239000004495 emulsifiable concentrate Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 description 28
239000000126 substance Substances 0.000 description 20
239000000203 mixture Substances 0.000 description 16
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 15
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 13
229920003171 Poly (ethylene oxide) Polymers 0.000 description 11
239000012456 homogeneous solution Substances 0.000 description 10
229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 10
150000001875 compounds Chemical class 0.000 description 9
229910019142 PO4 Inorganic materials 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
239000010452 phosphate Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
238000000034 method Methods 0.000 description 5
229920001214 Polysorbate 60 Polymers 0.000 description 4
239000013078 crystal Substances 0.000 description 4
201000010099 disease Diseases 0.000 description 4
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
238000001556 precipitation Methods 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000001346 alkyl aryl ethers Chemical class 0.000 description 3
239000012752 auxiliary agent Substances 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
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 3
150000003839 salts Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
239000008096 xylene Substances 0.000 description 3
FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
GNPWYHFXSMINJQ-UHFFFAOYSA-N 1,2-dimethyl-3-(1-phenylethyl)benzene Chemical compound C=1C=CC(C)=C(C)C=1C(C)C1=CC=CC=C1 GNPWYHFXSMINJQ-UHFFFAOYSA-N 0.000 description 2
QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 2
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 2
PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 2
239000004147 Sorbitan trioleate Substances 0.000 description 2
LWZFANDGMFTDAV-BURFUSLBSA-N [(2r)-2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O LWZFANDGMFTDAV-BURFUSLBSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
HNXNKTMIVROLTK-UHFFFAOYSA-N n,n-dimethyldecanamide Chemical compound CCCCCCCCCC(=O)N(C)C HNXNKTMIVROLTK-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
229950006451 sorbitan laurate Drugs 0.000 description 2
235000011067 sorbitan monolaureate Nutrition 0.000 description 2
229950004959 sorbitan oleate Drugs 0.000 description 2
229950011392 sorbitan stearate Drugs 0.000 description 2
235000019337 sorbitan trioleate Nutrition 0.000 description 2
229960000391 sorbitan trioleate Drugs 0.000 description 2
YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
WJYAJBDKANFOID-AWEZNQCLSA-N (2s)-2-(dodecylamino)propanoic acid Chemical compound CCCCCCCCCCCCN[C@@H](C)C(O)=O WJYAJBDKANFOID-AWEZNQCLSA-N 0.000 description 1
YQZBFMJOASEONC-UHFFFAOYSA-N 1-Methyl-2-propylbenzene Chemical compound CCCC1=CC=CC=C1C YQZBFMJOASEONC-UHFFFAOYSA-N 0.000 description 1
UVMGANPLBFFQIO-UHFFFAOYSA-N 1-dodecylnaphthalene Chemical compound C1=CC=C2C(CCCCCCCCCCCC)=CC=CC2=C1 UVMGANPLBFFQIO-UHFFFAOYSA-N 0.000 description 1
WDRZVZVXHZNSFG-UHFFFAOYSA-N 1-ethenylpyridin-1-ium Chemical class C=C[N+]1=CC=CC=C1 WDRZVZVXHZNSFG-UHFFFAOYSA-N 0.000 description 1
HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
ZADDSDYVJJAKCI-UHFFFAOYSA-N 1-tridecylnaphthalene Chemical compound C1=CC=C2C(CCCCCCCCCCCCC)=CC=CC2=C1 ZADDSDYVJJAKCI-UHFFFAOYSA-N 0.000 description 1
IZBZQUREHISXFJ-UHFFFAOYSA-N 2-[4-chloro-5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetic acid Chemical compound CC1=C(Cl)C(C(F)(F)F)=NN1CC(O)=O IZBZQUREHISXFJ-UHFFFAOYSA-N 0.000 description 1
PLLCCSYEGQDAIW-UHFFFAOYSA-N 5-ethyl-1,6-dimethyl-5-phenylcyclohexa-1,3-diene Chemical compound C=1C=CC=CC=1C1(CC)C=CC=C(C)C1C PLLCCSYEGQDAIW-UHFFFAOYSA-N 0.000 description 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
ZQISRDCJNBUVMM-YFKPBYRVSA-N L-histidinol Chemical compound OC[C@@H](N)CC1=CNC=N1 ZQISRDCJNBUVMM-YFKPBYRVSA-N 0.000 description 1
WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 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
CSWYKLRZFCSAHI-UHFFFAOYSA-N [O-]C(CC[N+]1=CC=CN=C1)=O Chemical compound [O-]C(CC[N+]1=CC=CN=C1)=O CSWYKLRZFCSAHI-UHFFFAOYSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
229960001950 benzethonium chloride Drugs 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
WYACBZDAHNBPPB-UHFFFAOYSA-N diethyl oxalate Chemical compound CCOC(=O)C(=O)OCC WYACBZDAHNBPPB-UHFFFAOYSA-N 0.000 description 1
GUVUOGQBMYCBQP-UHFFFAOYSA-N dmpu Chemical compound CN1CCCN(C)C1=O GUVUOGQBMYCBQP-UHFFFAOYSA-N 0.000 description 1
VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical class CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
239000008172 hydrogenated vegetable oil Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
LPEKGGXMPWTOCB-VKHMYHEASA-N methyl (S)-lactate Chemical compound COC(=O)[C@H](C)O LPEKGGXMPWTOCB-VKHMYHEASA-N 0.000 description 1
APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
WSVDSBZMYJJMSB-UHFFFAOYSA-N octadecylbenzene Chemical compound CCCCCCCCCCCCCCCCCCC1=CC=CC=C1 WSVDSBZMYJJMSB-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- 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
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/08—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D237/12—Halogen atoms or nitro radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Toxicology (AREA)
Dispersion Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Management, Administration, Business Operations System, And Electronic Commerce (AREA)
Apparatus Associated With Microorganisms And Enzymes (AREA)
Investigating Or Analysing Biological Materials (AREA)

