Description References
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Trifloxystrobin

Description References
Product Name
Trifloxystrobin
CAS No.
141517-21-7
Chemical Name
Trifloxystrobin
Synonyms
TEGA;Aprix;Swift;Dexter;Consist;STRATEGO;oxystrobin;rifloxystrobin;TRIFLOXYSTROBIN;Trifioxystrobin
CBNumber
CB3757745
Molecular Formula
C20H19F3N2O4
Formula Weight
408.37
MOL File
141517-21-7.mol
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Trifloxystrobin Property

Melting point:
72.9°
Boiling point:
bp~312°
Density 
1.21±0.1 g/cm3(Predicted)
Flash point:
>70 °C
storage temp. 
Sealed in dry,2-8°C
solubility 
Chloroform: Slightly Soluble; Methanol: Slightly Soluble
form 
Solid
color 
White to off-white
Stability:
Hygroscopic, Moisture Sensitive
InChI
InChI=1S/C20H19F3N2O4/c1-13(14-8-6-9-16(11-14)20(21,22)23)24-29-12-15-7-4-5-10-17(15)18(25-28-3)19(26)27-2/h4-11,24H,1,12H2,2-3H3/b25-18-
InChIKey
MGNJFZURPQVGJE-BWAHOGKJSA-N
SMILES
C1(=CC=CC=C1CONC(=C)C1C=CC=C(C(F)(F)F)C=1)/C(=N/OC)/C(=O)OC
LogP
5.112 (est)
EPA Substance Registry System
Trifloxystrobin (141517-21-7)
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Safety

Hazard Codes 
Xi,N
Risk Statements 
43-50/53
Safety Statements 
24-37-46-60-61
RIDADR 
UN3077 9/PG 3
WGK Germany 
2
Hazardous Substances Data
141517-21-7(Hazardous Substances Data)
Toxicity
LD50 in rats (mg/kg): >5000 orally; >2000 dermally; LC50 by inhalation in rats (mg/m3): >4646; LC50 in bobwhite quail (mg/kg): >2000; LC50 in rainbow trout (mg/l): 0.015 (Margot)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H317May cause an allergic skin reaction

H332Harmful if inhaled

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
46447
Product name
Trifloxystrobin
Purity
PESTANAL
Packaging
100mg
Price
$144
Updated
2025/07/31
TCI Chemical
Product number
T4071
Product name
Trifloxystrobin
Packaging
1G
Price
$114
Updated
2025/07/31
TCI Chemical
Product number
T4071
Product name
Trifloxystrobin
Packaging
5G
Price
$342
Updated
2025/07/31
Cayman Chemical
Product number
25825
Product name
Trifloxystrobin
Purity
≥98%
Packaging
25mg
Price
$36
Updated
2024/03/01
Cayman Chemical
Product number
25825
Product name
Trifloxystrobin
Purity
≥98%
Packaging
50mg
Price
$66
Updated
2024/03/01
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Trifloxystrobin Chemical Properties,Usage,Production

Description

Trifloxystrobin is a synthetic derivative of the naturally occurring strobilurins found in several genera of wood-decaying fungi such as Strobilurus tenacellus. It is a strobilurin foliar fungicide. Trifloxystrobin inhibits mitochondrial respiration by blocking electron transfer within the respirator chain. Therefore, trifloxystrobin is a potent inhibitor of 2 fungal spore germination and mycelial growth. It has a high level of activity against many fungal pathogens within the Ascomycete, Deuteromycete, Basidiomycete, and Oomycete classes.
Pests controlled by trifloxystrobin include grape and cucurbit powdery mildew, apple scab and powdery mildew, peanut leafspot, and brown patch of turfgrass. It could be applied to cereals, ornamental, vegetables (carrots, asparagus, cucurbits, fruiting vegetables, root vegetables (except radish)), fruits (apples, pears, grapes, strawberries) and tropical crops.

References

[1] http://sitem.herts.ac.uk/aeru/iupac/Reports/664.htm
[2] EPA Pesticide Fact Sheet

Chemical Properties

Off-White to Pale Beige Solid

Uses

Trifloxystrobin is a broad-spectrum foliar fungicide used in plant pritection. Trifloxystrobin functions by inhibiting fungal spore germination.

Uses

Agricultural fungicide.

Definition

ChEBI: Trifloxystrobin is the methyl ester of (2E)-(methoxyimino)[2-({[(E)-{1-[3-(trifluoromethyl)phenyl]ethylidene}amino]oxy}methyl)phenyl]acetic acid. A foliar applied fungicide for cereals which is particularly active against Ascomycetes, Deuteromycetes and Oomycetes It has a role as a mitochondrial cytochrome-bc1 complex inhibitor and an antifungal agrochemical. It is an oxime O-ether, an organofluorine compound, a methyl ester and a methoxyiminoacetate strobilurin antifungal agent.

Synthesis

99705-50-7

133409-72-0

43121-43-3

The general procedure for the synthesis of 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one from 3'-(trifluoromethyl)acetophenone oxime and (E)-2-(2-bromomethylphenyl)-2-methoxyiminoacetic acid methyl ester is as follows: Example 13: Synthesis of trioxamate 1. dissolve methyl (E)-2-(2-bromomethylphenyl)-2-methoxyiminoacetate (315 g, 1.10 mol) in 1500 ml of methyl isobutyl ketone. 2. To the above solution was added Intermediate-II (203.16 g, 1.0 mol) followed by potassium carbonate (145 g, 1.05 mol) at room temperature. 3. The reaction mixture was heated to 115°C and maintained for 12 hours. 4. After completion of the reaction, the mixture was cooled to room temperature and filtered to remove the potassium bromide by-products and excess potassium carbonate. 5. The solid from filtration is washed with methyl isobutyl ketone and can be recycled in the next batch for the preparation of trioxamate. 6. The filtrate was washed with water, dried over anhydrous sodium sulfate and subsequently concentrated under vacuum to give the crude product. 7. The crude product was recrystallized in methanol to give a white trioxamethyltriazine product weighing 348 g in 85% yield and >98% purity.

Metabolism

Trifloxystrobin is described as “mesostemic” due to its ability to redistribute to untreated plant parts through vapor action, limited but effective cuticular penetration, and translaminarmovement by diffusion (30). It is rainfast by virtue of its high affinity for the waxy cuticular layer.

Toxicity evaluation

Trifloxystrobin has an acute oral LD50 > 5,000 and an acute dermal LD50 > 2,000 mg/kg in rats. It is not a skin or eye irritant, is nonmutagenic and nonteratogenic. It shows rapid absorption and elimination in the rat. It has no toxicity to birds in acute studies (LD50 > 2,000 mg/kg) but has an LC50 of 0.015 mg/L in rainbow trout. The bee LD50 = 200 μg/bee. Environmental fate studies show it to be hydrolytically stable at pH 5, with a DT50 of 11.4 weeks at pH 7. It has a photolytic DT50 of 31.5 h at pH 7 (25 ?C) in water, a soil adsorption coefficient (Koc) of 1,642-3,745 ml/g, and a soil DT50 of 5.4 days under field conditions.

References

[1] Patent: WO2017/85747, 2017, A2. Location in patent: Page/Page column 21
[2] Patent: WO2013/144924, 2013, A1. Location in patent: Page/Page column 33; 34

Trifloxystrobin Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Trifloxystrobin manufacturers

Qingdao Trust Agri Chemical Co.,Ltd
Product
Trifloxystrobin 141517-21-7
Price
US $0.00/kg
Min. Order
1kg
Purity
95
Supply Ability
200000
Release date
2025-09-28
ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
trifloxystrobin 141517-21-7
Price
US $3.00-9.00/KG
Min. Order
0.01KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2025-06-21
Shaanxi Dideu New Materials Co. Ltd
Product
Trifloxystrobin 141517-21-7
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000KGS
Release date
2025-04-29

141517-21-7, TrifloxystrobinRelated Search:


