SK286830B6 - Kontinuálny spôsob prípravy stabilnej herbicídnej kompozície vodného suspenzného koncentrátu - Google Patents

Kontinuálny spôsob prípravy stabilnej herbicídnej kompozície vodného suspenzného koncentrátu Download PDF

Info

Publication number: SK286830B6
Authority: SK; Slovakia
Prior art keywords: group; pendimethalin; mixtures; condensation product; suspension concentrate
Prior art date: 2000-08-25

Application number

SK351-2003A

Other languages

English (en)

Slovak (sk)

Other versions

SK3512003A3 (en

Inventor

Jean-Paul Fafchamps

Jean-Michel Villanueva

Original Assignee

Basf Aktiengesellschaft

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.)

2000-08-25

Filing date

2001-08-24

Publication date

2009-06-05

2001-08-24 Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft

2003-09-11 Publication of SK3512003A3 publication Critical patent/SK3512003A3/sk

2009-06-05 Publication of SK286830B6 publication Critical patent/SK286830B6/sk

Links

239000000203 mixture Substances 0.000 title claims abstract description 38
239000007900 aqueous suspension Substances 0.000 title claims abstract description 20
239000012141 concentrate Substances 0.000 title claims abstract description 18
230000002363 herbicidal effect Effects 0.000 title claims description 11
238000002360 preparation method Methods 0.000 title abstract description 7
238000010924 continuous production Methods 0.000 title abstract description 4
239000005591 Pendimethalin Substances 0.000 claims abstract description 41
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical group CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims abstract description 41
239000013078 crystal Substances 0.000 claims abstract description 13
239000000575 pesticide Substances 0.000 claims abstract description 11
238000002156 mixing Methods 0.000 claims abstract description 8
238000000034 method Methods 0.000 claims description 34
239000003795 chemical substances by application Substances 0.000 claims description 10
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
239000007859 condensation product Substances 0.000 claims description 9
239000004094 surface-active agent Substances 0.000 claims description 8
ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 claims description 7
239000004009 herbicide Substances 0.000 claims description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
239000003755 preservative agent Substances 0.000 claims description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
239000007798 antifreeze agent Substances 0.000 claims description 4
238000011278 co-treatment Methods 0.000 claims description 4
230000002335 preservative effect Effects 0.000 claims description 4
239000002562 thickening agent Substances 0.000 claims description 4
SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 claims description 3
CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 claims description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
239000005981 Imazaquin Substances 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 3
239000002518 antifoaming agent Substances 0.000 claims description 3
239000004202 carbamide Substances 0.000 claims description 3
229920005610 lignin Polymers 0.000 claims description 3
229920005646 polycarboxylate Polymers 0.000 claims description 3
239000000377 silicon dioxide Substances 0.000 claims description 3
239000000375 suspending agent Substances 0.000 claims description 3
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 2
NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 claims description 2
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 2
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 2
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims description 2
PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 claims description 2
239000005504 Dicamba Substances 0.000 claims description 2
239000005561 Glufosinate Substances 0.000 claims description 2
239000005562 Glyphosate Substances 0.000 claims description 2
239000005566 Imazamox Substances 0.000 claims description 2
XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims description 2
239000005574 MCPA Substances 0.000 claims description 2
239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 2
150000001558 benzoic acid derivatives Chemical class 0.000 claims description 2
239000004927 clay Substances 0.000 claims description 2
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 2
235000011187 glycerol Nutrition 0.000 claims description 2
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 2
229940097068 glyphosate Drugs 0.000 claims description 2
239000004292 methyl p-hydroxybenzoate Substances 0.000 claims description 2
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims description 2
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims description 2
229960002216 methylparaben Drugs 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
229920002401 polyacrylamide Polymers 0.000 claims description 2
-1 polyoxyethylene phosphoric acid Polymers 0.000 claims description 2
229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
239000004405 propyl p-hydroxybenzoate Substances 0.000 claims description 2
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 claims description 2
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 claims description 2
150000003839 salts Chemical group 0.000 claims description 2
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims description 2
239000004299 sodium benzoate Substances 0.000 claims description 2
235000010234 sodium benzoate Nutrition 0.000 claims description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 2
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims 2
239000008098 formaldehyde solution Substances 0.000 claims 2
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 2
DBHODFSFBXJZNY-UHFFFAOYSA-N 2,4-dichlorobenzyl alcohol Chemical compound OCC1=CC=C(Cl)C=C1Cl DBHODFSFBXJZNY-UHFFFAOYSA-N 0.000 claims 1
ASKFWACWQQZSSS-UHFFFAOYSA-N 2-ethyl-1,2-thiazol-3-one Chemical compound CCN1SC=CC1=O ASKFWACWQQZSSS-UHFFFAOYSA-N 0.000 claims 1
SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 claims 1
229960004698 dichlorobenzyl alcohol Drugs 0.000 claims 1
235000010292 orthophenyl phenol Nutrition 0.000 claims 1
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims 1
PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 claims 1
159000000000 sodium salts Chemical class 0.000 claims 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 claims 1
230000008569 process Effects 0.000 description 14
239000000839 emulsion Substances 0.000 description 5
239000004546 suspension concentrate Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
238000010923 batch production Methods 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
150000003871 sulfonates Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000012010 growth Effects 0.000 description 2
238000009776 industrial production Methods 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000005648 plant growth regulator Substances 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000002794 2,4-DB Substances 0.000 description 1
101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
238000004220 aggregation Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
230000009418 agronomic effect Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
239000011324 bead Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
239000000571 coke Substances 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
NHFDKKSSQWCEES-UHFFFAOYSA-N dihydrogen phosphate;tris(2-hydroxyethyl)azanium Chemical compound OP(O)(O)=O.OCCN(CCO)CCO NHFDKKSSQWCEES-UHFFFAOYSA-N 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000003801 milling Methods 0.000 description 1
LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds

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)

SK351-2003A 2000-08-25 2001-08-24 Kontinuálny spôsob prípravy stabilnej herbicídnej kompozície vodného suspenzného koncentrátu SK286830B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US22831600P	2000-08-25	2000-08-25
PCT/EP2001/009787 WO2002015690A1 (en)	2000-08-25	2001-08-24	Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition

Publications (2)

Publication Number	Publication Date
SK3512003A3 SK3512003A3 (en)	2003-09-11
SK286830B6 true SK286830B6 (sk)	2009-06-05

Family

ID=22856665

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK351-2003A SK286830B6 (sk)	2000-08-25	2001-08-24	Kontinuálny spôsob prípravy stabilnej herbicídnej kompozície vodného suspenzného koncentrátu

Country Status (18)

Country	Link
US (1)	US6617280B2 (de)
EP (1)	EP1313366B1 (de)
AR (1)	AR030485A1 (de)
AT (1)	ATE274300T1 (de)
AU (1)	AU2001289832A1 (de)
BG (1)	BG66154B1 (de)
CZ (1)	CZ295651B6 (de)
DE (1)	DE60105174T2 (de)
DK (1)	DK1313366T3 (de)
ES (1)	ES2225604T3 (de)
HU (1)	HUP0300776A2 (de)
IL (2)	IL154303A0 (de)
PT (1)	PT1313366E (de)
RU (1)	RU2003107843A (de)
SK (1)	SK286830B6 (de)
TR (1)	TR200402441T4 (de)
WO (1)	WO2002015690A1 (de)
ZA (1)	ZA200302273B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP4580382B2 (ja) *	2003-04-14	2010-11-10	ビーエーエスエフソシエタス・ヨーロピア	ペンジメタンの水性流動性濃縮組成物
EP2346326B1 (de) *	2008-10-14	2014-03-26	Basf Se	Kristalline komplexe von pendimethalin und metazachlor
WO2010123851A1 (en) *	2009-04-20	2010-10-28	Valent Biosciences Corporation	Plant growth enhancement with combinations of pesa and herbicides
UA103689C2 (uk) †	2009-07-14	2013-11-11	Басф Се	Спосіб одержання водної суспензії органічної пестицидної сполуки
JP6189136B2 (ja) *	2013-08-22	2017-08-30	竹本油脂株式会社	水性懸濁農薬組成物
US10492490B2 (en) *	2015-03-06	2019-12-03	Board Of Trustees Of Michigan State University	Adjuvant compositions and related methods for reducing herbicide volatility
CN110699418B (zh) *	2019-11-14	2023-06-06	浙江星博生物科技股份有限公司	以非诊断为目的基于gc-ms精子计数的检测方法
WO2024108280A1 (pt) *	2022-11-24	2024-05-30	Iharabrás S.A. Indústrias Químicas	Processos contínuos para preparar uma formulação de glifosato

