DD293035A5 - Mittel zum anlocken von bastkaefern - Google Patents
Mittel zum anlocken von bastkaefern Download PDFInfo
- Publication number
- DD293035A5 DD293035A5 DD90339147A DD33914790A DD293035A5 DD 293035 A5 DD293035 A5 DD 293035A5 DD 90339147 A DD90339147 A DD 90339147A DD 33914790 A DD33914790 A DD 33914790A DD 293035 A5 DD293035 A5 DD 293035A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- bast
- beetle
- verbenol
- attracting
- cis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims abstract description 17
- 241000546120 Ips typographus Species 0.000 claims abstract description 14
- YTTFFPATQICAQN-UHFFFAOYSA-N 2-methoxypropan-1-ol Chemical compound COC(C)CO YTTFFPATQICAQN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000004480 active ingredient Substances 0.000 claims description 3
- 241000254173 Coleoptera Species 0.000 abstract description 16
- WONIGEXYPVIKFS-UHFFFAOYSA-N (+)-cis-Verbenol Natural products CC1=CC(O)C2C(C)(C)C1C2 WONIGEXYPVIKFS-UHFFFAOYSA-N 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 6
- WONIGEXYPVIKFS-YIZRAAEISA-N (1s,2s,5s)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol Chemical compound CC1=C[C@H](O)[C@@H]2C(C)(C)[C@H]1C2 WONIGEXYPVIKFS-YIZRAAEISA-N 0.000 abstract description 4
- 239000005667 attractant Substances 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 230000031902 chemoattractant activity Effects 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 8
- 241000218657 Picea Species 0.000 description 7
- 239000013543 active substance Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- NHMKYUHMPXBMFI-UHFFFAOYSA-N (s)-ipsdienol Chemical compound CC(C)=CC(O)CC(=C)C=C NHMKYUHMPXBMFI-UHFFFAOYSA-N 0.000 description 4
- HNVRRHSXBLFLIG-UHFFFAOYSA-N 3-hydroxy-3-methylbut-1-ene Chemical compound CC(C)(O)C=C HNVRRHSXBLFLIG-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- NHMKYUHMPXBMFI-SNVBAGLBSA-N (4s)-2-methyl-6-methylideneocta-2,7-dien-4-ol Chemical compound CC(C)=C[C@@H](O)CC(=C)C=C NHMKYUHMPXBMFI-SNVBAGLBSA-N 0.000 description 3
- 239000003016 pheromone Substances 0.000 description 3
- WONIGEXYPVIKFS-HRDYMLBCSA-N (1r,2r,5r)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol Chemical compound CC1=C[C@@H](O)[C@H]2C(C)(C)[C@@H]1C2 WONIGEXYPVIKFS-HRDYMLBCSA-N 0.000 description 2
- WONIGEXYPVIKFS-VGMNWLOBSA-N (1r,2s,5r)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol Chemical compound CC1=C[C@H](O)[C@H]2C(C)(C)[C@@H]1C2 WONIGEXYPVIKFS-VGMNWLOBSA-N 0.000 description 2
- RHAXCOKCIAVHPB-JTQLQIEISA-N (4s)-2-methyl-6-methylideneoct-7-en-4-ol Chemical compound CC(C)C[C@H](O)CC(=C)C=C RHAXCOKCIAVHPB-JTQLQIEISA-N 0.000 description 2
- RXBQNMWIQKOSCS-UHFFFAOYSA-N (7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)methanol Chemical compound C1C2C(C)(C)C1CC=C2CO RXBQNMWIQKOSCS-UHFFFAOYSA-N 0.000 description 2
- BZAZNULYLRVMSW-UHFFFAOYSA-N 2-Methyl-2-buten-3-ol Natural products CC(C)=C(C)O BZAZNULYLRVMSW-UHFFFAOYSA-N 0.000 description 2
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- LVSQXDHWDCMMRJ-UHFFFAOYSA-N 4-hydroxybutan-2-one Chemical compound CC(=O)CCO LVSQXDHWDCMMRJ-UHFFFAOYSA-N 0.000 description 2
- RHAXCOKCIAVHPB-UHFFFAOYSA-N Ipsenol-d Natural products CC(C)CC(O)CC(=C)C=C RHAXCOKCIAVHPB-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 244000007853 Sarothamnus scoparius Species 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- DCSCXTJOXBUFGB-JGVFFNPUSA-N (R)-(+)-Verbenone Natural products CC1=CC(=O)[C@@H]2C(C)(C)[C@H]1C2 DCSCXTJOXBUFGB-JGVFFNPUSA-N 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- DCSCXTJOXBUFGB-SFYZADRCSA-N (R)-(+)-verbenone Chemical compound CC1=CC(=O)[C@H]2C(C)(C)[C@@H]1C2 DCSCXTJOXBUFGB-SFYZADRCSA-N 0.000 description 1
- 240000000731 Fagus sylvatica Species 0.000 description 1
- 235000010099 Fagus sylvatica Nutrition 0.000 description 1
