DK174864B1 - Vandige herbicidpræparater indeholdende imidazolinonherbicider - Google Patents

Vandige herbicidpræparater indeholdende imidazolinonherbicider Download PDF

Info

Publication number: DK174864B1
Authority: DK; Denmark
Prior art keywords: acid; alkyl; methyl; composition according; halogen
Prior art date: 1986-08-15

Application number

DK198704257A

Other languages

Danish (da)

English (en)

Other versions

DK425787D0 (da

DK425787A (da

Inventor

William Steven Steller

Roger Charles Keintz

Original Assignee

American Cyanamid 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.)

1986-08-15

Filing date

1987-08-14

Publication date

2004-01-05

1987-08-14 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1987-08-14 Publication of DK425787D0 publication Critical patent/DK425787D0/da

1988-02-16 Publication of DK425787A publication Critical patent/DK425787A/da

2004-01-05 Application granted granted Critical

2004-01-05 Publication of DK174864B1 publication Critical patent/DK174864B1/da

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 10
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 title abstract description 3
238000002360 preparation method Methods 0.000 title description 13
239000004009 herbicide Substances 0.000 title description 6
239000002253 acid Substances 0.000 claims abstract description 30
239000000203 mixture Substances 0.000 claims abstract description 19
150000003839 salts Chemical class 0.000 claims abstract description 16
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 12
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 11
239000004202 carbamide Substances 0.000 claims abstract description 11
229910052736 halogen Inorganic materials 0.000 claims abstract description 11
150000002367 halogens Chemical class 0.000 claims abstract description 11
229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
239000001257 hydrogen Substances 0.000 claims abstract description 9
229910052717 sulfur Chemical group 0.000 claims abstract description 8
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 7
150000002431 hydrogen Chemical class 0.000 claims abstract description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
239000001301 oxygen Substances 0.000 claims abstract description 7
239000011593 sulfur Chemical group 0.000 claims abstract description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 7
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 5
125000003282 alkyl amino group Chemical group 0.000 claims abstract description 5
229910052799 carbon Inorganic materials 0.000 claims abstract description 4
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 3
125000003302 alkenyloxy group Chemical group 0.000 claims abstract description 3
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 3
125000005133 alkynyloxy group Chemical group 0.000 claims abstract description 3
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims abstract description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 11
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
-1 ammonium 2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) quinolin-3 carboxy-acrylate Chemical compound 0.000 claims description 3
150000001721 carbon Chemical group 0.000 claims description 3
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims description 2
235000019260 propionic acid Nutrition 0.000 claims description 2
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
FBJUTZMAUXJMMH-UHFFFAOYSA-N azane;5-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)pyridine-3-carboxylic acid Chemical compound [NH4+].N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C([O-])=O FBJUTZMAUXJMMH-UHFFFAOYSA-N 0.000 claims 1
125000001188 haloalkyl group Chemical group 0.000 claims 1
239000002563 ionic surfactant Substances 0.000 claims 1
238000010979 pH adjustment Methods 0.000 claims 1
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract description 5
239000002736 nonionic surfactant Substances 0.000 abstract description 4
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract description 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
150000007513 acids Chemical class 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
125000002636 imidazolinyl group Chemical group 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000003960 organic solvent Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
230000008014 freezing Effects 0.000 description 2
238000007710 freezing Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
238000000034 method Methods 0.000 description 2
239000011707 mineral Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
239000011591 potassium Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
QDXJFRHCHWDQSP-UHFFFAOYSA-N 1,4-dihydroimidazol-5-one;quinoline Chemical class O=C1CNC=N1.N1=CC=CC2=CC=CC=C21 QDXJFRHCHWDQSP-UHFFFAOYSA-N 0.000 description 1
VSGNJFMJPJJRTQ-UHFFFAOYSA-N 2-(4,5-dihydroimidazol-1-yl)benzoic acid Chemical class OC(=O)C1=CC=CC=C1N1C=NCC1 VSGNJFMJPJJRTQ-UHFFFAOYSA-N 0.000 description 1
101000713879 Homo sapiens T-complex protein 1 subunit eta Proteins 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
229920001213 Polysorbate 20 Polymers 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
102100036476 T-complex protein 1 subunit eta Human genes 0.000 description 1
230000032683 aging Effects 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000010257 thawing 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
- 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
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cosmetics (AREA)

