CS197727B1 - Insecticides,acaricides and ovicides - Google Patents
Insecticides,acaricides and ovicides Download PDFInfo
- Publication number
- CS197727B1 CS197727B1 CS778233A CS823377A CS197727B1 CS 197727 B1 CS197727 B1 CS 197727B1 CS 778233 A CS778233 A CS 778233A CS 823377 A CS823377 A CS 823377A CS 197727 B1 CS197727 B1 CS 197727B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- standard
- days
- diethyl
- mixture
- component
- Prior art date
Links
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 10
- 239000002917 insecticide Substances 0.000 title description 6
- 241000118205 Ovicides Species 0.000 title 1
- 239000000642 acaricide Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 8
- 239000004480 active ingredient Substances 0.000 claims abstract description 7
- 230000003151 ovacidal effect Effects 0.000 claims abstract description 7
- 231100000194 ovacidal Toxicity 0.000 claims abstract description 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 241000607479 Yersinia pestis Species 0.000 claims description 10
- JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 0.000 abstract description 4
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 abstract 1
- 239000002689 soil Substances 0.000 description 16
- 241001136249 Agriotes lineatus Species 0.000 description 9
- QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 9
- 239000013543 active substance Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- 235000013601 eggs Nutrition 0.000 description 5
- KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 5
- 238000007689 inspection Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 150000002903 organophosphorus compounds Chemical class 0.000 description 5
- -1 2-isopropyl-6-methylpyrimidin-4-yl Chemical group 0.000 description 4
- 241000255925 Diptera Species 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OVANCIHPSBMNEN-UHFFFAOYSA-N (2,2-dimethyl-3h-1-benzofuran-7-yl)methylcarbamic acid Chemical compound C1=CC(CNC(O)=O)=C2OC(C)(C)CC2=C1 OVANCIHPSBMNEN-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- 241001124076 Aphididae Species 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 241000905789 Lactobacillus larvae Species 0.000 description 2
- 241000255777 Lepidoptera Species 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 241000254109 Tenebrio molitor Species 0.000 description 2
- ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 description 2
- 241000526174 Trioza urticae Species 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000021186 dishes Nutrition 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- UAECOHJYXUJDOF-UHFFFAOYSA-N 2-methyl-1h-pyridazine-3,6-dione Chemical compound CN1N=C(O)C=CC1=O UAECOHJYXUJDOF-UHFFFAOYSA-N 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
- 239000004819 Drying adhesive Substances 0.000 description 1
- 241001427543 Elateridae Species 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- 241000700157 Rattus norvegicus Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- PKHDYSQMVVKCSM-UHFFFAOYSA-N [2-(dimethylamino)-1-(methylsulfanylmethylideneamino)-2-oxoethyl]carbamic acid Chemical compound CN(C)C(=O)C(NC(=O)O)N=CSC PKHDYSQMVVKCSM-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 231100000460 acute oral toxicity Toxicity 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000012272 crop production Methods 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 231100000517 death Toxicity 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- AVGQPNBPXNPEPF-UHFFFAOYSA-N ethylsulfanyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSP(O)(O)=S AVGQPNBPXNPEPF-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
- FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003992 organochlorine insecticide Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 230000000699 topical effect Effects 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS778233A CS197727B1 (en) | 1977-12-09 | 1977-12-09 | Insecticides,acaricides and ovicides |
| CH1246378A CH638951A5 (de) | 1977-12-09 | 1978-12-06 | Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten. |
| FR7834505A FR2410958A1 (fr) | 1977-12-09 | 1978-12-07 | Insecticides, acaricides et ovicides a base de dithiophosphates de o,o-dialcoyl-s-chloromethyle |
| DD78209588A DD140414A1 (de) | 1977-12-09 | 1978-12-07 | Insektizide,akarizide und ovizide |
| IT30677/78A IT1100790B (it) | 1977-12-09 | 1978-12-07 | Composizione insetticida,acaricida ed ovicida |
| BE192212A BE872626A (fr) | 1977-12-09 | 1978-12-08 | Insecticides, acaricides et ovicides |
| DE19782853124 DE2853124A1 (de) | 1977-12-09 | 1978-12-08 | Insektizide, akarizide und ovizide |
| JP15116478A JPS5495731A (en) | 1977-12-09 | 1978-12-08 | Pesticide * mitecide and egg killing agent |
| GB7847833A GB2012586B (en) | 1977-12-09 | 1978-12-08 | Insecticide acaricide and ovicide agents |
| HU78VI1220A HU184702B (en) | 1977-12-09 | 1978-12-08 | Insecticide, acaricide and ovicide composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS778233A CS197727B1 (en) | 1977-12-09 | 1977-12-09 | Insecticides,acaricides and ovicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS197727B1 true CS197727B1 (en) | 1980-05-30 |
Family
ID=5432638
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS778233A CS197727B1 (en) | 1977-12-09 | 1977-12-09 | Insecticides,acaricides and ovicides |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS5495731A (de) |
| BE (1) | BE872626A (de) |
| CH (1) | CH638951A5 (de) |
| CS (1) | CS197727B1 (de) |
| DD (1) | DD140414A1 (de) |
| DE (1) | DE2853124A1 (de) |
| FR (1) | FR2410958A1 (de) |
| GB (1) | GB2012586B (de) |
| HU (1) | HU184702B (de) |
| IT (1) | IT1100790B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113698430B (zh) * | 2021-10-29 | 2022-01-25 | 潍坊新绿化工有限公司 | 一种除草剂莎稗磷的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL105236C (de) * | 1955-08-18 | |||
| NL96707C (de) * | 1955-12-31 | |||
| GB1258922A (de) * | 1968-05-27 | 1971-12-30 | ||
| US3896219A (en) * | 1968-05-27 | 1975-07-22 | Murphy Chemical Ltd | S-chloromethyl diethyl phosphorothiolothionate as a soil insecticide |
| JPS5231414A (en) * | 1975-09-03 | 1977-03-09 | Hitachi Ltd | Safety device for electromobile |
-
1977
- 1977-12-09 CS CS778233A patent/CS197727B1/cs unknown
-
1978
- 1978-12-06 CH CH1246378A patent/CH638951A5/de not_active IP Right Cessation
- 1978-12-07 FR FR7834505A patent/FR2410958A1/fr active Granted
- 1978-12-07 DD DD78209588A patent/DD140414A1/de not_active IP Right Cessation
- 1978-12-07 IT IT30677/78A patent/IT1100790B/it active
- 1978-12-08 JP JP15116478A patent/JPS5495731A/ja active Pending
- 1978-12-08 DE DE19782853124 patent/DE2853124A1/de not_active Withdrawn
- 1978-12-08 GB GB7847833A patent/GB2012586B/en not_active Expired
- 1978-12-08 BE BE192212A patent/BE872626A/xx unknown
- 1978-12-08 HU HU78VI1220A patent/HU184702B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH638951A5 (de) | 1983-10-31 |
| DE2853124A1 (de) | 1979-06-13 |
| FR2410958B1 (de) | 1983-11-10 |
| GB2012586A (en) | 1979-08-01 |
| BE872626A (fr) | 1979-03-30 |
| GB2012586B (en) | 1982-07-28 |
| IT1100790B (it) | 1985-09-28 |
| HU184702B (en) | 1984-10-29 |
| DD140414A1 (de) | 1980-03-05 |
| JPS5495731A (en) | 1979-07-28 |
| FR2410958A1 (fr) | 1979-07-06 |
| IT7830677A0 (it) | 1978-12-07 |
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