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Merck

37876

Supelco

Anilofos

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C13H19ClNO3PS2
Número de CAS:
Peso molecular:
367.85
Beilstein/REAXYS Number:
2395778
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

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

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

InChI key

NXQDBZGWYSEGFL-UHFFFAOYSA-N

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General description

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.

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

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

>212.0 °F - closed cup

flash_point_c

> 100 °C - closed cup

ppe

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


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Certificados de análisis (COA)

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Visite la Librería de documentos

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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