HU188111B - Acricide compositions containing hydroquinone-diether derivatives as active agents,against surviveing eggs - Google Patents
Acricide compositions containing hydroquinone-diether derivatives as active agents,against surviveing eggs Download PDFInfo
- Publication number
- HU188111B HU188111B HU813623A HU362381A HU188111B HU 188111 B HU188111 B HU 188111B HU 813623 A HU813623 A HU 813623A HU 362381 A HU362381 A HU 362381A HU 188111 B HU188111 B HU 188111B
- Authority
- HU
- Hungary
- Prior art keywords
- eggs
- weight
- mineral oil
- alkyl
- active ingredient
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 43
- 235000013601 eggs Nutrition 0.000 title description 34
- 239000013543 active substance Substances 0.000 title description 3
- 239000002480 mineral oil Substances 0.000 claims description 29
- 235000010446 mineral oil Nutrition 0.000 claims description 23
- 239000004480 active ingredient Substances 0.000 claims description 21
- 230000000895 acaricidal effect Effects 0.000 claims description 19
- 239000004094 surface-active agent Substances 0.000 claims description 11
- -1 alkyl aromatic hydrocarbon Chemical class 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 239000003921 oil Substances 0.000 claims description 5
- 235000019198 oils Nutrition 0.000 claims description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
- 239000008158 vegetable oil Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 22
- 241000238876 Acari Species 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 238000011282 treatment Methods 0.000 description 8
- 239000000642 acaricide Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 241000488583 Panonychus ulmi Species 0.000 description 5
- 230000012447 hatching Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 101100402341 Caenorhabditis elegans mpk-1 gene Proteins 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 230000003151 ovacidal effect Effects 0.000 description 2
- 230000017448 oviposition Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 101150036453 sur-2 gene Proteins 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000488564 Bryobia Species 0.000 description 1
- 101100203596 Caenorhabditis elegans sol-1 gene Proteins 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 244000141359 Malus pumila Species 0.000 description 1
- 235000011430 Malus pumila Nutrition 0.000 description 1
- 235000015103 Malus silvestris Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000795633 Olea <sea slug> Species 0.000 description 1
- 241000488557 Oligonychus Species 0.000 description 1
- 241000488585 Panonychus Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 206010037742 Rabies Diseases 0.000 description 1
- 208000035415 Reinfection Diseases 0.000 description 1
- NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Polymers CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 210000001136 chorion Anatomy 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- LWJWGXUXSVJWBY-UHFFFAOYSA-N dihydroxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound OP(O)(=S)OC1=CC=CC=C1 LWJWGXUXSVJWBY-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 201000002266 mite infestation Diseases 0.000 description 1
- 230000016087 ovulation Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/215—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT26401/80A IT1141104B (it) | 1980-12-03 | 1980-12-03 | Acaricidi attivi contro le uova ibernanti |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU188111B true HU188111B (en) | 1986-03-28 |
Family
ID=11219408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU813623A HU188111B (en) | 1980-12-03 | 1981-12-02 | Acricide compositions containing hydroquinone-diether derivatives as active agents,against surviveing eggs |
Country Status (17)
| Country | Link |
|---|---|
| AR (1) | AR228883A1 (enExample) |
| AT (1) | AT376544B (enExample) |
| AU (1) | AU545108B2 (enExample) |
| CS (1) | CS228908B2 (enExample) |
| DK (1) | DK158697C (enExample) |
| DZ (1) | DZ355A1 (enExample) |
| GB (1) | GB2088214B (enExample) |
| GR (1) | GR81335B (enExample) |
| HU (1) | HU188111B (enExample) |
| IE (1) | IE51922B1 (enExample) |
| IT (1) | IT1141104B (enExample) |
| LU (1) | LU83799A1 (enExample) |
| MA (1) | MA19340A1 (enExample) |
| NZ (1) | NZ199100A (enExample) |
| PT (1) | PT74066B (enExample) |
| RO (1) | RO83146B (enExample) |
| TR (1) | TR21121A (enExample) |
-
1980
- 1980-12-03 IT IT26401/80A patent/IT1141104B/it active
-
1981
- 1981-11-26 DK DK524781A patent/DK158697C/da not_active IP Right Cessation
- 1981-11-27 AU AU77933/81A patent/AU545108B2/en not_active Expired
- 1981-11-27 MA MA19544A patent/MA19340A1/fr unknown
- 1981-11-27 NZ NZ199100A patent/NZ199100A/en unknown
- 1981-11-28 RO RO105894A patent/RO83146B/ro unknown
- 1981-11-28 DZ DZ816383A patent/DZ355A1/fr active
- 1981-11-30 PT PT74066A patent/PT74066B/pt unknown
- 1981-11-30 AT AT0514681A patent/AT376544B/de not_active IP Right Cessation
- 1981-11-30 LU LU83799A patent/LU83799A1/fr unknown
- 1981-11-30 AR AR287625A patent/AR228883A1/es active
- 1981-12-01 GB GB8136267A patent/GB2088214B/en not_active Expired
- 1981-12-01 GR GR66660A patent/GR81335B/el unknown
- 1981-12-01 CS CS818896A patent/CS228908B2/cs unknown
- 1981-12-02 HU HU813623A patent/HU188111B/hu unknown
- 1981-12-02 IE IE2821/81A patent/IE51922B1/en not_active IP Right Cessation
- 1981-12-02 TR TR21121A patent/TR21121A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NZ199100A (en) | 1984-12-14 |
| DK158697B (da) | 1990-07-09 |
| AU545108B2 (en) | 1985-06-27 |
| IE812821L (en) | 1982-06-03 |
| LU83799A1 (fr) | 1982-06-30 |
| CS228908B2 (en) | 1984-05-14 |
| PT74066A (en) | 1981-12-01 |
| ATA514681A (de) | 1984-05-15 |
| PT74066B (en) | 1983-10-31 |
| MA19340A1 (fr) | 1982-07-01 |
| IE51922B1 (en) | 1987-04-29 |
| RO83146A (ro) | 1984-02-21 |
| DK524781A (da) | 1982-06-04 |
| AT376544B (de) | 1984-11-26 |
| DZ355A1 (fr) | 2004-09-13 |
| GB2088214B (en) | 1984-02-15 |
| GB2088214A (en) | 1982-06-09 |
| IT8026401A0 (it) | 1980-12-03 |
| AU7793381A (en) | 1982-06-10 |
| IT1141104B (it) | 1986-10-01 |
| AR228883A1 (es) | 1983-04-29 |
| DK158697C (da) | 1990-11-26 |
| TR21121A (tr) | 1983-10-14 |
| GR81335B (enExample) | 1984-12-11 |
| RO83146B (ro) | 1984-02-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 |