SE407505B - Anvendning av vissa dicyklohexylfenyltennforeningar for bekempning av svampar och kvalster - Google Patents
Anvendning av vissa dicyklohexylfenyltennforeningar for bekempning av svampar och kvalsterInfo
- Publication number
- SE407505B SE407505B SE7316226A SE7316226A SE407505B SE 407505 B SE407505 B SE 407505B SE 7316226 A SE7316226 A SE 7316226A SE 7316226 A SE7316226 A SE 7316226A SE 407505 B SE407505 B SE 407505B
- Authority
- SE
- Sweden
- Prior art keywords
- compound
- compounds
- mites
- plants
- hydroxide
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 26
- 241000238876 Acari Species 0.000 claims description 19
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- 241000233866 Fungi Species 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 5
- RYXPMWYHEBGTRV-UHFFFAOYSA-N Omeprazole sodium Chemical compound [Na+].N=1C2=CC(OC)=CC=C2[N-]C=1S(=O)CC1=NC=C(C)C(OC)=C1C RYXPMWYHEBGTRV-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 241000196324 Embryophyta Species 0.000 description 23
- 239000007788 liquid Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 13
- 150000003606 tin compounds Chemical class 0.000 description 11
- 239000007787 solid Substances 0.000 description 10
- FKKGVNVVRBENQJ-UHFFFAOYSA-N dicyclohexyl(phenyl)tin;hydrate Chemical compound O.C1CCCCC1[Sn](C=1C=CC=CC=1)C1CCCCC1 FKKGVNVVRBENQJ-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 231100000167 toxic agent Toxicity 0.000 description 8
- 239000003440 toxic substance Substances 0.000 description 8
- 241000221785 Erysiphales Species 0.000 description 7
- -1 dicyclohexylphenyltin compound Chemical class 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- 244000046052 Phaseolus vulgaris Species 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 241000220225 Malus Species 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
- 230000004071 biological effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- PXQGTURWBNIMIM-UHFFFAOYSA-N dicyclohexyl(diphenyl)stannane Chemical compound C1CCCCC1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1CCCCC1 PXQGTURWBNIMIM-UHFFFAOYSA-N 0.000 description 3
- JHMPHVAGTPVBBX-UHFFFAOYSA-N dicyclohexyl(phenyl)tin Chemical class C1CCCCC1[Sn](C=1C=CC=CC=1)C1CCCCC1 JHMPHVAGTPVBBX-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003209 petroleum derivative Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 235000019987 cider Nutrition 0.000 description 2
- PJFLXRGZIMFEGW-UHFFFAOYSA-M dicyclohexyl(phenyl)stannanylium;bromide Chemical compound C1CCCCC1[Sn](C=1C=CC=CC=1)(Br)C1CCCCC1 PJFLXRGZIMFEGW-UHFFFAOYSA-M 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 231100000208 phytotoxic Toxicity 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 1
- 241000382353 Pupa Species 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 241001414987 Strepsiptera Species 0.000 description 1
- 244000186561 Swietenia macrophylla Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- WMJMABVHDMRMJA-UHFFFAOYSA-M [Cl-].[Mg+]C1CCCCC1 Chemical compound [Cl-].[Mg+]C1CCCCC1 WMJMABVHDMRMJA-UHFFFAOYSA-M 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 231100000460 acute oral toxicity Toxicity 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 235000021425 apple cider vinegar Nutrition 0.000 description 1
- 229940088447 apple cider vinegar Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000003181 biological factor Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- ISXUHJXWYNONDI-UHFFFAOYSA-L dichloro(diphenyl)stannane Chemical compound C=1C=CC=CC=1[Sn](Cl)(Cl)C1=CC=CC=C1 ISXUHJXWYNONDI-UHFFFAOYSA-L 0.000 description 1
- RHFTTZVNBAHQBF-UHFFFAOYSA-L dicyclohexyltin(2+);dibromide Chemical compound C1CCCCC1[Sn](Br)(Br)C1CCCCC1 RHFTTZVNBAHQBF-UHFFFAOYSA-L 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 231100000915 pathological change Toxicity 0.000 description 1
