FI68499C - Motgifter foer pyrrolidonherbicider - Google Patents
Motgifter foer pyrrolidonherbicider Download PDFInfo
- Publication number
- FI68499C FI68499C FI824390A FI824390A FI68499C FI 68499 C FI68499 C FI 68499C FI 824390 A FI824390 A FI 824390A FI 824390 A FI824390 A FI 824390A FI 68499 C FI68499 C FI 68499C
- Authority
- FI
- Finland
- Prior art keywords
- carbon atoms
- hydrogen
- chlorine
- antidote
- bromine
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 claims description 72
- 239000000729 antidote Substances 0.000 claims description 70
- 239000004009 herbicide Substances 0.000 claims description 67
- 241000196324 Embryophyta Species 0.000 claims description 51
- 239000000460 chlorine Chemical group 0.000 claims description 50
- 239000000203 mixture Substances 0.000 claims description 39
- 239000001257 hydrogen Substances 0.000 claims description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- -1 pyrrolidone compound Chemical class 0.000 claims description 32
- 229910052801 chlorine Inorganic materials 0.000 claims description 31
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 28
- 150000002431 hydrogen Chemical group 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 19
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 15
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 15
- 229910052794 bromium Chemical group 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 8
- 239000003094 microcapsule Substances 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 description 18
- 239000002689 soil Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 229940075522 antidotes Drugs 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 8
- 238000004061 bleaching Methods 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 244000038559 crop plants Species 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- YRZIQWSPMZZTOS-UHFFFAOYSA-N n-benzyl-2,2-dichloro-n-ethylacetamide Chemical compound ClC(Cl)C(=O)N(CC)CC1=CC=CC=C1 YRZIQWSPMZZTOS-UHFFFAOYSA-N 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
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- 235000009344 Chenopodium album Nutrition 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 244000236458 Panicum colonum Species 0.000 description 4
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- 231100000674 Phytotoxicity Toxicity 0.000 description 4
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
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- XRRXDEMRTNDOQJ-UHFFFAOYSA-N 2,2,2-trifluoroethyl n-(4-chlorophenyl)carbamate Chemical compound FC(F)(F)COC(=O)NC1=CC=C(Cl)C=C1 XRRXDEMRTNDOQJ-UHFFFAOYSA-N 0.000 description 3
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- JWOLLWQJKQOEOL-UHFFFAOYSA-N OOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOO JWOLLWQJKQOEOL-UHFFFAOYSA-N 0.000 description 3
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 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
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- UIQWBVPFHHQZHH-UHFFFAOYSA-N OOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOO UIQWBVPFHHQZHH-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241001533104 Tribulus terrestris Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
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- 230000035784 germination Effects 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
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- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 2
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- 241000894007 species Species 0.000 description 2
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- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- MUKYLHIZBOASDM-UHFFFAOYSA-N 2-[carbamimidoyl(methyl)amino]acetic acid 2,3,4,5,6-pentahydroxyhexanoic acid Chemical compound NC(=N)N(C)CC(O)=O.OCC(O)C(O)C(O)C(O)C(O)=O MUKYLHIZBOASDM-UHFFFAOYSA-N 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
- 241000207892 Convolvulus Species 0.000 description 1
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- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
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- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- GQWNECFJGBQMBO-UHFFFAOYSA-N Molindone hydrochloride Chemical compound Cl.O=C1C=2C(CC)=C(C)NC=2CCC1CN1CCOCC1 GQWNECFJGBQMBO-UHFFFAOYSA-N 0.000 description 1
- 206010028293 Muscle contractions involuntary Diseases 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- HFEFMUSTGZNOPY-UHFFFAOYSA-N OOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOO HFEFMUSTGZNOPY-UHFFFAOYSA-N 0.000 description 1
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- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
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- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
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- 235000009430 Thespesia populnea Nutrition 0.000 description 1
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
- 241000009298 Trigla lyra Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 240000005371 Urochloa ramosa Species 0.000 description 1
- 241000282458 Ursus sp. Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- LDVVMCZRFWMZSG-UHFFFAOYSA-N captan Chemical compound C1C=CCC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 LDVVMCZRFWMZSG-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
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- 230000018109 developmental process Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloro-acetic acid amide Natural products NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
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- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
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- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000036435 stunted growth Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
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- 239000007762 w/o emulsion Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
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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
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33578881A | 1981-12-30 | 1981-12-30 | |
| US06/335,789 US4416685A (en) | 1981-12-30 | 1981-12-30 | Trifluoroethyl-p-chlorophenylcarbamate herbicide antidote |
| US33578881 | 1981-12-30 | ||
| US33578981 | 1981-12-30 | ||
| US33595081 | 1981-12-30 | ||
| US06/335,949 US4439227A (en) | 1981-12-30 | 1981-12-30 | Diallyl dichloroacetmide herbicide antidote |
| US06/335,950 US4441914A (en) | 1981-12-30 | 1981-12-30 | Dichloroacetyl oxazolidine herbicide antidotes |
| US33594981 | 1981-12-30 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI824390A0 FI824390A0 (fi) | 1982-12-21 |
| FI824390L FI824390L (fi) | 1983-07-01 |
| FI68499B FI68499B (fi) | 1985-06-28 |
| FI68499C true FI68499C (fi) | 1985-10-10 |
Family
ID=27502527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI824390A FI68499C (fi) | 1981-12-30 | 1982-12-21 | Motgifter foer pyrrolidonherbicider |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0084253B1 (cs) |
| AU (1) | AU550535B2 (cs) |
| DD (1) | DD210188A5 (cs) |
| DE (1) | DE3273603D1 (cs) |
| DK (1) | DK159182C (cs) |
| FI (1) | FI68499C (cs) |
| GR (1) | GR78425B (cs) |
| HU (1) | HU188605B (cs) |
| IE (1) | IE54469B1 (cs) |
| IL (1) | IL67588A (cs) |
| NO (1) | NO156131C (cs) |
| NZ (1) | NZ202886A (cs) |
| PL (1) | PL135092B1 (cs) |
| PT (1) | PT76048B (cs) |
| SU (1) | SU1301301A3 (cs) |
| TR (1) | TR21550A (cs) |
| YU (1) | YU291782A (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ222993A (en) * | 1986-12-22 | 1989-09-27 | Stauffer Agricultural Chemical | Herbicidal compositions containing an acyl substituted oxazolidone antidote and two active herbicides |
| DE10022989A1 (de) * | 2000-05-11 | 2001-11-22 | Aventis Cropscience Gmbh | Kombinationen von Pflanzenschutzmitteln mit organischen oder anorganischen Trägermaterialien |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3959304A (en) * | 1974-07-01 | 1976-05-25 | Stauffer Chemical Company | Certain 3-haloacyl-2,2,5-trimethyl-oxazolidines |
| US4210589A (en) * | 1975-03-28 | 1980-07-01 | Stauffer Chemical Company | Method of preparation for aromatic N-substituted halo-substituted 2-pyrrolidinones |
| US4276078A (en) * | 1978-08-04 | 1981-06-30 | Stauffer Chemical Company | Herbicide compositions |
| AT363566B (de) * | 1978-08-08 | 1981-08-10 | Fleck Carl Maria Doz Dr | Verfahren und vorrichtung zur messung der lokalen leistung in kernreaktoren |
-
1982
- 1982-12-20 GR GR70108A patent/GR78425B/el unknown
- 1982-12-21 FI FI824390A patent/FI68499C/fi not_active IP Right Cessation
- 1982-12-22 NZ NZ202886A patent/NZ202886A/en unknown
- 1982-12-22 DK DK567282A patent/DK159182C/da not_active IP Right Cessation
- 1982-12-23 DE DE8282306906T patent/DE3273603D1/de not_active Expired
- 1982-12-23 EP EP82306906A patent/EP0084253B1/en not_active Expired
- 1982-12-24 AU AU91909/82A patent/AU550535B2/en not_active Ceased
- 1982-12-28 NO NO824397A patent/NO156131C/no unknown
- 1982-12-28 SU SU823558789A patent/SU1301301A3/ru active
- 1982-12-29 HU HU824228A patent/HU188605B/hu not_active IP Right Cessation
- 1982-12-29 PT PT76048A patent/PT76048B/pt not_active IP Right Cessation
- 1982-12-29 IL IL67588A patent/IL67588A/xx unknown
- 1982-12-30 PL PL1982239878A patent/PL135092B1/pl unknown
- 1982-12-30 YU YU02917/82A patent/YU291782A/xx unknown
- 1982-12-30 TR TR21550A patent/TR21550A/xx unknown
- 1982-12-30 IE IE3093/82A patent/IE54469B1/en not_active IP Right Cessation
- 1982-12-30 DD DD82246830A patent/DD210188A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FI824390L (fi) | 1983-07-01 |
| DK159182C (da) | 1991-02-25 |
| FI68499B (fi) | 1985-06-28 |
| DE3273603D1 (en) | 1986-11-06 |
| PT76048A (en) | 1983-01-01 |
| DK159182B (da) | 1990-09-17 |
| YU291782A (en) | 1985-06-30 |
| HU188605B (en) | 1986-04-28 |
| EP0084253B1 (en) | 1986-10-01 |
| GR78425B (cs) | 1984-09-27 |
| PL239878A1 (en) | 1983-08-15 |
| EP0084253A1 (en) | 1983-07-27 |
| DK567282A (da) | 1983-07-01 |
| PT76048B (en) | 1985-11-18 |
| TR21550A (tr) | 1984-09-28 |
| NZ202886A (en) | 1984-12-14 |
| PL135092B1 (en) | 1985-09-30 |
| DD210188A5 (de) | 1984-06-06 |
| AU9190982A (en) | 1983-07-07 |
| IE823093L (en) | 1983-06-30 |
| IL67588A (en) | 1986-01-31 |
| NO156131B (no) | 1987-04-21 |
| AU550535B2 (en) | 1986-03-27 |
| NO156131C (no) | 1987-09-02 |
| SU1301301A3 (ru) | 1987-03-30 |
| FI824390A0 (fi) | 1982-12-21 |
| NO824397L (no) | 1983-07-01 |
| IE54469B1 (en) | 1989-10-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: STAUFFER CHEMICAL COMPANY |