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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
Beilstein:
8787751
MDL number:
MFCD01751191
UNSPSC Code:
41116107
PubChem Substance ID:
329753899
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

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

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

InChI key

IANUJLZYFUDJIH-UHFFFAOYSA-N

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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.

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.

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Legal Information

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

Signal Word

Warning

Hazard Statements

H302,H317,H373,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF6599
BCBS9726V
SZBD038XV
SZBA029XV
SZBA029X

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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)
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
V T Gajbhiye et al.
Pest management science, 57(7), 633-639 (2001-07-24)
Adsorption-desorption of the herbicide flufenacet (FOE 5043) has been studied in five soils from different locations in India (Delhi, Ranchi, Nagpur, Kerala and Assam) varying in their physicochemical properties. The organic matter (OM) content varied from 0.072 to 0.864%, clay
Analysis and detection of the herbicides dimethenamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water.
Zimmerman LR, Schneider RJ, Thurman EM.
Journal of Agricultural and Food Chemistry, 50(5), 1045-1052 (2002)
W R Christenson et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 29(2), 251-259 (1996-02-01)
N-(4-Fluorophenyl)-N-(1-methylethyl)-2-[[5-(trifluoromethyl)-1,3, 4-thiadiazol-2-yl]oxy]acetamide (FOE 5043) is a new acetanilide-type herbicide undergoing regulatory testing. Previous work in this laboratory suggested that FOE 5043-induced reductions in serum thyroxine (T4) levels were mediated via an extrathyroidal site of action. The possibility that the alterations
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