DK141473B - Insekticidt middel indeholdende S-phthalimidomethyl-0, 0-dimethyldithiophosphat og en aktivator. - Google Patents
Insekticidt middel indeholdende S-phthalimidomethyl-0, 0-dimethyldithiophosphat og en aktivator. Download PDFInfo
- Publication number
- DK141473B DK141473B DK588875AA DK588875A DK141473B DK 141473 B DK141473 B DK 141473B DK 588875A A DK588875A A DK 588875AA DK 588875 A DK588875 A DK 588875A DK 141473 B DK141473 B DK 141473B
- Authority
- DK
- Denmark
- Prior art keywords
- pesticidal
- active
- activator
- agent
- compositions
- Prior art date
Links
- 239000012190 activator Substances 0.000 title claims description 16
- 239000002917 insecticide Substances 0.000 title claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 241000607479 Yersinia pestis Species 0.000 claims description 3
- 230000000361 pesticidal effect Effects 0.000 claims 8
- 239000000443 aerosol Substances 0.000 claims 2
- 239000000839 emulsion Substances 0.000 claims 2
- 239000007921 spray Substances 0.000 claims 2
- 239000000725 suspension Substances 0.000 claims 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- 239000011149 active material Substances 0.000 claims 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 239000010440 gypsum Substances 0.000 claims 1
- 229910052602 gypsum Inorganic materials 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000003208 petroleum Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000001766 physiological effect Effects 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000003380 propellant Substances 0.000 claims 1
- 229910052903 pyrophyllite Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000000454 talc Substances 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 claims 1
- 150000003738 xylenes Chemical class 0.000 claims 1
- 231100000167 toxic agent Toxicity 0.000 description 14
- 239000003440 toxic substance Substances 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- -1 methyl-O Chemical group 0.000 description 4
- 239000012747 synergistic agent Substances 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 3
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 3
- 230000003213 activating effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241000255925 Diptera Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 241000721621 Myzus persicae Species 0.000 description 2
- 244000088415 Raphanus sativus Species 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241001124076 Aphididae Species 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 235000011303 Brassica alboglabra Nutrition 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000011302 Brassica oleracea Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 244000064816 Brassica oleracea var. acephala Species 0.000 description 1
- 244000178937 Brassica oleracea var. capitata Species 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- 241000567412 Estigmene acrea Species 0.000 description 1
- 241000989913 Gunnera petaloidea Species 0.000 description 1
- 241000256244 Heliothis virescens Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 240000008436 Ipomoea aquatica Species 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 241000255908 Manduca sexta Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 241000255969 Pieris brassicae Species 0.000 description 1
- 235000019057 Raphanus caudatus Nutrition 0.000 description 1
- 235000011380 Raphanus sativus Nutrition 0.000 description 1
- 240000007113 Rumex obtusifolius Species 0.000 description 1
- 235000009422 Rumex obtusifolius Nutrition 0.000 description 1
- 235000001601 Sabal palmetto Nutrition 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- NUESSQYZNOVTAQ-UHFFFAOYSA-N chloro-ethoxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(Cl)(=S)OC1=CC=CC=C1 NUESSQYZNOVTAQ-UHFFFAOYSA-N 0.000 description 1
