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Pyrazosulfuron-ethyl

PESTANAL®, analytical standard

Synonym(s):

Ethyl 5-[(4,6-dimethoxy-2-pyrimidinyl)aminocarbonylaminosulfonyl]-1-methyl-1H-pyrazole-4-carboxylate

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About This Item

Empirical Formula (Hill Notation):
C14H18N6O7S
CAS Number:
Molecular Weight:
414.39
Beilstein/REAXYS Number:
8442639
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

SMILES string

CCOC(=O)c1cnn(C)c1S(=O)(=O)NC(=O)Nc2nc(OC)cc(OC)n2

InChI

1S/C14H18N6O7S/c1-5-27-12(21)8-7-15-20(2)11(8)28(23,24)19-14(22)18-13-16-9(25-3)6-10(17-13)26-4/h6-7H,5H2,1-4H3,(H2,16,17,18,19,22)

InChI key

BGNQYGRXEXDAIQ-UHFFFAOYSA-N

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General description

Pyrazosulfuron-ethyl belongs to the class of sulfonylurea herbicides.

Application

Pyrazosulfuron-ethyl may be used as an analytical standard for the analysis of pyrazosulfuron-ethyl in:
  • Environmental water samples by magnetic solid phase extraction (MSPE) using multi-walled carbon nanotubes as adsorbents, combined with high performance liquid chromatography-diode-array-detection (HPLC-DAD).
  • Rice paddy soils by dispersive-SPE as well as quick, easy, cheap, effective, rugged and safe (QuEChERS) extraction and liquid chromatography-tandem mass spectrometry (LC-MS/MS) equipped with electrospray ionization (ESI), and multiple reaction monitoring (MRM) detection.
  • Sandy loam soil by HPLC with ultraviolet (UV) detection.
  • Surface water samples by solvent demulsification dispersive liquid-liquid microextraction (SD-DLLME) in conjunction with ESI-LC-MS/MS with MRM detection.
  • Rice samples by QuEChERS extraction and ESI-LC-MS/MS with single reaction monitoring (SRM) detection.
  • Crop plants by QuEChERS extraction and ultra-high performance LC-MS/MS equipped with ESI, and SRM 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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Warning

hcodes

Hazard Classifications

Acute Tox. 4 Inhalation

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

>338.0 °F - closed cup

flash_point_c

> 170.00 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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Biochars mediated degradation, leaching and bioavailability of pyrazosulfuron-ethyl in a sandy loam soil.
Manna S and Singh N
Geoderma, 334, 63-71 (2019)
Determination of six sulfonylurea herbicides in environmental water samples by magnetic solid-phase extraction using multi-walled carbon nanotubes as adsorbents coupled with high-performance liquid chromatography.
Ma J, et al.
Journal of Chromatography A, 1466, 12-20 (2016)
Multiresidue determination of pesticides in crop plants by the quick, easy, cheap, effective, rugged, and safe method and ultra-high-performance liquid chromatography tandem mass spectrometry using a calibration based on a single level standard addition in the sample.
Viera MS, et al.
Journal of Chromatography A, 1526(1), 119-127 (2017)
Simultaneous determination of herbicides in rice by QuECHERS and LC-MS/MS using matrix-matched calibration.
Rebelo AM, et al.
Journal of the Brazilian Chemical Society, 27(1), 186-193 (2016)
Multi-residue method for determination of 58 pesticides, pharmaceuticals and personal care products in water using solvent demulsification dispersive liquid-liquid microextraction combined with liquid chromatography-tandem mass spectrometry.
Caldas SS, et al.
Talanta, 146, 676-688 (2016)

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