CH465320A - Verwendung von organischen Phosphorverbindungen zur Bekämpfung schädlicher Pflanzen oder Tiere - Google Patents
Verwendung von organischen Phosphorverbindungen zur Bekämpfung schädlicher Pflanzen oder TiereInfo
- Publication number
- CH465320A CH465320A CH167263A CH167263A CH465320A CH 465320 A CH465320 A CH 465320A CH 167263 A CH167263 A CH 167263A CH 167263 A CH167263 A CH 167263A CH 465320 A CH465320 A CH 465320A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- animals
- phosphonodithioate
- plants
- chloromethyl
- Prior art date
Links
- 241001465754 Metazoa Species 0.000 title claims description 15
- 150000002903 organophosphorus compounds Chemical class 0.000 title claims description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- ZOAMZFNAPHWBEN-UHFFFAOYSA-N 2-$l^{1}-oxidanylpropane Chemical compound CC(C)[O] ZOAMZFNAPHWBEN-UHFFFAOYSA-N 0.000 claims description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 230000008029 eradication Effects 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- WFQFIEFLHILPBF-UHFFFAOYSA-N chloromethyl-(4-chlorophenyl)sulfanyl-propan-2-yloxy-sulfanylidene-$l^{5}-phosphane Chemical compound CC(C)OP(=S)(CCl)SC1=CC=C(Cl)C=C1 WFQFIEFLHILPBF-UHFFFAOYSA-N 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 16
- 241000196324 Embryophyta Species 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- -1 chloronaphthyl Chemical group 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- FLQUDUCNBDGCRI-UHFFFAOYSA-N hydroxy-sulfanyl-sulfidophosphanium Chemical compound SP(S)=O FLQUDUCNBDGCRI-UHFFFAOYSA-N 0.000 description 8
- 241000238631 Hexapoda Species 0.000 description 7
- 244000046052 Phaseolus vulgaris Species 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000035784 germination Effects 0.000 description 5
- 230000002363 herbicidal effect Effects 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 235000005474 African couch grass Nutrition 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 4
- 241000219198 Brassica Species 0.000 description 4
- 235000003351 Brassica cretica Nutrition 0.000 description 4
- 235000003343 Brassica rupestris Nutrition 0.000 description 4
- 241001520106 Eustachys Species 0.000 description 4
- 241001674048 Phthiraptera Species 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 235000010460 mustard Nutrition 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000255777 Lepidoptera Species 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 244000062793 Sorghum vulgare Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000019713 millet Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000567412 Estigmene acrea Species 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- 241000257226 Muscidae Species 0.000 description 2
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 238000004166 bioassay Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 238000013101 initial test Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000008654 plant damage Effects 0.000 description 2
- 241000894007 species Species 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 125000004362 3,4,5-trichlorophenyl group Chemical group [H]C1=C(Cl)C(Cl)=C(Cl)C([H])=C1* 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000258913 Oncopeltus fasciatus Species 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241001454294 Tetranychus Species 0.000 description 1
- 241000254112 Tribolium confusum Species 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 240000006677 Vicia faba Species 0.000 description 1
- 238000001574 biopsy Methods 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- DXVBUJOATHQUCY-UHFFFAOYSA-N hydroxy-methyl-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CP(O)(S)=S DXVBUJOATHQUCY-UHFFFAOYSA-N 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4084—Esters with hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (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 |
|---|---|---|---|
| US17289062A | 1962-02-13 | 1962-02-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH465320A true CH465320A (de) | 1968-11-15 |
Family
ID=22629624
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH167263A CH465320A (de) | 1962-02-13 | 1963-02-11 | Verwendung von organischen Phosphorverbindungen zur Bekämpfung schädlicher Pflanzen oder Tiere |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE628296A (uk) |
| CH (1) | CH465320A (uk) |
| DE (1) | DE1184759B (uk) |
| FR (1) | FR1348127A (uk) |
| GB (1) | GB1034185A (uk) |
| NL (2) | NL139651B (uk) |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2714100A (en) * | 1952-08-05 | 1955-07-26 | Victor Chemical Works | Diallyl monochloromethanephosphonate and polymers |
| US2900405A (en) * | 1953-05-29 | 1959-08-18 | Eastman Kodak Co | Halomethanephosphonates |
| US2922810A (en) * | 1953-07-13 | 1960-01-26 | Victor Chemical Works | Chloromethanephosphonic acid esters |
| US2841604A (en) * | 1954-08-23 | 1958-07-01 | Victor Chemical Works | Dialkyl monochloromethanephosphonate esters containing from 3 to 10 carbon atoms in the hydrocarbon radicals |
| US2863903A (en) * | 1954-10-07 | 1958-12-09 | Victor Chemical Works | Alkyl aryl monochloromethane-phosphonate esters |
| US2960522A (en) * | 1954-10-07 | 1960-11-15 | Victor Chemical Works | Dicresyl monochloromethane-phosphonate |
| US2927014A (en) * | 1957-02-14 | 1960-03-01 | Virginia Carolina Chem Corp | Method for killing plants |
| US2910402A (en) * | 1958-02-21 | 1959-10-27 | Du Pont | Compositions and methods for destroying insects |
| US2988565A (en) * | 1958-11-14 | 1961-06-13 | Victor Chemical Works | O-ethyl-o-ethylmercaptoethyl chloromethylthionophosphonate |
| FR1280984A (fr) * | 1960-02-13 | 1962-01-08 | Bayer Ag | Esters dithiophosphoniques et leur procédé de préparation |
| NL267577A (uk) * | 1960-07-28 | |||
| FR1266440A (fr) * | 1960-09-03 | 1961-07-07 | Stauffer Chemical Co | Nouveaux thio-phosphonates, actifs en particulier comme acaricides et insecticides |
-
0
- BE BE628296D patent/BE628296A/xx unknown
- NL NL288842D patent/NL288842A/xx unknown
-
1963
- 1963-01-31 GB GB4033/63A patent/GB1034185A/en not_active Expired
- 1963-02-11 CH CH167263A patent/CH465320A/de unknown
- 1963-02-12 DE DEST20283A patent/DE1184759B/de active Pending
- 1963-02-12 NL NL63288842A patent/NL139651B/xx unknown
- 1963-02-13 FR FR924589A patent/FR1348127A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1348127A (fr) | 1964-01-04 |
| GB1034185A (en) | 1966-06-29 |
| DE1184759B (de) | 1965-01-07 |
| NL288842A (uk) | |
| NL139651B (nl) | 1973-09-17 |
| BE628296A (uk) |
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