BE897581A - Composition liquide stable a activite herbicide et procede pour sa preparation - Google Patents

Composition liquide stable a activite herbicide et procede pour sa preparation Download PDF

Info

Publication number: BE897581A
Authority: BE; Belgium
Prior art keywords: sep; composition according; urea; herbicidal activity; solvent
Prior art date: 1982-08-25

Application number

BE0/211395A

Other languages

English (en)

French (fr)

Original Assignee

Sintagro Sa

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.)

1982-08-25

Filing date

1983-08-23

Publication date

1983-12-16

1983-08-23 Application filed by Sintagro Sa filed Critical Sintagro Sa

1983-12-16 Publication of BE897581A publication Critical patent/BE897581A/fr

Links

239000000203 mixture Substances 0.000 title claims description 38
230000002363 herbicidal effect Effects 0.000 title claims description 25
239000007788 liquid Substances 0.000 title claims description 5
238000004519 manufacturing process Methods 0.000 title 1
239000002904 solvent Substances 0.000 claims description 22
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 15
SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 claims description 14
OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 claims description 8
RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical class OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 8
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 7
239000004202 carbamide Substances 0.000 claims description 7
239000003995 emulsifying agent Substances 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
125000000129 anionic group Chemical group 0.000 claims description 6
239000004009 herbicide Substances 0.000 claims description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
239000008096 xylene Substances 0.000 claims description 5
VACNDKUQVLNNLD-UHFFFAOYSA-N 2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O VACNDKUQVLNNLD-UHFFFAOYSA-N 0.000 claims description 4
125000004438 haloalkoxy group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 3
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims description 3
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims 1
150000002576 ketones Chemical class 0.000 claims 1
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 1
-1 wettables Substances 0.000 description 11
239000000839 emulsion Substances 0.000 description 7
229940078552 o-xylene Drugs 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000013543 active substance Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
241000196324 Embryophyta Species 0.000 description 4
235000008504 concentrate Nutrition 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
150000003738 xylenes Chemical class 0.000 description 4
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 3
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
150000004996 alkyl benzenes Chemical class 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
230000000694 effects Effects 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
235000011076 sorbitan monostearate Nutrition 0.000 description 3
NPDACUSDTOMAMK-UHFFFAOYSA-N 4-Chlorotoluene Chemical compound CC1=CC=C(Cl)C=C1 NPDACUSDTOMAMK-UHFFFAOYSA-N 0.000 description 2
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
BGTFWRDJZNCBCV-UHFFFAOYSA-N 4-methyl-3-hexen-2-one Natural products CCC(C)=CC(C)=O BGTFWRDJZNCBCV-UHFFFAOYSA-N 0.000 description 2
XVKRTNZGYNJYQX-UHFFFAOYSA-N 5-ethylhept-4-en-3-one Chemical compound CCC(=O)C=C(CC)CC XVKRTNZGYNJYQX-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
229920001213 Polysorbate 20 Polymers 0.000 description 2
229920001214 Polysorbate 60 Polymers 0.000 description 2
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000001587 sorbitan monostearate Substances 0.000 description 2
229940035048 sorbitan monostearate Drugs 0.000 description 2
UHEPJGULSIKKTP-UHFFFAOYSA-N sulcatone Chemical compound CC(C)=CCCC(C)=O UHEPJGULSIKKTP-UHFFFAOYSA-N 0.000 description 2
LABTWGUMFABVFG-ONEGZZNKSA-N (3E)-pent-3-en-2-one Chemical compound C\C=C\C(C)=O LABTWGUMFABVFG-ONEGZZNKSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
DHESKPVRPQXGRM-UHFFFAOYSA-N 1-ethyl-1-methoxy-3-phenylurea Chemical compound CCN(OC)C(=O)NC1=CC=CC=C1 DHESKPVRPQXGRM-UHFFFAOYSA-N 0.000 description 1
LABTWGUMFABVFG-UHFFFAOYSA-N 1-propenyl methyl ketone Natural products CC=CC(C)=O LABTWGUMFABVFG-UHFFFAOYSA-N 0.000 description 1
QXXIZJPWGJDHKR-UHFFFAOYSA-N 2,6-dinitro-n-propyl-4-(trifluoromethyl)aniline Chemical compound CCCNC1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O QXXIZJPWGJDHKR-UHFFFAOYSA-N 0.000 description 1
CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical class CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 1
SYTQFBVTZCYXOV-UHFFFAOYSA-N 3,5,5-trimethylcyclohex-2-en-1-one Chemical compound CC1=CC(=O)CC(C)(C)C1.CC1=CC(=O)CC(C)(C)C1 SYTQFBVTZCYXOV-UHFFFAOYSA-N 0.000 description 1
SIBULRZDICEHRZ-UHFFFAOYSA-N 3-(4-chlorophenyl)-1-ethoxy-1-methylurea Chemical compound CCON(C)C(=O)NC1=CC=C(Cl)C=C1 SIBULRZDICEHRZ-UHFFFAOYSA-N 0.000 description 1
GGBXJDKSEHTBLW-UHFFFAOYSA-N 5-methylhex-4-en-2-one Chemical compound CC(C)=CCC(C)=O GGBXJDKSEHTBLW-UHFFFAOYSA-N 0.000 description 1
125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
235000002566 Capsicum Nutrition 0.000 description 1
244000000626 Daucus carota Species 0.000 description 1
235000002767 Daucus carota Nutrition 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
239000006002 Pepper Substances 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
235000016761 Piper aduncum Nutrition 0.000 description 1
235000017804 Piper guineense Nutrition 0.000 description 1
244000203593 Piper nigrum Species 0.000 description 1
235000008184 Piper nigrum Nutrition 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
239000004147 Sorbitan trioleate Substances 0.000 description 1
PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
238000009835 boiling Methods 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
230000008021 deposition Effects 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000012535 impurity Substances 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
125000005394 methallyl group Chemical group 0.000 description 1
XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
MBGVPDOCIANUJN-UHFFFAOYSA-N n,n-bis(2-methylpropyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound CC(C)CN(CC(C)C)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O MBGVPDOCIANUJN-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
229920000053 polysorbate 80 Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical class C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
235000019337 sorbitan trioleate Nutrition 0.000 description 1
229960000391 sorbitan trioleate Drugs 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
244000045561 useful plants Species 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- 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<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

