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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

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Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, 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)
Belén Patiño et al.
International journal of food microbiology, 283, 45-51 (2018-08-14)
Filamentous fungi are an invaluable source for biocontrol strategies and for production and development of different antifungal polypeptides. Within this context, cysteine-rich antifungal AFP-like peptides stand out among many different antimicrobial compounds given their production easiness, stability, versatility, and efficacy.
Can Zhang et al.
Frontiers in microbiology, 8, 1779-1779 (2017-10-04)
The genus
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.
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