epoxiconazole (Ref: BAS 480F)
** Translations

Environmental Fate - Ecotoxicology - Human Health - A to Z Index - Home

GENERAL INFORMATION

Description: A broad-spectrum fungicide for control of diseases caused by Ascomycetes, Basidiomycetes and Deuteromycetes

Introduction: 1993, first registered

EC Directive 1107/2009 (repealing 91/414):
Status Annex 1
Dossier rapporteur/co-rapporteur Germany
Date inclusion expires 30/04/2019

Approved for use () or known to be used () in the following European countries:

AT

BE

BG

CY

CZ

DE

DK

EE

EL

ES

FI

FR

HU

IE

IT

LT

LU

LV

MT

NL

PL

PT

RO

SE

SI

SK

UK

Also registered in: Australia

General status:
Pesticide type Fungicide
Substance group Triazole
Substance origin Synthetic
Mode of action Preventative and curative action
CAS RN 133855-98-8/106325-08-0
EC number 406-850-2
CIPAC number 609
US EPA chemical code 123909
Chemical formula C17H13ClFN3O
SMILES Fc1ccc(cc1)C3(OC3c2ccccc2Cl)Cn4ncnc4
International Chemical Identifier (InChI) InChI=1/C17H13ClFN3O/c18-15-4-2-1-3-14(15)16-17(23-16,9-22-11-20-10-21-22)12-5-7-13(19)8-6-12/h1-8,10-11,16H,9H2/t16-,17-/m1/s1
Structure diagram/image available? Yes
Molecular mass (g mol-1) 329.76
IUPAC Name (2RS,3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fluorophenyl)propyl]-1H-1,2,4-triazole
CAS Name rel-1-[[(2R,3S)-3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiranyl]methyl]-1H-1,2,4-triazole
Other status information -
Herbicide Resistance Classification (HRAC) Not applicable
Insecticide Resistance Classification (IRAC) Not applicable
Fungicide Resistance Classification (FRAC) 3
Physical state Colourless crystalline solid
Related substances & organisms

Formulations:
Property Value
Example manufacturers of products using this active
  • AgriGuard
  • BASF
  • Bayer Environ
  • Landgold
  • Standon
Example products using this active
  • Epic
  • Opus
  • Splice
  • Swing Gold
  • Tango super
  • Venture
UK LERAP status LERAP Category B
Formulation and application details Often supplied as a soluble concentrate which is mixed with water and applied as a spray.


ENVIRONMENTAL FATE

Property Value Source/Quality Score/Other Information Interpretation
Solubility - In water at 20oC (mg l-1) 7.1 A5 Low
Solubility - In organic solvents at 20oC (mg l-1) 100000 A5 - Ethyl acetate -
140000 A5 - Acetone -
28800 C4 - Ethanol -
40000 A5 - Toluene -
Melting Point (oC) 136.7 A5 -
Boiling Point (oC) Decomposes before boiling A5 -
Degradation point (oC) 310 A5 -
Flashpoint (oC) Not highly flammable A5 -
Octanol-water partition coefficient at pH 7, 20oC P 2.00 X 1003 Calculated -
Log P 3.3 A5 High
Bulk density (g ml-1)/Specific gravity 1.38 A5 -
Dissociation constant (pKa) at 25oC Not applicable A5 -
Note: No dissociation
Vapour pressure at 25oC (mPa) 1.00 X 10-02 A5 Non-volatile
Henry's law constant at 25oC (Pa m3 mol-1) 4.71 X 10-04 A5 Non-volatile
Henry's law constant at 20oC (dimensionless) 2.04 X 10-07 Q2 Non-volatile
GUS leaching potential index 2.47 Calculated Transition state
SCI-GROW groundwater index (µg l-1) for a 1 kg ha-1 or 1 l ha-1 application rate Value 1.24 X 10-01 Calculated -
Note -
Potential for particle bound transport index - Calculated High
Maximum UV-vis absorption L mol-1 cm-1 204nm = 32000, 263nm = 390 A5 -
Surface tension (mN m-1) 72.9 A5 at 20oC, 6.4 mg l-1 -