SE1750195A 2016-03-04 2017-02-23 Liquid agrochemical SE540536C2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP2016041875A JP6589697B2 (ja)	2016-03-04	2016-03-04	液状農薬

Publications (2)

Publication Number	Publication Date
SE1750195A1 SE1750195A1 (en)	2017-09-05
SE540536C2 true SE540536C2 (en)	2018-09-25

Family

ID=58360766

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE1750195A SE540536C2 (en)	2016-03-04	2017-02-23	Liquid agrochemical

Country Status (11)

Country	Link
JP (1)	JP6589697B2 (de)
AT (1)	AT518360A3 (de)
BE (1)	BE1024292B1 (de)
DE (1)	DE102017002060A1 (de)
DK (1)	DK179289B1 (de)
ES (1)	ES2631752B1 (de)
FR (1)	FR3048333A1 (de)
GB (1)	GB2550245A (de)
NL (1)	NL1042280B1 (de)
PL (1)	PL230203B1 (de)
SE (1)	SE540536C2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP3603398A1 (de)	2018-07-31	2020-02-05	Rhodia Operations	Agrochemischzusammensetzung, seine herstellung und anwendung

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EP0278595B2 (de) *	1987-02-09	2000-01-12	Zeneca Limited	Fungizide
US5444078A (en) *	1993-10-01	1995-08-22	Rohm And Haas Company	Fully water-dilutable microemulsions
JP2000119263A (ja) *	1998-03-13	2000-04-25	Nippon Nohyaku Co Ltd	新規な１，３―チアジン誘導体又は１，３―セレナジン誘導体及びその用途並びに使用方法
EP1023833A3 (de) *	1999-01-29	2001-07-18	American Cyanamid Company	Ein oder mehrere Schädlingsbekämpfungsmittel und Zusätze enthaltendes Emulsionskonzentrat
EP1025757B1 (de) *	1999-01-29	2005-11-09	BASF Agro B.V., Arnhem (NL), Wädenswil-Branch	Entschäumer enthaltendes Pflanzenschutzmittel-Emulsionskonzentrat
JP4631010B2 (ja) *	1999-08-19	2011-02-16	日産化学工業株式会社	液状農薬組成物
AU2005252061B2 (en) *	2004-06-09	2010-02-11	Sumitomo Chemical Company, Limited	Pyridazine compound and use thereof
JP4792816B2 (ja) *	2004-06-09	2011-10-12	住友化学株式会社	ピリダジン化合物ならびにその用途
JP4747680B2 (ja) *	2004-06-28	2011-08-17	住友化学株式会社	ピリダジン化合物及びその用途
DE602005024814D1 (de) *	2004-06-28	2010-12-30	Sumitomo Chemical Co	Pyridazinverbindung und deren verwendung
EP1886560A1 (de) *	2006-08-05	2008-02-13	Bayer CropScience AG	Neue mikroemulgierbare Konzentrate
WO2008135413A1 (de) *	2007-05-02	2008-11-13	Basf Se	Fungizide pyridazine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel
GB0804619D0 (en) *	2008-03-12	2008-04-16	Norbrook Lab Ltd	A topical ectoparasiticide composition
UA106213C2 (ru) *	2008-10-10	2014-08-11	Басф Се	Жидкие препараты для защиты растений, содержащие пираклостробин
JP2012036142A (ja) *	2010-08-10	2012-02-23	Sumitomo Chemical Co Ltd	植物病害防除組成物およびその用途
JP2013142062A (ja) *	2012-01-10	2013-07-22	Sumitomo Chemical Co Ltd	植物病害防除組成物およびその用途
JP2013142063A (ja) *	2012-01-10	2013-07-22	Sumitomo Chemical Co Ltd	植物病害防除組成物およびその用途
JP2014019680A (ja)	2012-07-20	2014-02-03	Sumitomo Chemical Co Ltd	植物病害防除組成物およびその用途
JP6544523B2 (ja) *	2014-01-31	2019-07-17	日産化学株式会社	液状農薬組成物
JP2016041875A (ja)	2014-08-18	2016-03-31	旭化成ホームズ株式会社	建物

2016
- 2016-03-04 JP JP2016041875A patent/JP6589697B2/ja active Active
2017
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- 2017-03-01 ES ES201730271A patent/ES2631752B1/es not_active Expired - Fee Related
- 2017-03-01 PL PL420695A patent/PL230203B1/pl unknown
- 2017-03-02 FR FR1751694A patent/FR3048333A1/fr not_active Withdrawn
- 2017-03-02 GB GB1703381.2A patent/GB2550245A/en not_active Withdrawn
- 2017-03-02 BE BE2017/5131A patent/BE1024292B1/fr not_active IP Right Cessation
- 2017-03-03 AT ATA50170/2017A patent/AT518360A3/de not_active Application Discontinuation
- 2017-03-03 DE DE102017002060.4A patent/DE102017002060A1/de not_active Withdrawn
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Also Published As

Publication number	Publication date
BE1024292A1 (fr)	2018-01-16
NL1042280A (en)	2017-09-07
JP2017155015A (ja)	2017-09-07
ES2631752B1 (es)	2018-03-21
GB201703381D0 (en)	2017-04-19
IE20170047A1 (en)	2017-12-13
PL230203B1 (pl)	2018-10-31
AT518360A3 (de)	2018-06-15
JP6589697B2 (ja)	2019-10-16
BE1024292B1 (fr)	2018-01-23
GB2550245A (en)	2017-11-15
FR3048333A1 (fr)	2017-09-08
DE102017002060A1 (de)	2017-09-07
SE1750195A1 (en)	2017-09-05
ES2631752A1 (es)	2017-09-04
AT518360A2 (de)	2017-09-15
DK201770156A1 (en)	2017-10-02
NL1042280B1 (en)	2017-12-13
DK179289B1 (en)	2018-04-03
PL420695A1 (pl)	2017-09-11

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