ZA200205588B - Defoliation and minimization of plant regrowth following defoliation. - Google Patents

Defoliation and minimization of plant regrowth following defoliation. Download PDF

Info

Publication number: ZA200205588B
Authority: ZA; South Africa
Prior art keywords: plant; locus; ethephon; amount; composition
Prior art date: 1999-12-15

Application number

ZA200205588A

Other languages

English (en)

Inventor

John R Evans

Richard R Evans

Anita L Harrell

David L King

Wallace W Stewart

Original Assignee

Basf Corp

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.)

1999-12-15

Filing date

2002-07-12

Publication date

2003-10-07

2002-07-12 Application filed by Basf Corp filed Critical Basf Corp

2003-10-07 Publication of ZA200205588B publication Critical patent/ZA200205588B/en

Links

230000035613 defoliation Effects 0.000 title claims description 28
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical group OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 71
IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical group N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims description 58
239000005976 Ethephon Substances 0.000 claims description 54
241000196324 Embryophyta Species 0.000 claims description 38
239000003795 chemical substances by application Substances 0.000 claims description 23
230000004044 response Effects 0.000 claims description 22
239000000203 mixture Substances 0.000 claims description 20
238000000034 method Methods 0.000 claims description 18
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 13
239000005977 Ethylene Substances 0.000 claims description 13
244000046052 Phaseolus vulgaris Species 0.000 claims description 12
244000038559 crop plants Species 0.000 claims description 11
150000007659 semicarbazones Chemical group 0.000 claims description 11
230000001939 inductive effect Effects 0.000 claims description 10
239000003112 inhibitor Substances 0.000 claims description 9
229930192334 Auxin Natural products 0.000 claims description 8
239000002363 auxin Substances 0.000 claims description 8
SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims description 8
229920000742 Cotton Polymers 0.000 claims description 7
150000003007 phosphonic acid derivatives Chemical class 0.000 claims description 4
244000061456 Solanum tuberosum Species 0.000 claims description 3
244000299507 Gossypium hirsutum Species 0.000 claims description 2
LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims 4
108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims 2
102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
229920000136 polysorbate Polymers 0.000 claims 1
-1 semicarbazone compound Chemical class 0.000 description 25
238000011282 treatment Methods 0.000 description 13
239000002253 acid Substances 0.000 description 12
240000002024 Gossypium herbaceum Species 0.000 description 11
235000004341 Gossypium herbaceum Nutrition 0.000 description 11
239000004480 active ingredient Substances 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
229940093470 ethylene Drugs 0.000 description 8
HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
241000219146 Gossypium Species 0.000 description 5
230000012010 growth Effects 0.000 description 5
125000000623 heterocyclic group Chemical group 0.000 description 5
235000021332 kidney beans Nutrition 0.000 description 5
239000002671 adjuvant Substances 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 description 4
238000003306 harvesting Methods 0.000 description 4
125000003107 substituted aryl group Chemical group 0.000 description 4
UDBZUFZWXJJBAL-UHFFFAOYSA-N 4-chloro-5-methylpyrimidin-2-amine Chemical compound CC1=CN=C(N)N=C1Cl UDBZUFZWXJJBAL-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000835 fiber Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000007921 spray Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000001345 alkine derivatives Chemical class 0.000 description 2
230000008901 benefit Effects 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000036253 epinasty Effects 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
230000006872 improvement Effects 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
125000000547 substituted alkyl group Chemical group 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
ZFFPZOJIBMKDGH-UHFFFAOYSA-N 2-chloropropylphosphonic acid Chemical compound CC(Cl)CP(O)(O)=O ZFFPZOJIBMKDGH-UHFFFAOYSA-N 0.000 description 1
ZHNLTTJSGOZSMN-UHFFFAOYSA-N 2-fluoroethylphosphonic acid Chemical compound OP(O)(=O)CCF ZHNLTTJSGOZSMN-UHFFFAOYSA-N 0.000 description 1
NGADBMHGWDBFSS-UHFFFAOYSA-N 2-iodoethylphosphonic acid Chemical compound OP(O)(=O)CCI NGADBMHGWDBFSS-UHFFFAOYSA-N 0.000 description 1
125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 description 1
241000208140 Acer Species 0.000 description 1
235000009432 Gossypium hirsutum Nutrition 0.000 description 1
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 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
239000002837 defoliant Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
125000004969 haloethyl group Chemical group 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
210000003734 kidney Anatomy 0.000 description 1
229910003002 lithium salt Inorganic materials 0.000 description 1
159000000002 lithium salts Chemical class 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
YCIMNLLNPGFGHC-UHFFFAOYSA-N o-dihydroxy-benzene Natural products OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
125000000913 palmityl 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])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
239000000575 pesticide Substances 0.000 description 1
125000004437 phosphorous atom Chemical group 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000008569 process Effects 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000010076 replication Effects 0.000 description 1
DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
125000002889 tridecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000080 wetting agent 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
- 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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action

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)

ZA200205588A 1999-12-15 2002-07-12 Defoliation and minimization of plant regrowth following defoliation. ZA200205588B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US09/461,383 US6562758B1 (en)	1999-12-15	1999-12-15	Methods and compositions to defoliate crop plants and minimize plant regrowth following defoliation

Publications (1)

Publication Number	Publication Date
ZA200205588B true ZA200205588B (en)	2003-10-07

Family

ID=23832338

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200205588A ZA200205588B (en)	1999-12-15	2002-07-12	Defoliation and minimization of plant regrowth following defoliation.

Country Status (21)

Country	Link
US (1)	US6562758B1 (zh)
EP (1)	EP1237413B1 (zh)
JP (1)	JP2003517478A (zh)
KR (1)	KR100729326B1 (zh)
CN (1)	CN1225171C (zh)
AR (1)	AR026981A1 (zh)
AT (1)	ATE262792T1 (zh)
AU (1)	AU782800B2 (zh)
BR (1)	BR0016451B1 (zh)
CA (1)	CA2394238A1 (zh)
DE (1)	DE60009550D1 (zh)
EA (1)	EA006390B1 (zh)
ES (1)	ES2218262T3 (zh)
IL (2)	IL149773A0 (zh)
MX (1)	MXPA02005550A (zh)
NZ (1)	NZ519212A (zh)
PL (1)	PL357156A1 (zh)
TR (2)	TR200401643T4 (zh)
UA (1)	UA72950C2 (zh)
WO (1)	WO2001043552A2 (zh)
ZA (1)	ZA200205588B (zh)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2004006672A1 (en) *	2002-07-12	2004-01-22	Kristian Madsen	A method of removing phylloclades from phyllocacti
WO2007092184A2 (en) *	2006-02-02	2007-08-16	E. I. Du Pont De Nemours And Company	Method for improving harvestability of crops
SI2109641T1 (sl) *	2007-01-17	2017-08-31	Agrofresh Inc.	Dobava etilen blokirnega in promocijskega sedstva
KR101400969B1 (ko) *	2012-08-28	2014-05-29	강원대학교산학협력단	에테폰 또는 에틸렌을 이용한 가공용 감자의 저장 방법
ES2711980B2 (es)	2016-02-19	2021-02-09	Hazel Tech Inc	Composiciones para la liberación controlada de ingredientes activos y métodos de preparación de las mismas
US20200396993A1 (en)	2017-12-27	2020-12-24	Hazel Technologies, Inc.	Compositions and methods for release of cyclopropenes
CN109042727A (zh) *	2018-08-20	2018-12-21	福建农林大学	一种非农药药剂及其在榕树叶面病害虫防治上的应用

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US588931A (en) *		1897-08-24		Sachusetts
US4374661A (en)	1967-12-27	1983-02-22	Union Carbide Corporation	Growth regulation process
US4401454A (en)	1969-10-24	1983-08-30	Union Carbide Corporation	Growth regulation methods
US3879188A (en)	1969-10-24	1975-04-22	Amchem Prod	Growth regulation process
US4240819A (en)	1972-01-28	1980-12-23	Union Carbide Agricultural Products, Inc.	Method for the inhibition of plant growth
US4352869A (en)	1980-12-24	1982-10-05	Union Carbide Corporation	Solid state electrolytes
DE3222622A1 (de)	1982-06-11	1983-12-15	Schering AG, 1000 Berlin und 4709 Bergkamen	Mittel zur entblaetterung von pflanzen mit synergistischer wirkung
US5098466A (en) *	1985-08-20	1992-03-24	Sandoz Ltd.	Compounds
US5098462A (en)	1985-08-20	1992-03-24	Sandoz Ltd.	Substituted semi-carbazones and related compounds
US4840660A (en) *	1985-12-30	1989-06-20	Rhone Poulenc Nederlands B.V.	Plant growth regulator dispersions
US5123951A (en)	1986-03-31	1992-06-23	Rhone-Poulenc Nederland B.V.	Synergistic plant growth regulator compositions
DE3643657A1 (de)	1986-12-18	1988-06-30	Schering Ag	Mittel zur entblaetterung von pflanzen
DE3724399A1 (de)	1987-07-23	1989-02-02	Basf Ag	Phenylalkenylcarbonsaeuren und deren ester
US5665673A (en)	1988-12-29	1997-09-09	Anderson; Richard J.	Potentiating herbicidal compositions
US4960275A (en)	1989-11-06	1990-10-02	Imrych Magon	Water immersion amusement apparatus
DE19911165B4 (de) *	1999-03-12	2008-03-13	Bayer Cropscience Ag	Entlaubungsmittel

