CA1151890A - Methode pour inhiber la croissance des tiges de tournesol ou de coton - Google Patents

Methode pour inhiber la croissance des tiges de tournesol ou de coton

Info

Publication number: CA1151890A
Authority: CA; Canada
Prior art keywords: plants; hydrogen; sulfate; lll; compound
Prior art date: 1980-02-19
Legal status (The legal status 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 status listed.): Expired

Application number

CA000369468A

Other languages

English (en)

Inventor

Prithvi R. Bhalla

Neal E. Shafer

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Wyeth Holdings LLC

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.)

1980-02-19

Filing date

1981-01-28

Publication date

1983-08-16

1981-01-28 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1983-08-16 Application granted granted Critical

1983-08-16 Publication of CA1151890A publication Critical patent/CA1151890A/fr

Status Expired legal-status Critical Current

Links

235000003222 Helianthus annuus Nutrition 0.000 title claims abstract description 29
241000208818 Helianthus Species 0.000 title claims abstract description 25
238000000034 method Methods 0.000 title claims abstract description 18
229920000742 Cotton Polymers 0.000 title 1
241000196324 Embryophyta Species 0.000 claims abstract description 50
239000002689 soil Substances 0.000 claims abstract description 11
150000001875 compounds Chemical class 0.000 claims description 35
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
-1 alkylbenzene sulfonate Chemical class 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
229910052736 halogen Inorganic materials 0.000 claims description 8
150000002367 halogens Chemical class 0.000 claims description 8
XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 claims description 7
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
229910002651 NO3 Inorganic materials 0.000 claims description 4
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 4
229940077388 benzenesulfonate Drugs 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
230000001105 regulatory effect Effects 0.000 claims description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
230000012010 growth Effects 0.000 claims description 3
229910052740 iodine Inorganic materials 0.000 claims description 3
QSLPNSWXUQHVLP-UHFFFAOYSA-N $l^{1}-sulfanylmethane Chemical compound [S]C QSLPNSWXUQHVLP-UHFFFAOYSA-N 0.000 claims description 2
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 2
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
229910019142 PO4 Inorganic materials 0.000 claims description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 claims description 2
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 claims description 2
229940043264 dodecyl sulfate Drugs 0.000 claims description 2
QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical group C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
125000000262 haloalkenyl group Chemical group 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
239000010452 phosphate Substances 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
150000002431 hydrogen Chemical group 0.000 claims 5
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 2
125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 claims 1
150000005224 alkoxybenzenes Chemical class 0.000 claims 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
KEQTWHPMSVAFDA-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole Chemical class C1NNC=C1 KEQTWHPMSVAFDA-UHFFFAOYSA-N 0.000 abstract description 2
WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical class C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 abstract description 2
USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical class C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 abstract description 2
150000003839 salts Chemical class 0.000 abstract description 2
238000004904 shortening Methods 0.000 abstract 1
238000011282 treatment Methods 0.000 description 14
238000011156 evaluation Methods 0.000 description 13
235000013350 formula milk Nutrition 0.000 description 12
230000009467 reduction Effects 0.000 description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
241000131317 Capitulum Species 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
238000003306 harvesting Methods 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
239000012141 concentrate Substances 0.000 description 5
235000008504 concentrate Nutrition 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000203 mixture Substances 0.000 description 5
244000020551 Helianthus annuus Species 0.000 description 4
239000000243 solution Substances 0.000 description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
239000007921 spray Substances 0.000 description 3
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
230000009418 agronomic effect Effects 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
150000007942 carboxylates Chemical class 0.000 description 2
230000008859 change Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 2
LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
JARFAUHJHIUGCO-UHFFFAOYSA-N 1,2-dimethyl-3,5-diphenyl-3h-pyrazole Chemical compound CN1N(C)C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 JARFAUHJHIUGCO-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
MTCKPMRMUZIKPU-UHFFFAOYSA-N 3,5-diphenyl-1h-pyrazol-2-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C1=C(C=2C=CC=CC=2)N[NH+]=C1C1=CC=CC=C1 MTCKPMRMUZIKPU-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
101000657326 Homo sapiens Protein TANC2 Proteins 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
241000218922 Magnoliophyta Species 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
RRCYYLHJWRYWEI-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOOOOO RRCYYLHJWRYWEI-UHFFFAOYSA-N 0.000 description 1
241001503951 Phoma Species 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
102100034784 Protein TANC2 Human genes 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
230000008901 benefit Effects 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
230000008512 biological response Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000012677 causal agent Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
JCYWCSGERIELPG-UHFFFAOYSA-N imes Chemical class CC1=CC(C)=CC(C)=C1N1C=CN(C=2C(=CC(C)=CC=2C)C)[C]1 JCYWCSGERIELPG-UHFFFAOYSA-N 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000005082 stem growth Effects 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000012085 test solution Substances 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
General Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pretreatment Of Seeds And Plants (AREA)
Saccharide Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

