DE2855229C2 - Dichloracetamide und diese enthaltende Herbizide - Google Patents
Dichloracetamide und diese enthaltende HerbizideInfo
- Publication number
- DE2855229C2 DE2855229C2 DE2855229A DE2855229A DE2855229C2 DE 2855229 C2 DE2855229 C2 DE 2855229C2 DE 2855229 A DE2855229 A DE 2855229A DE 2855229 A DE2855229 A DE 2855229A DE 2855229 C2 DE2855229 C2 DE 2855229C2
- Authority
- DE
- Germany
- Prior art keywords
- udf54
- udf53
- maize
- dichloroacetamides
- dichloroallyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000004009 herbicide Substances 0.000 title claims description 18
- WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 title claims description 7
- 240000008042 Zea mays Species 0.000 claims description 20
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 14
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 14
- 235000009973 maize Nutrition 0.000 claims description 14
- 230000002363 herbicidal effect Effects 0.000 claims description 12
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002333 glycines Chemical class 0.000 claims description 2
- 231100000252 nontoxic Toxicity 0.000 claims description 2
- 230000003000 nontoxic effect Effects 0.000 claims description 2
- 239000004471 Glycine Substances 0.000 claims 1
- 239000000729 antidote Substances 0.000 description 17
- 229940075522 antidotes Drugs 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- WFKSADNZWSKCRZ-UHFFFAOYSA-N Diethatyl-ethyl Chemical compound CCOC(=O)CN(C(=O)CCl)C1=C(CC)C=CC=C1CC WFKSADNZWSKCRZ-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 150000002332 glycine derivatives Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000007832 Na2SO4 Substances 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KHMZDLNSWZGRDB-UHFFFAOYSA-N 1,3,3-trichloroprop-1-ene Chemical compound ClC=CC(Cl)Cl KHMZDLNSWZGRDB-UHFFFAOYSA-N 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 241000209764 Avena fatua Species 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
- 244000100545 Lolium multiflorum Species 0.000 description 2
- 244000115721 Pennisetum typhoides Species 0.000 description 2
- 235000007195 Pennisetum typhoides Nutrition 0.000 description 2
- 235000021501 Rumex crispus Nutrition 0.000 description 2
- 244000207667 Rumex vesicarius Species 0.000 description 2
- 235000008515 Setaria glauca Nutrition 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 240000006394 Sorghum bicolor Species 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 235000010726 Vigna sinensis Nutrition 0.000 description 2
- 241000219994 Vigna unguiculata subsp. unguiculata Species 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 231100000572 poisoning Toxicity 0.000 description 2
- 230000000607 poisoning effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- IHNGFMNOFGWIEZ-UHFFFAOYSA-N 2-(n-(2-chloroacetyl)-2,6-diethylanilino)butanoic acid Chemical compound CCC(C(O)=O)N(C(=O)CCl)C1=C(CC)C=CC=C1CC IHNGFMNOFGWIEZ-UHFFFAOYSA-N 0.000 description 1
- RRZDKGYPLSMZNJ-UHFFFAOYSA-N 2-(n-(2-chloroacetyl)-2-ethyl-6-methylanilino)-3-methylbutanoic acid Chemical compound CCC1=CC=CC(C)=C1N(C(C(C)C)C(O)=O)C(=O)CCl RRZDKGYPLSMZNJ-UHFFFAOYSA-N 0.000 description 1
- VUGCBIWQHSRQBZ-UHFFFAOYSA-N 2-methylbut-3-yn-2-amine Chemical compound CC(C)(N)C#C VUGCBIWQHSRQBZ-UHFFFAOYSA-N 0.000 description 1
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 241001295925 Gegenes Species 0.000 description 1
- 108010049175 N-substituted Glycines Proteins 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 150000003918 triazines Chemical class 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT31189/77A IT1114195B (it) | 1977-12-23 | 1977-12-23 | Due antidotti dicloroacetamidici per erbicidi non selettivi particolarmente attivi a proteggere il mais dall'azione tossica esercitata da esteri della glicina n,n disostituita erbicidi |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2855229A1 DE2855229A1 (de) | 1979-07-05 |
| DE2855229C2 true DE2855229C2 (de) | 1987-02-19 |
Family
ID=11233249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2855229A Expired DE2855229C2 (de) | 1977-12-23 | 1978-12-21 | Dichloracetamide und diese enthaltende Herbizide |
Country Status (14)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4258060A (en) * | 1979-08-13 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Substituted trichloropropylureas as plant disease control agents |
| CA1168056A (en) * | 1981-10-20 | 1984-05-29 | Attilio Formigoni | Weed-killer composition containing amides as antidotes for alpha-halo-acetanilides |
| JPS61293956A (ja) * | 1985-06-21 | 1986-12-24 | Tokuyama Soda Co Ltd | クロロアセトアミド化合物及びその製造方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4033756A (en) * | 1971-09-17 | 1977-07-05 | Gulf Research & Development Company | Dichloroacetamide treated rice seeds |
| US4021224A (en) * | 1971-12-09 | 1977-05-03 | Stauffer Chemical Company | Herbicide compositions |
| US3867444A (en) * | 1972-07-17 | 1975-02-18 | Stauffer Chemical Co | Schiff{3 s base dichloroacetamides |
| CH574207A5 (US20110232667A1-20110929-C00004.png) * | 1973-01-25 | 1976-04-15 | Ciba Geigy Ag | |
| US4053297A (en) * | 1975-04-21 | 1977-10-11 | Velsicol Chemical Corporation | Selective herbicidal compositions |
| IT1079199B (it) * | 1976-10-29 | 1985-05-08 | Montedison Spa | Antidoti,della classe delle dicloroacetamidi particolarmente attivi a proteggere il mais dalla azione tossica esercitata da esteri delle glicine n,n sostituite ebricide e associazione erbicida per culture di mais |
-
1977
- 1977-12-23 IT IT31189/77A patent/IT1114195B/it active
-
1978
- 1978-12-21 DE DE2855229A patent/DE2855229C2/de not_active Expired
- 1978-12-21 FR FR7835895A patent/FR2413362A2/fr active Granted
- 1978-12-21 ZA ZA00787170A patent/ZA787170B/xx unknown
- 1978-12-21 HU HU78MO1030A patent/HU182539B/hu not_active IP Right Cessation
- 1978-12-21 JP JP15693778A patent/JPS54106423A/ja active Granted
- 1978-12-21 US US05/971,713 patent/US4228101A/en not_active Expired - Lifetime
- 1978-12-21 YU YU3040/78A patent/YU40545B/xx unknown
- 1978-12-22 CA CA318,487A patent/CA1105055A/en not_active Expired
- 1978-12-22 PH PH21984A patent/PH15038A/en unknown
- 1978-12-22 IN IN1363/CAL/78A patent/IN149995B/en unknown
- 1978-12-22 BR BR7808460A patent/BR7808460A/pt unknown
- 1978-12-23 EG EG734/78A patent/EG13555A/xx active
-
1979
- 1979-01-03 MX MX797624U patent/MX6286E/es unknown
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| YU304078A (en) | 1983-12-31 |
| IT1114195B (it) | 1986-01-27 |
| DE2855229A1 (de) | 1979-07-05 |
| IN149995B (US20110232667A1-20110929-C00004.png) | 1982-06-26 |
| JPS54106423A (en) | 1979-08-21 |
| FR2413362B2 (US20110232667A1-20110929-C00004.png) | 1981-07-17 |
| ZA787170B (en) | 1979-12-27 |
| PH15038A (en) | 1982-05-20 |
| BR7808460A (pt) | 1979-08-07 |
| US4228101A (en) | 1980-10-14 |
| MX6286E (es) | 1985-03-18 |
| YU40545B (en) | 1986-02-28 |
| EG13555A (en) | 1981-12-31 |
| CA1105055A (en) | 1981-07-14 |
| FR2413362A2 (fr) | 1979-07-27 |
| JPS6319482B2 (US20110232667A1-20110929-C00004.png) | 1988-04-22 |
| HU182539B (en) | 1984-02-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1567212C3 (de) | Fungicides Mittel nut bactericider Nebenwirkung | |
| DE2433680A1 (de) | 2,3-dihydro-2,2-dimethyl-7-benzofuranylmethylcarbamat-n-aminosulfenyl-derivate, verfahren zu deren herstellung und diese verbindungen enthaltende insektizide zusammensetzungen | |
| DE2654331C2 (US20110232667A1-20110929-C00004.png) | ||
| DE2741437C2 (US20110232667A1-20110929-C00004.png) | ||
| DE2515113C2 (US20110232667A1-20110929-C00004.png) | ||
| DE2747814C2 (de) | Dichloracetamide, ihre Herstellung und diese enthaltende herbizide Mittel | |
| DE1169194B (de) | Mittel mit insektizider und akarizider Wirkung | |
| EP0031938A2 (de) | Verwendung von Aryloxy(thio)carbonsäurenitrilen und-amidoximen als Herbizid-Antidote | |
| DE2643403C2 (de) | Thiocarbonsäurederivate, Verfahren zu deren Herstellung und diese enthaltende Mittel | |
| DE2855229C2 (de) | Dichloracetamide und diese enthaltende Herbizide | |
| DE2015527C3 (de) | Cyanoalkylaldoximcarbamate und ihre Verwendung als Insektizide | |
| DD149935A5 (de) | Verfahren zur herstellung von racemen oder optisch aktivem 2-(propargyloxyimino)-1,7,7-trimethylbicyclo(2,2,1)heptan | |
| CH641175A5 (de) | Lacton-derivate und thiolacton-derivate und deren verwendung zur bekaempfung von pilzen. | |
| AT389625B (de) | Verwendung von substituierten glycinamiden als antidota in herbiziden mitteln und herbizide mittel | |
| DE1025203B (de) | Bekaempfung von Pflanzenparasiten | |
| DE2605586C2 (US20110232667A1-20110929-C00004.png) | ||
| DE1143668B (de) | Fungizide Mittel | |
| DE2362333C3 (de) | Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben | |
| DE4011781A1 (de) | Herbizides mittel | |
| DE2266035C2 (US20110232667A1-20110929-C00004.png) | ||
| DE2104857C3 (de) | N-Benzylcarboxamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide | |
| DE2441741C2 (de) | Saatschützende herbizide Zubereitung und ihre Verwendung | |
| AT380383B (de) | Fungizide zusammensetzung | |
| DE2112643B2 (de) | Formanüdin-Denvate und sie enthaltende Mittel | |
| DE2634278A1 (de) | Unkrautvertilgungsmittel, die dibromsubstituierte propionamide als antidots enthalten |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| AF | Is addition to no. |
Ref country code: DE Ref document number: 2747814 Format of ref document f/p: P |
|
| AF | Is addition to no. |
Ref country code: DE Ref document number: 2747814 Format of ref document f/p: P |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8340 | Patent of addition ceased/non-payment of fee of main patent |