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37044

Supelco

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:
83657-22-1
Molecular Weight:
291.78
MDL number:
MFCD01678674
UNSPSC Code:
41116107
PubChem Substance ID:
329755598
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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.

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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
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6673
BCCK6522
BCCF6467
BCBZ8723
BCBS3724V

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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)
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)
Kimio Uematsu et al.
Plant physiology and biochemistry : PPB, 46(8-9), 768-774 (2008-07-29)
Although adenosine 3',5'-cyclic monophosphate (cAMP) is known as a key second messenger in many living organisms, regulating a wide range of cellular responses, its biological function in higher plants is not well understood. In this study, the role and the
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
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