BE0/211395A 1982-08-25 1983-08-23 Composition liquide stable a activite herbicide et procede pour sa preparation BE897581A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH5044/82A CH652888A5 (de)	1982-08-25	1982-08-25	Stabile, fluessige zubereitung mit herbizider wirkung und verfahren zu ihrer herstellung.

Publications (1)

Publication Number	Publication Date
BE897581A true BE897581A (fr)	1983-12-16

Family

ID=4287005

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE0/211395A BE897581A (fr)	1982-08-25	1983-08-23	Composition liquide stable a activite herbicide et procede pour sa preparation

Country Status (5)

Country	Link
BE (1)	BE897581A (de)
CH (1)	CH652888A5 (de)
FR (1)	FR2532151A1 (de)
GB (1)	GB2126088B (de)
IT (1)	IT1164402B (de)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL87356C (de) *	1955-04-29
US3373010A (en) *	1964-10-08	1968-03-12	Du Pont	Herbicidal composition and method
GB1473105A (de) *	1973-08-10	1977-05-11
IT1131750B (it) *	1980-06-06	1986-06-25	Montedison Spa	Formulazioni stabili di n-(3,4-diclorofenil)-n'metossi-n'-metilurea (linorun) e 2,6-dinitor-n,n-dipropil-4-trifluoro metilanilina (trifluralin) in emulsione

1982
- 1982-08-25 CH CH5044/82A patent/CH652888A5/de not_active IP Right Cessation
1983
- 1983-08-03 GB GB08320961A patent/GB2126088B/en not_active Expired
- 1983-08-08 IT IT22479/83A patent/IT1164402B/it active
- 1983-08-23 FR FR8313597A patent/FR2532151A1/fr active Pending
- 1983-08-23 BE BE0/211395A patent/BE897581A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
FR2532151A1 (fr)	1984-03-02
IT8322479A0 (it)	1983-08-08
GB2126088A (en)	1984-03-21
GB8320961D0 (en)	1983-09-07
GB2126088B (en)	1986-01-02
IT1164402B (it)	1987-04-08
CH652888A5 (de)	1985-12-13

Legal Events

Date

Code

Title

Description

1989-02-28

RE

Patent lapsed

Owner name: SINTAGRO S.A.

Effective date: 19880831

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FR2530122A1 (fr)	1984-01-20	Compositions herbicides stables a base de m.bis-carbamates
CH470137A (fr)	1969-03-31	Composition acaricide
EP0290354A2 (de)	1988-11-09	Herbizide Mischung
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GB2176108A (en)	1986-12-17	Stabilised liquid herbicidal compositions
FI92789B (fi)	1994-09-30	Stabiloitu nestemäinen herbisidinen koostumus, joka käsittää metyyli-(3-(3-tolyyli-karbamoyylioksi)fenyyli)karbamaattia (fenmedifamia) tai etyyli-(3-fenyyli-karbamoyylioksifenyyli)karbamaattia (desmedifamia), menetelmä sen valmistamiseksi sekä tämän koostumuksen käyttö
FR2597720A1 (fr)	1987-10-30	Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation.
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WO1989000568A1 (fr)	1989-01-26	Compositions fongicides a base de derives nicotiniques, nouveaux derives nicotiniques et leur preparation
EP0273799A2 (de)	1988-07-06	Herbizide Emulsionskonzentrate auf Basis von Metabiscarbamaten
EP0080917B1 (de)	1985-01-23	Herbizide Zusammensetzungen auf der Basis von 4-Amino-6-chlor-5-methylthiopyrimidinderivaten und Pyridate und Verfahren zur Behandlung von Kulturen mit den genannten Zusammensetzungen
FR2599593A1 (fr)	1987-12-11	Compositions herbicides liquides stabilisees a base de m-bis-carbamates et leur utilisation
FR2589327A1 (fr)	1987-05-07	Melanges herbicides de derives d'acides pyridinoxyalcanoiques et de derives d'acides phenoxybenzoiques et leur utilisation pour le traitement des cultures
FR2590119A1 (fr)	1987-05-22	Compositions herbicides liquides stabilisees, a base de biscarbamate