CS268185B2 - Herbicide - Google Patents

Herbicide Download PDF

Info

Publication number: CS268185B2
Authority: CS; Czechoslovakia
Prior art keywords: diflufenican; compositions; herbicide; weed; weeds
Prior art date: 1986-07-21

Application number

CS875485A

Other languages

Czech (cs)

English (en)

Other versions

CS548587A2 (en

Inventor

Richard H Hewett

Brian M Luscombe

Original Assignee

May & Baker Ltd

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.)

1986-07-21

Filing date

1987-07-20

Publication date

1990-03-14

1987-07-20 Application filed by May & Baker Ltd filed Critical May & Baker Ltd

1989-04-14 Publication of CS548587A2 publication Critical patent/CS548587A2/cs

1990-03-14 Publication of CS268185B2 publication Critical patent/CS268185B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 56
239000004009 herbicide Substances 0.000 title claims abstract description 41
239000000203 mixture Substances 0.000 claims description 47
VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 claims description 31
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WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 abstract description 60
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244000111146 Sonchus arvensis Species 0.000 description 1
240000002439 Sorghum halepense Species 0.000 description 1
239000005625 Tri-allate Substances 0.000 description 1
MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 description 1
241001166549 Veronica hederifolia Species 0.000 description 1
241000219873 Vicia Species 0.000 description 1
244000105017 Vicia sativa Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 description 1
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000010775 animal oil Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000002152 aqueous-organic solution Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
230000002146 bilateral effect Effects 0.000 description 1
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
229960005286 carbaryl Drugs 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000007799 cork Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
229960005424 cypermethrin Drugs 0.000 description 1
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 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
239000012669 liquid formulation Substances 0.000 description 1
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
239000011859 microparticle Substances 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
VHLJOTFFKVPIAA-UHFFFAOYSA-N n-phenyl-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide Chemical compound FC(F)(F)C1=CC=CC(OC=2C(=CC=CN=2)C(=O)NC=2C=CC=CC=2)=C1 VHLJOTFFKVPIAA-UHFFFAOYSA-N 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
125000001400 nonyl 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])[H] 0.000 description 1
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000007170 pathology Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
238000011160 research Methods 0.000 description 1
238000012552 review Methods 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
JDVPQXZIJDEHAN-UHFFFAOYSA-N succinamic acid Chemical compound NC(=O)CCC(O)=O JDVPQXZIJDEHAN-UHFFFAOYSA-N 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
230000008961 swelling Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000012360 testing method Methods 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
125000005209 triethanolammonium group Chemical class 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

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)

CS875485A 1986-07-21 1987-07-20 Herbicide CS268185B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB868617740A GB8617740D0 (en)	1986-07-21	1986-07-21	Compositions of matter

Publications (2)

Publication Number	Publication Date
CS548587A2 CS548587A2 (en)	1989-04-14
CS268185B2 true CS268185B2 (en)	1990-03-14

Family

ID=10601421

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS875485A CS268185B2 (en)	1986-07-21	1987-07-20	Herbicide

Country Status (25)

