Endo-brevicomin |
Last updated: 12/06/2024
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(Also known as: Western balsam bark beetle aggregation pheromone) |
The following alerts are based on the data in the tables below. An absence of an alert does not imply the substance has no implications for human health, biodiversity or the environment but just that we do not have the data to form a judgement.
Environmental fate |
Ecotoxicity |
Human health |
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A volatile substance that is an insect pheromone and used, in conjunction with exo-brevicomin, as an attractant |
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Western balsam bark beetle (Dryocoetes confusus) |
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Fir trees |
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Current |
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Not approved |
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Not applicable |
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No UK approval for use as a pesticide |
EC Regulation 1107/2009 (repealing 91/414) |
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Not approved |
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Not applicable |
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Not applicable |
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Not applicable |
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No |
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ATAustria |
BEBelgium |
BGBulgaria |
CYCyprus |
CZCzech Republic |
DEGermany |
DKDenmark |
EEEstonia |
ELGreece |
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ESSpain |
FIFinland |
FRFrance |
HRCroatia |
HUHungary |
IEIreland |
ITItaly |
LTLithuania |
LULuxembourg |
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LVLatvia |
MTMalta |
NLNetherlands |
PLPoland |
PTPortugal |
RORomania |
SESweden |
SISlovenia |
SKSlovakia |
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ISIceland |
NONorway |
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(+/-)Endo-brevicomin is a chiral molecule and an isomer of brevicomin |
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C₉H₁₆O₂ |
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CCC1C2CCCC(O2)(O1)C |
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CC[C@H]1[C@H]2CCC[C@](O2)(O1)C |
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YONXEBYXWVCXIV-YIZRAAEISA-N |
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InChI=1S/C9H16O2/c1-3-7-8-5-4-6-9(2,10-7)11-8/h7-8H,3-6H2,1-2H3/t7-,8+,9-/m0/s1 |
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Yes |
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Insecticide, Semiochemical |
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Pheromone |
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>95% |
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- |
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Natural |
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Functions as an insect attractant - lure |
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Originally isolated from emergent and feeding adult Western balsam bark beetles (Dryocoetes confusus) |
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Chemically synthesised for commerical use |
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Forestry |
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Western balsam bark beetle (Dryocoetes confusus) |
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Fir trees |
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- |
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62532-53-0 |
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- |
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- |
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- |
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156.22 |
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- |
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(1S,5R,6R)-6-ethyl-1-methyl-7,8-dioxabicyclo[3.2.1]octane |
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endo-7-ethyl-5-methyl-6,8-dioxabicyclo[3.2.1]octane |
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- |
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- |
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Not applicable |
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Not applicable |
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UNM |
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Not applicable |
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- |
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Volatile colourless liquid |
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Western Balsam Bark Beetle Tree Bait |
Forestry Distributing, USA |
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Usually supplied in slow release formulations that are used within pheromone dispensers |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. |
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Soil adsorption and mobility |
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None
Terrestrial ecotoxicology |
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HUMAN HEALTH AND PROTECTION |
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High (class III) |
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Carcinogen |
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Endocrine disruptor |
XNo, known not to cause a problem |
A0 A = Chromosome aberration (EFSA database) 0 = No data ; B0 B = DNA damage/repair (EFSA database) 0 = No data ; C0 C = Gene mutation (EFSA database) 0 = No data ; D0 D = Genome mutation (EFSA database) 0 = No data ; E3 E = Unspecified genotoxicity type (miscellaneous data source) 3 = Negative |
XNo, known not to cause a problem |
Reproduction / development effects |
Acetyl cholinesterase inhibitor |
Neurotoxicant |
XNo, known not to cause a problem |
XNo, known not to cause a problem |
XNo, known not to cause a problem |
Respiratory tract irritant |
Skin irritant |
Skin sensitiser |
XNo, known not to cause a problem |
XNo, known not to cause a problem |
No data found |
Eye irritant |
Phototoxicant |
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XNo, known not to cause a problem |
No data found |
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No adverse human health effects noted |
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Not explosive or oxisiding |
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Not listed (Not listed) |
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endo-brevicomin |
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Record last updated: |
12/06/2024 |
Contact: |
aeru@herts.ac.uk |
Please cite as: |
Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |