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Merck
CN

34172

Triticonazole

PESTANAL®, analytical standard

Synonym(s):

(RS)-(E)-5-(4-Chlorobenzylidene)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol

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About This Item

Empirical Formula (Hill Notation):
C17H20ClN3O
CAS Number:
Molecular Weight:
317.81
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
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InChI

1S/C17H20ClN3O/c1-16(2)8-7-14(9-13-3-5-15(18)6-4-13)17(16,22)10-21-12-19-11-20-21/h3-6,9,11-12,22H,7-8,10H2,1-2H3/b14-9+

SMILES string

CC1(C)CCC(=C/c2ccc(Cl)cc2)\C1(O)Cn3cncn3

InChI key

PPDBOQMNKNNODG-NTEUORMPSA-N

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

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General description

Triticonazole is a triazole fungicide primarily used for cereal seed treatment.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Triticonazole may be used as an analytical reference standard for the determination of the analyte in sewage sludge, edible oils, soil and cereals and dry animal feed by various chromatography techniques.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - STOT RE 2

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

农药列管产品
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Dominik Bleša et al.
Plants (Basel, Switzerland), 10(2) (2021-03-07)
The use of biological control is becoming a common practice in plant production. One overlooked group of organisms potentially suitable for biological control are Rhizoctonia-like (Rh-like) fungi. Some of them are capable of forming endophytic associations with a large group
Qing Zhang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1009-1010, 130-137 (2016-01-03)
An efficient and novel enantioseparation and determination method was developed to quantify the enantiomers of chiral triazole fungicide triticonazole in fruit, vegetable, and soil samples. Under the optimal chromatographic conditions, the enantiomers of triticonazole were completely enantioseparated on a cellulose
Development of a multi-residue method for the determination of pesticides in cereals and dry animal feed using gas chromatography-tandem quadrupole mass spectrometry: II. Improvement and extension to new analytes.
Walorczyk S
Journal of Chromatography A, 1208(1-2), 202-214 (2008)
Jianfeng He et al.
Journal of separation science, 39(21), 4251-4257 (2016-09-03)
Enantiomeric pairs of triticonazole have been successfully separated by supercritical fluid chromatography coupled with a tris(3,5-dimethylphenylcarbamoyl) cellulose-coated chiral stationary phase in this work. The effects of co-solvent, dissolution solvent, flow rate, backpressure, and column temperature have been studied in detail
Degradation of formulated and unformulated triticonazole fungicide in soil: effect of application rate.
Beigel C, et al.
Soil Biology and Biochemistry, 31(4), 525-534 (1999)

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