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Supelco

Tebuconazole

PESTANAL®, analytical standard

Synonym(s):

1-(4-Chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)-3-pentanol

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About This Item

Empirical Formula (Hill Notation):
C16H22ClN3O
CAS Number:
Molecular Weight:
307.82
EC Number:
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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CC(C)(C)C(CO)(CCc1ccc(Cl)cc1)n2cncn2

InChI

1S/C16H22ClN3O/c1-15(2,3)16(10-21,20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7,11-12,21H,8-10H2,1-3H3

InChI key

UAJBSHCDOPGGBX-UHFFFAOYSA-N

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General description

Tebuconazole is a triazole fungicide. It is mostly used to control diseases in agricultural crops and is effective against diseases which are soil borne and foliar fungal based.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tebuconazole may have been used as reference standard in gas chromatography–mass spectrometry in selected ion monitoring mode (GC/MS, SIM) method for determination of pesticides from Hyptis pectinata, medicinal plant using [Zn(BDC)(H2O)2]n as adsorbent.

Legal Information

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Coordination polymer adsorbent for matrix solid-phase dispersion extraction of pesticides during analysis of dehydrated Hyptis pectinata medicinal plant by GC/MS.
Aquino A et.al.
Talanta, 83(2), 631-636 (2010)
Kristina Beijer et al.
Aquatic toxicology (Amsterdam, Netherlands), 198, 73-81 (2018-03-10)
Antifungal azoles are widely used in medicine, agriculture, and material protection and several antifungal azoles have been found in environmental samples. Although these compounds were designed to inhibit fungal enzymes such as lanosterol-14-demethylase (cytochrome P450 (CYP) 51), it is well
Can Zhang et al.
Frontiers in microbiology, 8, 1779-1779 (2017-10-04)
The genus
Tebuconazole application decreases soil microbial biomass and activity.
Mu?oz-Leoz, Borja, et al.
Soil Biology and Biochemistry, 43.10, 2176-2183 (2011)
Shuangyu Song et al.
Journal of agricultural and food chemistry, 66(20), 5031-5038 (2018-01-25)
In this study, a multi-residue analytical method using quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction and dispersive solid-phase extraction (d-SPE) cleanup, followed by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), was investigated for rapid determination of 60 pesticide residues

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