CH644351A5 - Herbizid wirksame 2-halogenacetanilide. - Google Patents

Herbizid wirksame 2-halogenacetanilide. Download PDF

Info

Publication number: CH644351A5
Authority: CH; Switzerland
Prior art keywords: methyl; compound; chloroacetanilide; ethyl; butyl
Prior art date: 1980-03-25

Application number

CH185181A

Other languages

German (de)

English (en)

Inventor

Gerhard Horst Alt

Original Assignee

Monsanto 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.)

1980-03-25

Filing date

1981-03-18

Publication date

1984-07-31

1981-03-18 Application filed by Monsanto Co filed Critical Monsanto Co

1984-07-31 Publication of CH644351A5 publication Critical patent/CH644351A5/de

Links

239000004009 herbicide Substances 0.000 title claims description 82
230000002363 herbicidal effect Effects 0.000 title claims description 62
229910052736 halogen Inorganic materials 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 146
241000196324 Embryophyta Species 0.000 claims description 80
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 38
238000002360 preparation method Methods 0.000 claims description 37
-1 1-methyl-pentyl Chemical group 0.000 claims description 35
235000010469 Glycine max Nutrition 0.000 claims description 26
244000068988 Glycine max Species 0.000 claims description 26
238000000034 method Methods 0.000 claims description 23
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 20
244000105624 Arachis hypogaea Species 0.000 claims description 13
229910052739 hydrogen Inorganic materials 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 13
235000020232 peanut Nutrition 0.000 claims description 13
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 12
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 12
240000002791 Brassica napus Species 0.000 claims description 8
229920000742 Cotton Polymers 0.000 claims description 8
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125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
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239000002671 adjuvant Substances 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
DVKFMXGJDGDPJC-UHFFFAOYSA-N n-(2-butoxy-6-methylphenyl)-2-chloro-n-methylacetamide Chemical group CCCCOC1=CC=CC(C)=C1N(C)C(=O)CCl DVKFMXGJDGDPJC-UHFFFAOYSA-N 0.000 claims description 5
235000013311 vegetables Nutrition 0.000 claims description 5
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 claims description 4
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125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 4
LVRSFIGNFVKIJZ-UHFFFAOYSA-N n-(2-butan-2-yloxy-6-methylphenyl)-2-chloro-n-methylacetamide Chemical group CCC(C)OC1=CC=CC(C)=C1N(C)C(=O)CCl LVRSFIGNFVKIJZ-UHFFFAOYSA-N 0.000 claims description 4
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
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NLJCMOJWDVMFPB-UHFFFAOYSA-N 2-chloro-n-methyl-n-(2-methyl-6-propoxyphenyl)acetamide Chemical group CCCOC1=CC=CC(C)=C1N(C)C(=O)CCl NLJCMOJWDVMFPB-UHFFFAOYSA-N 0.000 claims 4
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UBAGJCNJDBGZPW-UHFFFAOYSA-N 2-chloro-n-methyl-n-[2-methyl-6-(3-methylbutoxy)phenyl]acetamide Chemical group CC(C)CCOC1=CC=CC(C)=C1N(C)C(=O)CCl UBAGJCNJDBGZPW-UHFFFAOYSA-N 0.000 claims 4
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LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 4
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ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
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150000002367 halogens Chemical class 0.000 description 1
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239000003112 inhibitor Substances 0.000 description 1
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239000003350 kerosene Substances 0.000 description 1
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238000009533 lab test Methods 0.000 description 1
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical compound C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
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235000010981 methylcellulose Nutrition 0.000 description 1
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150000002825 nitriles Chemical class 0.000 description 1
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
INFDPOAKFNIJBF-UHFFFAOYSA-N paraquat Chemical compound C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 INFDPOAKFNIJBF-UHFFFAOYSA-N 0.000 description 1
239000008188 pellet Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Chemical class 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229910003446 platinum oxide Inorganic materials 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229940072033 potash Drugs 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
229940043267 rhodamine b Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000003334 secondary amides Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
230000036556 skin irritation Effects 0.000 description 1
231100000475 skin irritation Toxicity 0.000 description 1
ISGFBNPDKXKSLM-UHFFFAOYSA-M sodium 2-butan-2-yl-4,6-dinitrophenol 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound [N+](=O)([O-])C1=CC(=C(C(=C1)[N+](=O)[O-])O)C(C)CC.ClC1=C(OC=2C=CC(=C(C(=O)[O-])C2)[N+](=O)[O-])C=CC(=C1)C(F)(F)F.[Na+] ISGFBNPDKXKSLM-UHFFFAOYSA-M 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003463 sulfur Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000723 toxicological property Toxicity 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
238000009736 wetting Methods 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system

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)

CH185181A 1980-03-25 1981-03-18 Herbizid wirksame 2-halogenacetanilide. CH644351A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US13375880A	1980-03-25	1980-03-25

Publications (1)

Publication Number	Publication Date
CH644351A5 true CH644351A5 (de)	1984-07-31

Family

ID=22460176

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH185181A CH644351A5 (de)	1980-03-25	1981-03-18	Herbizid wirksame 2-halogenacetanilide.