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3337964A1 (de) *	1983-10-19	1985-05-02	Hoechst Ag, 6230 Frankfurt	Verfahren zur herstellung von pflanzenschutzmittel-dispersionen
US4871392A (en)	1986-05-23	1989-10-03	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
US5624884A (en)	1986-05-23	1997-04-29	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
DE3916465A1 (de) *	1989-05-20	1990-11-22	Bayer Ag	Herstellung kugelfoermiger dispersionen durch kristallisation von emulsionen
FR2670085B1 (fr) *	1990-12-10	1996-12-13	Rhone Poulenc Chimie	Suspensions phytosanitaires.

2001
- 2001-08-24 IL IL15430301A patent/IL154303A0/xx active IP Right Grant
- 2001-08-24 ES ES01969640T patent/ES2225604T3/es not_active Expired - Lifetime
- 2001-08-24 TR TR2004/02441T patent/TR200402441T4/xx unknown
- 2001-08-24 DE DE2001605174 patent/DE60105174T2/de not_active Expired - Lifetime
- 2001-08-24 US US09/938,371 patent/US6617280B2/en not_active Expired - Fee Related
- 2001-08-24 RU RU2003107843/15A patent/RU2003107843A/ru not_active Application Discontinuation
- 2001-08-24 CZ CZ2003862A patent/CZ295651B6/cs not_active IP Right Cessation
- 2001-08-24 SK SK351-2003A patent/SK286830B6/sk not_active IP Right Cessation
- 2001-08-24 WO PCT/EP2001/009787 patent/WO2002015690A1/en not_active Ceased
- 2001-08-24 AT AT01969640T patent/ATE274300T1/de active
- 2001-08-24 DK DK01969640T patent/DK1313366T3/da active
- 2001-08-24 AR ARP010104063A patent/AR030485A1/es unknown
- 2001-08-24 PT PT01969640T patent/PT1313366E/pt unknown
- 2001-08-24 AU AU2001289832A patent/AU2001289832A1/en not_active Abandoned
- 2001-08-24 EP EP01969640A patent/EP1313366B1/de not_active Expired - Lifetime
- 2001-08-24 HU HU0300776A patent/HUP0300776A2/hu unknown
2003
- 2003-02-05 IL IL154303A patent/IL154303A/en unknown
- 2003-02-18 BG BG107567A patent/BG66154B1/bg unknown
- 2003-03-24 ZA ZA200302273A patent/ZA200302273B/en unknown

Also Published As

Publication number	Publication date
AR030485A1 (es)	2003-08-20
DE60105174D1 (de)	2004-09-30
ZA200302273B (en)	2004-07-15
IL154303A0 (en)	2003-09-17
RU2003107843A (ru)	2004-07-27
ATE274300T1 (de)	2004-09-15
CZ295651B6 (cs)	2005-09-14
US20020128154A1 (en)	2002-09-12
BG66154B1 (bg)	2011-09-30
TR200402441T4 (tr)	2004-12-21
CZ2003862A3 (cs)	2003-06-18
IL154303A (en)	2007-06-03
EP1313366A1 (de)	2003-05-28
PT1313366E (pt)	2004-10-29
DK1313366T3 (da)	2004-10-04
AU2001289832A1 (en)	2002-03-04
DE60105174T2 (de)	2005-01-13
SK3512003A3 (en)	2003-09-11
ES2225604T3 (es)	2005-03-16
HUP0300776A2 (hu)	2005-11-28
PL361388A1 (en)	2004-10-04
WO2002015690A1 (en)	2002-02-28
EP1313366B1 (de)	2004-08-25
US6617280B2 (en)	2003-09-09
BG107567A (bg)	2004-08-31

Legal Events

Date	Code	Title	Description
2015-05-05	MM4A	Patent lapsed due to non-payment of maintenance fees	Effective date: 20140824

Publication	Publication Date	Title
EP0647096B1 (de)	1998-08-05	Landwirtschaftliche formulierungen enthaltend flüssige estern von fluroxypyr
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