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Supelco

Fenazox

PESTANAL®, analytical standard

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Synonym(s):
Azoxybenzene, Fenazox
Empirical Formula (Hill Notation):
C12H10N2O
CAS Number:
495-48-7
Molecular Weight:
198.22
Beilstein:
7462853
EC Number:
207-802-1
MDL number:
MFCD00019925
PubChem Substance ID:
329756942
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

SMILES string

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

InChI

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

InChI key

GAUZCKBSTZFWCT-YPKPFQOOSA-N

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Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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J P Tindall
Journal of the American Academy of Dermatology, 13(4), 539-558 (1985-10-01)
Chloracne, an acneform eruption resulting from poisoning by halogenated aromatic compounds, has been a considerable problem over the last 40 years. The condition is always a symptom of systemic poisoning and should be familiar to all practitioners, particularly dermatologists. It
Investigations of myelotoxic effects in rats.
T A Moeller
Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement, 14, 83-87 (1991-01-01)
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
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
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.
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