32431
Furilazole
PESTANAL®, analytical standard
Synonym(s):
(RS)-3-Dichloroacetyl-5-(2-furanyl)-2,2-dimethyl-1,3-oxazolidine
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C11H13Cl2NO3
CAS Number:
Molecular Weight:
278.13
Beilstein/REAXYS Number:
11343170
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade
analytical standard
Quality Level
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
storage temp.
2-8°C
SMILES string
CC1(C)OC(CN1C(=O)C(Cl)Cl)c2ccco2
InChI
1S/C11H13Cl2NO3/c1-11(2)14(10(15)9(12)13)6-8(17-11)7-4-3-5-16-7/h3-5,8-9H,6H2,1-2H3
InChI key
MCNOFYBITGAAGM-UHFFFAOYSA-N
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General description
Furilazole is classified under the dichloroacetamide group of herbicide safeners.
Application
Furilazole may be used as an analytical reference standard for the determination of the analyte in:
- Vegetables and a fruit samples by solid-phase extraction (SPE) and gas chromatography/multiphoton ionization/time-of-flight mass spectrometry (GC/MPI/TOFMS) as well as GC coupled to electron ionization (EI) MS.
- Food samples by GC/MS with multiple reaction monitoring (MRM) detection.
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
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Ionization of pesticides using a far-ultraviolet femtosecond laser in gas chromatography/time-of-flight mass spectrometry.
Hashiguchi Y, et al.
Analytical and Bioanalytical Chemistry, 405(22), 7053-7059 (2013)
Compensation of matrix effects in gas chromatography-mass spectrometry analysis of pesticides using a combination of matrix matching and multiple isotopically labeled internal standards.
Tsuchiyama T, et al.
Journal of Chromatography A, 1524(22), 233-245 (2017)
Solubility, partitioning, oxidation and photodegradation of dichloroacetamide herbicide safeners, benoxacor and furilazole.
Acharya SP and Weidhaas J
Chemosphere, 211, 1018-1024 (2018)
Analysis of pesticides by gas chromatography/multiphoton ionization/mass spectrometry using a femtosecond laser.
Li A, et al.
Analytica Chimica Acta, 701(1), 52-59 (2011)
Md Shiful Islam et al.
Gene, 639, 149-162 (2017-10-11)
Glutathione S-transferases (GSTs) are ubiquitous enzymes which play versatile functions including cellular detoxification and stress tolerance. In this study, a comprehensive genome-wide identification of GST gene family was carried out in potato (Solanum tuberosum L.). The result demonstrated the presence
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