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34172

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)

Lot/Batch Number

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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
Determination of polar pesticides in soil by micellar electrokinetic chromatography using QuEChERS sample preparation.
Bol?shakov DS, et al.
Journal of Analytical Chemistry, 69(1), 89-97 (2014)
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
Rui Liu et al.
Ecotoxicology and environmental safety, 185, 109691-109691 (2019-09-30)
The rational use and the environmental safety of chiral pesticides have attracted significant research interest. Here, enantioselective toxic effects and the selective toxic mechanism of triticonazole (TRZ) against the aquatic microalgae Chlorella pyrenoidosa were studied. The 96h-EC50 values of rac-
Determination of triazole pesticide residues in edible oils using air-assisted liquid-liquid microextraction followed by gas chromatography with flame ionization detection.
Farajzadeh MA, et al.
Journal of Separation Science, 38(6), 1002-1009 (2015)

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