CS258491B2 - Liquid insecticide and acaricide - Google Patents
Liquid insecticide and acaricide Download PDFInfo
- Publication number
- CS258491B2 CS258491B2 CS867418A CS741886A CS258491B2 CS 258491 B2 CS258491 B2 CS 258491B2 CS 867418 A CS867418 A CS 867418A CS 741886 A CS741886 A CS 741886A CS 258491 B2 CS258491 B2 CS 258491B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- amitraz
- composition according
- aluminum
- aluminum alkoxide
- carbon atoms
- Prior art date
Links
- 230000000895 acaricidal effect Effects 0.000 title claims description 4
- 239000007788 liquid Substances 0.000 title claims description 3
- 239000000642 acaricide Substances 0.000 title description 2
- 239000002917 insecticide Substances 0.000 title description 2
- -1 aluminium alkoxides Chemical class 0.000 claims abstract description 17
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- RDYMFSUJUZBWLH-UHFFFAOYSA-N endosulfan Chemical compound C12COS(=O)OCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl RDYMFSUJUZBWLH-UHFFFAOYSA-N 0.000 claims description 2
- 230000000749 insecticidal effect Effects 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 3
- QXAITBQSYVNQDR-UHFFFAOYSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1N=CN(C)C=NC1=CC=C(C)C=C1C QXAITBQSYVNQDR-UHFFFAOYSA-N 0.000 claims 2
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- WOZZOSDBXABUFO-UHFFFAOYSA-N tri(butan-2-yloxy)alumane Chemical compound [Al+3].CCC(C)[O-].CCC(C)[O-].CCC(C)[O-] WOZZOSDBXABUFO-UHFFFAOYSA-N 0.000 claims 1
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 abstract description 15
- 229960002587 amitraz Drugs 0.000 abstract description 15
- 239000000575 pesticide Substances 0.000 abstract description 9
- 239000012669 liquid formulation Substances 0.000 abstract description 2
- 239000004411 aluminium Substances 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000158500 Platanus racemosa Species 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 150000004703 alkoxides Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- WRMFBHHNOHZECA-UHFFFAOYSA-N butan-2-olate Chemical compound CCC(C)[O-] WRMFBHHNOHZECA-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- LRJOXARIJKBUFE-UHFFFAOYSA-N 1,2-diethyl-3-methylbenzene Chemical class CCC1=CC=CC(C)=C1CC LRJOXARIJKBUFE-UHFFFAOYSA-N 0.000 description 1
- BAMWORSGQSUNSC-UHFFFAOYSA-N 1-ethyl-2,3,4-trimethylbenzene Chemical class CCC1=CC=C(C)C(C)=C1C BAMWORSGQSUNSC-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical class CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 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
- 241001465754 Metazoa Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 229920013802 TRITON CF-10 Polymers 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes 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
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical class ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 150000005195 diethylbenzenes Chemical class 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- NSTORIOUDCABGP-UHFFFAOYSA-N ethanol;prop-1-ene Chemical class CCO.CC=C NSTORIOUDCABGP-UHFFFAOYSA-N 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- XLDBGFGREOMWSL-UHFFFAOYSA-N n,n'-bis[2,6-di(propan-2-yl)phenyl]methanediimine Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N=C=NC1=C(C(C)C)C=CC=C1C(C)C XLDBGFGREOMWSL-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- OGHBATFHNDZKSO-UHFFFAOYSA-N propan-2-olate Chemical compound CC(C)[O-] OGHBATFHNDZKSO-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000005201 tetramethylbenzenes Chemical class 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 150000005199 trimethylbenzenes Chemical class 0.000 description 1
- 150000003738 xylenes Chemical class 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compounds Of Unknown Constitution (AREA)
- Prostheses (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB858525447A GB8525447D0 (en) | 1985-10-16 | 1985-10-16 | Pesticidal compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS741886A2 CS741886A2 (en) | 1988-01-15 |
| CS258491B2 true CS258491B2 (en) | 1988-08-16 |
Family
ID=10586716
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS867418A CS258491B2 (en) | 1985-10-16 | 1986-10-14 | Liquid insecticide and acaricide |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US4710512A (de) |
| EP (1) | EP0226285B1 (de) |
| JP (1) | JPH0751483B2 (de) |
| KR (1) | KR950009174B1 (de) |
| CN (1) | CN1017957B (de) |
| AT (1) | ATE59528T1 (de) |
| AU (1) | AU570596B2 (de) |
| BR (1) | BR8605037A (de) |
| CA (1) | CA1266229A (de) |
| CS (1) | CS258491B2 (de) |
| DD (1) | DD250042A5 (de) |
| DE (1) | DE3676466D1 (de) |
| DK (1) | DK165434C (de) |
| EG (1) | EG18048A (de) |
| FI (1) | FI83470C (de) |
| GB (1) | GB8525447D0 (de) |
| GR (1) | GR3001672T3 (de) |
| HU (1) | HU203830B (de) |
| IE (1) | IE58898B1 (de) |
| IL (1) | IL80306A (de) |
| MW (1) | MW7086A1 (de) |
| NZ (1) | NZ217919A (de) |
| OA (1) | OA08428A (de) |
| PH (1) | PH21782A (de) |
| PT (1) | PT83545B (de) |
| RU (1) | RU1812944C (de) |
| TR (1) | TR22547A (de) |
| ZA (1) | ZA867811B (de) |
| ZM (1) | ZM9586A1 (de) |
| ZW (1) | ZW20786A1 (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7906128B2 (en) * | 2002-10-21 | 2011-03-15 | Wyeth Llc | Use of neuronal sodium channel antagonists for the control of ectoparasites in homeothermic animals |
| TWI350728B (en) * | 2004-10-08 | 2011-10-21 | Wyeth Corp | Amitraz compositions |
| US20080112993A1 (en) * | 2005-05-24 | 2008-05-15 | Wyeth | High-dose, long-lasting ectoparasiticide for extended control |
| TWI368505B (en) * | 2005-05-24 | 2012-07-21 | Wyeth Corp | Versatile high load concentrate compositions for control of ecto-parasites |
| TW200846029A (en) * | 2007-02-09 | 2008-12-01 | Wyeth Corp | High dose, long-acting ectoparasiticide for extended control |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1488906A (en) * | 1974-11-09 | 1977-10-19 | Boots Co Ltd | Pesticidal compositions |
| ZA804985B (en) * | 1979-09-20 | 1981-08-26 | Boots Co Ltd | Pesticidal compositions |
| GB2058570B (en) * | 1979-09-20 | 1983-02-23 | Boots Co Ltd | Pesticidal compositions |
| US4479968A (en) * | 1980-10-17 | 1984-10-30 | The Wellcome Foundation Ltd. | Control of ectoparasitic infestations of pigs |
-
1985
- 1985-10-16 GB GB858525447A patent/GB8525447D0/en active Pending
-
1986
- 1986-10-02 EP EP86307591A patent/EP0226285B1/de not_active Expired - Lifetime
- 1986-10-02 DE DE8686307591T patent/DE3676466D1/de not_active Expired - Lifetime
- 1986-10-02 AT AT86307591T patent/ATE59528T1/de not_active IP Right Cessation
- 1986-10-10 MW MW70/86A patent/MW7086A1/xx unknown
- 1986-10-13 ZM ZM95/86A patent/ZM9586A1/xx unknown
- 1986-10-13 OA OA58976A patent/OA08428A/xx unknown
- 1986-10-13 ZW ZW207/86A patent/ZW20786A1/xx unknown
- 1986-10-13 EG EG644/86A patent/EG18048A/xx active
- 1986-10-13 FI FI864116A patent/FI83470C/fi not_active IP Right Cessation
- 1986-10-14 DD DD86295261A patent/DD250042A5/de not_active IP Right Cessation
- 1986-10-14 DK DK490686A patent/DK165434C/da not_active IP Right Cessation
- 1986-10-14 NZ NZ217919A patent/NZ217919A/xx unknown
- 1986-10-14 CA CA000520358A patent/CA1266229A/en not_active Expired - Lifetime
- 1986-10-14 CS CS867418A patent/CS258491B2/cs not_active IP Right Cessation
- 1986-10-14 US US06/918,342 patent/US4710512A/en not_active Expired - Lifetime
- 1986-10-15 PH PH34372A patent/PH21782A/en unknown
- 1986-10-15 JP JP61243306A patent/JPH0751483B2/ja not_active Expired - Fee Related
- 1986-10-15 IE IE272386A patent/IE58898B1/en not_active IP Right Cessation
- 1986-10-15 HU HU864298A patent/HU203830B/hu unknown
- 1986-10-15 RU SU864028366A patent/RU1812944C/ru active
- 1986-10-15 AU AU64125/86A patent/AU570596B2/en not_active Expired
- 1986-10-15 BR BR8605037A patent/BR8605037A/pt not_active IP Right Cessation
- 1986-10-15 PT PT83545A patent/PT83545B/pt not_active IP Right Cessation
- 1986-10-15 ZA ZA867811A patent/ZA867811B/xx unknown
- 1986-10-15 IL IL80306A patent/IL80306A/xx not_active IP Right Cessation
- 1986-10-16 KR KR1019860008667A patent/KR950009174B1/ko not_active Expired - Lifetime
- 1986-10-16 TR TR38953/86A patent/TR22547A/xx unknown
- 1986-10-16 CN CN86106596A patent/CN1017957B/zh not_active Expired
-
1991
- 1991-03-27 GR GR91400385T patent/GR3001672T3/el unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| IF00 | In force as of 2000-06-30 in czech republic | ||
| MK4A | Patent expired |
Effective date: 20011014 |