Endo-brevicomin |

Last updated: 25/08/2025
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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. These hazard alerts do not take account of usage patterns or exposure, thus do not represent risk.
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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- |
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- |
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- |
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Not approved |
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Not applicable |
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No UK approval for use as a plant protection agent |
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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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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- |
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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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- |
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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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Current |
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- Forestry Distributing, USA
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- Western Balsam Bark Beetle Tree Bait
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Usually supplied in slow release formulations that are used within pheromone dispensers |
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The synthesis of endo-brevicomin begins with a suitable starting material, often a long-chain alkene or alkyne which undergoes hydroformylation, a process that adds a formyl group (CHO) to the carbon chain, resulting in an aldehyde intermediate. The aldehyde intermediate is then reduced to the corresponding alcohol using a reducing agent such as sodium borohydride or lithium aluminium hydride. The resulting alcohol undergoes cyclisation to form the bicyclic structure characteristic of endo-brevicomin before being purified. |
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While exact CO₂e values are not published for specific pheromones, some general information is available. The PHERA reported that biotechnological production (e.g. yeast fermentation) of pheromones can reduce GHG emissions by up to 90% compared to traditional chemical synthesis and GHG emissions are typically in the 5 to 10 kg CO₂e per kg of pheromone produced. Other sources suggest that small scale pheromone synthesis typically has emissions in the range 1 – 3 kg CO₂e per kg of pheromone produced. |
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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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> 1000 |
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source Rat |
Moderate |
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HUMAN HEALTH AND PROTECTION |
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High (class III) |
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> 1000 |
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source Rat |
Moderate |
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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: |
25/08/2025 |
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 |