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Key Documents

37876

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Anilofos

PESTANAL®, analytical standard

Synonyme(s) :

S-[2-(4-Chloro-N-isopropylanilino)-2-oxoethyl]-O,O′-dimethyl dithiophosphate

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About This Item

Formule empirique (notation de Hill):
C13H19ClNO3PS2
Numéro CAS:
Poids moléculaire :
367.85
Numéro Beilstein :
2395778
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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

Clé InChI

NXQDBZGWYSEGFL-UHFFFAOYSA-N

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Description générale

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.

Application

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.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

>212.0 °F - closed cup

Point d'éclair (°C)

> 100 °C - closed cup

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

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)
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
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

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