CA1123220A - Herbicidal compositions - Google Patents

Herbicidal compositions

Info

Publication number: CA1123220A
Authority: CA; Canada
Prior art keywords: formula; chlorine; herbicidal compositions; bromine; compound
Prior art date: 1977-12-14
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

CA317,863A

Other languages

English (en)

French (fr)

Inventor

Hans Schumacher

Konrad Albrecht

Peter Langeluddeke

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.)

Hoechst AG

Original Assignee

Hoechst AG

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.)

1977-12-14

Filing date

1978-12-13

Publication date

1982-05-11

1978-12-13 Application filed by Hoechst AG filed Critical Hoechst AG

1982-05-11 Application granted granted Critical

1982-05-11 Publication of CA1123220A publication Critical patent/CA1123220A/en

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 17
230000002363 herbicidal effect Effects 0.000 title claims abstract description 11
150000001875 compounds Chemical class 0.000 claims abstract description 20
241000196324 Embryophyta Species 0.000 claims abstract description 12
239000000460 chlorine Substances 0.000 claims abstract description 12
239000004480 active ingredient Substances 0.000 claims abstract description 9
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052794 bromium Chemical group 0.000 claims abstract description 8
229910052801 chlorine Inorganic materials 0.000 claims abstract description 8
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 8
235000013339 cereals Nutrition 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
125000001246 bromo group Chemical group Br* 0.000 claims abstract description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052783 alkali metal Inorganic materials 0.000 claims abstract description 3
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims abstract description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract 2
150000001340 alkali metals Chemical class 0.000 claims abstract 2
WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims description 4
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
239000011734 sodium Substances 0.000 claims description 2
159000000000 sodium salts Chemical class 0.000 claims description 2
229940074995 bromine Drugs 0.000 claims 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical class N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 1
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
238000000034 method Methods 0.000 claims 1
230000002195 synergetic effect Effects 0.000 abstract description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
230000000694 effects Effects 0.000 description 9
235000013350 formula milk Nutrition 0.000 description 8
-1 4-(4'-chlorophenoxy)-phenoxy Chemical group 0.000 description 7
230000006378 damage Effects 0.000 description 6
229920000151 polyglycol Polymers 0.000 description 5
239000010695 polyglycol Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
241001621841 Alopecurus myosuroides Species 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000004009 herbicide Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
235000007320 Avena fatua Nutrition 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
241000209504 Poaceae Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000013543 active substance Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
241000602336 Anthemis arvensis Species 0.000 description 2
244000022181 Atriplex patula Species 0.000 description 2
235000009066 Atriplex patula Nutrition 0.000 description 2
244000075850 Avena orientalis Species 0.000 description 2
FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
235000004443 Ricinus communis Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
235000005373 Uvularia sessilifolia Nutrition 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000000996 additive effect Effects 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
239000012876 carrier material Substances 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000005624 silicic acid group Chemical class 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 2
HJHVQCXHVMGZNC-JCJNLNMISA-M sodium;(2z)-2-[(3r,4s,5s,8s,9s,10s,11r,13r,14s,16s)-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12,13,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoate Chemical compound [Na+].O[C@@H]([C@@H]12)C[C@H]3\C(=C(/CCC=C(C)C)C([O-])=O)[C@@H](OC(C)=O)C[C@]3(C)[C@@]2(C)CC[C@@H]2[C@]1(C)CC[C@@H](O)[C@H]2C HJHVQCXHVMGZNC-JCJNLNMISA-M 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000002699 waste material Substances 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical class [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
244000192528 Chrysanthemum parthenium Species 0.000 description 1
240000005702 Galium aparine Species 0.000 description 1
235000014820 Galium aparine Nutrition 0.000 description 1
235000017945 Matricaria Nutrition 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
244000062793 Sorghum vulgare Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
125000003118 aryl group Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
244000038559 crop plants Species 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 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
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA317,863A 1977-12-14 1978-12-13 Herbicidal compositions Expired CA1123220A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DEP2755617.8		1977-12-14
DE19772755617 DE2755617A1 (de)	1977-12-14	1977-12-14	Herbizide mischungen

Publications (1)

Publication Number	Publication Date
CA1123220A true CA1123220A (en)	1982-05-11

Family

ID=6026062

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA317,863A Expired CA1123220A (en)	1977-12-14	1978-12-13	Herbicidal compositions

Country Status (21)

Country	Link
JP (1)	JPS5489023A (cs)
AT (1)	AT364192B (cs)
AU (1)	AU525418B2 (cs)
BE (1)	BE872765A (cs)
CA (1)	CA1123220A (cs)
CS (1)	CS203025B2 (cs)
DD (1)	DD157750A5 (cs)
DE (1)	DE2755617A1 (cs)
DK (1)	DK545078A (cs)
FR (1)	FR2411565A1 (cs)
GB (1)	GB2011787B (cs)
GR (1)	GR65232B (cs)
IL (1)	IL56195A0 (cs)
IT (1)	IT1101737B (cs)
NL (1)	NL7812145A (cs)
PL (1)	PL112150B1 (cs)
PT (1)	PT68909A (cs)
RO (1)	RO75105A (cs)
SE (1)	SE7812782L (cs)
SU (1)	SU884549A3 (cs)
ZA (1)	ZA786972B (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3415069A1 (de) *	1983-11-19	1985-05-30	Hoechst Ag, 6230 Frankfurt	Herbizide mittel

1977
- 1977-12-14 DE DE19772755617 patent/DE2755617A1/de not_active Withdrawn
1978
- 1978-11-22 DD DDAPA01N/209248A patent/DD157750A5/de unknown
- 1978-11-30 DK DK545078A patent/DK545078A/da not_active Application Discontinuation
- 1978-12-09 GR GR57833A patent/GR65232B/el unknown
- 1978-12-12 IT IT30757/78A patent/IT1101737B/it active
- 1978-12-12 IL IL56195A patent/IL56195A0/xx unknown
- 1978-12-12 AT AT0882578A patent/AT364192B/de not_active IP Right Cessation
- 1978-12-12 SU SU782696353A patent/SU884549A3/ru active
- 1978-12-12 RO RO7895883A patent/RO75105A/ro unknown
- 1978-12-13 JP JP15325578A patent/JPS5489023A/ja active Pending
- 1978-12-13 GB GB7848278A patent/GB2011787B/en not_active Expired
- 1978-12-13 CS CS788287A patent/CS203025B2/cs unknown
- 1978-12-13 ZA ZA00786972A patent/ZA786972B/xx unknown
- 1978-12-13 NL NL7812145A patent/NL7812145A/xx not_active Application Discontinuation
- 1978-12-13 SE SE7812782A patent/SE7812782L/xx unknown
- 1978-12-13 AU AU42458/78A patent/AU525418B2/en not_active Expired
- 1978-12-13 PT PT68909A patent/PT68909A/pt unknown
- 1978-12-13 CA CA317,863A patent/CA1123220A/en not_active Expired
- 1978-12-14 FR FR7835211A patent/FR2411565A1/fr active Pending
- 1978-12-14 PL PL1978211747A patent/PL112150B1/pl unknown
- 1978-12-14 BE BE192321A patent/BE872765A/xx unknown

Also Published As

Publication number	Publication date
ATA882578A (de)	1981-02-15
FR2411565A1 (fr)	1979-07-13
ZA786972B (en)	1979-11-28
AT364192B (de)	1981-09-25
NL7812145A (nl)	1979-06-18
SU884549A3 (ru)	1981-11-23
IL56195A0 (en)	1979-03-12
SE7812782L (sv)	1979-06-15
PL112150B1 (en)	1980-09-30
PT68909A (en)	1979-01-01
AU4245878A (en)	1979-06-21
GB2011787B (en)	1982-05-12
DE2755617A1 (de)	1979-06-21
CS203025B2 (en)	1981-02-27
IT7830757A0 (it)	1978-12-12
DD157750A5 (de)	1982-12-08
BE872765A (fr)	1979-06-14
GB2011787A (en)	1979-07-18
JPS5489023A (en)	1979-07-14
RO75105A (ro)	1980-10-30
DK545078A (da)	1979-06-15
PL211747A1 (pl)	1979-07-30
GR65232B (en)	1980-07-30
AU525418B2 (en)	1982-11-04
IT1101737B (it)	1985-10-07

Legal Events

Date	Code	Title	Description
1999-05-11	MKEX	Expiry

Publication	Publication Date	Title
DE2640730C2 (de)	1983-08-25	Benzoxazolyloxy- und Benzothiazolyloxy-phenoxy-Verbindungen und diese enthaltende herbizide Mittel
AU646560B2 (en)	1994-02-24	Herbicidal compositions with increased crop safety
US4692181A (en)	1987-09-08	Herbicidal compositions
EP0837632B1 (en)	1999-09-22	Selective herbicidal composition
US4047928A (en)	1977-09-13	Wild oat herbicide mixture
US2863754A (en)	1958-12-09	Method of weed control
US4336057A (en)	1982-06-22	Herbicides
US4488896A (en)	1984-12-18	Methods and compositions for the selective control of undesirable weed species in the presence of wet-land crops
IL29284A (en)	1971-07-28	N-(1,1-dimethylpropynyl)-3,5-disubstituted benzamides and herbicidal compositions containing them
US3112342A (en)	1963-11-26	1-methoxy-1-methyl-3-(3-chloro-4-cumenyl) urea
CA1123220A (en)	1982-05-11	Herbicidal compositions
US4749812A (en)	1988-06-07	N-(3-chloro-4-isopropylphenyl) carboxamide derivative and selective herbicide
CA1099126A (en)	1981-04-14	Herbicidal compositions
CA1168884A (en)	1984-06-12	Synergistic composition and method of selectively controlling weeds, especially in cereals
US4047932A (en)	1977-09-13	Herbicidal agents
CA1236315A (en)	1988-05-10	Herbicidal agents
CA2082845A1 (en)	1993-05-16	Synergistic composition and method of selective weed control
CA1058903A (en)	1979-07-24	Herbicidal compositions
US4272281A (en)	1981-06-09	Composition for and method of selectively controlling weeds in cereals
US4256482A (en)	1981-03-17	Herbicidal composition
US4645526A (en)	1987-02-24	Herbicidal agents
CA1167270A (en)	1984-05-15	Synergistic composition and method of selectively controlling weeds, especially in cereals and soybeans
US4032324A (en)	1977-06-28	Synergistic herbicidal composition for the control of weeds
US3228762A (en)	1966-01-11	Method of killing weeds
US4272283A (en)	1981-06-09	Herbicidal composition and method for controlling weeds