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Propiconazol solution

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

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About This Item

Fórmula empírica (notación de Hill):
C15H17Cl2N3O2
Número de CAS:
60207-90-1
Peso molecular:
342.22
Beilstein:
9349305
Número CE:
200-659-6
Número MDL:
MFCD00055299
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329757008
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

concentración

100 ng/μL in methanol

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

formato

single component solution

temp. de almacenamiento

2-8°C

cadena SMILES

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

Clave InChI

STJLVHWMYQXCPB-UHFFFAOYSA-N

Aplicación

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

Información legal

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

Palabra de señalización

Danger

Clasificaciones de peligro

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

Órganos de actuación

Eyes,Central nervous system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

51.8 °F - closed cup

Punto de inflamabilidad (°C)

11 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves

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Certificados de análisis (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
Fuxing Zhu et al.
Pest management science, 68(7), 1003-1009 (2012-02-22)
The long-term preservation of interesting phenotypes in plant pathogenic fungi allows for follow-up studies in the future. Twelve storage approaches were investigated to determine their effects on instability of propiconazole resistance for three demethylation inhibitor (DMI) fungicide-resistant and two DMI-sensitive
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
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