Degradation:
Property Value Source/Quality Score/Other Information Interpretation
Soil degradation (days) (aerobic) DT50 (typical) 354 B5 Persistent
DT50 (lab at 20oC) 226 A5 Persistent
DT50 (field) 120 A5 Persistent
DT90 (lab at 20oC) - - -
DT90 (field) - - -
Note EU dossier lab studies DT50 range 98-649 days, field studies DT50 range 44-124 days; Other studies: lab DT50 range 224-2236 days, field range 52-226 days
Aqueous photolysis DT50 (days) at pH 7 Value 52 A5 Stable
Note -
Aqueous hydrolysis DT50 (days) at 20oC and pH 7 Value Stable A5 Very persistent
Note Stable pH 5 to pH 9 at 25 degC, some hydrolysis at elevated temperatures
Water-Sediment DT50 (days) 119.8 A5 Slow
Water phase only DT50 (days) 65.8 A5 Stable

Soil adsorption and mobility:
Property Value Source/Quality Score/Other Information Interpretation
Linear Kd - - -
Koc -
Notes and range -
Freundlich Kf 12.18 A5 Slightly mobile
Kfoc 1073
1/n 0.836
Notes and range EU dossier Kf range 4.79-21.78 mL/g, Kfoc range 280-2647 mL/g, 1/n range 0.766-0.910, Soils=5
pH sensitivity No

Key metabolites:
Metabolite Formation Medium Estimated Maximum Occurrence Fraction 91/414 Relevancy
1,2,4-triazole (Ref: CGA 71019) Soil   0.066   Minor fraction, Relevant

Other known metabolites:
Metabolite name and reference Aliases Formation Medium / Rate Estimated Maximum Occurrence Fraction Metabolising Enzymes
triazole alanine TA Plant - -
triazole acetic acid - Plant - -
triazoly hydroxyl propionic acid THPA Plant - -
1-(2-chlorophenyl)-2-(4-fluorophenyl)-1-hydroxy-3-(1H-1,2,4-triazol-1-yl)propane
(Ref: BF480-alcohol)
- Soil - -
1-[(2Z)-3-(2-chlorophenyl)-2-(4-fluorophenyl)-2 propenyl]-1H-1,2,4-triazole
(Ref: BF480-entriazole)
- Water/sediment; Soil - -
1H-1,2,4-triazol-1-ylacetic acid
(Ref: CGA 142856)
TAA Plant - -


ECOTOXICOLOGY

Property Value Source/Quality Score/Other Information Interpretation
Bio-concentration factor BCF 70 A5 Whole fish Low potential
CT50 (days) 0.72 -
Bioaccumulation potential - Calculated Low
Mammals - Acute oral LD50 (mg kg-1) 3160 A5 Rat Low
Mammals - Short term dietary NOEL (mg kg-1) 7.5 B5 Rat High
(ppm diet) 90 -
Birds - Acute LD50 (mg kg-1) > 2000 A5 Colinus virginianus Moderate
Birds - Short term dietary (LC50/LD50) > 907 mg kg bw-1 day-1 A5 Colinus virginianus -
Fish - Acute 96 hour LC50 (mg l-1) 3.14 A5 Oncorhynchus mykiss Moderate
Fish - Chronic 21 day NOEC (mg l-1) 0.01 A5 Oncorhynchus mykiss, 28 day -
Aquatic invertebrates - Acute 48 hour EC50 (mg l-1) 8.69 A5 Daphnia magna Moderate
Aquatic invertebrates - Chronic 21 day NOEC (mg l-1) 0.63 Q2 Daphnia magna -
Aquatic crustaceans - Acute 96 hour LC50 (mg l-1) - - -
Sediment dwelling organisms - Acute 96 hour LC50 (mg l-1) 0.0625 A5 Chironomus riparius, emergence High
Sediment dwelling organisms - Chronic 28 day NOEC, static, water (mg l-1) 0.0625 A4 Chironomus riparius, emergence Moderate
Sediment dwelling organisms - Chronic 28 day NOEC, sediment (mg kg-1) - - -
Aquatic plants - Acute 7 day EC50, biomass (mg l-1) 0.014 A5 Lemna gibba Moderate
Algae - Acute 72 hour EC50, growth (mg l-1) 1.19 A5 Pseudokirchneriella subcapitata Moderate
Algae - Chronic 96 hour NOEC, growth (mg l-1) 0.0078 A5 Pseudokirchneriella subcapitata Moderate
Honeybees - Acute 48 hour LD50 (µg bee-1) > 83 A5 Oral Moderate
Earthworms - Acute 14 day LC50 (mg kg-1) > 500 A5 Eisenia foetida, corr Moderate
Earthworms - Chronic 14 day NOEC, reproduction (mg kg-1) 0.084 A5 Esenia foetida, corr High
Other soil macro-organisms - e.g. Collembola LR50product ha
EC50product ha
NOECproduct ha
% Effect
- - -
Other arthropod (1) LR50 g ha-1 246 246A5 Aphidius rhopalosiphi Moderately harmful at 1 kg ha-1
% Effect - - -
Other arthropod (2) LR50 g ha-1 258 A5 Typhlodromus pyri Moderately harmful at 1 kg ha-1
% Effect - - -
Soil micro-organisms Nitrogen mineralisation: No significant effect
Carbon mineralisation: No significant effect
A5
Dose: 1.88 kg/ha
-
Mesocosm study data NOEAEC mg l-1 - - -
NOEAEC mg l-1 - - -


HUMAN HEALTH AND PROTECTION

General:
Property Value Source/Quality Score/Other Information Interpretation
Mammals - Acute oral LD50 (mg kg-1) 3160 A5 Rat Low
Mammals - Dermal LD50 (mg kg-1 body weight) > 2000 A5 Rat -
Mammals - Inhalation LC50 (mg l-1) > 5.3 A5 Rat, 4hr -
Other Mammal toxicity endpoints - -
ADI - Acceptable Daily Intake (mg kg-1bw day-1) 0.008 A5 Mice, SF=100 -
ARfD - Acute Reference Dose (mg kg-1bw day-1) 0.023 A5 Rat, SF=100 -
AOEL - Acceptable Operator Exposure Level - Systemic (mg kg-1bw day-1) 0.008 A5 Rat, SF=100 -
Dermal penetration studies (%) 50 A5 -
Dangerous Substances Directive 76/464 List II - -
Exposure Limits - - -
Exposure Routes Public Acceptable risk for proposed uses
Occupational Acceptable risk for proposed uses
Examples of European MRLs (mg kg-1) Value Barley, oats: 1.0; Wheat, rye, triticale: 0.2; Sugar beet: 0.05
Note A5 EU dossier proposals
For the EU pesticides database click here
Drinking Water MAC (µg l-1) - - -

Health issues:
Carcinogen Mutagen Endocrine disrupter Reproduction / development effects Acetyl cholinesterase inhibitor Neurotoxicant Respiratory tract irritant Skin irritant Eye irritant

-

-

General human health issues Possible liver toxicant

: Yes, known to cause a problem
: No, known not to cause a problem
: Possibly, status not identified
- : No data

Handling issues:
Property Value Source/Quality Score/Other Information Interpretation
General Not explosive or oxidising
IMDG Transport Code is usually 9
CLP classification 2013 -
EC Risk Classification Carcinogen category 3: R40
Reproduction risk category 3: R62, R63
N - Dangerous for the environment: R51, R53
EC Safety Classification S2, S36/37, S46, S61
WHO Classification NL - Not listed
US EPA Classification (formulation) No consensus across products or no products available - -
UN Number Usually 3077 or 3082
Waste disposal & packaging Usually Packaging Group III (minor danger)


TRANSLATIONS

Language Name
English epoxiconazole
French epoxiconazole
German Epoxiconazol
Danish epoxiconazol
Italian epossiconazolo
Spanish epoxiconazol
Greek epoxiconazole
Slovenian epoksikonazol
Polish epoksykonazol
Swedish -
Hungarian epoxikonazol
Dutch epoxiconazool

Record last updated: Tuesday 07 August 2012
Contact: aeru@herts.ac.uk
© Copyright University of Hertfordshire