- HVGRATIHPILWBY-UHFFFAOYSA-N chloro-hydroxy-(2-methoxyphenoxy)-sulfanylidene-lambda5-phosphane Chemical compound COC1=CC=CC=C1OP(O)(Cl)=S HVGRATIHPILWBY-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- OOFVSLAKBNBEEH-UHFFFAOYSA-N dichloro-hydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound OP(Cl)(Cl)=S OOFVSLAKBNBEEH-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000004591 piperonyl group Chemical group C(C1=CC=2OCOC2C=C1)* 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 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
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl compounds
-
- 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
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/537,143 US3956486A (en) | 1974-12-30 | 1974-12-30 | Insecticidal phthalimidothiophosphates activated with certain phosphorothionates |
| US53714374 | 1974-12-30 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DK588875A DK588875A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-07-01 |
| DK141473B true DK141473B (da) | 1980-03-24 |
| DK141473C DK141473C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1980-09-22 |
Family
ID=24141403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK588875AA DK141473B (da) | 1974-12-30 | 1975-12-23 | Insekticidt middel indeholdende S-phthalimidomethyl-0, 0-dimethyldithiophosphat og en aktivator. |
Country Status (20)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3236431A1 (de) * | 1982-10-01 | 1984-04-05 | Basf Ag, 6700 Ludwigshafen | Cyclopropyl-methyl-(thio)-phosphorsaeureamide, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2767194A (en) * | 1955-03-18 | 1956-10-16 | Stauffer Chemical Co | Compositions of matter |
| NL100594C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1958-02-24 | |||
| JPS4833372B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1969-03-27 | 1973-10-13 | ||
| JPS5123567B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-07-10 | 1976-07-17 |
-
1974
- 1974-12-30 US US05/537,143 patent/US3956486A/en not_active Expired - Lifetime
-
1975
- 1975-12-18 FR FR7538814A patent/FR2309143A1/fr active Granted
- 1975-12-22 DE DE19752557829 patent/DE2557829A1/de active Pending
- 1975-12-22 AT AT976875A patent/AT344453B/de not_active IP Right Cessation
- 1975-12-23 JP JP50153851A patent/JPS5188638A/ja active Pending
- 1975-12-23 DK DK588875AA patent/DK141473B/da unknown
- 1975-12-23 BR BR7508611*A patent/BR7508611A/pt unknown
- 1975-12-24 AU AU87855/75A patent/AU504259B2/en not_active Expired
- 1975-12-27 ES ES443916A patent/ES443916A1/es not_active Expired
- 1975-12-29 BE BE7000755A patent/BE837162A/xx unknown
- 1975-12-29 SU SU752304452A patent/SU665771A3/ru active
- 1975-12-29 EG EG770/75A patent/EG11851A/xx active
- 1975-12-29 IL IL48754A patent/IL48754A/xx unknown
- 1975-12-29 CA CA242,666A patent/CA1050881A/en not_active Expired
- 1975-12-29 AR AR261785A patent/AR217046A1/es active
- 1975-12-29 NL NL7515130A patent/NL7515130A/xx not_active Application Discontinuation
- 1975-12-30 RO RO7584378A patent/RO70334A/ro unknown
- 1975-12-30 PL PL1975186093A patent/PL97386B1/pl unknown
- 1975-12-30 DD DD190654A patent/DD122472A5/xx unknown
- 1975-12-30 GB GB53130/75A patent/GB1493889A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EG11851A (en) | 1977-12-31 |
| DD122472A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-10-12 |
| DE2557829A1 (de) | 1976-07-08 |
| DK141473C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1980-09-22 |
| GB1493889A (en) | 1977-11-30 |
| PL97386B1 (pl) | 1978-02-28 |
| IL48754A0 (en) | 1976-02-29 |
| FR2309143B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1980-02-08 |
| IL48754A (en) | 1979-10-31 |
| DK588875A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-07-01 |
| US3956486A (en) | 1976-05-11 |
| RO70334A (ro) | 1982-03-24 |
| AR217046A1 (es) | 1980-02-29 |
| FR2309143A1 (fr) | 1976-11-26 |
| SU665771A3 (ru) | 1979-05-30 |
| AU8785575A (en) | 1977-06-30 |
| AT344453B (de) | 1978-07-25 |
| CA1050881A (en) | 1979-03-20 |
| JPS5188638A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-08-03 |
| BR7508611A (pt) | 1976-09-08 |
| ATA976875A (de) | 1977-11-15 |
| ES443916A1 (es) | 1978-04-16 |
| BE837162A (nl) | 1976-06-29 |
| AU504259B2 (en) | 1979-10-11 |
| NL7515130A (nl) | 1976-07-02 |
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