Trifloxystrobin - analytical standard , CAS No.141517-21-7

CAS: 141517-21-7 Cat. No.: T129128 Molecular Weight: 408.37 EC Number: 604-237-6 PubChem CID: 11664966
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
methyl (2E)-2-methoxyimino-2-[2-[[(Z)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate | methyl (2E)-(methoxyimino)[2-({[(E)-{1-[3-(trifluoromethyl)phenyl]ethylidene}amino]oxy}methyl)phenyl]acetate | NCGC00163847-01 | Benzeneacetic ac
Storage
Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
100mg
T129128-100mg
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Why this grade

analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Trifloxystrobin is a broad spectrum fungicide that inhibits fungal spore germination.
A strobilurin class fungicide.

Specifications

Synonyms
methyl (2E)-2-methoxyimino-2-[2-[[(Z)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate | methyl (2E)-(methoxyimino)[2-({[(E)-{1-[3-(trifluoromethyl)phenyl]ethylidene}amino]oxy}methyl)phenyl]acetate | NCGC00163847-01 | Benzeneacetic ac
Specifications & Purity
analytical standard
Storage
Room temperature
Shipped In
Normal
Grade
Analytical standard
Names and Identifiers
Canonical SmilesCC(=NOCC1=CC=CC=C1C(=NOC)C(=O)OC)C2=CC(=CC=C2)C(F)(F)F
IUPAC Namemethyl (2E)-2-methoxyimino-2-[2-[[(E)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate
InChIKeyONCZDRURRATYFI-TVJDWZFNSA-N
INCHI1S/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/h4-11H,12H2,1-3H3/b24-13+,25-18+
Isomeric SMILES C/C(=N\OCC1=CC=CC=C1/C(=N\OC)/C(=O)OC)/C2=CC(=CC=C2)C(F)(F)F
WGK Germany 2
PubChem CID 11664966
Molecular Weight 408.37

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassTrifluoromethylbenzenes
Intermediate Tree Nodes Not available
Direct ParentTrifluoromethylbenzenes
Alternative Parents Methyl esters  Monocarboxylic acids and derivatives  Organopnictogen compounds  Organonitrogen compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl fluorides  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Trifluoromethylbenzene - Methyl ester - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alkyl halide - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
External Descriptors Strobilurin fungicides
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Cercospora beticola (433 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Blumeria graminis (462 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colletotrichum lagenaria (239 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pyricularia oryzae (1832 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Solanum lycopersicum (493 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fulvia fulva (138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Verticillium dahliae (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Solanum melongena (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Erysiphe necator (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudoperonospora cubensis (1623 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDateItem
J2509825Certificate of AnalysisSep 24, 2025 T129128
A2009120Certificate of AnalysisOct 07, 2023 T129128
Chemical and Physical Properties
Flash Point(°F)70 °C
Flash Point(°C)70°C
Boil Point(°C)312 °C
Melt Point(°C)72.9°C
Molecular Weight408.400 g/mol
XLogP34.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count9
Rotatable Bond Count8
Exact Mass408.13 Da
Monoisotopic Mass408.13 Da
Topological Polar Surface Area69.500 Ų
Heavy Atom Count29
Formal Charge0
Complexity607.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Wenhui Li, Ying Gu, Zikun Liu, Rimao Hua, Xiangwei Wu, Jiaying Xue.  (2022)  Development of a polyurethane-coated thin film solid phase microextraction device for multi-residue monitoring of pesticides in fruit and tea beverages.  JOURNAL OF SEPARATION SCIENCE,  46  (2): (2200661).  [PMID:36373185] [10.1002/jssc.202200661]
2. Kun Jia, Guilan Chen, Junquan Zeng, Fasheng Liu, Xinjun Liao, Chen Guo, Jiaqi Luo, Guanghua Xiong, Huiqiang Lu.  (2022)  Low trifloxystrobin-tebuconazole concentrations induce cardiac and developmental toxicity in zebrafish by regulating notch mediated‐oxidative stress generation.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:35709675] [10.1016/j.ecoenv.2022.113752]
3. Qian Wang, Yujie Wu, Wei Guo, Feifang Zhang, Feng Zhang.  (2022)  A magnetic covalent organic framework as selective adsorbent for preconcentration of multi strobilurin fungicides in foods.  FOOD CHEMISTRY,      [PMID:35636183] [10.1016/j.foodchem.2022.133190]
4. Xiao Y. Li, Ying J. Qin, Yue Wang, Tao Huang, Yuan H. Zhao, Xiao H. Wang, Christopher J. Martyniuk, Bing Yan.  (2021)  Relative comparison of strobilurin fungicides at environmental levels: Focus on mitochondrial function and larval activity in early staged zebrafish (Danio rerio).  TOXICOLOGY,      [PMID:33548355] [10.1016/j.tox.2021.152706]
5. Min Wang, Yajie Yue, Xiaoning Wei, Jinyuan Zhang, Xinyuan Bi, Liyan Jia, Xu Jing.  (2024)  Chitosan-based emulsive liquid-liquid microextraction for the determination of strobilurin fungicides in water samples.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39486720] [10.1016/j.ijbiomac.2024.137136]
6. Weitao Hu, Guilan Chen, Wenbin Yuan, Chen Guo, Fasheng Liu, Shouhua Zhang, Zigang Cao.  (2024)  Iprodione induces hepatotoxicity in zebrafish by mediating ROS generation and upregulating p53 signalling pathway.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:38181604] [10.1016/j.ecoenv.2023.115911]
7. Yuxin Wang, Yulin Wang, Jizhen Fu, Suzhen Li, Yawen Zhang, Xiaojiao Zheng, Jin Liu, Li Li, Xu Jing.  (2025)  Semi-automatic emulsification liquid-liquid microextraction with deep eutectic solvent for the determination of strobilurin fungicides in food samples.  TALANTA,      [PMID:39923671] [10.1016/j.talanta.2025.127692]
8. Weifan Pan, Peng Zhang, Qi Wang, Liangguang Du, Xue Yang, Xiaowei Guo, Jiamin Yu.  (2025)  Detection and classification of lambda-cyhalothrin and iprodione residues in tobacco leaves by SERS combined with supervised machine learning.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.113959]
9. Jing Yang, Guy Smagghe, Xiaomao Wu, Wanping Zhang, Xiangsheng Chen.  (2026)  Divergent impacts of conventional and biodegradable microplastics on pesticide fate and toxicity in a soil–chive system, underscoring a soil-plant-microbe disruption.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:41629037] [10.1016/j.pestbp.2026.106971]
10. Ru Liang, Qianxue Shao, Yongming Ruan, Min Wang, Jiarong Cui, Jiaojiao Xia, Yanfei Zhu, Ziyao Liu, Zengpei Lin, Hongxing Xu, Zhongxian Lu, Pingyang Zhu.  (2026)  Toxicological impacts of paddy field pesticides on red claw crayfish (Cherax quadricarinatus) and implications for integrated rice-crayfish farming.  Aquaculture Reports,      [PMID:] [10.1016/j.aqrep.2026.103532]
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