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Merck
CN

45763

Fenazox

PESTANAL®, analytical standard

Synonym(s):

Azoxybenzene, Fenazox

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About This Item

Empirical Formula (Hill Notation):
C12H10N2O
CAS Number:
Molecular Weight:
198.22
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
207-802-1
Beilstein/REAXYS Number:
7462853
MDL number:
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Product Name

Fenazox, PESTANAL®, analytical standard

InChI key

GAUZCKBSTZFWCT-YPKPFQOOSA-N

InChI

1S/C12H10N2O/c15-14(12-9-5-2-6-10-12)13-11-7-3-1-4-8-11/h1-10H/b14-13-

SMILES string

[O-]\[N+](=N/c1ccccc1)c2ccccc2

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

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Legal Information

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

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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M Kujawa et al.
Zeitschrift fur die gesamte Hygiene und ihre Grenzgebiete, 35(5), 255-257 (1989-05-01)
No sex differences could been shown after absorption and distribution of azoxybenzen in the rat. The highest level occur in the thyroid gland, the adrenals and in the fat tissues. The maximum level was reached 30 min. after application.
Sławomir Piliszek et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(4), 275-287 (2012-03-21)
The quantitative structure - property relationship (QSPR) and the artificial neural networks (ANNs) methods were used to estimate aqueous solubility (log S and μg/L) of polychlorinated trans-azoxybenzenes (PCt-ABs). These QSPR and ANN models are based on geometry optimalization and quantum-chemical
M Stock et al.
Die Nahrung, 29(5), 473-479 (1985-01-01)
Results from investigations on the metabolism of 14C-Fenazox show that in 6-8 weeks old tomato-plants (sort "Harzfeuer") the agent undergoes a biotransformation. After chromatographic separation the structure of the biotransformation products was elucidated by comparison to authentic test substances, by
R Plass et al.
Die Nahrung, 32(10), 989-997 (1988-01-01)
Oral administrations of azoxybenzene (0, 25, 50 and 100 mg/kg b.w.) over a period up to 7 days caused a time and dose dependent decrease in the amount of cytochrome P-450 as well as in the ability of aminopyrine-N-demethylation and
Investigations of myelotoxic effects in rats.
T A Moeller
Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement, 14, 83-87 (1991-01-01)

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