SE461433B - Vaextskyddskomposition med fungicid aktivitet innehaallande som aktiv bestaandsdel vissa alkoxikarbonylditiokarbamat samt foerfarande foer framstaellning av naemnda alkoxikarbonylditiokarbamat - Google Patents
Vaextskyddskomposition med fungicid aktivitet innehaallande som aktiv bestaandsdel vissa alkoxikarbonylditiokarbamat samt foerfarande foer framstaellning av naemnda alkoxikarbonylditiokarbamatInfo
- Publication number
- SE461433B SE461433B SE8307028A SE8307028A SE461433B SE 461433 B SE461433 B SE 461433B SE 8307028 A SE8307028 A SE 8307028A SE 8307028 A SE8307028 A SE 8307028A SE 461433 B SE461433 B SE 461433B
- Authority
- SE
- Sweden
- Prior art keywords
- formula
- weight
- alkoxycarbonyldithiocarbamates
- carbon atoms
- butoxypropyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 21
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 6
- 239000000470 constituent Substances 0.000 title abstract description 4
- 238000004519 manufacturing process Methods 0.000 title description 3
- -1 methoxyethyl Chemical group 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims abstract description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 4
- 239000000654 additive Substances 0.000 claims abstract description 4
- 239000003085 diluting agent Substances 0.000 claims abstract description 4
- 125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims abstract description 4
- 150000001412 amines Chemical group 0.000 claims abstract description 3
- 239000012736 aqueous medium Substances 0.000 claims abstract description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 2
- 239000004094 surface-active agent Substances 0.000 claims abstract 2
- 239000012990 dithiocarbamate Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000005059 halophenyl group Chemical group 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 150000004659 dithiocarbamates Chemical class 0.000 claims description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical class NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 abstract description 3
- 230000000996 additive effect Effects 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract description 2
- 150000002148 esters Chemical class 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 239000002609 medium Substances 0.000 description 6
- 235000015097 nutrients Nutrition 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920001817 Agar Polymers 0.000 description 4
- 241000223195 Fusarium graminearum Species 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000010419 agar Nutrition 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 241000206672 Gelidium Species 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000002054 inoculum Substances 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 238000004362 fungal culture Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241001465180 Botrytis Species 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- NPPQSCRMBWNHMW-UHFFFAOYSA-N Meprobamate Chemical compound NC(=O)OCC(C)(CCC)COC(N)=O NPPQSCRMBWNHMW-UHFFFAOYSA-N 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 210000004197 pelvis Anatomy 0.000 description 1
- ICNCMCHAPLUNBG-UHFFFAOYSA-N propyl carbamodithioate Chemical compound CCCSC(N)=S ICNCMCHAPLUNBG-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (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 |
|---|---|---|---|
| HU821205A HU187452B (en) | 1982-04-20 | 1982-04-20 | Fungicides containing - as reagent - alkoxicarbonile ditiocarbamata and process for production of the reagent |
| PCT/HU1983/000017 WO1983003603A1 (fr) | 1982-04-20 | 1983-04-20 | Agent protecteur de plantes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8307028L SE8307028L (sv) | 1983-12-19 |
| SE8307028D0 SE8307028D0 (sv) | 1983-12-19 |
| SE461433B true SE461433B (sv) | 1990-02-19 |
Family
ID=10953330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8307028A SE461433B (sv) | 1982-04-20 | 1983-12-19 | Vaextskyddskomposition med fungicid aktivitet innehaallande som aktiv bestaandsdel vissa alkoxikarbonylditiokarbamat samt foerfarande foer framstaellning av naemnda alkoxikarbonylditiokarbamat |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4613615A (ro) |
| JP (1) | JPS59500766A (ro) |
| AT (1) | AT386927B (ro) |
| CH (1) | CH660482A5 (ro) |
| DE (1) | DE3340214D2 (ro) |
| GB (1) | GB2129805B (ro) |
| HU (1) | HU187452B (ro) |
| NL (1) | NL8320114A (ro) |
| RO (1) | RO88377A (ro) |
| SE (1) | SE461433B (ro) |
| SU (1) | SU1318155A3 (ro) |
| WO (1) | WO1983003603A1 (ro) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101618369B (zh) * | 2009-07-24 | 2013-01-23 | 东北大学 | 一种赤铁矿低温浮选药剂及其制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2457674A (en) * | 1944-12-02 | 1948-12-28 | Rohm & Haas | Fungicidal compositions |
| US2695901A (en) * | 1953-06-23 | 1954-11-30 | Monsanto Chemicals | Thiocarbamyl cyanuryl derivatives |
| US2974156A (en) * | 1958-08-29 | 1961-03-07 | Rohm & Haas | Method for stabilization of manganese salts of alkylene bisdithiocarbamic acids and the products thereof |
| NL277376A (ro) * | 1961-05-09 | |||
| GB1038727A (en) * | 1964-02-13 | 1966-08-10 | Monsanto Chemicals | Vulcanisation process and novel bis(dithiocarbamates) for use therein |
| US3352815A (en) * | 1965-03-08 | 1967-11-14 | Ciba Geigy Corp | Aralkyl-phenyl nu-aryl-thiocarbamates |
| CH508339A (de) * | 1969-05-08 | 1971-06-15 | Ciba Geigy Ag | Mittel zur Bekämpfung von Insekten und Vertretern der Ordnung Acarina |
| BE788711A (fr) * | 1971-09-13 | 1973-03-12 | Azote & Prod Chim | Derives thiocarbamiques et compositions pesticides contenant ces derives |
-
1982
- 1982-04-20 HU HU821205A patent/HU187452B/hu not_active IP Right Cessation
-
1983
- 1983-04-20 AT AT0902183A patent/AT386927B/de not_active IP Right Cessation
- 1983-04-20 NL NL8320114A patent/NL8320114A/nl unknown
- 1983-04-20 WO PCT/HU1983/000017 patent/WO1983003603A1/de not_active Ceased
- 1983-04-20 DE DE83HU8300017T patent/DE3340214D2/de not_active Expired
- 1983-04-20 GB GB08333833A patent/GB2129805B/en not_active Expired
- 1983-04-20 JP JP58501365A patent/JPS59500766A/ja active Pending
- 1983-04-20 US US06/568,210 patent/US4613615A/en not_active Expired - Fee Related
- 1983-04-20 CH CH6923/83A patent/CH660482A5/de not_active IP Right Cessation
- 1983-12-16 RO RO83112908A patent/RO88377A/ro unknown
- 1983-12-19 SU SU833682651A patent/SU1318155A3/ru active
- 1983-12-19 SE SE8307028A patent/SE461433B/sv not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US4613615A (en) | 1986-09-23 |
| GB8333833D0 (en) | 1984-02-01 |
| DE3340214D2 (en) | 1984-05-17 |
| JPS59500766A (ja) | 1984-05-04 |
| AT386927B (de) | 1988-11-10 |
| GB2129805A (en) | 1984-05-23 |
| WO1983003603A1 (fr) | 1983-10-27 |
| SE8307028L (sv) | 1983-12-19 |
| ATA902183A (de) | 1988-04-15 |
| RO88377A (ro) | 1986-02-28 |
| GB2129805B (en) | 1987-02-25 |
| SE8307028D0 (sv) | 1983-12-19 |
| NL8320114A (nl) | 1984-03-01 |
| SU1318155A3 (ru) | 1987-06-15 |
| HU187452B (en) | 1986-01-28 |
| CH660482A5 (de) | 1987-04-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NUG | Patent has lapsed |
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