SK285677B6 - Kompozícia obsahujúca činidlo na potlačenie vyzrážania chlóracetamidov vhodná ako herbicíd a spôsobjej prípravy - Google Patents

Kompozícia obsahujúca činidlo na potlačenie vyzrážania chlóracetamidov vhodná ako herbicíd a spôsobjej prípravy Download PDF

Info

Publication number: SK285677B6
Authority: SK; Slovakia
Prior art keywords: dimetenamide; composition; precipitation temperature; dicamba; reducing agent
Prior art date: 1997-11-03

Application number

SK574-2000A

Other languages

English (en)

Slovak (sk)

Other versions

SK5742000A3 (en

Inventor

George Luteri

Raad Yacoub

Charles Gallagher

Steven Bowe

Original Assignee

Basf Corporation

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.)

1997-11-03

Filing date

1998-10-22

Publication date

2007-06-07

1998-10-22 Application filed by Basf Corporation filed Critical Basf Corporation

2000-12-11 Publication of SK5742000A3 publication Critical patent/SK5742000A3/sk

2007-06-07 Publication of SK285677B6 publication Critical patent/SK285677B6/sk

Links

239000000203 mixture Substances 0.000 title claims abstract description 75
238000001556 precipitation Methods 0.000 title claims abstract description 70
VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical class NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 title claims abstract description 32
230000002363 herbicidal effect Effects 0.000 title claims abstract description 32
239000004009 herbicide Substances 0.000 title claims abstract description 24
238000000034 method Methods 0.000 title claims abstract description 12
239000003795 chemical substances by application Substances 0.000 title claims abstract description 10
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims abstract description 60
239000005504 Dicamba Substances 0.000 claims abstract description 59
239000007787 solid Substances 0.000 claims abstract description 40
MRUDNSFOFOQZDA-UHFFFAOYSA-N 2,6-dichlorobenzoic acid Chemical compound OC(=O)C1=C(Cl)C=CC=C1Cl MRUDNSFOFOQZDA-UHFFFAOYSA-N 0.000 claims abstract description 16
JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 14
239000003085 diluting agent Substances 0.000 claims description 14
239000003638 chemical reducing agent Substances 0.000 claims description 12
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 5
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
150000005215 alkyl ethers Chemical class 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
150000001350 alkyl halides Chemical class 0.000 claims description 4
230000000994 depressogenic effect Effects 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 3
239000005580 Metazachlor Substances 0.000 claims description 3
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 3
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 claims description 3
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 claims description 3
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 2
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical compound NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims 1
239000000243 solution Substances 0.000 description 28
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 23
238000009472 formulation Methods 0.000 description 21
239000002244 precipitate Substances 0.000 description 20
238000010790 dilution Methods 0.000 description 11
239000012895 dilution Substances 0.000 description 11
238000010438 heat treatment Methods 0.000 description 10
239000000126 substance Substances 0.000 description 9
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
239000008096 xylene Substances 0.000 description 8
230000002829 reductive effect Effects 0.000 description 7
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
230000000694 effects Effects 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000003849 aromatic solvent Substances 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
-1 dimetenamide Chemical class 0.000 description 4
239000003209 petroleum derivative Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
235000010233 benzoic acid Nutrition 0.000 description 3
150000001559 benzoic acids Chemical class 0.000 description 3
238000002329 infrared spectrum Methods 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
238000010899 nucleation Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241000196324 Embryophyta Species 0.000 description 2
230000003247 decreasing effect Effects 0.000 description 2
239000003966 growth inhibitor Substances 0.000 description 2
230000003993 interaction Effects 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000005648 plant growth regulator Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
ISERORSDFSDMDV-UHFFFAOYSA-N 2-(n-(2-chloroacetyl)-2,6-diethylanilino)acetic acid Chemical compound CCC1=CC=CC(CC)=C1N(CC(O)=O)C(=O)CCl ISERORSDFSDMDV-UHFFFAOYSA-N 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000002547 anomalous effect Effects 0.000 description 1
230000002605 anti-dotal effect Effects 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
238000003556 assay Methods 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000012470 diluted sample Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
230000012010 growth Effects 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
229940060367 inert ingredients Drugs 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
230000002147 killing effect Effects 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
KJLLKLRVCJAFRY-UHFFFAOYSA-N mebutizide Chemical compound ClC1=C(S(N)(=O)=O)C=C2S(=O)(=O)NC(C(C)C(C)CC)NC2=C1 KJLLKLRVCJAFRY-UHFFFAOYSA-N 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000004001 molecular interaction Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
239000002373 plant growth inhibitor Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000001629 suppression Effects 0.000 description 1
238000010257 thawing Methods 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000009736 wetting Methods 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/46—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom rings with more than six members

Landscapes

Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)

