CH669712A5 - - Google Patents
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- Publication number
- CH669712A5 CH669712A5 CH1624/86A CH162486A CH669712A5 CH 669712 A5 CH669712 A5 CH 669712A5 CH 1624/86 A CH1624/86 A CH 1624/86A CH 162486 A CH162486 A CH 162486A CH 669712 A5 CH669712 A5 CH 669712A5
- Authority
- CH
- Switzerland
- Prior art keywords
- springworm
- iii
- acetate
- male
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- YJINQJFQLQIYHX-SNAWJCMRSA-N 11E-Tetradecenyl acetate Chemical compound CC\C=C\CCCCCCCCCCOC(C)=O YJINQJFQLQIYHX-SNAWJCMRSA-N 0.000 claims description 9
- 241001465754 Metazoa Species 0.000 claims description 8
- YJINQJFQLQIYHX-PLNGDYQASA-N 11Z-Tetradecenyl acetate Chemical compound CC\C=C/CCCCCCCCCCOC(C)=O YJINQJFQLQIYHX-PLNGDYQASA-N 0.000 claims description 6
- 241000277984 Sparganothis pilleriana Species 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 230000006378 damage Effects 0.000 claims description 4
- 239000002917 insecticide Substances 0.000 claims description 3
- 241000894007 species Species 0.000 claims description 3
- GJNNIRNIXNLOJP-ONEGZZNKSA-N 9-Dodecen-1-ol Chemical compound CC\C=C\CCCCCCCCO GJNNIRNIXNLOJP-ONEGZZNKSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- -1 compounds E 9-dodecenyl acetate Chemical class 0.000 claims 1
- 238000001514 detection method Methods 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 13
- 239000003016 pheromone Substances 0.000 description 8
- 239000005667 attractant Substances 0.000 description 6
- 230000031902 chemoattractant activity Effects 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000000877 Sex Attractant Substances 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 241000255777 Lepidoptera Species 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- VZWGRQBCURJOMT-UHFFFAOYSA-N Dodecyl acetate Chemical compound CCCCCCCCCCCCOC(C)=O VZWGRQBCURJOMT-UHFFFAOYSA-N 0.000 description 3
- 241000510032 Ellipsaria lineolata Species 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- MFFQOUCMBNXSBK-SNAWJCMRSA-N 9E-Dodecenyl acetate Chemical compound CC\C=C\CCCCCCCCOC(C)=O MFFQOUCMBNXSBK-SNAWJCMRSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- IOUUIFSIQMVYKP-UHFFFAOYSA-N Tetradecyl acetate Chemical compound CCCCCCCCCCCCCCOC(C)=O IOUUIFSIQMVYKP-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000007963 capsule composition Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
- FWWOMPFHMRPXIH-UHFFFAOYSA-N 11-tetradecenoic acid Chemical compound CCC=CCCCCCCCCCC(O)=O FWWOMPFHMRPXIH-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000005698 Dodecyl acetate Substances 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 241001261102 Lobesia Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001341014 Sparganothis Species 0.000 description 1
- 230000021736 acetylation Effects 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008827 biological function Effects 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000002975 chemoattractant Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000004920 integrated pest control Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000017448 oviposition Effects 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 230000019617 pupation Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 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
- 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
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3516469 | 1985-05-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH669712A5 true CH669712A5 (fr) | 1989-04-14 |
Family
ID=6270093
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1624/86A CH669712A5 (fr) | 1985-05-08 | 1986-04-22 |
Country Status (5)
| Country | Link |
|---|---|
| AT (1) | AT395506B (fr) |
| CH (1) | CH669712A5 (fr) |
| DE (1) | DE3614601C2 (fr) |
| FR (1) | FR2581507B1 (fr) |
| IT (1) | IT1204335B (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100021417A1 (en) * | 2008-07-24 | 2010-01-28 | Shin-Etsu Chemical Co., Ltd. | Acetate-containing mating disruptant and mating disruption method using the same |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2933749A1 (de) * | 1979-08-21 | 1981-03-26 | Hoechst Ag, 65929 Frankfurt | Insektenlockstoff |
| NL8101118A (nl) * | 1981-03-09 | 1982-10-01 | Tno | Lokmiddel voor de florida-mot. |
-
1986
- 1986-04-22 CH CH1624/86A patent/CH669712A5/de not_active IP Right Cessation
- 1986-04-30 DE DE3614601A patent/DE3614601C2/de not_active Expired - Fee Related
- 1986-04-30 FR FR868606296A patent/FR2581507B1/fr not_active Expired
- 1986-05-05 IT IT20302/86A patent/IT1204335B/it active
- 1986-05-07 AT AT0122886A patent/AT395506B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2581507B1 (fr) | 1989-12-01 |
| IT1204335B (it) | 1989-03-01 |
| IT8620302A0 (it) | 1986-05-05 |
| AT395506B (de) | 1993-01-25 |
| DE3614601A1 (de) | 1986-11-13 |
| ATA122886A (de) | 1992-06-15 |
| FR2581507A1 (fr) | 1986-11-14 |
| DE3614601C2 (de) | 1994-12-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |