SU521843A3 - Пестицидна композици на основе производных 1,2,4-тиадиазола - Google Patents
Пестицидна композици на основе производных 1,2,4-тиадиазолаInfo
- Publication number
- SU521843A3 SU521843A3 SU1816228A SU1816228A SU521843A3 SU 521843 A3 SU521843 A3 SU 521843A3 SU 1816228 A SU1816228 A SU 1816228A SU 1816228 A SU1816228 A SU 1816228A SU 521843 A3 SU521843 A3 SU 521843A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- thiadiazole
- composition based
- pesticide composition
- water
- thiadiazole derivatives
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 15
- YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical class C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 title description 2
- 239000000575 pesticide Substances 0.000 title 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 241000196324 Embryophyta Species 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 241000607479 Yersinia pestis Species 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 241000255925 Diptera Species 0.000 description 5
- -1 dusts Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 240000008100 Brassica rapa Species 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000003440 toxic substance Substances 0.000 description 4
- 235000011293 Brassica napus Nutrition 0.000 description 3
- 235000000540 Brassica rapa subsp rapa Nutrition 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 241000238876 Acari Species 0.000 description 2
- 241000239290 Araneae Species 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- LAKQZMOFHIMETE-UHFFFAOYSA-N 5-(4-chlorophenyl)-1,2,4-thiadiazol-3-one Chemical compound C1=CC(Cl)=CC=C1C1=NC(=O)NS1 LAKQZMOFHIMETE-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000239223 Arachnida Species 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- DGTHFTXUCGRIQO-UHFFFAOYSA-N C[ClH]P(=O)(Cl)[ClH]C Chemical compound C[ClH]P(=O)(Cl)[ClH]C DGTHFTXUCGRIQO-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 241000171274 Megoura Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241001136616 Methone Species 0.000 description 1
- 241000255972 Pieris <butterfly> Species 0.000 description 1
- 241000255969 Pieris brassicae Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000000254 damaging effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 description 1
- NOIJEDJHAHUJCB-UHFFFAOYSA-N dimethoxy-[(5-phenyl-1,2,4-thiadiazol-3-yl)oxy]-sulfanylidene-lambda5-phosphane Chemical compound COP(=S)(OC1=NSC(=N1)C1=CC=CC=C1)OC NOIJEDJHAHUJCB-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000021552 granulated sugar Nutrition 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 230000037303 wrinkles Effects 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
- C07F9/6539—Five-membered rings
- C07F9/65392—Five-membered rings containing two nitrogen atoms
- C07F9/65397—Five-membered rings containing two nitrogen atoms having the two nitrogen atoms in positions 1 and 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3521471 | 1971-07-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU521843A3 true SU521843A3 (ru) | 1976-07-15 |
Family
ID=10375167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1816228A SU521843A3 (ru) | 1971-07-27 | 1972-07-25 | Пестицидна композици на основе производных 1,2,4-тиадиазола |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3801586A (OSRAM) |
| AU (1) | AU461861B2 (OSRAM) |
| CH (1) | CH574213A5 (OSRAM) |
| DE (1) | DE2236459A1 (OSRAM) |
| FR (1) | FR2147168A1 (OSRAM) |
| GB (1) | GB1334418A (OSRAM) |