- 101000711237 Homo sapiens Serpin I2 Proteins 0.000 description 1
- RXBQNMWIQKOSCS-RKDXNWHRSA-N Myrtenol Natural products C1[C@H]2C(C)(C)[C@@H]1CC=C2CO RXBQNMWIQKOSCS-RKDXNWHRSA-N 0.000 description 1
- 241000545593 Scolytinae Species 0.000 description 1
- 102100034076 Serpin I2 Human genes 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- GKPOMITUDGXOSB-UHFFFAOYSA-N but-3-yn-2-ol Chemical compound CC(O)C#C GKPOMITUDGXOSB-UHFFFAOYSA-N 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229930003658 monoterpene Natural products 0.000 description 1
- 150000002773 monoterpene derivatives Chemical class 0.000 description 1
- 235000002577 monoterpenes Nutrition 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 229930004725 sesquiterpene Natural products 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- -1 trans-myrtenol Chemical compound 0.000 description 1
- DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 239000000341 volatile oil 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/06—Oxygen or sulfur directly attached to a cycloaliphatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
- Polyesters Or Polycarbonates (AREA)
- Financial Or Insurance-Related Operations Such As Payment And Settlement (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS891869A CS277444B6 (en) | 1989-03-28 | 1989-03-28 | Agent for attraction of bark beetles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD293035A5 true DD293035A5 (de) | 1991-08-22 |
Family
ID=5354144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD90339147A DD293035A5 (de) | 1989-03-28 | 1990-03-28 | Mittel zum anlocken von bastkaefern |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0390074B1 (cs) |
| AT (1) | ATE115829T1 (cs) |
| BG (1) | BG49922A3 (cs) |
| CS (1) | CS277444B6 (cs) |
| DD (1) | DD293035A5 (cs) |
| DE (1) | DE59008051D1 (cs) |
| FI (1) | FI95189C (cs) |
| NO (1) | NO173762C (cs) |
| PL (1) | PL161881B1 (cs) |
| RU (1) | RU1774848C (cs) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010060923A1 (de) | 2010-12-01 | 2012-06-06 | Basf Se | Vorrichtung zur Abgabe von Pheromonen und dessen Verwendung |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO138235C (no) * | 1977-01-13 | 1978-08-02 | Borregaard Ind | Preparat for tiltrekning av granbarkbiller |
| DE2945655A1 (de) * | 1979-11-12 | 1981-05-21 | Celamerck Gmbh & Co Kg, 6507 Ingelheim | Vorrichtung fuer die abgabe von phermonen |
| DE3541467A1 (de) * | 1985-11-23 | 1987-05-27 | Celamerck Gmbh & Co Kg | Insektenlockstoff |
-
1989
- 1989-03-28 CS CS891869A patent/CS277444B6/cs unknown
-
1990
- 1990-03-27 AT AT90105817T patent/ATE115829T1/de not_active IP Right Cessation
- 1990-03-27 NO NO901400A patent/NO173762C/no unknown
- 1990-03-27 DE DE59008051T patent/DE59008051D1/de not_active Expired - Fee Related
- 1990-03-27 EP EP90105817A patent/EP0390074B1/de not_active Expired - Lifetime
- 1990-03-28 DD DD90339147A patent/DD293035A5/de not_active IP Right Cessation
- 1990-03-28 RU SU904743707A patent/RU1774848C/ru active
- 1990-03-28 FI FI901553A patent/FI95189C/fi not_active IP Right Cessation
- 1990-03-28 PL PL90284509A patent/PL161881B1/pl unknown
- 1990-03-28 BG BG091604A patent/BG49922A3/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO901400L (no) | 1990-10-01 |
| NO173762C (no) | 1994-02-02 |
| CS277444B6 (en) | 1993-03-17 |
| RU1774848C (ru) | 1992-11-07 |
| ATE115829T1 (de) | 1995-01-15 |
| FI95189B (fi) | 1995-09-29 |
| CS8901869A2 (en) | 1991-03-12 |
| PL161881B1 (pl) | 1993-08-31 |
| EP0390074A1 (de) | 1990-10-03 |
| FI901553A0 (fi) | 1990-03-28 |
| EP0390074B1 (de) | 1994-12-21 |
| NO173762B (no) | 1993-10-25 |
| FI95189C (fi) | 1996-01-10 |
| BG49922A3 (en) | 1992-03-16 |
| NO901400D0 (no) | 1990-03-27 |
| DE59008051D1 (de) | 1995-02-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |