CH654465A5 - Lockstoffpraeparat fuer maennliche wintersaateule. - Google Patents

Lockstoffpraeparat fuer maennliche wintersaateule. Download PDF

Info

Publication number: CH654465A5
Authority: CH; Switzerland
Prior art keywords: weight; formula; compound; owls; attractant
Prior art date: 1982-08-10

Application number

CH4319/83A

Other languages

German (de)

English (en)

Inventor

Csaba Dr Szantay

Lajos Dr Novak

Miklos Dr Toth

Bela Dr Majoros

Gabor Szocs

Attila-Tamas Dr Kis

Ferenc Jurak

Istvan Ujvary

Original Assignee

Egyt Gyogyszervegyeszeti Gyar

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-08-10

Filing date

1983-08-09

Publication date

1986-02-28

1983-08-09 Application filed by Egyt Gyogyszervegyeszeti Gyar filed Critical Egyt Gyogyszervegyeszeti Gyar

1986-02-28 Publication of CH654465A5 publication Critical patent/CH654465A5/de

Links

238000002360 preparation method Methods 0.000 title claims description 30
239000005667 attractant Substances 0.000 title claims description 22
230000031902 chemoattractant activity Effects 0.000 title claims description 22
241001415849 Strigiformes Species 0.000 title claims description 20
150000001875 compounds Chemical class 0.000 claims description 33
239000004480 active ingredient Substances 0.000 claims description 26
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 22
238000000034 method Methods 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 21
241000238631 Hexapoda Species 0.000 claims description 13
JVUSAMNTRVLYOT-KHPPLWFESA-N [(Z)-dec-1-enyl] acetate Chemical compound CCCCCCCC\C=C/OC(C)=O JVUSAMNTRVLYOT-KHPPLWFESA-N 0.000 claims description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
UECPLNNAVLEZGO-PFONDFGASA-N [(z)-tetradec-1-enyl] acetate Chemical compound CCCCCCCCCCCC\C=C/OC(C)=O UECPLNNAVLEZGO-PFONDFGASA-N 0.000 claims description 9
239000007788 liquid Substances 0.000 claims description 9
MAAMIILYYYQTQW-SEYXRHQNSA-N [(z)-dodec-1-enyl] acetate Chemical compound CCCCCCCCCC\C=C/OC(C)=O MAAMIILYYYQTQW-SEYXRHQNSA-N 0.000 claims description 8
239000005662 Paraffin oil Substances 0.000 claims description 7
239000012442 inert solvent Substances 0.000 claims description 6
241000218475 Agrotis segetum Species 0.000 claims description 5
235000019486 Sunflower oil Nutrition 0.000 claims description 5
239000002775 capsule Substances 0.000 claims description 5
239000002600 sunflower oil Substances 0.000 claims description 5
230000013011 mating Effects 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 3
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 3
239000007787 solid Substances 0.000 claims description 2
239000003701 inert diluent Substances 0.000 claims 1
239000000877 Sex Attractant Substances 0.000 description 13
230000000694 effects Effects 0.000 description 10
-1 methanol Chemical class 0.000 description 10
241000607479 Yersinia pestis Species 0.000 description 6
238000002474 experimental method Methods 0.000 description 5
239000002917 insecticide Substances 0.000 description 5
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 4
241000196324 Embryophyta Species 0.000 description 4
241000255777 Lepidoptera Species 0.000 description 4
241001465754 Metazoa Species 0.000 description 4
239000004698 Polyethylene Substances 0.000 description 4
239000013543 active substance Substances 0.000 description 4
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
229920000573 polyethylene Polymers 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
150000001450 anions Chemical class 0.000 description 3
230000006378 damage Effects 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000003016 pheromone Substances 0.000 description 3
WYPQHXVMNVEVEB-UHFFFAOYSA-N (Z)-1-hydroxy-5-decene Natural products CCCCC=CCCCCO WYPQHXVMNVEVEB-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
241000510032 Ellipsaria lineolata Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000002955 isolation Methods 0.000 description 2
239000003350 kerosene Substances 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 2
125000006239 protecting group Chemical group 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
241000894007 species Species 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
239000004322 Butylated hydroxytoluene Substances 0.000 description 1
241000905957 Channa melasoma Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
241000251539 Vertebrata <Metazoa> Species 0.000 description 1
239000012345 acetylating agent Substances 0.000 description 1
238000007171 acid catalysis Methods 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
229940095259 butylated hydroxytoluene Drugs 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000003912 environmental pollution Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
125000005905 mesyloxy group Chemical group 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
239000002420 orchard Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000003442 weekly effect Effects 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)