| HU (1) | HU166010B (OSRAM) |
| IT (1) | IT963263B (OSRAM) |
| NL (1) | NL7210216A (OSRAM) |
| PL (1) | PL90347B1 (OSRAM) |
| SU (1) | SU521843A3 (OSRAM) |
| ZA (1) | ZA725147B (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7403327A (OSRAM) * | 1973-04-19 | 1974-10-22 | ||
| US4069319A (en) * | 1973-10-26 | 1978-01-17 | Roussel Uclaf | Novel thiadiazoles |
-
1971
- 1971-07-27 GB GB3521471A patent/GB1334418A/en not_active Expired
-
1972
- 1972-07-06 US US00269342A patent/US3801586A/en not_active Expired - Lifetime
- 1972-07-21 IT IT27299/72A patent/IT963263B/it active
- 1972-07-25 PL PL1972156909A patent/PL90347B1/pl unknown
- 1972-07-25 DE DE2236459A patent/DE2236459A1/de active Pending
- 1972-07-25 ZA ZA725147A patent/ZA725147B/xx unknown
- 1972-07-25 CH CH1108872A patent/CH574213A5/xx not_active IP Right Cessation
- 1972-07-25 FR FR7226723A patent/FR2147168A1/fr not_active Withdrawn
- 1972-07-25 NL NL7210216A patent/NL7210216A/xx not_active Application Discontinuation
- 1972-07-25 SU SU1816228A patent/SU521843A3/ru active
- 1972-07-25 AU AU44950/72A patent/AU461861B2/en not_active Expired
- 1972-07-27 HU HUSE1636A patent/HU166010B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7210216A (OSRAM) | 1973-01-30 |
| DE2236459A1 (de) | 1973-02-08 |
| PL90347B1 (OSRAM) | 1977-01-31 |
| IT963263B (it) | 1974-01-10 |
| GB1334418A (en) | 1973-10-17 |
| CH574213A5 (OSRAM) | 1976-04-15 |
| ZA725147B (en) | 1973-04-25 |
| HU166010B (OSRAM) | 1974-12-28 |
| AU461861B2 (en) | 1975-06-05 |
| FR2147168A1 (OSRAM) | 1973-03-09 |
| AU4495072A (en) | 1974-01-31 |
| US3801586A (en) | 1974-04-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR840000764B1 (ko) | 벤조페논 히드라존의 제조방법 | |
| DE1542909A1 (de) | Insekticides Mittel | |
| SU521843A3 (ru) | Пестицидна композици на основе производных 1,2,4-тиадиазола | |
| US4297496A (en) | Nitrimine derivatives | |
| DE2054512A1 (de) | Pyranverbindungen, Verfahren zu ih rer Herstellung und ihre Verwendung als Pflanzenschutzmittel | |
| DE2637886A1 (de) | 3-pyridyl-oxy-alkancarbonsaeureamide | |
| US4237168A (en) | N-(4-Chloro-2-methylphenyl)-N-hydroxy methanimidamide and its pesticidal use | |
| HU184822B (en) | Insecticide and nematocide compositions containing asymmetric thiophosphonates | |
| US2403495A (en) | Insecticide | |
| US4330321A (en) | Compounds and method for selectively controlling grassy weeds in broadleaved crops | |
| US4045575A (en) | Thioamide pesticides | |
| CA1128539A (en) | Furylmethyloxime ethers, their preparation and their use as pesticides | |
| DE2524578A1 (de) | Barbitursaeurederivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide | |
| EP0056807A4 (en) | DETERMINED 2- (4 - ((5-TRIFLUORMETHYL) -2-PYRIDINYL) OXY) PHENOXY) -N-PYRIDINYL PROPANAMIDES AND THEIR SCRUBBERS AND A METHOD FOR SELECTIVELY CONTROLLING GRASS WEED IN RICE. | |
| US4297370A (en) | Insecticidal compositions | |
| DE2211706A1 (de) | Thiazol-Derivate | |
| CH516909A (de) | Mittel zur Bekämpfung von Schädlingen in der Landwirtschaft, Verfahren zu dessen Herstellung sowie Verwendung des Mittels | |
| US4788217A (en) | Pesticidal carbamates | |
| AT368681B (de) | Herbizide zusammensetzungen | |
| US3830921A (en) | Pyridine insecticides | |
| US4288611A (en) | N-Methyl-carbamates of 3,5-dimethyl-4-(N'-monosubstituted)-aminophenols exerting an insecticidal and acaricidal action | |
| CA1052386A (en) | Selective herbicides | |
| US4096275A (en) | Thioamide pesticides | |
| CA1093563A (en) | Pesticidal carboxylates | |
| KR910002882B1 (ko) | N-메틸카르밤산염의 유도체, 그 제조방법 및 그것을 함유한 살충제 |