  • STRATEGO
  • TEGA
  • Benzeneacetic acid, .alpha.-(methoxyimino)-2-(E)-1-3-(trifluoromethyl)phenylethylideneaminooxymethyl-, methyl ester, (.alpha.E)-
  • methyl (e)-α-methoxyimino-2-[(e)-1-(3-trifluoromethylphenyl)ethylidenaminooxymethyl]phenylacetate
  • trifloxystrobin (bsi, pa iso)
  • TRIFLOXYSTROBIN
  • Methyl (2Z)-2-methoxyimino-2-[2-[[1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate
  • alpha-(Methoxyimino)-2-[[[(E)-[1-[3-(trifluoromethyl)phenyl]ethylidene]amino]oxy]methylbenzene acetic acid, (E,E)-Methyl ester
  • Trifloxystrobin 100mg [141517-21-7]
  • trifloxystrobin (ISO) (E,E)-α-methoxyimino-{2-[[[[1-[3-(trifluoromethyl)phenyl]ethylidene]amino]oxy]methyl]benzeneacetic acid methyl ester
  • Trifloxystrobin Solution in Acetone
  • Trifioxystrobin
  • Bacteria oxiMe esters
  • FREE SAMPLE NCV TRIFLOXYSTROBIN TECHNICAL
  • Trifloxystrobin Solution, 1000ppm
  • oxystrobin
  • (E)-Methyl 2-(methoxyimino)-2-(2-((((E)-(1-(3-(trifluoromethyl)phenyl)ethylidene)amino)oxy)methyl)phenyl)acetate
  • TrifloxystrobinSolution,1,000mg/L,1ml
  • TrifloxystrobinSolution,100mg/L,1ml
  • Trifloxystrobin Reference Material
  • Trifloxystrobin@1000 ug/mL in Acetonitrile
  • TrifloxystrobinSolution,100mg/L,5x1ml
  • Benzeneacetic acid, α-(methoxyimino)-2-[[[(E)-[1-[3-(trifluoromethyl)phenyl]ethylidene]amino]oxy]methyl]-, methyl ester, (αE)-
  • trifloxystrobin 96%
  • rifloxystrobin
  • Methyl (E)-2-(methoxyimino)-2-(2-(((((E)-1-(3-(trifluoromethyl)phenyl)ethylidene)amino)oxy)methyl)phenyl)acetate
  • Aprix
  • Consist
  • Dexter
  • Swift
  • Kresoxim-methyl Impurity 4
  • Trapinamine hydrochloride
  • C17842000 Trifloxystrobin
  • L17842000CY Trifloxystrobin 10μg/mLin Cyclohe
  • Trifloxystrobin 10 μg/ml Ethyl acetate
  • Trifloxystrobin 10.0 μg/ml Acetonitrile
  • Trifloxystrobin 100 μg/ml Ethyl acetate
  • Fruquintinib Impurity 14
  • Trifloxystrobin, 10 mM in DMSO
  • Maryland Pesticide Mixture 2 1000 μg/mL in Acetonitrile
  • Pesticide Mixture 205 100 μg/mL in Acetonitrile
  • Trifloxystrobin 10 μg/mL in Cyclohexane
  • California Pesticides Class 2B Mixture 1035 100 μg/mL in Acetonitrile, Second Source
  • Pennsylvania Pesticide Mixture 333 10 μg/mL in Acetonitrile
  • Ohio Pesticide Mixture 335 10-100 μg/mL in Acetonitrile
  • HJ 909-2017 PBDE Mixture 265 200 μg/mL in n-Hexane:Toluene
  • Montana Pesticide Mixture 270 10 μg/mL in Acetonitrile
  • Michigan Pesticide Mixture 2 100 μg/mL in Acetonitrile
  • Massachusetts Residual Pesticide Mixture 100 μg/mL in Acetonitrile
  • Oregon Pesticide Mixture 3 100x AL 100-200 μg/mL in Acetonitrile
  • GC PestiMix 3 10 μg/mL in Isooctane:Toluene (50:50)
  • Pesticide Mixture, 22-7558, 10 mg/L
  • Nevada Pesticide Mixture 62 100 μg/mL in Acetonitrile
  • Oregon Cannabis Pesticide Mixture 10x AL 2-20 μg/mL in Acetonitrile
  • Oregon Pesticide Mixture 100 μg/mL in Acetonitrile
  • Pesticide Mixture 651 600 μg/mL?in Acetonitrile
  • Maryland Pesticide Mixture 2 1000 μg/mL in Acetonitrile Second Source
  • Pesticide Mix 18-1472, 200 ug/mL