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Pyrasulfotole

PESTANAL®, analytical standard

Synonym(s):

(5-Hydroxy-1,3-dimethyl-1H-pyrazol-4-yl)[2-(methylsulfonyl)-4-(trifluoromethyl)phenyl]methanone, (5-Hydroxy-1,3-dimethylpyrazol-4-yl)(α,α,α-trifluoro-2-mesyl-p-tolyl)methanone

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About This Item

Empirical Formula (Hill Notation):
C14H13F3N2O4S
CAS Number:
Molecular Weight:
362.32
MDL number:
UNSPSC Code:
41116107
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

Cc1nn(C)c(O)c1C(=O)c2cc(ccc2S(C)(=O)=O)C(F)(F)F

InChI

1S/C14H13F3N2O4S/c1-7-11(13(21)19(2)18-7)12(20)9-5-4-8(14(15,16)17)6-10(9)24(3,22)23/h4-6,21H,1-3H3

InChI key

DWSPRBSLSXQIEJ-UHFFFAOYSA-N

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General description

Pyrasulfotole, a 4-hydroxyphenylpyruvate dioxygenase inhibitor, is well-known for its role in weed control, as well as excellent crop selectivity.

Application

Pyrasulfotole may be used as an analytical reference standard for the determination of the analyte in:
  • Agricultural products by liquid chromatography-time of flight mass spectrometry (LC-TOF-MS).
  • Vegetables and fruits by LC coupled to tandem mass spectrometry (MS/MS).

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

Health hazardEnvironment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2 Oral

Target Organs

Liver,Urinary system,Pancreas

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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An efficient one-pot synthesis of 2-(aryloxyacetyl) cyclohexane-1, 3-diones as herbicidal 4-hydroxyphenylpyruvate dioxygenase inhibitors.
Wang DW, et al.
Journal of Agricultural and Food Chemistry, 64(47), 8986-8993 (2016)
Simultaneous determination of acidic pesticides in vegetables and fruits by liquid chromatography-tandem mass spectrometry.
Shida SS, et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 50(3), 151-162 (2015)
Multi-residue screening method of acidic pesticides in agricultural products by liquid chromatography/time of flight mass spectrometry.
Akiyama Y, et al.
Journal of Pesticide Science, 0909020093-0909020093 (2009)
Bo He et al.
Journal of agricultural and food chemistry, 67(39), 10844-10852 (2019-09-19)
The discovery of 4-hydroxyphenylpyruvate dioxygenase (HPPD, EC 1.13.11.27) inhibitors has been an active area of research due to their great potential as herbicides for weed control. Starting from the binding mode of known inhibitors of HPPD, a series of HPPD
Chandrima Shyam et al.
Frontiers in plant science, 11, 614618-614618 (2021-02-02)
Evolution of multiple herbicide resistance in Palmer amaranth across the United States is a serious challenge for its management. Recently, a Palmer amaranth population (KCTR; Kansas Conservation Tillage Resistant) from a long-term conservation tillage research project in Kansas, United States

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