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Supelco

Propiconazole solution

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

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About This Item

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

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

concentração

100 ng/μL in methanol

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

single component solution

temperatura de armazenamento

2-8°C

cadeia de caracteres 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

chave InChI

STJLVHWMYQXCPB-UHFFFAOYSA-N

Aplicação

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

Informações legais

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

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Eyes,Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

51.8 °F - closed cup

Ponto de fulgor (°C)

11 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves

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Certificados de análise (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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