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Merck

37876

Supelco

Anilofos

PESTANAL®, analytical standard

Synonym(e):

S-[2-(4-Chlor-N-isopropylanilino)-2-oxoethyl]-O,O′-dimethyl-dithiophosphat

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About This Item

Empirische Formel (Hill-System):
C13H19ClNO3PS2
CAS-Nummer:
Molekulargewicht:
367.85
Beilstein:
2395778
EG-Nummer:
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

COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1

InChI

1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3

InChIKey

NXQDBZGWYSEGFL-UHFFFAOYSA-N

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Allgemeine Beschreibung

Anilofos is a pre-emergence, organophosphorus herbicide, which is commonly used for the control of various annual grass weeds and sedges such as barnyard grasses in rice-based cropping system. Its mode of action involves the inhibition of cell division stage in weeds.

Anwendung

Anilofos may be used as an analytical reference standard for the quantification of the analyte in environmental samples using stir bar sorptive extraction and thermal desorption combined with gas chromatography coupled to mass spectrometry.
Anilofos may be used as an analytical reference standard for the quantification of the analyte in environmental samples using stir bar-sorptive extraction and thermal desorption combined with gas chromatography coupled to mass spectrometry.
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 2

Flammpunkt (°F)

>212.0 °F - closed cup

Flammpunkt (°C)

> 100 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Bioefficacy and determination of terminal residues of a herbicide anilofos in field soil and plants following an application to the transplanted rice crop
Sondhia S and Dixit A
Communications in Soil Science and Plant Analysis, 46(20), 2576-2584 (2015)
Dilek Akyil et al.
Cytotechnology, 69(6), 865-874 (2017-06-14)
We aimed to evaluate the mutagenic effect of Anilofos, organophosphate pesticide, by using Ames/Salmonella/microsome test. Its cytotoxic and genotoxic effects were also determined by chromosome aberration (CA), sister chromatid exchange (SCE) and micronucleus (MN) test in human peripheral blood lymphocytes.
Simultaneous determination of 64 pesticides in river water by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry
Nakamura S and Daishima S
Analytical and Bioanalytical Chemistry, 382(1), 99-107 (2005)
Jishi Wang et al.
Journal of chromatography. A, 1521, 10-18 (2017-09-25)
In this research, the manual two-step QuEChERS approach has been streamlined and automated into a one-step method using a cleanup tube fitted within an extraction tube. A novel automatic QuEChERS combination have been developed to simplify the QuEChERS procedures and
Jaswant Singh et al.
Food chemistry, 327, 127080-127080 (2020-05-27)
A hydrazone based Schiff base (SB) has been synthesized and investigated for the detection, quantification and degradation of selective organophosphates (i.e diethyl chlorophosphate, diethyl cyanophosphonate, tris (2-chloroethyl) phosphate and dichlorvos). The organophosphates (OPs) form a covalent bond with -OH groups

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