DD216377A5 - Antidotum-praeparat - Google Patents

Antidotum-praeparat Download PDF

Info

Publication number: DD216377A5
Authority: DD; German Democratic Republic
Prior art keywords: group; carbon atoms; antidote; alkyl group; antidotum
Prior art date: 1982-07-14

Application number

DD83262629A

Other languages

German (de)

English (en)

Inventor

Gyoergy Matolcsy

Barna Bordas

Antal Gimesi

Magdolna Kovacs

Marton Tueske

Original Assignee

Eszakmagyar Vegyimuevek

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.)

1982-07-14

Filing date

1983-07-13

Publication date

1984-12-12

1983-07-13 Application filed by Eszakmagyar Vegyimuevek filed Critical Eszakmagyar Vegyimuevek

1984-12-12 Publication of DD216377A5 publication Critical patent/DD216377A5/de

Links

239000000729 antidote Substances 0.000 title claims abstract description 51
238000002360 preparation method Methods 0.000 title claims abstract description 27
239000004480 active ingredient Substances 0.000 claims abstract description 19
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
125000000217 alkyl group Chemical group 0.000 claims abstract description 9
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims abstract description 6
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 5
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
150000003869 acetamides Chemical class 0.000 claims abstract description 3
125000003342 alkenyl group Chemical group 0.000 claims abstract description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 20
241000196324 Embryophyta Species 0.000 description 17
240000008042 Zea mays Species 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
235000002017 Zea mays subsp mays Nutrition 0.000 description 15
239000004009 herbicide Substances 0.000 description 14
230000002363 herbicidal effect Effects 0.000 description 13
239000000203 mixture Substances 0.000 description 13
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 11
235000005822 corn Nutrition 0.000 description 11
229910052757 nitrogen Inorganic materials 0.000 description 11
239000000243 solution Substances 0.000 description 11
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
229940075522 antidotes Drugs 0.000 description 10
230000000694 effects Effects 0.000 description 9
-1 nitrogen-containing heterocyclic compounds Chemical class 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
DFCAFRGABIXSDS-UHFFFAOYSA-N Cycloate Chemical compound CCSC(=O)N(CC)C1CCCCC1 DFCAFRGABIXSDS-UHFFFAOYSA-N 0.000 description 7
239000000839 emulsion Substances 0.000 description 7
240000004713 Pisum sativum Species 0.000 description 6
235000010582 Pisum sativum Nutrition 0.000 description 6
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 6
230000009931 harmful effect Effects 0.000 description 6
239000002689 soil Substances 0.000 description 6
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 5
235000021536 Sugar beet Nutrition 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000012141 concentrate Substances 0.000 description 5
235000008504 concentrate Nutrition 0.000 description 5
238000002474 experimental method Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
230000001681 protective effect Effects 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000004576 sand Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 4
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 4
239000000969 carrier Substances 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
229940079593 drug Drugs 0.000 description 4
239000003814 drug Substances 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
239000007789 gas Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
235000009973 maize Nutrition 0.000 description 4
239000003921 oil Substances 0.000 description 4
238000009331 sowing Methods 0.000 description 4
238000005507 spraying Methods 0.000 description 4
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
244000075850 Avena orientalis Species 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
240000005979 Hordeum vulgare Species 0.000 description 3
235000007340 Hordeum vulgare Nutrition 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
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
238000001816 cooling Methods 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
229940093475 2-ethoxyethanol Drugs 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
235000005781 Avena Nutrition 0.000 description 2
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 2
241000192043 Echinochloa Species 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
