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N13576

Propiconazole

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H17Cl2N3O2
CAS Number:
Molecular Weight:
342.22
Beilstein:
9349305
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-1075

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

SMILES string

CCCC1COC(Cn2cncn2)(O1)c3ccc(Cl)cc3Cl

InChI

1S/C15H17Cl2N3O2/c1-2-3-12-7-21-15(22-12,8-20-10-18-9-19-20)13-5-4-11(16)6-14(13)17/h4-6,9-10,12H,2-3,7-8H2,1H3

InChI key

STJLVHWMYQXCPB-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

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Deepika Somani et al.
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Cochliobolus sativus (anamorph: Bipolaris sorokiniana) is a filamentous fungus from the class Dothideomycetes. It is a pathogen of cereals including wheat and barley, and causes foliar spot blotch, root rot, black point on grains, head blight, leaf blight, and seedling
Sarah Y Skolness et al.
Toxicological sciences : an official journal of the Society of Toxicology, 132(2), 284-297 (2013-01-23)
Conazoles are designed to inhibit cytochrome P450 (CYP) 14α-demethylase, an enzyme key to fungal cell wall formation. In vertebrates, conazoles may inhibit other CYPs, potentially disrupting processes like sex steroid synthesis. Propiconazole is a current-use pesticide that is among the
Maryline Calonne et al.
Chemosphere, 87(4), 376-383 (2012-01-14)
The increasing concentrations impact (0.02, 0.2 and 2 mg L(-1)) of a Sterol Biosynthesis Inhibitor (SBI) fungicide, propiconazole, was evaluated on development and sterol metabolism of two non-target organisms: mycorrhizal or non-mycorrhizal transformed chicory roots and the arbuscular mycorrhizal fungus
Anna-Maija Nyman et al.
Ecotoxicology (London, England), 21(7), 1828-1840 (2012-05-09)
Toxicokinetic-toxicodynamic (TKTD) models quantify the time-course of internal concentration, which is defined by uptake, elimination and biotransformation (TK), and the processes which lead to the toxic effects (TD). TKTD models show potential in predicting pesticide effects in fluctuating concentrations, but
Thomas Hartwig et al.
PloS one, 7(5), e36625-e36625 (2012-05-17)
Brassinosteroids (BRs) are steroidal hormones that play pivotal roles during plant development. In addition to the characterization of BR deficient mutants, specific BR biosynthesis inhibitors played an essential role in the elucidation of BR function in plants. However, high costs

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