Tralomethrin (Ref: OMS 3048) |

Last updated: 13/02/2025
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(Also known as: tralomethrine; HAG 107; RU 25474) |
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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An insecticide used to control a wide range of agronomic pests and household insects |
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Ants; Cockroaches; Fleas; Termites |
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Cotton; Non-crop situations including houses, commercial buildings, offices and industrial sites |
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- |
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Current |
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1993, first registration USA; 2023, withdrawn UK |
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Not approved |
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Expired |
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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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Expired |
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Not applicable |
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Yes |
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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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A chiral molecule. Epimeric stereochemistry |
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C₂₂H₁₉Br₄NO₃ |
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CC1(C(C1C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C(C(Br)(Br)Br)Br)C |
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CC1([C@H]([C@H]1C(=O)O[C@H](C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C(C(Br)(Br)Br)Br)C |
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YWSCPYYRJXKUDB-KAKFPZCNSA-N |
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InChI=1S/C22H19Br4NO3/c1-21(2)17(19(23)22(24,25)26)18(21)20(28)30-16(12-27)13-7-6-10-15(11-13)29-14-8-4-3-5-9-14/h3-11,16-19H,1-2H3/t16-,17-,18+,19+/m1/s1 |
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Yes |
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Insecticide, Veterinary substance |
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Pyrethroid insecticide; Pyrethroid ester insecticide |
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- |
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- |
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Synthetic |
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Non-systemic with contact and stomach action. Sodium channel modulator. |
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66841-25-6 |
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266-493-1 |
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- |
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121501 |
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48132 |
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No data found |
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665.0 |
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(S)-cyano(3-phenoxyphenyl)methyl (1R,3S)-2,2-dimethyl-3-[(1?)-1,2,2,2-tetrabromoethyl]cyclopropane-1-carboxylate |
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(S)-α-cyano-3-phenoxybenzyl (1R,3S)-2,2-dimethyl-3-[(RS)-1,2,2,2-tetrabromoethyl]cyclopropanecarboxylate |
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(S)-cyano(3-phenoxyphenyl)methyl (1R,3S)-2,2-dimethyl-3-(1,2,2,2-tetrabromoethyl)cyclopropanecarboxylate |
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PAN listed Highly Hazardous Chemical |
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- |
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Not applicable |
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Not applicable |
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3A |
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Not applicable |
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Alabama argillacea, Heliothis virescens |
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Yellow resinous solid |
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- Scout-X-TRA
- Hotshot
- Rid a bug
- Spectracide
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- |
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0.08 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
Low |
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1000000 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Xylene |
- |
1000000 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Toluene |
- |
1000000 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Acetone |
- |
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143 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
- |
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- |
- |
- |
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- |
- |
- |
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26 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
- |
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1.00 X 1005 |
Calculated |
- |
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5 |
L2 L = Pesticide manuals and hard copy reference books / other sources 2 = Unverified data of unknown source |
High |
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- |
- |
- |
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- |
- |
- |
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1.7 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
- |
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- |
- |
- |
- |
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4.80 X 10-06 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
Low volatility |
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1.60 X 10-10 |
H4 H = The US ARS pesticide properties database. Dataset is no longer available. 4 = Verified data |
Non-volatile |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
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3 |
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Non-persistent |
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27 |
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Non-persistent |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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Best available data |
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- |
- |
- |
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- |
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5.0 |
R4 R = Peer reviewed scientific publications 4 = Verified data |
- |
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Published literature RL₅₀ range 0.3-14.0, 3 field & undercover grown crops, various matrices, n=3 |
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0.05 |
R3 R = Peer reviewed scientific publications 3 = Unverified data of known source |
Fast |
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- |
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Stable |
W4 W = French database provided by ARVALIS-Institut du Végétal. Dataset no longer available. 4 = Verified data |
Stable |
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- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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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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- |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
Non-mobile |
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359732 |
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Best available data |
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- |
- |
- |
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- |
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- |
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- |
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- |
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-2.23 |
Calculated |
Low leachability |
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5.35 X 10-03 |
Calculated |
- |
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Estimated concentrations of chemicals with Koc values greater than 9995 ml g⁻¹ are beyond the scope of the regression data used in SCI-GROW development. If there are concerns for such chemicals, a higher tier groundwater exposure assessment should be considered, regardless of the concentration returned by SCI-GROW |
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Medium |
Calculated |
- |
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Non-mobile |
Calculated |
- |
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- |
- |
- |
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1200 |
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Threshold for concern |
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Not available |
- |
Known groundwater metabolites |
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None
None
Terrestrial ecotoxicology |
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99 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Rat |
High |
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0.75 |
L2 L = Pesticide manuals and hard copy reference books / other sources 2 = Unverified data of unknown source Rat 2 yr |
High |
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- |
- |
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- |
- |
- |
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> 2510 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Phasianidae |
Low |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
- |
- |
- |
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0.13 |
Apis mellifera |
High |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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[The residual time to 25% mortality (RT25) value for honeybees is 0.5 hrs - USEPA data] |
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- |
- |
- |
- |
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- |
- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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0.011 |
R4 R = Peer reviewed scientific publications 4 = Verified data Megachile rotundata |
High |
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Contact |
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1.27 |
R4 R = Peer reviewed scientific publications 4 = Verified data Nomia melanderi |
Moderate |
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contact |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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0.0016 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Oncorhynchus mykiss |
High |
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0.000088 |
P3 P = Other non-EU, UK or US Governments and Regulators 3 = Unverified data of known source Pimephales promelas survival |
High |
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- |
- |
- |
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0.000038 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Daphnia magna |
High |
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0.0000544 |
P3 P = Other non-EU, UK or US Governments and Regulators 3 = Unverified data of known source Daphnia magna |
High |
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> 0.00014 |
R4 R = Peer reviewed scientific publications 4 = Verified data Ceriodaphnia dubia |
High |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
HUMAN HEALTH AND PROTECTION |
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High (class III) |
- |
- |
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99 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Rat |
High |
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2000 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Rabbit |
- |
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0.4 |
L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source Rat |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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- |
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- |
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EU MRL pesticide database |
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- |
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- |
- |
- |
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- |
- |
- |
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- |
- |
- |
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Carcinogen |
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Endocrine disruptor |
XNo, known not to cause a problem |
A3 A = Chromosome aberration (EFSA database) 3 = Negative ; 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 ; E0 E = Unspecified genotoxicity type (miscellaneous data source) 0 = No data |
No data found |
Reproduction / development effects |
Acetyl cholinesterase inhibitor |
Neurotoxicant |
?Possibly, status not identified |
XNo, known not to cause a problem |
XNo, known not to cause a problem |
Respiratory tract irritant |
Skin irritant |
Skin sensitiser |
No data found |
✓Yes, known to cause a problem |
No data found |
Eye irritant |
Phototoxicant |
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✓Yes, known to cause a problem |
No data found |
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No further information available |
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IMDG Transport Hazard Class 6.1 |
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Health: H302, H315, H319 Environment: H400, H410 |
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II (Moderately hazardous) |
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UN3349 |
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- |
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- |
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tralomethrin |
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tralomethrine |
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Tralomethrin |
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tralomethrin |
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tralometrina |
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tralometrina |
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- |
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tralometryna |
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- |
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- |
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- |
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- |
Record last updated: |
13/02/2025 |
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 |