239000006004 Quartz sand Substances 0.000 description 2
241000220261 Sinapis Species 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
230000002159 abnormal effect Effects 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
230000002605 anti-dotal effect Effects 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
238000007865 diluting Methods 0.000 description 2
238000011156 evaluation Methods 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
239000000463 material Substances 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 2
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 2
WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical class CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
COAABSMONFNYQH-TTWCUHKNSA-N (2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(oxiran-2-ylmethylsulfanyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1SCC1OC1 COAABSMONFNYQH-TTWCUHKNSA-N 0.000 description 1
LPVPNRSVMLNXGQ-UHFFFAOYSA-N 1-(azepan-1-yl)-2,2-dichloroethanone Chemical compound ClC(Cl)C(=O)N1CCCCCC1 LPVPNRSVMLNXGQ-UHFFFAOYSA-N 0.000 description 1
CSJXXXVSKOYFEM-UHFFFAOYSA-N 2,2-dichloro-n-(2-ethoxyethoxymethyl)-n-(3-methylbutyl)acetamide Chemical compound CCOCCOCN(C(=O)C(Cl)Cl)CCC(C)C CSJXXXVSKOYFEM-UHFFFAOYSA-N 0.000 description 1
QUTCNOUBSBYDKI-UHFFFAOYSA-N 2,2-dichloro-n-(2-ethoxyethoxymethyl)-n-propylacetamide Chemical compound CCCN(C(=O)C(Cl)Cl)COCCOCC QUTCNOUBSBYDKI-UHFFFAOYSA-N 0.000 description 1
SXEBYDPDAWIBRV-UHFFFAOYSA-N 2,2-dichloro-n-(2-methoxyethoxymethyl)-n-prop-2-enylacetamide Chemical compound COCCOCN(CC=C)C(=O)C(Cl)Cl SXEBYDPDAWIBRV-UHFFFAOYSA-N 0.000 description 1
OULUTVKIEJPRQG-UHFFFAOYSA-N 2,2-dichloro-n-[ethoxy(methoxy)methyl]-n-propylacetamide Chemical compound CCCN(C(=O)C(Cl)Cl)C(OC)OCC OULUTVKIEJPRQG-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
RGBTVAFCTYXACZ-UHFFFAOYSA-N 2-chloro-4-methoxy-3-methyl-n-phenylbutanamide Chemical compound COCC(C)C(Cl)C(=O)NC1=CC=CC=C1 RGBTVAFCTYXACZ-UHFFFAOYSA-N 0.000 description 1
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
101150106303 AHSG gene Proteins 0.000 description 1
235000006760 Acer pensylvanicum Nutrition 0.000 description 1
240000002245 Acer pensylvanicum Species 0.000 description 1
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
241000251730 Chondrichthyes Species 0.000 description 1
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
241001057636 Dracaena deremensis Species 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
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
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 description 1
241000209510 Liliopsida Species 0.000 description 1
241001092142 Molina Species 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
244000115721 Pennisetum typhoides Species 0.000 description 1
235000007195 Pennisetum typhoides Nutrition 0.000 description 1
241001310793 Podium Species 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
241000218201 Ranunculaceae Species 0.000 description 1
235000008515 Setaria glauca Nutrition 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
235000007244 Zea mays Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000002671 adjuvant Substances 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
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003139 biocide Substances 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
239000002734 clay mineral Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000011161 development Methods 0.000 description 1
229940058963 dichloroacetamide derivative drug for amoebiasis and other protozoal diseases Drugs 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000003203 everyday effect Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
244000230030 foxtail bristlegrass Species 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000000034 method Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
229940044654 phenolsulfonic acid Drugs 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 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
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D309/06—Radicals substituted by oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Toxicology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD83262629A 1982-07-14 1983-07-13 Antidotum-praeparat DD216377A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU822288A HU183997B (en)	1982-07-14	1982-07-14	Herbicide and antidote composition resp. containing thiolcarba mate derivative and/or chloroacetanilide derivatives as herbicide and/or substituted acetamide antidote

Publications (1)

Publication Number	Publication Date
DD216377A5 true DD216377A5 (de)	1984-12-12

Family

ID=10958696

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD83262629A DD216377A5 (de)	1982-07-14	1983-07-13	Antidotum-praeparat
DD25303783A DD210827A5 (de)	1982-07-14	1983-07-13	Antidotierte Herbizide Zusammensetzungen

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD25303783A DD210827A5 (de)	1982-07-14	1983-07-13	Antidotierte Herbizide Zusammensetzungen

Country Status (21)

Country	Link
US (2)	US4605764A (xx)
BE (1)	BE897291A (xx)
CS (1)	CS235330B2 (xx)
DD (2)	DD216377A5 (xx)
DE (1)	DE3325152A1 (xx)
DK (1)	DK323783A (xx)
ES (1)	ES8504669A1 (xx)
FR (1)	FR2530237B1 (xx)
GB (1)	GB2124222B (xx)
GR (1)	GR77574B (xx)
HU (1)	HU183997B (xx)
IE (1)	IE55597B1 (xx)
IT (1)	IT1200929B (xx)
LU (1)	LU84897A1 (xx)
NL (1)	NL8302514A (xx)
PL (1)	PL137023B1 (xx)
PT (1)	PT77022B (xx)
RO (1)	RO86849B (xx)
SU (2)	SU1482506A3 (xx)
TR (1)	TR22313A (xx)
YU (1)	YU43830B (xx)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0174278B1 (de) *	1984-09-03	1989-04-19	Ciba-Geigy Ag	Neue N-(substituierte Alkyl)-dichloracetamid-derivate
HUT49981A (en) *	1988-05-31	1989-12-28	Eszakmagyar Vegyimuevek	Antidotal herbicide comprising chloroacetanilide derivative as active ingredient
US5201933A (en) *	1988-08-01	1993-04-13	Monsanto Company	Safening herbicidal benzoic acid derivatives
US20050203176A1 (en) *	2004-03-12	2005-09-15	Wyeth	Carbamates as HIV anti-viral agents

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3287106A (en) *	1963-11-15	1966-11-22	Monsanto Co	Method for inhibiting the growth of grass type weeds
US3268324A (en) *	1965-10-11	1966-08-23	Monsanto Co	Herbicidal composition and method employing oxa aliphatic acetamide
US4021224A (en) *	1971-12-09	1977-05-03	Stauffer Chemical Company	Herbicide compositions
IN144916B (xx) *	1975-08-08	1978-07-29	Stauffer Chemical Co
FR2399408A1 (fr) *	1977-08-03	1979-03-02	Ugine Kuhlmann	Derives de dichloroacetamide et trichloroacetamide antidotes d'herbicides
DE2832950A1 (de) *	1978-07-27	1980-02-21	Basf Ag	Herbizide mittel
US4443628A (en) *	1979-12-26	1984-04-17	Ppg Industries, Inc.	Antidotal compounds for use with herbicides

1982
- 1982-07-14 HU HU822288A patent/HU183997B/hu not_active IP Right Cessation
1983
- 1983-07-04 LU LU84897A patent/LU84897A1/de unknown
- 1983-07-06 IE IE1580/83A patent/IE55597B1/en unknown
- 1983-07-12 RO RO111610A patent/RO86849B/ro unknown
- 1983-07-12 DE DE19833325152 patent/DE3325152A1/de not_active Withdrawn
- 1983-07-12 YU YU1505/83A patent/YU43830B/xx unknown
- 1983-07-12 FR FR8311597A patent/FR2530237B1/fr not_active Expired
- 1983-07-12 IT IT48672/83A patent/IT1200929B/it active
- 1983-07-13 DD DD83262629A patent/DD216377A5/de unknown
- 1983-07-13 US US06/513,215 patent/US4605764A/en not_active Expired - Fee Related
- 1983-07-13 DK DK323783A patent/DK323783A/da not_active Application Discontinuation
- 1983-07-13 GR GR71934A patent/GR77574B/el unknown
- 1983-07-13 DD DD25303783A patent/DD210827A5/de unknown
- 1983-07-13 GB GB08318948A patent/GB2124222B/en not_active Expired
- 1983-07-13 PT PT77022A patent/PT77022B/pt unknown
- 1983-07-14 CS CS835326A patent/CS235330B2/cs unknown
- 1983-07-14 PL PL1983243008A patent/PL137023B1/pl unknown
- 1983-07-14 NL NL8302514A patent/NL8302514A/nl not_active Application Discontinuation
- 1983-07-14 SU SU833622526A patent/SU1482506A3/ru active
- 1983-07-14 ES ES524122A patent/ES8504669A1/es not_active Expired
- 1983-07-14 BE BE0/211174A patent/BE897291A/fr not_active IP Right Cessation
- 1983-07-15 TR TR4550A patent/TR22313A/xx unknown
1984
- 1984-07-23 SU SU843765008A patent/SU1251799A3/ru active
1986
- 1986-03-10 US US06/838,271 patent/US4843177A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
RO86849A (ro)	1985-05-20
YU150583A (en)	1986-08-31
PL137023B1 (en)	1986-04-30
GB8318948D0 (en)	1983-08-17
IT8348672A0 (it)	1983-07-12
DE3325152A1 (de)	1984-01-19
DK323783D0 (da)	1983-07-13
ES524122A0 (es)	1985-05-01
CS235330B2 (en)	1985-05-15
FR2530237B1 (fr)	1986-04-18
BE897291A (fr)	1983-11-03
GB2124222B (en)	1986-03-05
PT77022B (en)	1986-01-24
HU183997B (en)	1984-06-28
DD210827A5 (de)	1984-06-27
TR22313A (tr)	1987-01-30
IT1200929B (it)	1989-01-27
GR77574B (xx)	1984-09-24
LU84897A1 (de)	1983-12-05
US4605764A (en)	1986-08-12
RO86849B (ro)	1985-05-31
PL243008A1 (en)	1984-07-16
DK323783A (da)	1984-01-15
FR2530237A1 (fr)	1984-01-20
GB2124222A (en)	1984-02-15
IE831580L (en)	1984-01-14
YU43830B (en)	1989-12-31
PT77022A (en)	1983-08-01
US4843177A (en)	1989-06-27
ES8504669A1 (es)	1985-05-01
SU1482506A3 (ru)	1989-05-23
IE55597B1 (en)	1990-11-21
NL8302514A (nl)	1984-02-01
SU1251799A3 (ru)	1986-08-15

Publication	Publication Date	Title
EP0191736B1 (de)	1991-07-17	Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen
DE2639405C2 (de)	1983-12-29	Phenylglyoxylnitril-2-oximcyanmethyläther, Verfahren zu dessen Herstellung und Mittel, welche diesen als Gegenmittel für Kulturpflanzen schädigende Herbizide enthalten
EP0139613A1 (de)	1985-05-02	N-(2-Nitrophenyl)-4-aminopyrimidin-Derivate, deren Herstellung und Verwendung
EP0172786A2 (de)	1986-02-26	Pyrimidinderivate wirksam als Schädlingsbekämpfungsmittel
DE1913726C3 (de)	1981-12-03	Mittel zur Bekämpfung von Pilzen auf Basis von Pyrazinderivaten
EP0159287B1 (de)	1989-10-11	Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen
EP0149974A2 (de)	1985-07-31	Mittel zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von Herbiziden
DE2628384A1 (de)	1978-04-13	Herbizide und fungizide mittel
DE3520760A1 (de)	1986-03-20	Mittel zur verzoegerung der wirkung herbizider praeparate und herbizide praeparate mit verzoegerter wirkung und verfahren zu deren herstellung
DD216377A5 (de)	1984-12-12	Antidotum-praeparat
DE2123277A1 (de)	1971-12-02	Insektizide Mittel
AT391587B (de)	1990-10-25	Herbizides mittel
DE2813335C2 (de)	1987-04-09	N-acylierte N-Alkylaniline, Verfahren zu ihrer Herstellung sowie mikrobizide Mittel enthaltend diese als Wirkstoffe
DD149889A5 (de)	1981-08-05	Verfahren zur verringerung der schaedigung von kulturpflanzen
EP0065483A1 (de)	1982-11-24	Mikrobizide Acylanilin- und Acylnaphthylamin-Derivate, Verfahren zu deren Herstellung und ihre Verwendung
US3352750A (en)	1967-11-14	Alkyl-substituted-benzoquinone-4-oximinyl nu-alkyl carbamates and use as fungicides
EP0126710A1 (de)	1984-11-28	Mittel zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von Herbiziden
EP0174278B1 (de)	1989-04-19	Neue N-(substituierte Alkyl)-dichloracetamid-derivate
DD149455A5 (de)	1981-07-15	Fungizide zusammensetzung
CH643240A5 (de)	1984-05-30	2-hydroxybenzamidderivate mit fungizider wirkung.
EP0101404A2 (de)	1984-02-22	Organozinnester mit acylierten Aminocarbonsäuren und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0170905B1 (de)	1988-04-27	alpha-Acyloximino-alkanphosphon-(und-phosphin)-säureester, ihre Herstellung und Verwendung im Pflanzenschutz
DE1810581C3 (de)	1977-12-29	N-Acyl-p-dialkylamino-phenylhydrazone, Verfahren zu ihrer Herstellung und deren Verwendung zur Bekämpfung von phytopathogene Pilzen
DD149991A5 (de)	1981-08-12	Fungizide mittel
DE2917893A1 (de)	1980-11-13	N-(alkoxy- bzw. alkoxycarbonalalkyl)- n-hydroxyacetyl- bzw. propionyl-anilin- derivate als pflanzenfungizide