Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

31718

Supelco

Flufenacet

PESTANAL®, analytical standard

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Looking for similar products? Visit Product Comparison Guide

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.

Recommended products

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

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCF6599
BCBS9726V
SZBD038XV
SZBA029XV
SZBA029X

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Chlorothalonil PESTANAL®, analytical standard

Supelco

36791

Chlorothalonil

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
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)
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
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
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-
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service