CS209930B2 - Herbicide means - Google Patents

Herbicide means Download PDF

Info

Publication number: CS209930B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; compound; bifenox; mecoprop; range
Prior art date: 1978-07-15

Application number

CS794899A

Other languages

Czech (cs)

English (en)

Inventor

Jean M Beraud

James L Glasgow

George Skylakakis

Original Assignee

Lilly Industries 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.)

1978-07-15

Filing date

1979-07-12

Publication date

1981-12-31

1979-07-12 Application filed by Lilly Industries Ltd filed Critical Lilly Industries Ltd

1981-12-31 Publication of CS209930B2 publication Critical patent/CS209930B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims description 13
239000004009 herbicide Substances 0.000 title description 4
150000001875 compounds Chemical class 0.000 claims abstract description 46
235000013339 cereals Nutrition 0.000 claims abstract description 11
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims abstract description 9
239000000203 mixture Substances 0.000 claims description 37
150000002148 esters Chemical class 0.000 claims description 11
150000003839 salts Chemical class 0.000 claims description 10
239000004480 active ingredient Substances 0.000 claims description 9
239000007900 aqueous suspension Substances 0.000 claims description 7
239000007864 aqueous solution Substances 0.000 claims description 5
239000004563 wettable powder Substances 0.000 claims description 5
231100001184 nonphytotoxic Toxicity 0.000 claims description 4
241000196324 Embryophyta Species 0.000 abstract description 18
230000002195 synergetic effect Effects 0.000 abstract description 7
244000042664 Matricaria chamomilla Species 0.000 abstract description 6
235000007232 Matricaria chamomilla Nutrition 0.000 abstract description 5
235000017945 Matricaria Nutrition 0.000 abstract description 4
239000005484 Bifenox Substances 0.000 description 32
SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 description 32
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 21
-1 alkali metal salts Chemical class 0.000 description 20
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
238000000034 method Methods 0.000 description 10
239000002253 acid Substances 0.000 description 8
239000004094 surface-active agent Substances 0.000 description 8
239000012141 concentrate Substances 0.000 description 7
241000209140 Triticum Species 0.000 description 6
235000021307 Triticum Nutrition 0.000 description 6
239000011734 sodium Substances 0.000 description 6
230000001629 suppression Effects 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
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 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical group CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
240000005979 Hordeum vulgare Species 0.000 description 4
235000007340 Hordeum vulgare Nutrition 0.000 description 4
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
239000002904 solvent Substances 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
240000005702 Galium aparine Species 0.000 description 3
235000014820 Galium aparine Nutrition 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000003755 preservative agent Substances 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
239000005574 MCPA Substances 0.000 description 2
239000005575 MCPB Substances 0.000 description 2
101150039283 MCPB gene Proteins 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 2
240000005592 Veronica officinalis Species 0.000 description 2
241000990144 Veronica persica Species 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 2
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
229920005610 lignin Polymers 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
235000019333 sodium laurylsulphate Nutrition 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
LYCAIKOWRPUZTN-NMQOAUCRSA-N 1,2-dideuteriooxyethane Chemical compound [2H]OCCO[2H] LYCAIKOWRPUZTN-NMQOAUCRSA-N 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical class OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
UGDWWCJKEUBONY-UHFFFAOYSA-N 6-chloro-6-methylcyclohexa-1,3-dien-1-ol Chemical compound CC1(Cl)CC=CC=C1O UGDWWCJKEUBONY-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241000208479 Anagallis arvensis Species 0.000 description 1
240000000662 Anethum graveolens Species 0.000 description 1
235000007227 Anethum graveolens Nutrition 0.000 description 1
235000017311 Anethum sowa Nutrition 0.000 description 1
235000007319 Avena orientalis Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 1
229920000896 Ethulose Polymers 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
244000182930 Matricaria sp Species 0.000 description 1
235000008885 Matricaria sp Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
240000004674 Papaver rhoeas Species 0.000 description 1
235000007846 Papaver rhoeas Nutrition 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
244000286177 Raphanus raphanistrum Species 0.000 description 1
235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
235000021501 Rumex crispus Nutrition 0.000 description 1
244000207667 Rumex vesicarius Species 0.000 description 1
235000007238 Secale cereale Nutrition 0.000 description 1
244000082988 Secale cereale Species 0.000 description 1
241000219289 Silene Species 0.000 description 1
244000111146 Sonchus arvensis Species 0.000 description 1
235000006731 Sonchus arvensis Nutrition 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
241001166549 Veronica hederifolia Species 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
239000001264 anethum graveolens Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000007798 antifreeze agent Substances 0.000 description 1
239000010692 aromatic oil Substances 0.000 description 1
ZXVOCOLRQJZVBW-UHFFFAOYSA-N azane;ethanol Chemical compound N.CCO ZXVOCOLRQJZVBW-UHFFFAOYSA-N 0.000 description 1
150000001555 benzenes Chemical group 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000004720 fertilization Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000003349 gelling agent Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000005764 inhibitory process Effects 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
235000019357 lignosulphonate Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 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
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
VSXGXPNADZQTGQ-UHFFFAOYSA-N oxirane;phenol Chemical class C1CO1.OC1=CC=CC=C1 VSXGXPNADZQTGQ-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
PDTFCHSETJBPTR-UHFFFAOYSA-N phenylmercuric nitrate Chemical compound [O-][N+](=O)O[Hg]C1=CC=CC=C1 PDTFCHSETJBPTR-UHFFFAOYSA-N 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
230000002265 prevention Effects 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
238000005245 sintering Methods 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof

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)

CS794899A 1978-07-15 1979-07-12 Herbicide means CS209930B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB7829989A GB2027344A (en)	1978-07-15	1978-07-15	Herbicidal formulation

Publications (1)

Publication Number	Publication Date
CS209930B2 true CS209930B2 (en)	1981-12-31

Family

ID=10498452

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS794899A CS209930B2 (en)	1978-07-15	1979-07-12	Herbicide means

Country Status (6)

Country	Link
JP (1)	JPS5515483A (fr)
BE (1)	BE877675A (fr)
CA (1)	CA1129664A (fr)
CS (1)	CS209930B2 (fr)
GB (2)	GB2027344A (fr)
ZA (1)	ZA793515B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0231657Y2 (fr) *	1986-10-15	1990-08-27

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5635164B2 (fr) *	1973-11-28	1981-08-15
JPS50125030A (fr) *	1974-03-23	1975-10-01

1978
- 1978-07-15 GB GB7829989A patent/GB2027344A/en not_active Withdrawn
1979
- 1979-07-11 GB GB7924150A patent/GB2031279B/en not_active Expired
- 1979-07-12 ZA ZA00793515A patent/ZA793515B/xx unknown
- 1979-07-12 CS CS794899A patent/CS209930B2/cs unknown
- 1979-07-12 BE BE6/46892A patent/BE877675A/fr not_active IP Right Cessation
- 1979-07-13 CA CA331,753A patent/CA1129664A/fr not_active Expired
- 1979-07-13 JP JP8920679A patent/JPS5515483A/ja active Pending

Also Published As

Publication number	Publication date
BE877675A (fr)	1980-01-14
GB2031279B (en)	1983-02-16
CA1129664A (fr)	1982-08-17
JPS5515483A (en)	1980-02-02
GB2031279A (en)	1980-04-23
GB2027344A (en)	1980-02-20
ZA793515B (en)	1981-02-25

Publication	Publication Date	Title
US6090750A (en)	2000-07-18	Herbicidal combinations
CZ227897A3 (en)	1997-10-15	Synergetic herbicidal agents based on gluphosinate and nitrodiphenyl ethers as well as process for preparing thereof
US6274535B1 (en)	2001-08-14	Defoliant
KR100738764B1 (ko)	2007-07-12	인 함유 엽 제초제, 이미다졸리논 및 호르몬 제초제를 포함하는 상승작용 제초 조성물
KR100195565B1 (ko)	1999-06-15	제초 조성물
CA1129665A (fr)	1982-08-17	Methode de destruction des mauvaises herbes dans les champs cerealiers et preparation herbicide a cette fin
CS209930B2 (en)	1981-12-31	Herbicide means
CN100388885C (zh)	2008-05-21	用于稻田的除草组合物
AU594853B2 (en)	1990-03-15	Herbicidal composition
FI62204B (fi)	1982-08-31	Foerfarande foer bekaempning av ograes pao vaextplatsen av saedesvaexter och vid foerfarandet anvaendbar herbicidkomposition
RU2035141C1 (ru)	1995-05-20	Гербицидная композиция и способ уничтожения сорняков
CA1308928C (fr)	1992-10-20	Composition herbicide
AU2024231139A1 (en)	2025-07-17	Herbicidal compositions comprising fluazifop and triclopyr
US4755214A (en)	1988-07-05	Composition for regulating plant growth
HU206593B (en)	1992-12-28	Synergetic herbicide compositions containing phenoxy- and imidazolinyl groups-containing benzoic acid derivatives and process for extirpating weeds with the composition
CS268692B2 (en)	1990-04-11	Synergetc herbicide
JPS58154503A (ja)	1983-09-14	選択的ビ−ト除草剤
MXPA97001836A (en)	1999-10-14	Herbici combinations
JPH11302112A (ja)	1999-11-02	植物生長調節剤組成物
JPS6141490B2 (fr)	1986-09-16
JPH07233005A (ja)	1995-09-05	除草剤組成物
JPH09175914A (ja)	1997-07-08	除草剤組成物
JPS5993006A (ja)	1984-05-29	除草組成物
JPH0637370B2 (ja)	1994-05-18	除草剤組成物
JPS63190803A (ja)	1988-08-08	除草組成物