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Merck
CN

31718

Flufenacet

PESTANAL®, analytical standard

Synonym(s):

N-(4-Fluorophenyl)-N-isopropyl-2-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yloxy]acetamide

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About This Item

Empirical Formula (Hill Notation):
C14H13F4N3O2S
CAS Number:
142459-58-3
Molecular Weight:
363.33
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753899
MDL number:
MFCD01751191
Beilstein/REAXYS Number:
8787751

Key Documents

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Product Name

Flufenacet, PESTANAL®, analytical standard

InChI

1S/C14H13F4N3O2S/c1-8(2)21(10-5-3-9(15)4-6-10)11(22)7-23-13-20-19-12(24-13)14(16,17)18/h3-6,8H,7H2,1-2H3

SMILES string

CC(C)N(C(=O)COc1nnc(s1)C(F)(F)F)c2ccc(F)cc2

InChI key

IANUJLZYFUDJIH-UHFFFAOYSA-N

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Quality Level

100

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Application

Flufenacet has been used as reference standard for identification of pesticide from food and water samples using liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Flufenacet is an acetamide herbicide. It is used as a pesticide when combined with triazine compounds. They help in controlling the growth of weeds.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN5905
BCCF6599
BCBS9726V

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María J Carpio et al.
Journal of environmental management, 260, 110161-110161 (2020-02-25)
This paper reports the mobility and total balance of chlorotoluron (CTL), flufenacet (FNC) and bromide ion (Br-) throughout a sandy soil profile after the application of spent mushroom substrate (SMS) and green compost (GC). Obtaining mobility dataset is crucial to
Adsorption-desorption, persistence, and leaching behavior of flufenacet in alluvial soil of India.
S Gupta et al.
Bulletin of environmental contamination and toxicology, 66(1), 9-16 (2000-11-18)
Persistence, mobility, and adsorption of the herbicide flufenacet in the soil of winter wheat crops.
J Rouchaud et al.
Bulletin of environmental contamination and toxicology, 67(4), 609-616 (2002-01-10)
W R Christenson et al.
Toxicology and applied pharmacology, 132(2), 253-262 (1995-06-01)
Evidence of increased hepatic metabolizing capacity coupled with reductions in serum thyroxine (T4) levels were noted in the rat during preliminary toxicity studies with FOE 5043, an oxyacetamide with herbicidal properties. These findings were consistent with reports in the literature
Suman Gupta et al.
Chemosphere, 47(9), 901-906 (2002-07-11)
Effect of concentration, moisture and soil type on dissipation of flufenacet from soil has been studied under laboratory condition. The treated soil samples (1 and 10 microg/g levels) were incubated at 25+/-1 degrees C. The effect of moisture was studied
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