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Supelco

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
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

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

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+

InChI key

PPDBOQMNKNNODG-NTEUORMPSA-N

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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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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
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)
Determination of azoles in sewage sludge from Spanish wastewater treatment plants by liquid chromatography-tandem mass spectrometry.
Garcia?Valcarcel AI, et al.
Journal of Separation Science, 34(11), 1228-1235 (2011)
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)

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