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45349

Supelco

Bitertanol

PESTANAL®, analytical standard

Sinônimo(s):

3,3-Dimethyl-1-(4-phenylphenoxy)-1-(1,2,4-triazol-1-yl)butan-2-ol

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About This Item

Fórmula empírica (Notação de Hill):
C20H23N3O2
Número CAS:
55179-31-2
Peso molecular:
337.42
Beilstein:
620948
Número CE:
259-513-5
Número MDL:
MFCD00055508
Código UNSPSC:
41116107
ID de substância PubChem:
329756665
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

descrição

mixture of stereo isomers

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

CC(C)(C)C(O)C(Oc1ccc(cc1)-c2ccccc2)n3cncn3

InChI

1S/C20H23N3O2/c1-20(2,3)18(24)19(23-14-21-13-22-23)25-17-11-9-16(10-12-17)15-7-5-4-6-8-15/h4-14,18-19,24H,1-3H3

chave InChI

VGPIBGGRCVEHQZ-UHFFFAOYSA-N

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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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302

Declarações de precaução

P264 - P270 - P301 + P312 - P501

Classificações de perigo

Acute Tox. 4 Oral

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

No data available

Ponto de fulgor (°C)

No data available

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCC9372
BCBX0123
SZBD184XV
SZBC066XV
SZB7177XV

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Visite a Biblioteca de Documentos

Tatiana Zamora et al.
Journal of separation science, 27(9), 645-652 (2004-09-25)
Coupled-column liquid chromatography with fluorescence detection was applied to the determination of o-phenylphenol and bitertanol residues in orange and banana fruits. After extraction with a mixture of acetone, dichloromethane-petroleum ether, and ethyl acetate, an extract aliquot of 100 microL was
Y Yamazaki et al.
Journal of AOAC International, 81(6), 1252-1256 (1998-12-16)
A simple and rapid method was developed for determining bitertanol residues in strawberries. Bitertanol was extracted from samples with ethyl acetate. Bitertanol acetate was added prior to extraction as a surrogate standard. The ethyl acetate extract was cleaned up by
Marc Bourgin et al.
Chemosphere, 90(4), 1387-1395 (2012-09-25)
The degradation of bitertanol by ozone treatment is investigated. Solutions of bitertanol (8.4 μg mL(-1)) were prepared either by dissolution of the standard or by dilution of Gaucho Blé seed loading solution and then ozonated under different conditions. Evolution of
Ping-Kun Chan et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 44(12), 2047-2057 (2006-09-15)
The effects of fungicide bitertanol on cytochrome P450-dependent monooxygenases were studied using rats treated intraperitoneally with the N-substituted triazole for 4 days. Treatment with 10, 25, and 100 mg/kg bitertanol produced 2-, 4-, and 14-fold increases of 7-ethoxyresorufin O-deethylation activity
A R Allen et al.
Neurotoxicology and teratology, 15(4), 237-242 (1993-07-01)
Several recent reports indicate that triadimefon, a triazole fungicide, has effects on behavior that are similar to those of psychomotor stimulants. For example, triadimefon increases overall fixed-interval (FI) response rate, disrupts FI response patterning, increases motor activity, and produces stereotypies
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