Country	Link
US (1)	US4875925A (fr)
EP (1)	EP0257771B1 (fr)
JP (1)	JP2655648B2 (fr)
AR (1)	AR243725A1 (fr)
AT (1)	ATE103138T1 (fr)
AU (1)	AU604487B2 (fr)
BG (1)	BG60241B1 (fr)
BR (1)	BR8703764A (fr)
CA (1)	CA1300914C (fr)
CS (1)	CS268185B2 (fr)
DD (1)	DD266020A5 (fr)
DE (1)	DE3789410T2 (fr)
DK (1)	DK174200B1 (fr)
ES (1)	ES2052566T3 (fr)
FI (1)	FI91822C (fr)
GB (1)	GB8617740D0 (fr)
HU (1)	HU201446B (fr)
IE (1)	IE63868B1 (fr)
IL (1)	IL83196A (fr)
NZ (1)	NZ221108A (fr)
PL (1)	PL149888B1 (fr)
PT (1)	PT85376B (fr)
RU (1)	RU1836013C (fr)
TR (1)	TR23145A (fr)
ZA (1)	ZA875276B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5461027A (en) *	1989-01-24	1995-10-24	Griffin Corporation	Microencapsulated pendimethalin and method of making and using same
DE4223465A1 (de) *	1992-07-16	1994-01-20	Bayer Ag	Herbizide Mittel auf Basis von Heteroaryloxyacetamiden
CN1074646C (zh) *	1992-10-06	2001-11-14	国际壳牌研究有限公司	除草剂混合物
US6894003B2 (en) *	2000-06-23	2005-05-17	Basf Aktiengesellschaft	Enhancement of the activity of carotenoid biosynthesis inhibitor herbicides
DE10334300A1 (de) *	2003-07-28	2005-03-03	Bayer Cropscience Gmbh	Ölsuspensionskonzentrat
PT2198712T (pt) *	2004-12-17	2018-10-18	Syngenta Participations Ag	Composições herbicidas compreendendo prossulfocarbe
AU2006200731B2 (en) *	2005-03-31	2011-05-19	Sumitomo Chemical Company, Limited	Emulsifiable concentrate
CN101228869B (zh) *	2007-01-25	2011-03-09	浙江禾田化工有限公司	氟节胺和二甲戊乐灵烟草抑芽复配制剂
HUE029537T2 (en)	2009-12-17	2017-03-28	Bayer Ip Gmbh	Flufenacet based herbicide preparation
US8153556B2 (en) *	2009-12-18	2012-04-10	Dow Agrosciences Llc	Synergistic herbicidal compositions containing benfluralin
CN102599162A (zh) *	2011-12-20	2012-07-25	青岛瀚生生物科技股份有限公司	一种复合除草剂
AU2013363890B2 (en) *	2012-12-18	2017-03-30	Bayer Cropscience Ag	Herbicidal agents containing aclonifen
CN106259345A (zh) *	2016-08-08	2017-01-04	江苏辉丰农化股份有限公司	具有增效作用的除草组合物
CN109819987A (zh) *	2019-03-21	2019-05-31	河南瀚斯作物保护有限公司	一种含有吡氟酰草胺、二甲戊灵和乙氧氟草醚的除草组合物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3920742A (en) *	1971-08-25	1975-11-18	American Cyanamid Co	N-sec-alkyl-2,6-dinitro-3,4-xylidine herbicides
US4082537A (en) *	1977-03-23	1978-04-04	American Cyanamid Company	2,6-dinitroaniline herbicidal compositions
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
IL64220A (en) *	1980-11-21	1985-06-30	May & Baker Ltd	Nicotinamide derivatives,their preparation and their use as herbicides
GR861640B (en) *	1985-07-02	1986-10-24	May & Baker Ltd	Insecticide method by using diflufenican

