CH652888A5 - Stabile, fluessige zubereitung mit herbizider wirkung und verfahren zu ihrer herstellung. - Google Patents

Stabile, fluessige zubereitung mit herbizider wirkung und verfahren zu ihrer herstellung. Download PDF

Info

Publication number: CH652888A5
Authority: CH; Switzerland
Prior art keywords: dinitro; atoms; trifluoromethyl; aniline; urea
Prior art date: 1982-08-25

Application number

CH5044/82A

Other languages

German (de)

English (en)

Inventor

Willi Dr-Chem Luethy

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

1982-08-25

Publication date

1985-12-13

1982-08-25 Application filed by Sintagro Sa filed Critical Sintagro Sa

1982-08-25 Priority to CH5044/82A priority Critical patent/CH652888A5/de

1983-08-03 Priority to GB08320961A priority patent/GB2126088B/en

1983-08-08 Priority to IT22479/83A priority patent/IT1164402B/it

1983-08-23 Priority to BE0/211395A priority patent/BE897581A/fr

1983-08-23 Priority to FR8313597A priority patent/FR2532151A1/fr

1985-12-13 Publication of CH652888A5 publication Critical patent/CH652888A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims description 22
238000002360 preparation method Methods 0.000 title claims description 21
238000000034 method Methods 0.000 title claims description 12
239000007788 liquid Substances 0.000 title claims description 6
238000004519 manufacturing process Methods 0.000 title 1
239000002904 solvent Substances 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 18
239000000203 mixture Substances 0.000 claims description 18
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 16
SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 claims description 16
239000003995 emulsifying agent Substances 0.000 claims description 9
RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical class OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 8
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 7
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 7
125000000129 anionic group Chemical group 0.000 claims description 6
239000004009 herbicide Substances 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
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 6
150000001875 compounds Chemical class 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
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
QFUSCYRJMXLNRB-UHFFFAOYSA-N 2,6-dinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O QFUSCYRJMXLNRB-UHFFFAOYSA-N 0.000 claims description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
239000003945 anionic surfactant Substances 0.000 claims description 2
239000004202 carbamide Substances 0.000 claims description 2
125000004438 haloalkoxy group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000002736 nonionic surfactant Substances 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims 2
239000008096 xylene Substances 0.000 claims 2
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
125000001931 aliphatic group Chemical group 0.000 claims 1
150000001448 anilines Chemical class 0.000 claims 1
-1 aliphatic ketones Chemical class 0.000 description 29
239000004480 active ingredient Substances 0.000 description 8
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
239000012141 concentrate Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
150000003738 xylenes Chemical class 0.000 description 5
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
UHEPJGULSIKKTP-UHFFFAOYSA-N sulcatone Chemical compound CC(C)=CCCC(C)=O UHEPJGULSIKKTP-UHFFFAOYSA-N 0.000 description 4
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
241000196324 Embryophyta Species 0.000 description 3
229920001213 Polysorbate 20 Polymers 0.000 description 3
229920001214 Polysorbate 60 Polymers 0.000 description 3
150000004996 alkyl benzenes 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
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 3
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 3
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 3
235000010989 polyoxyethylene 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
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
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
230000000885 phytotoxic effect Effects 0.000 description 2
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 2
OHEFFKYYKJVVOX-UHFFFAOYSA-N sulcatol Natural products CC(O)CCC=C(C)C OHEFFKYYKJVVOX-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
BGTFWRDJZNCBCV-AATRIKPKSA-N (e)-4-methylhex-3-en-2-one Chemical compound CC\C(C)=C\C(C)=O BGTFWRDJZNCBCV-AATRIKPKSA-N 0.000 description 1
MLAPCZAEMSPIHB-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-methoxy-1-(2-methoxyethyl)-3-methylurea Chemical compound ClC1=CC=C(C=C1)N(C(=O)N(C)OC)CCOC MLAPCZAEMSPIHB-UHFFFAOYSA-N 0.000 description 1
DMJWIYNOTAWVOH-UHFFFAOYSA-N 1-butoxy-1-butyl-3-(4-chloro-3-methylsulfanylphenyl)-3-ethylurea Chemical compound CCCCON(CCCC)C(=O)N(CC)C1=CC=C(Cl)C(SC)=C1 DMJWIYNOTAWVOH-UHFFFAOYSA-N 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
OWRHJTUZVUYYNA-UHFFFAOYSA-N 1-methoxy-3-methylurea Chemical compound CNC(=O)NOC OWRHJTUZVUYYNA-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
LIOVBQHDFPHDSP-UHFFFAOYSA-N 3-(3-chloro-4-ethoxyphenyl)-1-methoxy-1-methylurea Chemical compound CCOC1=CC=C(NC(=O)N(C)OC)C=C1Cl LIOVBQHDFPHDSP-UHFFFAOYSA-N 0.000 description 1
HMOULFHNQQZLDV-UHFFFAOYSA-N 3-(4-bromophenyl)-1-methoxy-1-methylurea 3-(4-chlorophenyl)-1-methoxy-1-methylurea 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea Chemical compound ClC=1C=C(C=CC1Cl)NC(=O)N(OC)C.BrC1=CC=C(C=C1)NC(=O)N(OC)C.ClC1=CC=C(C=C1)NC(=O)N(OC)C HMOULFHNQQZLDV-UHFFFAOYSA-N 0.000 description 1
UMOOQQMJNZVVKB-UHFFFAOYSA-N 3-(4-chloro-2-methylphenyl)-1-methoxy-1-methylurea Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1C UMOOQQMJNZVVKB-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
BGTFWRDJZNCBCV-UHFFFAOYSA-N 4-methyl-3-hexen-2-one Natural products CCC(C)=CC(C)=O BGTFWRDJZNCBCV-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
LIXZPXRZBOQNBU-UHFFFAOYSA-N C(C)(C)C1=CC=C(C=C1)N(C(=O)N(OC)CC)CC.ClC1=CC=C(C=C1)N(C(=O)N(OC)C)C Chemical compound C(C)(C)C1=CC=C(C=C1)N(C(=O)N(OC)CC)CC.ClC1=CC=C(C=C1)N(C(=O)N(OC)C)C LIXZPXRZBOQNBU-UHFFFAOYSA-N 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
BNQNEUPEQYLJGJ-UHFFFAOYSA-N FC(C1=CC(=C(N(C)C)C(=C1)[N+](=O)[O-])[N+](=O)[O-])(F)F.FC(C1=CC(=C(NCCC)C(=C1)[N+](=O)[O-])[N+](=O)[O-])(F)F Chemical compound FC(C1=CC(=C(N(C)C)C(=C1)[N+](=O)[O-])[N+](=O)[O-])(F)F.FC(C1=CC(=C(NCCC)C(=C1)[N+](=O)[O-])[N+](=O)[O-])(F)F BNQNEUPEQYLJGJ-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
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
229920003171 Poly (ethylene oxide) Polymers 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
239000013543 active substance Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 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
235000013339 cereals Nutrition 0.000 description 1
239000000470 constituent Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000004744 fabric Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
125000005394 methallyl group Chemical group 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
KNTOUMMLMPJOSR-UHFFFAOYSA-N n,n-di(butan-2-yl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound CCC(C)N(C(C)CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O KNTOUMMLMPJOSR-UHFFFAOYSA-N 0.000 description 1
IFCKWWXWJYTNCS-UHFFFAOYSA-N n-ethyl-2,6-dinitro-n-propyl-4-(trifluoromethyl)aniline Chemical compound CCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O IFCKWWXWJYTNCS-UHFFFAOYSA-N 0.000 description 1
UCGLSBJMKKXNCO-UHFFFAOYSA-N n-hexan-3-yl-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound CCCC(CC)NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O UCGLSBJMKKXNCO-UHFFFAOYSA-N 0.000 description 1
VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
CDZOGLJOFWFVOZ-UHFFFAOYSA-N n-propylaniline Chemical compound CCCNC1=CC=CC=C1 CDZOGLJOFWFVOZ-UHFFFAOYSA-N 0.000 description 1
125000001400 nonyl 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])[H] 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
239000000249 polyoxyethylene sorbitan monopalmitate Substances 0.000 description 1
235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002689 soil 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
239000004563 wettable powder 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
- 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)

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

Priority Applications (5)