DK198704257A 1986-08-15 1987-08-14 Vandige herbicidpræparater indeholdende imidazolinonherbicider DK174864B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/896,775 US4816060A (en)	1986-08-15	1986-08-15	Herbicidal aqueous compositions of imidazolinone herbicides
US89677586		1986-08-15

Publications (3)

Publication Number	Publication Date
DK425787D0 DK425787D0 (da)	1987-08-14
DK425787A DK425787A (da)	1988-02-16
DK174864B1 true DK174864B1 (da)	2004-01-05

Family

ID=25406812

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK198704257A DK174864B1 (da)	1986-08-15	1987-08-14	Vandige herbicidpræparater indeholdende imidazolinonherbicider

Country Status (26)

Country	Link
US (1)	US4816060A (fr)
EP (1)	EP0256414B1 (fr)
JP (1)	JP2512759B2 (fr)
KR (1)	KR950006916B1 (fr)
AT (1)	ATE72727T1 (fr)
AU (1)	AU597407B2 (fr)
BG (1)	BG48203A3 (fr)
BR (1)	BR8704215A (fr)
CA (1)	CA1297695C (fr)
CS (1)	CS271478B2 (fr)
DD (1)	DD261518A5 (fr)
DE (1)	DE3776833D1 (fr)
DK (1)	DK174864B1 (fr)
EG (1)	EG18433A (fr)
ES (1)	ES2037686T3 (fr)
GE (1)	GEP19970806B (fr)
GR (1)	GR3003891T3 (fr)
HU (1)	HU200888B (fr)
IE (1)	IE61158B1 (fr)
IL (1)	IL83461A (fr)
IN (1)	IN166550B (fr)
SU (1)	SU1723994A3 (fr)
TR (1)	TR24598A (fr)
UA (1)	UA6153A1 (fr)
YU (1)	YU46560B (fr)
ZA (1)	ZA876050B (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4936902A (en) *	1989-04-25	1990-06-26	American Cyanamid Company	Selective control of sicklepod in the presence of leguminous crops
US5268352A (en) *	1989-11-22	1993-12-07	American Cyanamid Company	Herbicidal emulsifiable suspension concentrate compositions
EP0454968A1 (fr) *	1990-04-30	1991-11-06	American Cyanamid Company	Procédé pour l'augmentation de l'activité biologique de formulations contenant les esters de l'acide imidazolinyl benzoique solides
US5250502A (en) *	1990-04-30	1993-10-05	American Cyanamid Company	Method for enhancing the herbicidal activity of formulations containing solid imidazolinyl benzoic acid esters with bisulfate
EP0473890A1 (fr) *	1990-08-28	1992-03-11	American Cyanamid Company	Compositions herbicides aqueuses de 2-(2-imidazolin-2-yl)-pyridines et quinoléines
ZA912722B (en) *	1990-08-31	1992-01-29	American Cyanamid Co	Herbicidal 2-(-imidazolin-2-yl)-benzo-(6-membered)-heterocycles
EP0554015B1 (fr) *	1992-01-28	1995-03-22	Ishihara Sangyo Kaisha, Ltd.	Suspension herbicide à base d'huile chimiquement stabilisée
US5696024A (en) *	1995-06-06	1997-12-09	American Cyanmid	Herbicidal water soluble granular compositions
TW471950B (en) *	1997-09-17	2002-01-11	American Cyanamid Co	Concentrated, aqueous herbicidal compositions containing an imidazolinyl acid salt and a glyphosate salt
US6127317A (en) *	1997-09-17	2000-10-03	American Cyanamid Company	Concentrated, aqueous herbicidal compositions containing an imidazolinyl acid salt and a glyphosate salt
IL126572A (en) *	1997-10-31	2003-07-31	American Cyanamid Co	Methods and compositions for enhancing herbicidal activity
US6060430A (en) *	1997-10-31	2000-05-09	American Cyanamid Company	Methods and compositions for enhancing herbicidal activity
US6277787B1 (en)	1998-09-14	2001-08-21	American Cyanamid Co.	Synergistic herbicidal methods and compositions
US6214768B1 (en)	1998-09-14	2001-04-10	American Cyanamid Co.	Synergistic herbicidal methods and compositions
US8232230B2 (en) *	2000-12-01	2012-07-31	Helena Holding Company	Manufacture and use of a herbicide formulation
ATE362314T1 (de) *	2001-09-26	2007-06-15	Platte Chemical Co	Herbizidzusammensetzungen umfassend imidazolinonsäure
AU2003229178A1 (en) *	2002-05-13	2003-11-11	Ceres Environmental Solution Industry Incorporated	Urea based natural herbicide compositions
US20050288188A1 (en) *	2004-06-28	2005-12-29	Helena Holding Company	Manufacture and use of a plant growth regulating compound
US8426341B2 (en) *	2005-05-27	2013-04-23	Helena Holding Company	Herbicide formulation
UA120654C2 (uk)	2018-01-15	2020-01-10	Олександр Юрійович Микитюк	Спосіб очистки рідких вуглеводневих моторних палив або вуглеводневих паливних фракцій від сірки

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4188487A (en)	1977-08-08	1980-02-12	American Cyanamid Company	Imidazolinyl benzoic acids, esters and salts and their use as herbicidal agents
US4297128A (en)	1978-06-09	1981-10-27	American Cyanamid Co.	Use of imidazolinyl benzoates as herbicidal agents
US4488896A (en) *	1980-03-13	1984-12-18	American Cyanamid Company	Methods and compositions for the selective control of undesirable weed species in the presence of wet-land crops
EP0041624B1 (fr) *	1980-06-02	1984-02-01	American Cyanamid Company	Méthode pour la régulation de la croissance des plantes à l'aide de certaines 2-(2-imidazolin-2-yle)pyridines et quinoléines
FI860449A7 (fi) *	1985-02-04	1986-08-05	American Cyanamid Co	Komposition foer behandling av graesmatta.
ES2046167T3 (es) *	1985-12-13	1994-02-01	American Cyanamid Company	Procedimiento para la preparacion de composiciones herbicidas de (2-imidazolin-2-il)-heteropiridina condensadas.

1986
- 1986-08-15 US US06/896,775 patent/US4816060A/en not_active Expired - Lifetime
1987
- 1987-08-04 EP EP87111215A patent/EP0256414B1/fr not_active Expired - Lifetime
- 1987-08-04 DE DE8787111215T patent/DE3776833D1/de not_active Expired - Lifetime
- 1987-08-04 ES ES198787111215T patent/ES2037686T3/es not_active Expired - Lifetime
- 1987-08-04 AT AT87111215T patent/ATE72727T1/de not_active IP Right Cessation
- 1987-08-06 IL IL83461A patent/IL83461A/xx not_active IP Right Cessation
- 1987-08-11 IN IN624/CAL/87A patent/IN166550B/en unknown
- 1987-08-12 TR TR87/0569A patent/TR24598A/xx unknown
- 1987-08-13 CA CA000544404A patent/CA1297695C/fr not_active Expired - Lifetime
- 1987-08-13 EG EG469/87A patent/EG18433A/xx active
- 1987-08-13 YU YU151187A patent/YU46560B/sh unknown
- 1987-08-13 CS CS875979A patent/CS271478B2/cs not_active IP Right Cessation
- 1987-08-14 KR KR1019870008947A patent/KR950006916B1/ko not_active Expired - Lifetime
- 1987-08-14 DD DD87306062A patent/DD261518A5/de unknown
- 1987-08-14 AU AU76892/87A patent/AU597407B2/en not_active Expired
- 1987-08-14 IE IE217687A patent/IE61158B1/en not_active IP Right Cessation
- 1987-08-14 UA UA4203183A patent/UA6153A1/uk unknown
- 1987-08-14 HU HU873684A patent/HU200888B/hu unknown
- 1987-08-14 DK DK198704257A patent/DK174864B1/da not_active IP Right Cessation
- 1987-08-14 BR BR8704215A patent/BR8704215A/pt not_active IP Right Cessation
- 1987-08-14 SU SU874203183A patent/SU1723994A3/ru active
- 1987-08-14 ZA ZA876050A patent/ZA876050B/xx unknown
- 1987-08-14 JP JP62201952A patent/JP2512759B2/ja not_active Expired - Lifetime
- 1987-08-14 BG BG080934A patent/BG48203A3/xx unknown
1992
- 1992-02-27 GR GR910401738T patent/GR3003891T3/el unknown
1994
- 1994-01-20 GE GEAP19941747A patent/GEP19970806B/en unknown