SK574-2000A 1997-11-03 1998-10-22 Kompozícia obsahujúca činidlo na potlačenie vyzrážania chlóracetamidov vhodná ako herbicíd a spôsobjej prípravy SK285677B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US08/963,280 US5977024A (en)	1997-11-03	1997-11-03	Mixtures and methods for suppressing precipitation of chloroacetamides
PCT/EP1998/006704 WO1999022594A1 (fr)	1997-11-03	1998-10-22	Melanges de chloroacetamides permettant de supprimer la precipitation

Publications (2)

Publication Number	Publication Date
SK5742000A3 SK5742000A3 (en)	2000-12-11
SK285677B6 true SK285677B6 (sk)	2007-06-07

Family

ID=25507010

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK574-2000A SK285677B6 (sk)	1997-11-03	1998-10-22	Kompozícia obsahujúca činidlo na potlačenie vyzrážania chlóracetamidov vhodná ako herbicíd a spôsobjej prípravy

Country Status (22)

Country	Link
US (1)	US5977024A (fr)
EP (1)	EP1043929B1 (fr)
JP (1)	JP4578677B2 (fr)
KR (1)	KR100554590B1 (fr)
CN (1)	CN1264405C (fr)
AR (1)	AR013745A1 (fr)
AT (1)	ATE318516T1 (fr)
AU (1)	AU758051B2 (fr)
BG (1)	BG64883B1 (fr)
BR (1)	BR9814840B1 (fr)
CA (1)	CA2250262C (fr)
CZ (1)	CZ296392B6 (fr)
DE (1)	DE69833677T2 (fr)
HU (1)	HU229669B1 (fr)
IL (1)	IL135665A (fr)
NZ (1)	NZ504391A (fr)
PL (1)	PL194322B1 (fr)
RU (1)	RU2216936C2 (fr)
SK (1)	SK285677B6 (fr)
UA (1)	UA57116C2 (fr)
WO (1)	WO1999022594A1 (fr)
ZA (1)	ZA989978B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN104604872B (zh) *	2013-11-04	2016-08-17	南京华洲药业有限公司	一种含麦草畏与吡草胺的除草组合物及其应用
WO2016142280A1 (fr)	2015-03-06	2016-09-15	Cheminova A/S	Composition de concentré émulsionnable contenant du péthoxamide

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3013054A (en) *	1958-08-04	1961-12-12	Velsicol Chemical Corp	2-methoxy-3, 6-dichlorobenzoates
US4411694A (en) *	1980-06-03	1983-10-25	American Cyanamid Company	Emulsifiable concentrates of 2-chloro-N-isopropyl-2',3'-dimethylacetanilide with improved resistance to crystallization and process for preparing the same
BE895815A (fr) *	1982-02-09	1983-08-04	Sandoz Sa	Chloracetamides heteroaromatiques, leur preparation, leur utilisation en tant qu'herbicides.
US4666502A (en) *	1982-02-09	1987-05-19	Sandoz Ltd.	Herbicidal N-thienyl-chloroacetamides
US4460406A (en) *	1982-04-19	1984-07-17	Monsanto Company	Herbicidal concentrated emulsions
US4695673A (en) *	1985-11-20	1987-09-22	Stauffer Chemical Company	Process for the production of acylated 1,3-dicarbonyl compounds
EP0230596B1 (fr) *	1985-12-30	1992-01-02	Stauffer Chemical Company	Combinaisons herbicides synergiques et méthode d'application
US4789393A (en) *	1986-03-07	1988-12-06	E. I. Du Pont De Nemours And Company	Herbicidal pyridine sulfonamides
US4923501A (en) *	1987-11-04	1990-05-08	Kumiai Chemical Industry Co., Ltd.	Pyrimidine derivatives, processes for their production, and herbicidal method and compositions
HU206242B (en) *	1988-04-18	1992-10-28	Sandoz Ag	Herbicidal compositions comprising substituted benzoyl bicyclodione derivatives as active ingredient
GB8901516D0 (en) *	1989-01-24	1989-03-15	Sandoz Ltd	Improvements in or relating to herbicides
TR24452A (tr) *	1989-04-25	1991-11-01	Sandoz Ltd	Pestisidler ve bitki bueyueme duezenleyicileri olarak heterosiklik dionlar
AU7077091A (en) *	1990-01-11	1991-08-05	E.I. Du Pont De Nemours And Company	Herbicidal pyrimidines and triazines
HU212435B (en) *	1990-06-07	1996-06-28	Sandoz Ag	Herbicidal compositions containing substituted phthalides and heterocyclic phthalides as active ingredient and process for preparation of their active ingredients.
HU9203730D0 (en) *	1991-12-06	1993-03-29	Sandoz Ag	Substituted phthalides and heterocyclic ones
US5457085A (en) *	1992-11-16	1995-10-10	Sandoz Ltd.	Optical isomer of dimethenamid
US5721191A (en) *	1993-02-18	1998-02-24	Sandoz Ltd.	Synergistic herbicidal compositions of dimethenamid and sulfonylureas
EP2050338B1 (fr) *	1993-02-18	2011-05-25	Basf Se	Compositions herbicides

