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Merck

37044

Supelco

Uniconazole

PESTANAL®, analytical standard

Sinónimos:

(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

Fórmula empírica (notación de Hill):
C15H18ClN3O
Número de CAS:
Peso molecular:
291.78
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

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

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General description

Uniconazole is a vinyl triazole fungicide with plant growth regulatory activity.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Uniconazole may be used as an analytical reference standard for the quantification of the analyte in fruits and vegetables using various chromatographic techniques.

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 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Certificados de análisis (COA)

Lot/Batch Number

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Visite la Librería de documentos

Enantiomeric separation of diniconazole and uniconazole by cyclodextrin-modified micellar electrokinetic chromatography
Furuta R and Doi T
Journal of Chromatography A, 676(2), 431-436 (1994)
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)
Fast enantiomeric separation of uniconazole and diniconazole by electrokinetic chromatography using an anionic cyclodextrin: Application to the determination of analyte-selector apparent binding constants for enantiomers
Martin-Biosca Y, et al.
Electrophoresis, 21(15), 3240-3248 (2000)
Yasushi Todoroki et al.
Bioorganic & medicinal chemistry, 16(6), 3141-3152 (2008-01-01)
The plant growth retardant S-(+)-uniconazole (UNI-OH) is a strong inhibitor of abscisic acid (ABA) 8'-hydroxylase, a key enzyme in the catabolism of ABA, a plant hormone involved in stress tolerance, stomatal closure, flowering, seed dormancy, and other physiological events. In

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