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Dinoseb

PESTANAL®, analytical standard

Synonym(s):

2-sec-Butyl-4,6-dinitrophenol

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About This Item

Empirical Formula (Hill Notation):
C10H12N2O5
CAS Number:
88-85-7
Molecular Weight:
240.21
EC Number:
201-861-7
MDL number:
MFCD00024246
UNSPSC Code:
41116107
PubChem Substance ID:
329756747
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Restricted to professional users. Attention − Avoid exposure − obtain special instructions before use.

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

EUH044

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCM0929
BCCH5434
BCBW3273
SZBD030XV
SZBA246XV

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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.
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
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.
Reproductive toxicology (Elmsford, N.Y.), 25(3), 327-334 (2008-05-09)
The present review paper summarizes the data available in the literature concerning prenatal exposure to dinoseb (2-sec-butyl-4,6-dinitrophenol; CAS No. 88-85-7), evaluating reported developmental toxicity in experimental animals. In particular, we have focused on the variable factors in the manifestation of
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