1997
- 1997-11-03 US US08/963,280 patent/US5977024A/en not_active Expired - Lifetime
1998
- 1998-10-22 AU AU12312/99A patent/AU758051B2/en not_active Expired
- 1998-10-22 HU HU0004263A patent/HU229669B1/hu not_active IP Right Cessation
- 1998-10-22 JP JP2000518551A patent/JP4578677B2/ja not_active Expired - Lifetime
- 1998-10-22 CZ CZ20001631A patent/CZ296392B6/cs not_active IP Right Cessation
- 1998-10-22 KR KR1020007004763A patent/KR100554590B1/ko not_active Expired - Fee Related
- 1998-10-22 UA UA2000063198A patent/UA57116C2/uk unknown
- 1998-10-22 RU RU2000114822/04A patent/RU2216936C2/ru not_active IP Right Cessation
- 1998-10-22 EP EP98955509A patent/EP1043929B1/fr not_active Expired - Lifetime
- 1998-10-22 IL IL13566598A patent/IL135665A/en not_active IP Right Cessation
- 1998-10-22 SK SK574-2000A patent/SK285677B6/sk not_active IP Right Cessation
- 1998-10-22 DE DE69833677T patent/DE69833677T2/de not_active Expired - Lifetime
- 1998-10-22 WO PCT/EP1998/006704 patent/WO1999022594A1/fr not_active Ceased
- 1998-10-22 BR BRPI9814840-0A patent/BR9814840B1/pt not_active IP Right Cessation
- 1998-10-22 PL PL98340252A patent/PL194322B1/pl unknown
- 1998-10-22 CN CNB988107368A patent/CN1264405C/zh not_active Expired - Fee Related
- 1998-10-22 AT AT98955509T patent/ATE318516T1/de active
- 1998-10-22 NZ NZ504391A patent/NZ504391A/xx not_active IP Right Cessation
- 1998-11-02 ZA ZA9809978A patent/ZA989978B/xx unknown
- 1998-11-02 CA CA002250262A patent/CA2250262C/fr not_active Expired - Lifetime
- 1998-11-03 AR ARP980105520A patent/AR013745A1/es active IP Right Grant
2000
- 2000-05-04 BG BG104401A patent/BG64883B1/bg unknown

Also Published As

Publication number	Publication date
BR9814840B1 (pt)	2010-06-01
CZ296392B6 (cs)	2006-03-15
EP1043929B1 (fr)	2006-03-01
AR013745A1 (es)	2001-01-10
HUP0004263A3 (en)	2004-03-01
RU2216936C2 (ru)	2003-11-27
DE69833677D1 (de)	2006-04-27
AU758051B2 (en)	2003-03-13
NZ504391A (en)	2002-09-27
ATE318516T1 (de)	2006-03-15
EP1043929A1 (fr)	2000-10-18
CN1278140A (zh)	2000-12-27
ZA989978B (en)	2000-05-02
JP2001521877A (ja)	2001-11-13
KR100554590B1 (ko)	2006-03-03
IL135665A0 (en)	2001-05-20
AU1231299A (en)	1999-05-24
WO1999022594A1 (fr)	1999-05-14
BR9814840A (pt)	2000-10-03
CZ20001631A3 (en)	2001-06-13
JP4578677B2 (ja)	2010-11-10
BG104401A (en)	2001-08-31
CA2250262A1 (fr)	1999-05-03
CA2250262C (fr)	2004-01-20
PL194322B1 (pl)	2007-05-31
DE69833677T2 (de)	2006-08-31
IL135665A (en)	2004-07-25
HUP0004263A2 (hu)	2001-04-28
UA57116C2 (uk)	2003-06-16
CN1264405C (zh)	2006-07-19
SK5742000A3 (en)	2000-12-11
PL340252A1 (en)	2001-01-29
US5977024A (en)	1999-11-02
KR20010031700A (ko)	2001-04-16
BG64883B1 (bg)	2006-08-31
HU229669B1 (hu)	2014-04-28

Legal Events

Date	Code	Title	Description
2016-07-01	MM4A	Patent lapsed due to non-payment of maintenance fees	Effective date: 20151022

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US8871683B2 (en)	2014-10-28	Dicamba herbicide composition
US6030923A (en)	2000-02-29	Liquid agricultural chemical composition
BRPI0705235B1 (pt)	2016-05-17	composição agroquímica e método de fabricação e uso da mesma
AU781074B2 (en)	2005-05-05	Herbicidal emulsifiable concentrates
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