CH4319/83A 1982-08-10 1983-08-09 Lockstoffpraeparat fuer maennliche wintersaateule. CH654465A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU822569A HU187779B (en)	1982-08-10	1982-08-10	Composition for enticing turnip moth males

Publications (1)

Publication Number	Publication Date
CH654465A5 true CH654465A5 (de)	1986-02-28

Family

ID=10960037

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH4319/83A CH654465A5 (de)	1982-08-10	1983-08-09	Lockstoffpraeparat fuer maennliche wintersaateule.

Country Status (12)

Country	Link
JP (1)	JPS5998007A (it)
BE (1)	BE897483A (it)
CH (1)	CH654465A5 (it)
DD (1)	DD222765A5 (it)
DE (1)	DE3328891A1 (it)
FR (1)	FR2531612A1 (it)
GB (1)	GB2126481B (it)
HU (1)	HU187779B (it)
IT (1)	IT1194367B (it)
NL (1)	NL8302798A (it)
NO (1)	NO832861L (it)
SE (1)	SE8304338L (it)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3805751A1 (de) *	1988-02-24	1989-09-07	Basf Ag	Verfahren und mittel zur bekaempfung der pfirsichmotte
US5030660A (en) *	1989-11-01	1991-07-09	Wisconsin Alumni Research Foundation	Insect repellent containing 1-dodecene

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2834872A1 (de) *	1978-08-09	1980-02-21	Hoechst Ag	Insektenlockstoff
SU999973A3 (ru) *	1979-12-29	1983-02-23	Хиноин Дьедьсер Еш Ведьесети Термекек Дьяра Рт (Инопредприятие)	Способ получени производных пиридо (1,2-а) пиримидина или их фармацевтически приемлемых солей или их оптически активных изомеров

1982
- 1982-08-10 HU HU822569A patent/HU187779B/hu not_active IP Right Cessation
1983
- 1983-08-08 BE BE1/10848A patent/BE897483A/fr not_active IP Right Cessation
- 1983-08-09 SE SE8304338A patent/SE8304338L/xx not_active Application Discontinuation
- 1983-08-09 NO NO832861A patent/NO832861L/no unknown
- 1983-08-09 FR FR8313077A patent/FR2531612A1/fr not_active Withdrawn
- 1983-08-09 GB GB08321395A patent/GB2126481B/en not_active Expired
- 1983-08-09 CH CH4319/83A patent/CH654465A5/de not_active IP Right Cessation
- 1983-08-09 JP JP58144536A patent/JPS5998007A/ja active Pending
- 1983-08-09 IT IT22487/83A patent/IT1194367B/it active
- 1983-08-09 NL NL8302798A patent/NL8302798A/nl not_active Application Discontinuation
- 1983-08-10 DE DE19833328891 patent/DE3328891A1/de not_active Withdrawn
- 1983-08-10 DD DD83253859A patent/DD222765A5/de unknown

Also Published As

Publication number	Publication date
IT8322487A0 (it)	1983-08-09
BE897483A (fr)	1984-02-08
DD222765A5 (de)	1985-05-29
GB8321395D0 (en)	1983-09-07
HU187779B (en)	1986-02-28
FR2531612A1 (fr)	1984-02-17
SE8304338D0 (sv)	1983-08-09
JPS5998007A (ja)	1984-06-06
GB2126481B (en)	1985-10-30
IT1194367B (it)	1988-09-22
NO832861L (no)	1984-02-13
GB2126481A (en)	1984-03-28
SE8304338L (sv)	1984-02-11
DE3328891A1 (de)	1984-02-16
NL8302798A (nl)	1984-03-01

Legal Events

Date	Code	Title	Description
1987-04-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

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