Country Status (31)

Country	Link
JP (1)	JPS56145255A (fr)
AR (1)	AR228450A1 (fr)
AT (1)	AT374661B (fr)
AU (1)	AU536795B2 (fr)
BE (1)	BE888000A (fr)
BG (1)	BG35892A3 (fr)
BR (1)	BR8101606A (fr)
CA (1)	CA1206165A (fr)
CH (1)	CH644351A5 (fr)
CS (1)	CS223996B2 (fr)
DD (1)	DD157297A5 (fr)
DE (1)	DE3110452C2 (fr)
DK (1)	DK121081A (fr)
EG (1)	EG14782A (fr)
FR (1)	FR2479206A1 (fr)
GB (1)	GB2072178B (fr)
GR (1)	GR73574B (fr)
HU (1)	HU189496B (fr)
IE (1)	IE51697B1 (fr)
IL (1)	IL62415A (fr)
IT (1)	IT1144664B (fr)
LU (1)	LU83234A1 (fr)
MA (1)	MA19104A1 (fr)
NL (1)	NL8101322A (fr)
NZ (1)	NZ196545A (fr)
PL (1)	PL125722B1 (fr)
PT (1)	PT72680B (fr)
RO (2)	RO86072B (fr)
SE (1)	SE8101732L (fr)
TR (1)	TR20886A (fr)
ZA (1)	ZA811804B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2542736B1 (fr) *	1983-03-16	1986-06-06	Kumiai Chemical Industry Co	Derive de chloracetanilide, procede de production et composition herbicide le contenant

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3268584A (en) *	1961-08-28	1966-08-23	Monsanto Co	Herbicidal alpha-haloacetanilides
US3442945A (en) *	1967-05-22	1969-05-06	Monsanto Co	Phytotoxic alpha-halo-acetanilides
DE1921464A1 (de) *	1969-04-26	1970-12-17	Basf Ag	Herbizid
US4152137A (en) *	1975-09-04	1979-05-01	Ciba-Geigy Corporation	Phenylglyoxylonitrile-2-oxime-cyanomethyl ether as a crop safener
US4146387A (en) *	1977-11-25	1979-03-27	Stauffer Chemical Company	Synergistic herbicidal compositions
US4258196A (en) *	1978-04-17	1981-03-24	Monsanto Company	Process for the production of tertiary 2-haloacetamides

1981
- 1981-03-18 CA CA000373316A patent/CA1206165A/fr not_active Expired
- 1981-03-18 DE DE3110452A patent/DE3110452C2/de not_active Expired
- 1981-03-18 HU HU81692A patent/HU189496B/hu unknown
- 1981-03-18 AR AR284649A patent/AR228450A1/es active
- 1981-03-18 PL PL1981230204A patent/PL125722B1/pl unknown
- 1981-03-18 IE IE593/81A patent/IE51697B1/en unknown
- 1981-03-18 BR BR8101606A patent/BR8101606A/pt unknown
- 1981-03-18 JP JP3807781A patent/JPS56145255A/ja active Granted
- 1981-03-18 RO RO111088A patent/RO86072B/ro unknown
- 1981-03-18 MA MA19310A patent/MA19104A1/fr unknown
- 1981-03-18 IT IT20416/81A patent/IT1144664B/it active
- 1981-03-18 DK DK121081A patent/DK121081A/da unknown
- 1981-03-18 GR GR64435A patent/GR73574B/el unknown
- 1981-03-18 NL NL8101322A patent/NL8101322A/nl not_active Application Discontinuation
- 1981-03-18 TR TR20886A patent/TR20886A/xx unknown
- 1981-03-18 NZ NZ196545A patent/NZ196545A/en unknown
- 1981-03-18 FR FR8105444A patent/FR2479206A1/fr active Granted
- 1981-03-18 CS CS811983A patent/CS223996B2/cs unknown
- 1981-03-18 DD DD81228406A patent/DD157297A5/de unknown
- 1981-03-18 IL IL62415A patent/IL62415A/xx unknown
- 1981-03-18 SE SE8101732A patent/SE8101732L/ not_active Application Discontinuation
- 1981-03-18 AU AU68486/81A patent/AU536795B2/en not_active Ceased
- 1981-03-18 PT PT72680A patent/PT72680B/pt unknown
- 1981-03-18 BG BG051259A patent/BG35892A3/xx unknown
- 1981-03-18 RO RO81103740A patent/RO82131A/fr unknown
- 1981-03-18 CH CH185181A patent/CH644351A5/de not_active IP Right Cessation
- 1981-03-18 EG EG141/81A patent/EG14782A/xx active
- 1981-03-18 GB GB8108379A patent/GB2072178B/en not_active Expired
- 1981-03-18 LU LU83234A patent/LU83234A1/fr unknown
- 1981-03-18 AT AT0126281A patent/AT374661B/de not_active IP Right Cessation
- 1981-03-18 BE BE0/204167A patent/BE888000A/fr not_active IP Right Cessation
1982
- 1982-03-18 ZA ZA00811804A patent/ZA811804B/xx unknown

Also Published As

Publication number	Publication date
AU6848681A (en)	1981-10-01
MA19104A1 (fr)	1981-10-01
NZ196545A (en)	1984-02-03
BR8101606A (pt)	1981-09-29
AR228450A1 (es)	1983-03-15
BG35892A3 (en)	1984-07-16
GB2072178B (en)	1984-02-29
GR73574B (fr)	1984-03-19
ZA811804B (en)	1982-04-28
HU189496B (en)	1986-07-28
PL230204A1 (fr)	1981-11-13
AU536795B2 (en)	1984-05-24
CA1206165A (fr)	1986-06-17
IL62415A (en)	1984-03-30
RO82131B (ro)	1983-06-30
IT1144664B (it)	1986-10-29
FR2479206B1 (fr)	1984-05-11
DD157297A5 (de)	1982-11-03
EG14782A (en)	1985-06-30
DE3110452A1 (de)	1981-12-24
LU83234A1 (fr)	1981-10-30
ATA126281A (de)	1983-10-15
PT72680B (en)	1982-03-24
JPS56145255A (en)	1981-11-11
JPH0148261B2 (fr)	1989-10-18
RO86072B (ro)	1985-03-02
IT8120416A0 (it)	1981-03-18
SE8101732L (sv)	1981-11-09
FR2479206A1 (fr)	1981-10-02
PL125722B1 (en)	1983-06-30
NL8101322A (nl)	1981-10-16
IE810593L (en)	1981-09-25
TR20886A (tr)	1982-11-22
AT374661B (de)	1984-05-25
IE51697B1 (en)	1987-02-18
GB2072178A (en)	1981-09-30
BE888000A (fr)	1981-09-18
PT72680A (en)	1981-04-01
RO86072A (fr)	1985-02-25
DE3110452C2 (de)	1986-10-16
DK121081A (da)	1981-09-26
RO82131A (fr)	1983-07-07
CS223996B2 (en)	1983-11-25
IL62415A0 (en)	1981-05-20

Publication	Publication Date	Title
DE69321439T2 (de)	1999-03-04	Verfahren zur Steigerung der heroiziden Wirksamkeit und herbizeiden Zusammensetzungen mit gesteigerter Wirksamkeit
RU2083107C1 (ru)	1997-07-10	Гербицидное синергитическое средство, способ поражения нежелательных растений
DE69723750T2 (de)	2004-06-03	Herbizide Kombinationen
DE69702968T2 (de)	2000-12-28	Herbizide zusammensetzung und deren verwendung zur unkrautbekämpfung
DE69606044T2 (de)	2000-09-14	Synergistische herbizide zusammensetzung und verfahren zu ihre verwendung
DE69509649T2 (de)	1999-09-16	Synergistische herbizide zusammensetzung und verfahren zu ihrer anwendung
DE69222638T2 (de)	1998-02-19	Verfahren und herbizide zusammensetzungen, die substituierte cyclohexandione und stickstoffdünger enthalten
DE69329531T2 (de)	2001-02-08	Triazolinone enthaltende herbizide zusammensetzungen
EP2238835B1 (fr)	2016-04-06	Défoliant à base de thidiazuron et de flufénacet
DE60109408T2 (de)	2006-01-26	Verfahren zum schutz von kulturpflanzen vor der phytotoxischen wirkung von herbiziden durch verwendung von phosphorierten estern
DE3110473C2 (de)	1986-02-13	N-Alkyl-2'-n-butoxy-6'-ethyl-2-chloracetanilide und Herbizide, welche diese Verbindungen enthalten
DE69214998T2 (de)	1997-03-06	Herbizide Zusammensetzungen mit reduzierter Phytoxitität
CH644351A5 (de)	1984-07-31	Herbizid wirksame 2-halogenacetanilide.
DE3110525C2 (de)	1986-10-30	2-Chloracetanilide und sie enthaltende Herbizide
DE3110451C2 (de)	1986-10-23	2-Chloracetanilide und sie enthaltende Herbizide
DE3110523C2 (de)	1986-02-06	2'-Trifluor-methyl-2-chloracetanilide und sie enthaltende Herbizide
DE69216905T2 (de)	1997-05-15	Herbizide Zusammensetzungen mit verbesserter Getreide-Sicherheit
CH644350A5 (de)	1984-07-31	Herbizide 2-halogenacetanilide.
DE69123486T2 (de)	1997-04-03	Herbizide Zusammensetzung und Verfahren zur Unkrautvernichtung
CH644587A5 (de)	1984-08-15	Herbizid wirksame 2-halogenacetanilide.
DD157293A5 (de)	1982-11-03	Herbizidzubereitung
DE2638069A1 (de)	1977-12-15	Herbizid und/oder insektizid wirksames pflanzenschutzmittel
DE2735001A1 (de)	1978-02-09	Herbicides mittel
DE2261431A1 (de)	1974-06-27	Herbizide mittel
DE3936664A1 (de)	1990-05-10	Herbizid und wachstumsregulierend wirksames synergistisches mittel

Legal Events

Date	Code	Title	Description
1989-11-30	PL	Patent ceased
2024-10-31	PL	Patent ceased