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Merck

32431

Supelco

Furilazol

PESTANAL®, analytical standard

Synonym(e):

(RS)-3-Dichloracetyl-5-(2-furanyl)-2,2-dimethyl-1,3-oxazolidin

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About This Item

Empirische Formel (Hill-System):
C11H13Cl2NO3
CAS-Nummer:
Molekulargewicht:
278.13
Beilstein:
11343170
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

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

InChIKey

MCNOFYBITGAAGM-UHFFFAOYSA-N

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Allgemeine Beschreibung

Furilazole is classified under the dichloroacetamide group of herbicide safeners.

Anwendung

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.

Empfohlene Produkte

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

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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