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Merck

45453

Supelco

Dinoseb

PESTANAL®, analytical standard

Sinónimos:

2-sec-Butyl-4,6-dinitrophenol

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About This Item

Fórmula empírica (notación de Hill):
C10H12N2O5
Número de CAS:
Peso molecular:
240.21
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CCC(C)c1cc(cc(c1O)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C10H12N2O5/c1-3-6(2)8-4-7(11(14)15)5-9(10(8)13)12(16)17/h4-6,13H,3H2,1-2H3

InChI key

OWZPCEFYPSAJFR-UHFFFAOYSA-N

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Application

Dinoseb may be used as a reference standard in the analysis of dinoseb residues in samples of raspberry extract using high performance liquid chromatography coupled with ultraviolet-visible light detector (HPLC-UV).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Caution

Restringido a usuarios profesionales. Atención − Evitar exposición − obtener instrucciones especiales antes de usar

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Irrit. 2 - Skin Sens. 1

supp_hazards

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

306.9 °F - closed cup

flash_point_c

152.7 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificados de análisis (COA)

Lot/Batch Number

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Visite la Librería de documentos

High-performance liquid chromatography method for the determination of dinoseb: application to the analysis of residues in raspberries
Szeto.YS and Price.MP
Journal of Agricultural and Food Chemistry, 39, 1614-1617 (1991)
Mark R Viant et al.
Aquatic toxicology (Amsterdam, Netherlands), 76(3-4), 329-342 (2005-11-18)
Changes in metabolism of Japanese medaka (Oryzias latipes) embryos exposed to dinoseb (2-sec-butyl-4,6-dinitrophenol), a substituted dinitrophenol herbicide, were determined by in vivo (31)P NMR, high-pressure liquid chromatography (HPLC)-UV, and (1)H NMR metabolomics. ATP and phosphocreatine (PCr) metabolism were characterized within
Mariko Matsumoto et al.
Reproductive toxicology (Elmsford, N.Y.), 29(3), 292-297 (2010-02-06)
This study evaluated the prenatal developmental toxicity of the pesticide 2-sec-butyl-4,6-dinitrophenol (dinoseb). Pregnant rats were given dinoseb by gavage at 0, 8.0 or 10 mg/kg bw/day on days 6-15 of gestation, or in the diet at 0, 120 or 200
Mariko Matsumoto et al.
Environmental toxicology, 23(2), 169-183 (2008-01-25)
In a combined repeated dose toxicity study with reproduction/developmental toxicity screening test, Crj:CD(SD)IGS rats were dosed with dinoseb, 2-sec-butyl-4,6-dinitrophenol, by gavage at 0 (vehicle), 0.78, 2.33, or 7.0 mg/kg bw/day. Six males per group were dosed for a total of
Toshikazu Takahagi et al.
Bioscience, biotechnology, and biochemistry, 70(1), 266-268 (2006-01-24)
In atrazine-tolerant tobacco cells with Ser to Thr mutation at the 264th amino acid of PsbA polypeptide in photosystem II (PSII), electron trannsport around the secondary quinone acceptor (Q(B)) site was inhibited to a greater extent by barbatic acid than

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