31718

Supelco

Flufenacet

PESTANAL®, analytical standard

Synonym(s):
N-(4-Fluorophenyl)-N-isopropyl-2-5-(trifluoromethyl)-1,3,4-thiadiazol-2-yloxyacetamide
Empirical Formula (Hill Notation):
C14H13F4N3O2S
CAS Number:
Molecular Weight:
363.33
Beilstein/REAXYS Number:
8787751
MDL number:
PubChem Substance ID:
NACRES:
NA.24
Pricing and availability is not currently available.

Quality Level

grade

analytical standard

product line

PESTANAL®

form

neat

CofA

certificate is enclosed in each package

shelf life

limited shelf life, expiry date on the label

application(s)

HPLC: suitable
gas chromatography (GC): suitable

Featured Industry

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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Related Categories

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.

Legal Information

PESTANAL is a registered trademark of Sigma-Aldrich International GmbH

Signal Word

Warning

Hazard Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Hazard Codes

Xn,N

Risk Statement

22-43-48/22-50/53

Safety Statement

13-24-37-60-61

RIDADR

UN 3077 9 / PGIII

WGK Germany

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
M Bazoobandi et al.
Journal of chromatography. A, 886(1-2), 319-322 (2000-08-19)
An analytical procedure for detecting residues of a new herbicide, flufenacet, in soil, wheat grain and straw by gas chromatographic method using various solvents and extraction methods was standardized. The best results were obtained when samples fortified with flufenacet and...
Sara Tucci et al.
The Journal of eukaryotic microbiology, 57(1), 63-69 (2009-12-18)
Euglena gracilis is able to synthesize adenosine triphosphate under anaerobic conditions through a malonyl-independent fatty acid synthesis leading to wax ester fermentation. Mitochondrial fatty acid synthesis uses acetyl-CoA and propionyl-CoA as C2- and C3-donors for de novo synthesis of even-...
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...
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)

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