Also Published As

Publication number	Publication date
EP0256414A2 (fr)	1988-02-24
EP0256414A3 (en)	1988-09-07
DE3776833D1 (de)	1992-04-02
ZA876050B (en)	1988-04-27
GEP19970806B (en)	1997-02-10
JP2512759B2 (ja)	1996-07-03
CS597987A2 (en)	1990-02-12
UA6153A1 (uk)	1994-12-29
DK425787D0 (da)	1987-08-14
YU46560B (sh)	1993-11-16
US4816060A (en)	1989-03-28
YU151187A (en)	1989-04-30
ATE72727T1 (de)	1992-03-15
EG18433A (en)	1993-04-30
DK425787A (da)	1988-02-16
CS271478B2 (en)	1990-10-12
BG48203A3 (en)	1990-12-14
KR880002440A (ko)	1988-05-09
IL83461A (en)	1991-09-16
IE872176L (en)	1988-02-15
ES2037686T3 (es)	1993-07-01
IE61158B1 (en)	1994-10-05
DD261518A5 (de)	1988-11-02
GR3003891T3 (fr)	1993-03-16
AU597407B2 (en)	1990-05-31
BR8704215A (pt)	1988-04-12
SU1723994A3 (ru)	1992-03-30
HUT44892A (en)	1988-05-30
IN166550B (fr)	1990-06-02
HU200888B (en)	1990-09-28
AU7689287A (en)	1988-02-18
KR950006916B1 (ko)	1995-06-26
CA1297695C (fr)	1992-03-24
TR24598A (tr)	1991-12-06
JPS6372602A (ja)	1988-04-02
IL83461A0 (en)	1988-01-31
EP0256414B1 (fr)	1992-02-26

Legal Events

Date	Code	Title	Description
2009-11-23	PUP	Patent expired

Publication	Publication Date	Title
KR0120741B1 (ko)	1997-10-30	살균제
US6458748B1 (en)	2002-10-01	Di- or tri-fluoromethanesulfonyl anilide derivatives, process for the preparation of them and herbicides containing them as the active ingredient
KR950006151B1 (ko)	1995-06-09	살균제
KR100631307B1 (ko)	2006-10-04	피리미디닐벤즈이미다졸 및 트리아지닐벤즈이미다졸유도체및 농원예용 살균제
AU597407B2 (en)	1990-05-31	Herbicidal aqueous compositions of imidazolinone herbicides
KR950011415B1 (ko)	1995-10-04	살균제
KR890002044A (ko)	1989-04-07	2-페톡시 피리미딘 유도체 및 제초조성물
KR950702541A (ko)	1995-07-29	살충제 피리미딘 화합물(pesticidal pyrimidine compounds)
KR890005066A (ko)	1989-05-11	2-아닐리노 피리미딘 유도체
KR920014771A (ko)	1992-08-25	제초제
KR920014770A (ko)	1992-08-25	제초제
BR0013251B1 (pt)	2010-11-30	derivado de isoxazolina e herbicida que contém o mesmo como ingrediente ativo.
CS235308B2 (en)	1985-05-15	Fungicide and acaracide agent and method of efficient matters production
RU2013132601A (ru)	2015-01-27	6-(2-аминофенил)пиколинаты и их применение в качестве гербицидов
CN101875639A (zh)	2010-11-03	取代嘧啶醚类化合物及其应用
JP2002193710A (ja)	2002-07-10	ピリミジン又はトリアジン誘導体及び農園芸用殺菌剤
EP0694538A2 (fr)	1996-01-31	Dérivés de 2-benzyloxy-4-phénoxy pyrimidine, procédé pour leur préparation et compositions herbicides les contenant
JPH101478A (ja)	1998-01-06	インダゾールスルホニル尿素誘導体及び除草剤
JPS61103873A (ja)	1986-05-22	新規な２‐シアノベンズイミダゾール誘導体
EP1162962B1 (fr)	2004-12-01	Sulfone d'alkynyle aryle
KR900006809B1 (ko)	1990-09-21	피리미딘 유도체의 제조방법
EP0707001A1 (fr)	1996-04-17	Dérivés de benzyloxypyrimidine, procédé de préparation de ces composés et composition herbicide
KR960012180B1 (ko)	1996-09-16	신규 6-클로로-2-(4,6-디메톡시피리미딘-2-일)옥시벤조익산의 페닐이미노 에스테르 유도체 및 그의 제조방법
CA2368458A1 (fr)	2000-10-19	Uraciles de propynyle
AU2019345216A1 (en)	2021-04-15	Dicyclanil salt with dodecylbenzenesulfonate and use of such a salt in combating and controlling of parasites