DD253566A5 - Insektizides, mitizides, nematizides oder bodenpestizides mittel - Google Patents
Insektizides, mitizides, nematizides oder bodenpestizides mittel Download PDFInfo
- Publication number
- DD253566A5 DD253566A5 DD85285351A DD28535185A DD253566A5 DD 253566 A5 DD253566 A5 DD 253566A5 DD 85285351 A DD85285351 A DD 85285351A DD 28535185 A DD28535185 A DD 28535185A DD 253566 A5 DD253566 A5 DD 253566A5
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- DD
- German Democratic Republic
- Prior art keywords
- group
- item
- ethyl
- butyl
- composition according
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- 239000002917 insecticide Substances 0.000 title description 13
- 239000000642 acaricide Substances 0.000 title description 6
- 239000005645 nematicide Substances 0.000 title description 6
- 239000000203 mixture Substances 0.000 claims abstract description 61
- -1 phosphate compound Chemical class 0.000 claims abstract description 53
- 150000002903 organophosphorus compounds Chemical class 0.000 claims abstract description 25
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 19
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 230000001069 nematicidal effect Effects 0.000 claims abstract description 10
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 7
- 230000003129 miticidal effect Effects 0.000 claims abstract description 7
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims abstract description 4
- 125000004434 sulfur atom Chemical group 0.000 claims abstract description 3
- 241000238631 Hexapoda Species 0.000 claims description 29
- 239000002689 soil Substances 0.000 claims description 28
- 241000607479 Yersinia pestis Species 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 241000238876 Acari Species 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 16
- 241000244206 Nematoda Species 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000004414 alkyl thio group Chemical group 0.000 claims description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 230000001681 protective effect Effects 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 8
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical group S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 abstract description 4
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- 230000000694 effects Effects 0.000 abstract description 2
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- 125000000547 substituted alkyl group Chemical group 0.000 abstract 2
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- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
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- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
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- 239000002728 pyrethroid Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003252 quinoxalines Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-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
- 239000004455 soybean meal Substances 0.000 description 1
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- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000007944 thiolates Chemical class 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 241000701366 unidentified nuclear polyhedrosis viruses Species 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/80—Two oxygen atoms, e.g. hydantoin with hetero atoms or acyl radicals directly attached to ring nitrogen atoms
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
- A01N57/32—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27848184 | 1984-12-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD253566A5 true DD253566A5 (de) | 1988-01-27 |
Family
ID=17597928
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD85285351A DD253566A5 (de) | 1984-12-27 | 1985-12-24 | Insektizides, mitizides, nematizides oder bodenpestizides mittel |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4645761A (fr) |
| EP (1) | EP0186124B1 (fr) |
| JP (1) | JPH066597B2 (fr) |
| KR (1) | KR920004981B1 (fr) |
| CN (1) | CN1007981B (fr) |
| AR (1) | AR242584A1 (fr) |
| AU (1) | AU583870B2 (fr) |
| BR (1) | BR8506556A (fr) |
| CA (1) | CA1261851A (fr) |
| DD (1) | DD253566A5 (fr) |
| DE (1) | DE3569116D1 (fr) |
| ES (1) | ES8703889A1 (fr) |
| MX (1) | MX168931B (fr) |
| PH (1) | PH21820A (fr) |
| PL (1) | PL148149B1 (fr) |
| RO (1) | RO93255B (fr) |
| SU (1) | SU1553008A3 (fr) |
| ZA (1) | ZA859758B (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3670292D1 (de) * | 1985-06-25 | 1990-05-17 | Ishihara Sangyo Kaisha | Organophosphorverbindungen, verfahren zu ihrer herstellung und sie enthaltende insektizide, mitizide, nematozide oder bodenpestizide praeparate. |
| US5705176A (en) * | 1986-12-09 | 1998-01-06 | Stapleton; Billy J. | Insecticidal bait composition for cockroaches |
| US5346700A (en) * | 1986-12-09 | 1994-09-13 | Stapleton Billy J | Insecticidal bait composition for cockroaches |
| US6007832A (en) * | 1987-02-24 | 1999-12-28 | Stapleton; Billy J. | Insecticidal bait composition for cockroaches |
| US4839349A (en) * | 1988-06-03 | 1989-06-13 | Uniroyal Chemical Company, Inc. | Phosphorus substituted tetrazolinones and pesticidal use |
| JPH0739430B2 (ja) * | 1990-07-06 | 1995-05-01 | アグロカネショウ株式会社 | 有機リン化合物、その製造法および該化合物を含有する殺虫、殺ダニ、殺線虫剤 |
| JP2700743B2 (ja) * | 1992-09-16 | 1998-01-21 | アグロカネショウ株式会社 | 有機リン化合物、その製造法および該化合物を含有する殺虫、殺ダニ、殺線虫剤 |
| CN1088344C (zh) * | 1997-10-17 | 2002-07-31 | 青岛市卫生防疫站 | 富硒或富锌蚯蚓干粉或提取物的制造方法 |
| US9540330B2 (en) * | 2010-12-15 | 2017-01-10 | Nektar Therapeutics | Oligomer-containing hydantoin compounds |
| CN102246818A (zh) * | 2011-08-08 | 2011-11-23 | 陕西美邦农药有限公司 | 一种含有机磷类化合物的杀虫组合物 |
| CN105777647B (zh) * | 2016-04-06 | 2018-06-01 | 江苏快达农化股份有限公司 | 一种合成1-异丙基氨基甲酰胺-3-(3,5-二氯苯基)乙内酰脲的方法 |
| FR3115475A1 (fr) | 2020-10-23 | 2022-04-29 | IFP Energies Nouvelles | Procede de preparation d’un catalyseur a base d’izm-2 par un traitement thermique specifique et utilisation dudit catalyseur pour l’isomerisation de charges paraffiniques en distillats moyens |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH439306A (fr) * | 1965-07-09 | 1967-07-15 | Sandoz Ag | Procédé de préparation de nouvelles N-phosphamides de 2-imidazolidine-thione |
| US4237122A (en) * | 1978-06-22 | 1980-12-02 | Sumitomo Chemical Company, Limited | Imidazolidinedione compounds, and their production and use |
-
1985
- 1985-12-11 AU AU51121/85A patent/AU583870B2/en not_active Ceased
- 1985-12-18 MX MX001019A patent/MX168931B/es unknown
- 1985-12-18 US US06/810,266 patent/US4645761A/en not_active Expired - Lifetime
- 1985-12-18 EP EP85116176A patent/EP0186124B1/fr not_active Expired
- 1985-12-18 DE DE8585116176T patent/DE3569116D1/de not_active Expired
- 1985-12-20 ZA ZA859758A patent/ZA859758B/xx unknown
- 1985-12-23 CA CA000498489A patent/CA1261851A/fr not_active Expired
- 1985-12-24 DD DD85285351A patent/DD253566A5/de unknown
- 1985-12-25 JP JP60290789A patent/JPH066597B2/ja not_active Expired - Lifetime
- 1985-12-26 ES ES550443A patent/ES8703889A1/es not_active Expired
- 1985-12-26 RO RO121423A patent/RO93255B/ro unknown
- 1985-12-26 SU SU854004201A patent/SU1553008A3/ru active
- 1985-12-26 CN CN85109754A patent/CN1007981B/zh not_active Expired
- 1985-12-27 PH PH33242A patent/PH21820A/en unknown
- 1985-12-27 BR BR8506556A patent/BR8506556A/pt not_active IP Right Cessation
- 1985-12-27 KR KR1019850009898A patent/KR920004981B1/ko not_active IP Right Cessation
- 1985-12-27 AR AR85302737A patent/AR242584A1/es active
- 1985-12-27 PL PL1985257173A patent/PL148149B1/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SU1553008A3 (ru) | 1990-03-23 |
| RO93255A (fr) | 1987-12-31 |
| MX168931B (es) | 1993-06-15 |
| EP0186124B1 (fr) | 1989-03-29 |
| BR8506556A (pt) | 1986-09-09 |
| ZA859758B (en) | 1986-09-24 |
| CN85109754A (zh) | 1986-10-22 |
| CN1007981B (zh) | 1990-05-16 |
| PL257173A1 (en) | 1987-06-15 |
| RO93255B (ro) | 1988-01-01 |
| KR920004981B1 (ko) | 1992-06-22 |
| JPS61267594A (ja) | 1986-11-27 |
| PH21820A (en) | 1988-03-04 |
| AU5112185A (en) | 1986-07-03 |
| DE3569116D1 (en) | 1989-05-03 |
| EP0186124A1 (fr) | 1986-07-02 |
| ES8703889A1 (es) | 1987-03-01 |
| KR860004858A (ko) | 1986-07-14 |
| CA1261851A (fr) | 1989-09-26 |
| AU583870B2 (en) | 1989-05-11 |
| US4645761A (en) | 1987-02-24 |
| JPH066597B2 (ja) | 1994-01-26 |
| PL148149B1 (en) | 1989-09-30 |
| ES550443A0 (es) | 1987-03-01 |
| AR242584A1 (es) | 1993-04-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| IF04 | In force in the year 2004 |
Expiry date: 20051225 |