CH500664A - Composition pesticide - Google Patents
Composition pesticideInfo
- Publication number
- CH500664A CH500664A CH1253568A CH1253568A CH500664A CH 500664 A CH500664 A CH 500664A CH 1253568 A CH1253568 A CH 1253568A CH 1253568 A CH1253568 A CH 1253568A CH 500664 A CH500664 A CH 500664A
- Authority
- CH
- Switzerland
- Prior art keywords
- composition
- substituted
- test
- results
- ovicidal
- Prior art date
Links
- 125000003118 aryl group Chemical group 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
- 239000002917 insecticide Substances 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 7
- 230000000895 acaricidal effect Effects 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 230000003151 ovacidal effect Effects 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 241000244206 Nematoda Species 0.000 claims description 5
- 230000002506 adulticidal effect Effects 0.000 claims description 5
- 235000013601 eggs Nutrition 0.000 claims description 5
- 230000001069 nematicidal effect Effects 0.000 claims description 5
- 239000000575 pesticide Substances 0.000 claims description 5
- 241001454294 Tetranychus Species 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 231100000194 ovacidal Toxicity 0.000 claims description 4
- 241000244205 Panagrellus Species 0.000 claims description 3
- 241001454293 Tetranychus urticae Species 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 3
- 238000011109 contamination Methods 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 241000244198 Panagrellus silusiae Species 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 238000003898 horticulture Methods 0.000 claims description 2
- 239000005645 nematicide Substances 0.000 claims description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 abstract description 4
- 241000254179 Sitophilus granarius Species 0.000 abstract 1
- 241001233957 eudicotyledons Species 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- OVJCAYMARFNMQB-UHFFFAOYSA-M potassium;diethoxy-oxido-sulfanylidene-$l^{5}-phosphane Chemical compound [K+].CCOP([O-])(=S)OCC OVJCAYMARFNMQB-UHFFFAOYSA-M 0.000 description 6
- 230000000361 pesticidal effect Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical group NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 4
- 230000037406 food intake Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 241001124076 Aphididae Species 0.000 description 3
- 241000238631 Hexapoda Species 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 2
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- -1 N, N-dimethylthiocarbamoylthiomethyl Chemical group 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000000974 larvacidal effect Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 125000003107 substituted aryl group Chemical group 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
- KRTBZJBLNRDSGZ-UHFFFAOYSA-N 1-[chloromethylsulfanyl(ethoxy)phosphoryl]oxyethane Chemical compound CCOP(=O)(OCC)SCCl KRTBZJBLNRDSGZ-UHFFFAOYSA-N 0.000 description 1
- GSFSVEDCYBDIGW-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)-6-chlorophenol Chemical compound OC1=C(Cl)C=CC=C1C1=NC2=CC=CC=C2S1 GSFSVEDCYBDIGW-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000255601 Drosophila melanogaster Species 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
- 240000008415 Lactuca sativa Species 0.000 description 1
- 241000256259 Noctuidae Species 0.000 description 1
- PEPLNASCGCOBKK-UHFFFAOYSA-N OP(O)(SCCl)=O Chemical compound OP(O)(SCCl)=O PEPLNASCGCOBKK-UHFFFAOYSA-N 0.000 description 1
- 241001013804 Peridroma saucia Species 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 241000482268 Zea mays subsp. mays Species 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material 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 |
|---|---|---|---|
| FR119575A FR1542675A (fr) | 1967-08-31 | 1967-08-31 | Nouveaux thiophosphates organiques et procédé de préparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH500664A true CH500664A (fr) | 1970-12-31 |
Family
ID=8637593
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1253568A CH500664A (fr) | 1967-08-31 | 1968-08-21 | Composition pesticide |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE719369A (ref) |
| CH (1) | CH500664A (ref) |
| FR (1) | FR1542675A (ref) |
| NL (1) | NL6812210A (ref) |
-
1967
- 1967-08-31 FR FR119575A patent/FR1542675A/fr not_active Expired
-
1968
- 1968-08-12 BE BE719369D patent/BE719369A/xx unknown
- 1968-08-21 CH CH1253568A patent/CH500664A/fr not_active IP Right Cessation
- 1968-08-28 NL NL6812210A patent/NL6812210A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR1542675A (fr) | 1968-10-18 |
| NL6812210A (ref) | 1969-03-04 |
| BE719369A (ref) | 1969-02-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |