Fluvalinate |

Last updated: 26/08/2024
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(Not known by any other names) |
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 broad range of pests |
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Moths, Aphids, Thrips, Leafhoppers, Beetles, Hemipteran spp. |
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Cotton; Cereals; Fruit trees; Grapes; Vegetables |
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- |
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Considered obsolete but may be available in some countries |
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1980, first reported |
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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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Fluvalinate is a chiral molecule. Technical fluvalinate material is an isomeric mixture of the R- and S-isomers. However, commerical products now only use the R-isomer (tau-fluvalinate) |
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C₂₆H₂₂ClF₃N₂O₃ |
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CC(C)C(C(=O)OC(C#N)C1=CC(=CC=C1)OC2=CC=CC=C2)NC3=C(C=C(C=C3)C(F)(F)F)Cl |
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No data |
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INISTDXBRIBGOC-UHFFFAOYSA-N |
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InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3 |
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Yes |
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Insecticide, Acaricide, Veterinary substance |
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Pyrethroid insecticide; Pyrethroid acaricide; Pyrethroid ester insecticide; Pyrethroid ester acaricide |
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- |
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- |
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Synthetic |
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Contact and stomach action. Sodium channel modulator. |
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69409-94-5 |
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805-993-1 |
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432 |
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109302 |
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50516 |
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No data found |
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502.91 |
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(RS)-a-cyano-3-phenoxybenzyl N-(2-chloro-a,a,a-trifluoro-p-tolyl)-DL-valinate |
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(RS)-α-cyano-3-phenoxybenzyl N-(2-chloro-α,α,α-trifluoro-p-tolyl)-DL-valinate |
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cyano(3-phenoxyphenyl)methyl N-[2-chloro-4-(trifluoromethyl)phenyl]-DL-valinate |
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Potential groundwater pollutant; PAN Bad Chemical Actor |
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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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Blattella germanica, Ctenocephalides felis, Heliothis virescens, Myzus persicae, Phyllonorycter blancardella, many others |
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Viscous, yellow oil |
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- Apistan
- Klartan
- Minadox
- Yardex
- Mavrik
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Available in a range of formulations including emulsifiable concentrates, suspensions and flowable formulations |
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0.002 |
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Low |
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- |
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- |
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25 |
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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- |
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- |
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7.08 X 1003 |
Calculated |
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3.85 |
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High |
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Soluble |
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- |
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Regulatory data - observed in metabolism and farm animal feeding studies |
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- |
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- |
- |
- |
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- |
- |
- |
- |
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0.013 |
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Low volatility |
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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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7 |
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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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- |
- |
- |
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General literature gives DT₅₀ 6-8 days |
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3.0 |
R4 R = Peer reviewed scientific publications 4 = Verified data |
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Chickpea pods, n=1 |
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1.95 |
R4 R = Peer reviewed scientific publications 4 = Verified data |
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Published literature RL₅₀ range 1.7-2.4, field grown okra & pepper, n=3 |
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1 |
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Moderately fast |
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- |
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Stable |
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Stable |
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Stable under normal environmental temperatures and pH |
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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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1000000 |
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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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- |
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Cannot be calculated |
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- |
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- |
- |
- |
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- |
- |
- |
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- |
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Known soil and groundwater metabolites |
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None
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3-phenoxy benzoic acid |
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Water (photolysis) |
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anilino acid |
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Water (photolysis) |
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Terrestrial ecotoxicology |
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261 |
Rat |
Moderate |
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- |
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- |
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- |
- |
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- |
- |
- |
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> 2510 |
Colinus virginianus |
Low |
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[The residual time to 25% mortality (RT25) value for honeybees is 8 hrs (range 2-24 hrs) - USEPA data] |
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- |
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- |
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- |
- |
- |
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- |
- |
- |
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0.0009 |
Lepomis macrochirus |
High |
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0.000033 |
P3 P = Other non-EU, UK or US Governments and Regulators 3 = Unverified data of known source Pimephales promelas 30 day |
High |
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- |
- |
- |
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0.074 |
Daphnia magna |
High |
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- |
- |
- |
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- |
- |
- |
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0.0029 |
Americamysis bahia |
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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HUMAN HEALTH AND PROTECTION |
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High (class III) |
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- |
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261 |
Rat |
Moderate |
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20000 |
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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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- |
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EU MRL pesticide database |
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- |
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- |
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Mainly metabolised and excreated in urine but a proportion is excreted unchanged in faeces |
Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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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 |
✓Yes, known to cause a problem |
Reproduction / development effects |
Acetyl cholinesterase inhibitor |
Neurotoxicant |
✓Yes, known 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 |
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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Liver and kidney toxicant Endocrine issues - Binding to human sex hormone, inhibition of progesterone production |
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Not explosive |
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- |
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II (Moderately hazardous) |
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- |
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- |
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- |
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fluvalinate |
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fluvalinate |
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Fluvalinate |
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fluvalinat |
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fluvalinato |
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fluvalinate |
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fluvalinate |
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fluwalinat |
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fluvalinat |
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- |
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fluvalinaat |
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- |
Record last updated: |
26/08/2024 |
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 |