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45899

Supelco

Propiconazole solution

100 ng/μL in methanol, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H17Cl2N3O2
CAS Number:
60207-90-1
Molecular Weight:
342.22
Beilstein/REAXYS Number:
9349305
EC Number:
200-659-6
MDL number:
MFCD00055299
UNSPSC Code:
41116107
PubChem Substance ID:
329757008
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 ng/μL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

single component solution

storage temp.

2-8°C

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

Application

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

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBX4665
SZBF236XV
SZBD179XV
SZBD106XV
SZB9079XV

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Stephen Nesnow et al.
Chemico-biological interactions, 194(1), 79-89 (2011-08-26)
Propiconazole induces hepatocellular carcinomas and hepatocellular adenomas in mice and promotes liver tumors in rats. Transcriptional, proteomic, metabolomic and biochemical studies of hepatic tissues from mice treated with propiconazole under the conditions of the chronic bioassay indicated that propiconazole induced
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
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
Jon Hulvey et al.
Applied and environmental microbiology, 78(18), 6674-6682 (2012-07-17)
We investigated genetic factors that govern the reduced propiconazole sensitivity of Sclerotinia homoeocarpa field isolates collected during a 2-year field efficacy study on dollar spot disease of turf in five New England sites. These isolates displayed a >50-fold range of
Jes Jessen Rasmussen et al.
Aquatic toxicology (Amsterdam, Netherlands), 118-119, 54-61 (2012-04-21)
Previously, laboratory experiments have revealed that freely diluted azole fungicides potentiate the direct toxic effect of pyrethroid insecticides on Daphnia magna. More ecologically relevant exposure scenarios where pesticides are adsorbed have not been addressed. In this study we exposed beech
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