37044
烯效唑
PESTANAL®, analytical standard
别名:
(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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关于此项目
经验公式（希尔记法）:
C15H18ClN3O
化学文摘社编号:
分子量:
291.78
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
InChI key
YNWVFADWVLCOPU-MDWZMJQESA-N
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+
grade
analytical standard
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
Quality Level
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.
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
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)
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)
Sha Liu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(3), 332-335 (2011-08-10)
To study the effects of spraying uniconazole on plant morphology and total alkaloid content of Aconitum carmichaeli for providing theory base for establishment of planting measure. The mainly morphological character and total alkaloid content of Radix Aconiti Lateralis Praeparata were
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
Rika Kodaka et al.
Environmental toxicology and chemistry, 25(2), 310-316 (2006-03-08)
Aerobic soil metabolism of uniconazole-P ([S]-E-1-[4-chlorophenyl]-4,4-dimethyl-2-[1,2,4-triazole-1-yl]-penten-3-ol) and the effect of illumination on metabolic profiles were studied in the water-sediment system when spiked to water. Uniconazole-P was gradually partitioned to the sediment with an aquatic half-life of 6.9 d in darkness
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