DD283758A5 - Unkrautvernichtungsmittel und verfahren zur vernichtung von unkraut - Google Patents

Unkrautvernichtungsmittel und verfahren zur vernichtung von unkraut Download PDF

Info

Publication number: DD283758A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; antidote; derivatives; group; general formula
Prior art date: 1988-05-31

Application number

DD89329058A

Other languages

German (de)

English (en)

Inventor

Karoly Balogh

Angela Bartfai

Barna Bordas

Antal Gimesi

Erzsebet Grega

Eva Janos

Gyoergy Matolcsy

Jozsef Nagy

Csaba Pavliscsak

Istvan Toth

Original Assignee

��@��k��

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.)

1988-05-31

Filing date

1989-05-30

Publication date

1990-10-24

1989-05-30 Application filed by ��@��k�� filed Critical ��@��k��

1990-10-24 Publication of DD283758A5 publication Critical patent/DD283758A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 6
230000006378 damage Effects 0.000 title description 8
239000000729 antidote Substances 0.000 claims abstract description 51
230000002363 herbicidal effect Effects 0.000 claims abstract description 43
239000004480 active ingredient Substances 0.000 claims abstract description 31
239000004009 herbicide Substances 0.000 claims abstract description 19
239000003223 protective agent Substances 0.000 claims abstract description 18
241000196324 Embryophyta Species 0.000 claims abstract description 14
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims abstract description 13
125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 claims abstract description 4
WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 claims abstract 4
229940058963 dichloroacetamide derivative drug for amoebiasis and other protozoal diseases Drugs 0.000 claims abstract 4
239000000203 mixture Substances 0.000 claims description 35
-1 methoxyethyl Chemical group 0.000 claims description 11
229920006395 saturated elastomer Polymers 0.000 claims description 6
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 claims description 4
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 4
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims 3
150000008064 anhydrides Chemical class 0.000 claims 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
POBHZXUQLPHXDO-UHFFFAOYSA-N 2-(dichloromethyl)-4-ethyl-2-methyl-1,3-dioxolane Chemical compound CCC1COC(C)(C(Cl)Cl)O1 POBHZXUQLPHXDO-UHFFFAOYSA-N 0.000 claims 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 abstract description 22
239000000126 substance Substances 0.000 abstract description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
238000002360 preparation method Methods 0.000 description 26
239000013543 active substance Substances 0.000 description 12
229940075522 antidotes Drugs 0.000 description 11
240000008042 Zea mays Species 0.000 description 9
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 8
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 8
235000002017 Zea mays subsp mays Nutrition 0.000 description 8
230000001681 protective effect Effects 0.000 description 7
239000000654 additive Substances 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
239000007788 liquid Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 5
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
230000008901 benefit Effects 0.000 description 5
235000005822 corn Nutrition 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
230000000254 damaging effect Effects 0.000 description 4
239000000243 solution Substances 0.000 description 4
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 4
KTFNPLHWDYECSQ-UHFFFAOYSA-N 2-chloro-n-(ethoxymethyl)-n-[2-methyl-6-(trifluoromethyl)phenyl]acetamide Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1C(F)(F)F KTFNPLHWDYECSQ-UHFFFAOYSA-N 0.000 description 3
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-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
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
239000008187 granular material Substances 0.000 description 3
235000009973 maize Nutrition 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000009331 sowing Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229920001214 Polysorbate 60 Polymers 0.000 description 2
230000009471 action Effects 0.000 description 2
229920000180 alkyd Polymers 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000000969 carrier Substances 0.000 description 2
244000038559 crop plants Species 0.000 description 2
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000012895 dilution Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
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 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
230000002335 preservative effect Effects 0.000 description 2
230000021749 root development Effects 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical class CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
RBFKNKLYUXDMQT-UHFFFAOYSA-N 2-chloro-3-ethoxy-n-phenylpropanamide Chemical compound CCOCC(Cl)C(=O)NC1=CC=CC=C1 RBFKNKLYUXDMQT-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
235000006760 Acer pensylvanicum Nutrition 0.000 description 1
241000219318 Amaranthus Species 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
GTSSFGPSIKYACK-UHFFFAOYSA-N C(CC)OC(NC=1SC=CC1)=O Chemical compound C(CC)OC(NC=1SC=CC1)=O GTSSFGPSIKYACK-UHFFFAOYSA-N 0.000 description 1
VGEOGXDEBIKNPL-UHFFFAOYSA-O CCCOC(NC1=CC=C[S+]1CC)=O Chemical compound CCCOC(NC1=CC=C[S+]1CC)=O VGEOGXDEBIKNPL-UHFFFAOYSA-O 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
241000219312 Chenopodium Species 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
241000122235 Junco hyemalis Species 0.000 description 1
241001490213 Milium Species 0.000 description 1
235000005052 Milium effusum Nutrition 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
240000008114 Panicum miliaceum Species 0.000 description 1
235000007199 Panicum miliaceum Nutrition 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical class CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
244000062793 Sorghum vulgare Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
235000007244 Zea mays Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000005089 alkenylaminocarbonyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
235000012735 amaranth Nutrition 0.000 description 1
239000004178 amaranth Substances 0.000 description 1
239000005557 antagonist Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
RMRJXGBAOAMLHD-IHFGGWKQSA-N buprenorphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]11CC[C@]3([C@H](C1)[C@](C)(O)C(C)(C)C)OC)CN2CC1CC1 RMRJXGBAOAMLHD-IHFGGWKQSA-N 0.000 description 1
230000008859 change Effects 0.000 description 1
239000002734 clay mineral Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000001784 detoxification Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil 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
239000003960 organic solvent Substances 0.000 description 1
238000010422 painting Methods 0.000 description 1
125000000913 palmityl 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])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
239000002245 particle Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
229940044654 phenolsulfonic acid Drugs 0.000 description 1
238000005554 pickling Methods 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
230000008569 process Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
230000000630 rising effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent 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
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- 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
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring

Landscapes

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

DD89329058A 1988-05-31 1989-05-30 Unkrautvernichtungsmittel und verfahren zur vernichtung von unkraut DD283758A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU882756A HUT49981A (en)	1988-05-31	1988-05-31	Antidotal herbicide comprising chloroacetanilide derivative as active ingredient

Publications (1)

Publication Number	Publication Date
DD283758A5 true DD283758A5 (de)	1990-10-24

Family

ID=10960960

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD89329058A DD283758A5 (de)	1988-05-31	1989-05-30	Unkrautvernichtungsmittel und verfahren zur vernichtung von unkraut

Country Status (9)

Country	Link
DD (1)	DD283758A5 (it)
DE (1)	DE3917577A1 (it)
GR (1)	GR890100359A (it)
HU (1)	HUT49981A (it)
IT (1)	IT1237400B (it)
NL (1)	NL8901385A (it)
PL (1)	PL279674A1 (it)
RO (1)	RO105051B1 (it)
ZA (1)	ZA893794B (it)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU178064B (en) *	1978-05-31	1982-02-28	Noevenyvedelmi Kutato Intezet	Antidote composition containing n-/trimethyl-cyclopentillidene /-ethanol-amine-dichloracetate and process for preparing the active material
HU183997B (en) *	1982-07-14	1984-06-28	Noevenyvedelmi Kutato Intezet	Herbicide and antidote composition resp. containing thiolcarba mate derivative and/or chloroacetanilide derivatives as herbicide and/or substituted acetamide antidote

1988
- 1988-05-31 HU HU882756A patent/HUT49981A/hu unknown
1989
- 1989-05-19 ZA ZA893794A patent/ZA893794B/xx unknown
- 1989-05-30 GR GR890100359A patent/GR890100359A/el unknown
- 1989-05-30 DD DD89329058A patent/DD283758A5/de not_active IP Right Cessation
- 1989-05-30 IT IT8920688A patent/IT1237400B/it active
- 1989-05-30 DE DE3917577A patent/DE3917577A1/de not_active Withdrawn
- 1989-05-30 PL PL27967489A patent/PL279674A1/xx unknown
- 1989-05-30 RO RO139979A patent/RO105051B1/ro unknown
- 1989-05-31 NL NL8901385A patent/NL8901385A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
IT8920688A0 (it)	1989-05-30
ZA893794B (en)	1990-02-28
GR890100359A (el)	1990-03-12
PL279674A1 (en)	1990-01-08
HUT49981A (en)	1989-12-28
DE3917577A1 (de)	1989-12-07
NL8901385A (nl)	1989-12-18
RO105051B1 (en)	1994-12-19
IT1237400B (it)	1993-06-01

Legal Events

Date	Code	Title	Description
1996-06-20	ENJ	Ceased due to non-payment of renewal fee

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DE2857693C2 (de)	1986-10-09	Verfahren zur selektiven Bekämpfung bzw. Vernichtung von unerwünschtem Pflanzenwuchs in Nutzpflanzenkulturen
DE972405C (de)	1959-07-16	Mittel zur Regelung des Pflanzenwachstums
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