- 230000036285 pathological change Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 229910000498 pewter Inorganic materials 0.000 description 1
- 239000010957 pewter Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- CVNKFOIOZXAFBO-UHFFFAOYSA-J tin(4+);tetrahydroxide Chemical class [OH-].[OH-].[OH-].[OH-].[Sn+4] CVNKFOIOZXAFBO-UHFFFAOYSA-J 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000041 toxicology testing Toxicity 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Plant Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31150972A | 1972-12-04 | 1972-12-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE407505B true SE407505B (sv) | 1979-04-02 |
Family
ID=23207216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7316226A SE407505B (sv) | 1972-12-04 | 1973-11-30 | Anvendning av vissa dicyklohexylfenyltennforeningar for bekempning av svampar och kvalster |
Country Status (16)
| Country | Link |
|---|---|
| JP (1) | JPS5715564B2 (de) |
| AT (1) | AT322573B (de) |
| BE (1) | BE808132A (de) |
| CA (1) | CA1055039A (de) |
| CH (1) | CH587007A5 (de) |
| DE (1) | DE2360419C2 (de) |
| DK (1) | DK140682B (de) |
| ES (1) | ES421100A1 (de) |
| FR (1) | FR2208605B1 (de) |
| GB (1) | GB1406556A (de) |
| IT (1) | IT1047473B (de) |
| MX (1) | MX4090E (de) |
| NL (1) | NL178384C (de) |
| NO (1) | NO139149C (de) |
| SE (1) | SE407505B (de) |
| ZA (1) | ZA739200B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR243195A1 (es) * | 1985-09-03 | 1993-07-30 | Shionogi & Co Ltd Y Nitto Kase | Compuestos de tri-organo-estano y composiciones pesticidas que los contienen |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1542863A1 (de) * | 1966-08-19 | 1970-07-02 | Dow Chemical Co | Arachnizides Mittel |
| US3552945A (en) * | 1967-11-15 | 1971-01-05 | Ethyl Corp | Herbitoxic organotin compounds and method using same |
-
1973
- 1973-11-16 NO NO4413/73A patent/NO139149C/no unknown
- 1973-11-29 NL NLAANVRAGE7316314,A patent/NL178384C/xx not_active IP Right Cessation
- 1973-11-30 SE SE7316226A patent/SE407505B/sv unknown
- 1973-12-03 ES ES421100A patent/ES421100A1/es not_active Expired
- 1973-12-03 IT IT9707/73A patent/IT1047473B/it active
- 1973-12-03 BE BE138438A patent/BE808132A/xx not_active IP Right Cessation
- 1973-12-03 MX MX732120U patent/MX4090E/es unknown
- 1973-12-03 GB GB5589273A patent/GB1406556A/en not_active Expired
- 1973-12-03 DK DK652673AA patent/DK140682B/da unknown
- 1973-12-03 CH CH1692273A patent/CH587007A5/xx not_active IP Right Cessation
- 1973-12-03 CA CA187,182A patent/CA1055039A/en not_active Expired
- 1973-12-04 FR FR7343281A patent/FR2208605B1/fr not_active Expired
- 1973-12-04 DE DE2360419A patent/DE2360419C2/de not_active Expired
- 1973-12-04 AT AT1015673A patent/AT322573B/de not_active IP Right Cessation
- 1973-12-04 JP JP13491873A patent/JPS5715564B2/ja not_active Expired
- 1973-12-04 ZA ZA739200A patent/ZA739200B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1406556A (en) | 1975-09-17 |
| FR2208605A1 (de) | 1974-06-28 |
| AT322573B (de) | 1975-05-26 |
| CH587007A5 (de) | 1977-04-29 |
| BE808132A (nl) | 1974-03-29 |
| ES421100A1 (es) | 1976-04-16 |
| DE2360419A1 (de) | 1974-08-15 |
| DK140682C (de) | 1980-04-08 |
| NO139149C (no) | 1979-01-31 |
| NL7316314A (de) | 1974-06-06 |
| IT1047473B (it) | 1980-09-10 |
| NL178384C (nl) | 1986-03-17 |
| CA1055039A (en) | 1979-05-22 |
| FR2208605B1 (de) | 1978-09-15 |
| NL178384B (nl) | 1985-10-16 |
| ZA739200B (en) | 1974-11-27 |
| DE2360419C2 (de) | 1982-06-03 |
| NO139149B (no) | 1978-10-09 |
| JPS49116224A (de) | 1974-11-06 |
| MX4090E (es) | 1981-12-08 |
| DK140682B (da) | 1979-10-29 |
| JPS5715564B2 (de) | 1982-03-31 |
| AU6313073A (en) | 1975-06-05 |
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