NZ199100A - Acaricidal hydroquinone diether compositions - Google Patents
Acaricidal hydroquinone diether compositionsInfo
- Publication number
- NZ199100A NZ199100A NZ199100A NZ19910081A NZ199100A NZ 199100 A NZ199100 A NZ 199100A NZ 199100 A NZ199100 A NZ 199100A NZ 19910081 A NZ19910081 A NZ 19910081A NZ 199100 A NZ199100 A NZ 199100A
- Authority
- NZ
- New Zealand
- Prior art keywords
- weight
- acaricidal
- eggs
- mites
- compositions according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 230000000895 acaricidal effect Effects 0.000 title claims description 29
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 title description 4
- 235000013601 eggs Nutrition 0.000 claims abstract description 50
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 12
- 201000002266 mite infestation Diseases 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 4
- 244000045561 useful plants Species 0.000 claims abstract description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- 239000002480 mineral oil Substances 0.000 claims description 30
- 241000238876 Acari Species 0.000 claims description 24
- 235000010446 mineral oil Nutrition 0.000 claims description 20
- 239000004480 active ingredient Substances 0.000 claims description 13
- 239000004094 surface-active agent Substances 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 10
- 239000003960 organic solvent Substances 0.000 claims description 8
- 241000488583 Panonychus ulmi Species 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 5
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 3
- 241000488585 Panonychus Species 0.000 claims description 2
- 241001454295 Tetranychidae Species 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
- 150000001298 alcohols Chemical class 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 230000000694 effects Effects 0.000 description 20
- 239000000642 acaricide Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 5
- 239000013543 active substance Substances 0.000 description 5
- 230000012447 hatching Effects 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-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
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Polymers CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- 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 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Polymers CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 101100402341 Caenorhabditis elegans mpk-1 gene Proteins 0.000 description 2
- 101100203596 Caenorhabditis elegans sol-1 gene Proteins 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 241000118205 Ovicides Species 0.000 description 2
- 231100000674 Phytotoxicity Toxicity 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- -1 hydrocarbons alcohols Chemical class 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
- 230000035515 penetration Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229950004959 sorbitan oleate Drugs 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 101150036453 sur-2 gene Proteins 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Polymers OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
- JNYAEWCLZODPBN-UHFFFAOYSA-N 2-(1,2-dihydroxyethyl)oxolane-3,4-diol Polymers OCC(O)C1OCC(O)C1O JNYAEWCLZODPBN-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
- 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
- NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Polymers CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 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
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004888 barrier function 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
- 239000011575 calcium Substances 0.000 description 1
- HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
- 210000001136 chorion Anatomy 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009792 diffusion process Methods 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
- 239000000839 emulsion Substances 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
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-CTQIIAAMSA-N sorbitan Polymers OCC(O)C1OCC(O)[C@@H]1O JNYAEWCLZODPBN-CTQIIAAMSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 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 |
|---|---|
| NZ199100A true NZ199100A (en) | 1984-12-14 |
Family
ID=11219408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ199100A NZ199100A (en) | 1980-12-03 | 1981-11-27 | Acaricidal hydroquinone diether compositions |
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 |
|---|---|
| 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 |
| HU188111B (en) | 1986-03-28 |
| 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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