37044
Uniconazole
PESTANAL®, analytical standard
Synonym(s):
(E)-(RS)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol
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About This Item
Empirical Formula (Hill Notation):
C15H18ClN3O
CAS Number:
Molecular Weight:
291.78
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
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
CC(C)(C)C(O)C(=C/c1ccc(Cl)cc1) 2cncn2
InChI
1S/C15H18ClN3O/c1-15(2,3)14(20)13(19-10-17-9-18-19)8-11-4-6-12(16)7-5-11/h4-10,14,20H,1-3H3/b13-8+
InChI key
YNWVFADWVLCOPU-MDWZMJQESA-N
General description
Uniconazole is a vinyl triazole fungicide with plant growth regulatory activity.
Application
Uniconazole may be used as an analytical reference standard for the quantification of the analyte in fruits and vegetables using various chromatographic techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
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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Analytical method for 44 pesticide residues in spinach using multi-plug-filtration cleanup based on multiwalled carbon nanotubes with liquid chromatography and tandem mass spectrometry detection
Qin Y, et al.
Journal of Separation Science, 39(9), 1757-1765 (2016)
Multi-residue determination of plant growth regulators in apples and tomatoes by liquid chromatography/tandem mass spectrometry
Xue J, et al.
Rapid Communications in Mass Spectrometry, 25(21), 3289-3297 (2011)
Peng Wang et al.
Journal of chromatographic science, 46(9), 787-792 (2008-11-15)
The amylose-tris(3,5-dimethylphenylcarbamate) chiral stationary phase was synthesized and used to separate the enantiomers of triazole pesticides by high-performance liquid chromatography. The mobile phase was n-hexane-isopropanol applying a flow rate of 1.0 mL/min. Six triazole pesticides were enantioselectively separated. Myclobutanil, paclobutrazol
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 456179-5ML | 04061832341200 |
| 37044-50MG | 04061831833485 |