19701
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®
assay
≥98.0% (HPLC)
shelf life
limited shelf life, expiry date on the label
composition
carbon content, 61.57% , hydrogen content, 6.22% , nitrogen content, 14.40%
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
150-160 °C
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 triazole compound which have plant growth regulating and fungitoxic properties. It protects plants from temperature fluctuations, drought and air pollutants.
Application
Uniconazole may have been used as racemic pesticide standard to determine pesticides from soil using achiral and chiral liquid chromatography in combination with matrix solid-phase dispersion.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Improvement of uniconazole-induced protection in wheat seedlings.
Fletcher, R. A. and G. Hofstra
Journal of Plant Growth Regulation, 9.1-4, 207-212 (1990)
Zhao-Yang Li et al.
Journal of AOAC International, 86(3), 521-528 (2003-07-11)
The separation of enantiomers and diastereomers of 8 commonly used pesticides was investigated by liquid chromatography (LC) using a Chiralcel OD column (cellulose tris-3,5-dimethylphenylcarbamate as the chiral stationary phase) and a Pirkle-type Chirex 3020 column (urea derivative from the reaction
Makiko Sugiura et al.
Magnetic resonance in chemistry : MRC, 44(2), 121-126 (2005-12-17)
An NMR method for discriminating among enantiomers by using a chiral liquid crystalline solution was applied to chiral triazole compounds, uniconazole (1) and diniconazole (2), which exhibit antifungal and plant growth regulating activities. These chiral compounds were dissolved in PBLG