1986
- 1986-07-21 GB GB868617740A patent/GB8617740D0/en active Pending
1987
- 1987-07-15 IL IL83196A patent/IL83196A/xx not_active IP Right Cessation
- 1987-07-17 ZA ZA875276A patent/ZA875276B/xx unknown
- 1987-07-17 TR TR496/87A patent/TR23145A/xx unknown
- 1987-07-17 AU AU75781/87A patent/AU604487B2/en not_active Ceased
- 1987-07-17 CA CA000542390A patent/CA1300914C/fr not_active Expired - Fee Related
- 1987-07-17 US US07/074,578 patent/US4875925A/en not_active Expired - Fee Related
- 1987-07-17 IE IE193687A patent/IE63868B1/en not_active IP Right Cessation
- 1987-07-17 ES ES87306356T patent/ES2052566T3/es not_active Expired - Lifetime
- 1987-07-17 NZ NZ221108A patent/NZ221108A/xx unknown
- 1987-07-17 AT AT87306356T patent/ATE103138T1/de not_active IP Right Cessation
- 1987-07-17 EP EP87306356A patent/EP0257771B1/fr not_active Expired - Lifetime
- 1987-07-17 DE DE3789410T patent/DE3789410T2/de not_active Expired - Lifetime
- 1987-07-20 CS CS875485A patent/CS268185B2/cs unknown
- 1987-07-20 DD DD86305158A patent/DD266020A5/de not_active IP Right Cessation
- 1987-07-20 BR BR8703764A patent/BR8703764A/pt not_active Application Discontinuation
- 1987-07-20 JP JP62180913A patent/JP2655648B2/ja not_active Expired - Lifetime
- 1987-07-20 DK DK198703771A patent/DK174200B1/da not_active IP Right Cessation
- 1987-07-20 HU HU873341A patent/HU201446B/hu not_active IP Right Cessation
- 1987-07-20 AR AR87308191A patent/AR243725A1/es active
- 1987-07-20 FI FI873191A patent/FI91822C/fi not_active IP Right Cessation
- 1987-07-20 RU SU874203029A patent/RU1836013C/ru active
- 1987-07-21 PT PT85376A patent/PT85376B/pt unknown
- 1987-07-21 BG BG080682A patent/BG60241B1/bg unknown
- 1987-07-21 PL PL1987266931A patent/PL149888B1/pl unknown

Also Published As

Publication number	Publication date
DK377187A (da)	1988-01-22
HU201446B (en)	1990-11-28
PL149888B1 (en)	1990-03-31
CS548587A2 (en)	1989-04-14
IL83196A (en)	1992-03-29
NZ221108A (en)	1989-08-29
FI873191A0 (fi)	1987-07-20
DD266020A5 (de)	1989-03-22
JP2655648B2 (ja)	1997-09-24
EP0257771A1 (fr)	1988-03-02
CA1300914C (fr)	1992-05-19
IE63868B1 (en)	1995-06-14
US4875925A (en)	1989-10-24
HUT47380A (en)	1989-03-28
BG60241B2 (en)	1994-03-24
AR243725A1 (es)	1993-09-30
DK377187D0 (da)	1987-07-20
PT85376A (fr)	1987-08-01
TR23145A (tr)	1989-04-17
RU1836013C (ru)	1993-08-23
AU604487B2 (en)	1990-12-20
DE3789410T2 (de)	1994-10-13
PT85376B (pt)	1990-04-30
FI873191L (fi)	1988-01-22
BG60241B1 (bg)	1994-03-24
ES2052566T3 (es)	1994-07-16
DE3789410D1 (de)	1994-04-28
AU7578187A (en)	1988-01-28
IL83196A0 (en)	1987-12-31
BR8703764A (pt)	1988-03-29
DK174200B1 (da)	2002-09-16
ATE103138T1 (de)	1994-04-15
FI91822C (fi)	1994-08-25
GB8617740D0 (en)	1986-08-28
FI91822B (fi)	1994-05-13
IE871936L (en)	1988-01-21
JPS6333306A (ja)	1988-02-13
ZA875276B (en)	1988-03-30
EP0257771B1 (fr)	1994-03-23
PL266931A1 (en)	1988-08-18

Publication	Publication Date	Title
CS268185B2 (en)	1990-03-14	Herbicide
CZ275892A3 (en)	1993-05-12	Herbicidal composition
DK170870B1 (da)	1996-02-26	Fremgangsmåde til bekæmpelse af ukrudt under anvendelse af bromoxynil eller ioxynil og diflufenican samt produkt og herbicidt præparat omfattende bromoxynil eller ioxynil og diflufenican
FI93600C (fi)	1995-05-10	Rikkakasvien torjuntamenetelmä, jossa käytetään diflufenikaania, ja herbisidikoostumus
US6660692B1 (en)	2003-12-09	Herbicidal compositions comprising picolinafen
JP2554501B2 (ja)	1996-11-13	ジフルフエニカンを使用する除草方法
FI83832B (fi)	1991-05-31	Foerfarande foer bekaempning av ograes genom anvaendning av diflufenican.
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