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P14815

Sigma-Aldrich

4-Ethoxyaniline

98%

Synonym(s):

p-Phenetidine, 4-Ethoxyaniline

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About This Item

Linear Formula:
C2H5OC6H4NH2
CAS Number:
156-43-4
Molecular Weight:
137.18
Beilstein:
606666
EC Number:
205-855-5
MDL number:
MFCD00007865
UNSPSC Code:
12352100
PubChem Substance ID:
24898204
NACRES:
NA.22

Quality Level

200

Assay

98%

refractive index

n20/D 1.559 (lit.)

bp

250 °C (lit.)

mp

2-5 °C (lit.)

density

1.065 g/mL at 25 °C (lit.)

SMILES string

CCOc1ccc(N)cc1

InChI

1S/C8H11NO/c1-2-10-8-5-3-7(9)4-6-8/h3-6H,2,9H2,1H3

InChI key

IMPPGHMHELILKG-UHFFFAOYSA-N

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Related Categories

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Muta. 2 - Skin Sens. 1

Storage Class Code

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

WGK

WGK 1

Flash Point(F)

251.6 °F - closed cup

Flash Point(C)

122 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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D Ross et al.
The Journal of biological chemistry, 260(28), 15028-15032 (1985-12-05)
Horseradish peroxidase-catalyzed oxidation of p-phenetidine in the presence of either glutathione (GSH), cysteine, or N-acetylcysteine led to the production of the appropriate thioyl radical which could be observed using EPR spectroscopy in conjunction with the spin trap 5,5-dimethyl-1-pyrroline-N-oxide. This confirms
V V Subrahmanyam et al.
Chemico-biological interactions, 61(1), 45-59 (1987-01-01)
The peroxidase catalyzed oxidation of certain drugs in the presence of glutathione (GSH) resulted in extensive oxidation to oxidized glutathione (GSSG). Extensive oxygen uptake ensued and thiyl radicals could be trapped. Only catalytic amounts of drugs were required indicating a
J A Hinson et al.
The Journal of pharmacology and experimental therapeutics, 238(1), 106-112 (1986-07-01)
Addition of p-[3H]nitrosophenetole to protein incubations resulted in quantitative binding of radiolabel to protein. Preincubation of protein with N-methylmaleimide to derivatize sulfhydryl groups followed by addition of p-[3H]nitrosophenetole resulted in a 90% decrease in covalent binding. Treatment of the p-[3H]nitrosophenetole
Co-oxidation of xenobiotics.
P Moldéus et al.
Biochemical Society transactions, 13(5), 847-850 (1985-10-01)
C B Jensen et al.
Toxicology and applied pharmacology, 111(1), 1-12 (1991-10-01)
Phenacetin is well known to cause hemolytic anemia and methemoglobinemia in humans. Early mechanistic studies clearly established a causal role for active/reactive drug metabolites in the process but did not unequivocally identify these metabolite(s) or resolve the question of whether
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