1999
- 1999-12-15 US US09/461,383 patent/US6562758B1/en not_active Expired - Lifetime
2000
- 2000-12-05 ES ES00985133T patent/ES2218262T3/es not_active Expired - Lifetime
- 2000-12-05 KR KR1020027007623A patent/KR100729326B1/ko not_active IP Right Cessation
- 2000-12-05 CA CA002394238A patent/CA2394238A1/en not_active Abandoned
- 2000-12-05 BR BRPI0016451-8A patent/BR0016451B1/pt not_active IP Right Cessation
- 2000-12-05 AU AU21650/01A patent/AU782800B2/en not_active Ceased
- 2000-12-05 WO PCT/EP2000/012202 patent/WO2001043552A2/en active Search and Examination
- 2000-12-05 JP JP2001544501A patent/JP2003517478A/ja active Pending
- 2000-12-05 AT AT00985133T patent/ATE262792T1/de not_active IP Right Cessation
- 2000-12-05 PL PL00357156A patent/PL357156A1/xx not_active Application Discontinuation
- 2000-12-05 TR TR2004/01643T patent/TR200401643T4/xx unknown
- 2000-12-05 NZ NZ519212A patent/NZ519212A/en unknown
- 2000-12-05 MX MXPA02005550A patent/MXPA02005550A/es active IP Right Grant
- 2000-12-05 EP EP00985133A patent/EP1237413B1/en not_active Expired - Lifetime
- 2000-12-05 TR TR2004/00727T patent/TR200400727T4/xx unknown
- 2000-12-05 CN CNB008171785A patent/CN1225171C/zh not_active Expired - Fee Related
- 2000-12-05 EA EA200200679A patent/EA006390B1/ru not_active IP Right Cessation
- 2000-12-05 UA UA2002075746A patent/UA72950C2/uk unknown
- 2000-12-05 IL IL14977300A patent/IL149773A0/xx active IP Right Grant
- 2000-12-05 DE DE60009550T patent/DE60009550D1/de not_active Expired - Lifetime
- 2000-12-15 AR ARP000106691A patent/AR026981A1/es active IP Right Grant
2002
- 2002-05-21 IL IL149773A patent/IL149773A/en not_active IP Right Cessation
- 2002-07-12 ZA ZA200205588A patent/ZA200205588B/en unknown

Also Published As

Publication number	Publication date
AR026981A1 (es)	2003-03-05
TR200401643T4 (tr)	2004-08-23
EA006390B1 (ru)	2005-12-29
ES2218262T3 (es)	2004-11-16
EP1237413B1 (en)	2004-03-31
EA200200679A1 (ru)	2003-02-27
NZ519212A (en)	2005-01-28
TR200400727T4 (tr)	2004-06-21
WO2001043552A3 (en)	2001-11-15
DE60009550D1 (de)	2004-05-06
WO2001043552A2 (en)	2001-06-21
CN1409599A (zh)	2003-04-09
AU782800B2 (en)	2005-09-01
IL149773A (en)	2007-05-15
UA72950C2 (uk)	2005-05-16
US6562758B1 (en)	2003-05-13
BR0016451B1 (pt)	2013-02-19
BR0016451A (pt)	2002-09-10
PL357156A1 (en)	2004-07-12
AU2165001A (en)	2001-06-25
IL149773A0 (en)	2002-11-10
KR100729326B1 (ko)	2007-06-15
ATE262792T1 (de)	2004-04-15
EP1237413A2 (en)	2002-09-11
KR20020065907A (ko)	2002-08-14
CA2394238A1 (en)	2001-06-21
CN1225171C (zh)	2005-11-02
JP2003517478A (ja)	2003-05-27
MXPA02005550A (es)	2002-10-23

Publication	Publication Date	Title
AU782800B2 (en)	2005-09-01	Methods and compositions to defoliate crop plants and minimize plant regrowth following defoliation
US8906828B2 (en)	2014-12-09	Compositions and methods for post emergent weed control with clethodim and gibberellic acid
AU2013337723B2 (en)	2017-07-06	Compositions and methods for post emergent weed control with dim herbicides and gibberellic acid
DE2362333C3 (de)	1978-07-13	Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben
US4932995A (en)	1990-06-12	Process for increasing rice crop yield
US6022830A (en)	2000-02-08	Crop harvesting method using a benzyloxphenyl uracil
US11839211B2 (en)	2023-12-12	Clethodim compositions and methods of use thereof
US5270287A (en)	1993-12-14	Method for defoliating and desiccating cotton
DE3018289A1 (de)	1980-11-27	N-alkinylanilide
DE102004017981A1 (de)	2005-11-03	Fungizide Wirkstoffkombinationen
AU643238B2 (en)	1993-11-11	Method for defoliating and desiccating cotton
US20030158041A1 (en)	2003-08-21	Methods of and compositions for plant defoliation
Guthrie	1951	Control of the Corn Earworm Amd Corn Leaf Aphid on Bagged Sorghum Heads
JPH0564922B2 (zh)	1993-09-16
GB2064960A (en)	1981-06-24	Fungicidal composition
JPS58144308A (ja)	1983-08-27	殺虫・殺ダニ組成物
DD262790A1 (de)	1988-12-14	Akarizide mittel
WO2000004774A1 (en)	2000-02-03	Crop harvesting method using a benzyloxyphenyl uracil
CH658243A5 (de)	1986-10-31	Dinitrophenole, verfahren zu ihrer herstellung und diese verbindungen enthaltende pflanzenschutzkompositionen.