CA000369468A 1980-02-19 1981-01-28 Methode pour inhiber la croissance des tiges de tournesol ou de coton Expired CA1151890A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US12264280A	1980-02-19	1980-02-19
US122,642		1980-02-19

Publications (1)

Publication Number	Publication Date
CA1151890A true CA1151890A (fr)	1983-08-16

Family

ID=22403930

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000369468A Expired CA1151890A (fr)	1980-02-19	1981-01-28	Methode pour inhiber la croissance des tiges de tournesol ou de coton

Country Status (7)

Country	Link
AR (1)	AR229840A1 (fr)
AU (1)	AU6740981A (fr)
BR (1)	BR8100964A (fr)
CA (1)	CA1151890A (fr)
ES (1)	ES499545A0 (fr)
FR (1)	FR2475853A1 (fr)
ZA (1)	ZA811086B (fr)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE795534A (fr) *	1972-02-18	1973-08-16	Basf Ag	Agents pour la regulation de la croissance des plantes, contenant comme principe actif un sel azote
IN141872B (fr) *	1974-07-01	1977-04-30	American Cyanamid Co
DE2523144A1 (de) *	1975-05-24	1976-12-09	Bayer Ag	Mittel zur regulierung des pflanzenwachstums

1981
- 1981-01-28 CA CA000369468A patent/CA1151890A/fr not_active Expired
- 1981-02-18 FR FR8103167A patent/FR2475853A1/fr active Pending
- 1981-02-18 AR AR284343A patent/AR229840A1/es active
- 1981-02-18 BR BR8100964A patent/BR8100964A/pt unknown
- 1981-02-18 ZA ZA00811086A patent/ZA811086B/xx unknown
- 1981-02-18 AU AU67409/81A patent/AU6740981A/en not_active Abandoned
- 1981-02-18 ES ES499545A patent/ES499545A0/es active Granted

Also Published As

Publication number	Publication date
FR2475853A1 (fr)	1981-08-21
AR229840A1 (es)	1983-12-30
ZA811086B (en)	1982-03-31
BR8100964A (pt)	1981-08-25
ES8207146A1 (es)	1982-09-01
AU6740981A (en)	1981-08-27
ES499545A0 (es)	1982-09-01

Legal Events

Date	Code	Title	Description
2000-08-16	MKEX	Expiry

Publication	Publication Date	Title
SU967257A3 (ru)	1982-10-15	Гербицидный состав
JP4578506B2 (ja)	2010-11-10	植物の成長を調節するためのｎ−アリールピラゾール又はｎ−ヘテロアリールピラゾール化合物の使用
JPH01135702A (ja)	1989-05-29	多置換酪酸類、それらのエステル類および誘導体類を使用する植物の生長を調節する方法
EP0466353B1 (fr)	1995-08-30	Composition pour inhiber la floraison des plantes et pour prolonger la durée de la floraison
CA1151890A (fr)	1983-08-16	Methode pour inhiber la croissance des tiges de tournesol ou de coton
JP2832482B2 (ja)	1998-12-09	殺虫殺菌剤組成物
JPS61200968A (ja)	1986-09-05	複素環式化合物、その製造方法およびこれを含有する、殺菌または植物生長調整剤組成物
US3989502A (en)	1976-11-02	Method for controlling growth of tobacco suckers
JPH0242067A (ja)	1990-02-13	ピリミジン誘導体、その製造法、及びそれの用途
JPS62249978A (ja)	1987-10-30	トリアゾール化合物、その製造法及びそれを含有する植物生長調節組成物
JP3176418B2 (ja)	2001-06-18	農園芸用殺菌剤
CS268195B2 (en)	1990-03-14	Plant growth regulator
KR0168853B1 (ko)	1999-01-15	살진균 및 살충 조성물
US5585329A (en)	1996-12-17	Plant growth promotion using 3-cyano-1-phenylpyrazoles such as fipronil
JP3560620B2 (ja)	2004-09-02	農園芸用殺菌剤組成物
KR100314196B1 (ko)	2002-11-23	농원예용살진균제조성물
JPH0328401B2 (fr)	1991-04-19
JP4994619B2 (ja)	2012-08-08	植物用矮化剤および植物の矮化方法
JPH04275201A (ja)	1992-09-30	除草剤組成物
EP1304037A1 (fr)	2003-04-23	Regulateurs de floraison
JP3195109B2 (ja)	2001-08-06	農園芸用殺菌剤組成物
JPH01207211A (ja)	1989-08-21	除草剤組成物
JPH0314802B2 (fr)	1991-02-27
JPS6348843B2 (fr)	1988-09-30
JPS61176503A (ja)	1986-08-08	芝生用除草剤組成物