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.
GB08320961A GB2126088B (en)	1982-08-25	1983-08-03	Herbcidal liquid preparation and method for its production
IT22479/83A IT1164402B (it)	1982-08-25	1983-08-08	Preparato liquido stabile con azione erbicida e processo per la sua preparazione
BE0/211395A BE897581A (fr)	1982-08-25	1983-08-23	Composition liquide stable a activite herbicide et procede pour sa preparation
FR8313597A FR2532151A1 (fr)	1982-08-25	1983-08-23	Composition liquide stable a activite herbicide et procede pour sa preparation

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
CH652888A5 true CH652888A5 (de)	1985-12-13

Family

ID=4287005

Family Applications (1)

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

Country Status (5)

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

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE547357A (fr) *	1955-04-29
US3373010A (en) *	1964-10-08	1968-03-12	Du Pont	Herbicidal composition and method
GB1473105A (fr) *	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 BE BE0/211395A patent/BE897581A/fr not_active IP Right Cessation
- 1983-08-23 FR FR8313597A patent/FR2532151A1/fr active Pending

Also Published As

Publication number	Publication date
GB8320961D0 (en)	1983-09-07
BE897581A (fr)	1983-12-16
IT8322479A0 (it)	1983-08-08
GB2126088B (en)	1986-01-02
GB2126088A (en)	1984-03-21
IT1164402B (it)	1987-04-08
FR2532151A1 (fr)	1984-03-02

Legal Events

Date	Code	Title	Description
1994-04-29	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0077759B1 (fr)	1987-12-09	Phénylurées
DE68907650T2 (de)	1994-01-27	Oberflächenaktiver Stoff auf der Basis von oxyethylierten und oxypropylierten Phenyl-1-ethylphenolen, Verfahren zu ihrer Herstellung und ihre Verwendung zum Erhalten von konzentrierten Lösungen von aktiven Verbindungen.
EP0175649B1 (fr)	1991-01-02	Carbodiimides substituées
EP0179021A2 (fr)	1986-04-23	Benzoylphénylurées
EP0235089B1 (fr)	1991-11-21	N-Benzoyl-N'-phenylurées, leur préparation et leur utilisation pour la destruction de parasites
DE2213057A1 (de)	1972-09-28	Herbizide und pestizide Arylaminopyridinverbindungen, deren Herstellung und deren Verwendung
DE2928410A1 (de)	1981-01-29	Acylharnstoffe, insektizide mittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung
EP0055213B1 (fr)	1986-02-26	Phénylurées
EP0495748A1 (fr)	1992-07-22	Agents acaricides
EP0044278B1 (fr)	1983-10-26	Phénylurées
EP0098800B1 (fr)	1985-08-14	Carbamates
EP0174274B1 (fr)	1988-11-23	Dérivés de phénylbenzoylurée
EP0014674B1 (fr)	1983-10-05	Urées N-phényl-N'-benzoyliques substituées, procédés pour leur préparation, agents contenant ces composés et leur utilisation pour combattre les organismes nuisibles; 4-(propényloxy)-anilines substituées
EP0219460A2 (fr)	1987-04-22	Benzoylphénylurées
DE3110473C2 (de)	1986-02-13	N-Alkyl-2'-n-butoxy-6'-ethyl-2-chloracetanilide und Herbizide, welche diese Verbindungen enthalten
DE2061133A1 (de)	1971-06-24	Pestizide Verbindung,Verfahren zu ihrer Herstellung und Verwendung
DE1542972B2 (de)	1973-02-15	Herbicide mittel
DE2048660A1 (de)	1971-06-24	N o Fluorphenylharnstoffe zur Schad hngsbekampfung
DE3045770C2 (fr)	1989-04-20
DE3235419A1 (de)	1983-04-14	Phenylharnstoffe
EP0065487A1 (fr)	1982-11-24	Dérivé de phénylurée
DE3637341A1 (de)	1987-05-07	Herbizide gemische und ihre verwendung zur behandlung von kulturen
DE1809838C3 (de)	1978-01-05	N-(3-Brom-4-chlorphenyl)-N'methoxy-N'-methylharnstoff und seine Verwendung als Herbizid
DE3406992A1 (de)	1984-09-13	Chinazoline und ihre anwendung bei der schaedlingsbekaempfung
AT211603B (de)	1960-10-25	Selektive herbizide Mischungen