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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:
107534-96-3
Molecular Weight:
307.82
EC Number:
403-640-2
MDL number:
MFCD00145350
UNSPSC Code:
41116107
PubChem Substance ID:
329753956
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

H302,H361d,H410

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8341
BCCL2536
BCCL2398
BCCJ9429
BCCH6660

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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
Hsuan-Chen Wang et al.
Environmental microbiology, 20(1), 270-280 (2017-11-11)
Emerging azole resistance in Aspergillus fumigatus poses a serious threat to human health. This nationwide surveillance study investigated the prevalence and molecular characteristics of azole-resistant A. fumigatus environmental isolates in Taiwan, an island country with increasing use of azole fungicides.
Can Zhang et al.
Frontiers in microbiology, 8, 1779-1779 (2017-10-04)
The genus
Andres Mäe et al.
Frontiers in plant science, 11, 385-385 (2020-05-01)
Septoria tritici blotch (STB) is caused by the ascomycete Zymoseptoria tritici and one of the predominating diseases in wheat (Triticum aestivum) in Europe. The control of STB is highly reliant on frequent fungicide applications. The primary objective of this study
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