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P14815

Sigma-Aldrich

4-Ethoxyaniline

98%

Sinônimo(s):

p-Phenetidine, 4-Ethoxyaniline

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About This Item

Fórmula linear:
C2H5OC6H4NH2
Número CAS:
156-43-4
Peso molecular:
137.18
Beilstein:
606666
Número CE:
205-855-5
Número MDL:
MFCD00007865
Código UNSPSC:
12352100
ID de substância PubChem:
24898204
NACRES:
NA.22

Nível de qualidade

200

Ensaio

98%

índice de refração

n20/D 1.559 (lit.)

p.e.

250 °C (lit.)

pf

2-5 °C (lit.)

densidade

1.065 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCOc1ccc(N)cc1

InChI

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

chave InChI

IMPPGHMHELILKG-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

251.6 °F - closed cup

Ponto de fulgor (°C)

122 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
MKCR0015
MKCN1138
MKCL4829
MKCJ1259
MKCD9225

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L-Valine ethyl ester hydrochloride 99%

Sigma-Aldrich

220698

L-Valine ethyl ester hydrochloride

R Larsson et al.
The Journal of pharmacology and experimental therapeutics, 235(2), 475-480 (1985-11-01)
The metabolism of p-phenetidine in microsomes from rabbit kidney and the metabolism of acetaminophen and p-phenetidine in human kidney microsomes to protein binding metabolites were examined. Microsomal preparations from rabbit kidney medulla catalyzed the irreversible arachidonic acid-dependent binding of p-[14C]phenetidine
V Fischer et al.
Chemico-biological interactions, 60(2), 115-127 (1986-11-01)
The oxidation of the phenacetin metabolites p-phenetidine and acetaminophen by peroxidases was investigated. Free radical intermediates from both metabolites were detected using fast-flow ESR spectroscopy. Oxidation of acetaminophen with either lactoperoxidase and hydrogen peroxide or horseradish peroxidase and hydrogen peroxide
R Larsson et al.
Chemico-biological interactions, 60(3), 317-330 (1986-12-01)
The interaction of N-(4-ethoxyphenyl)p-benzoquinone imine (NEPBQI), a metabolite formed during peroxidase catalyzed metabolism of p-phenetidine, with GSH and its effects in isolated rat hepatocytes were investigated. When reacted with GSH NEPBQI formed both a mono- and a diglutathione conjugate as
T Nohmi et al.
Japanese journal of cancer research : Gann, 78(2), 153-161 (1987-02-01)
Metabolic activation of phenacetin by liver microsomes proceeds via both phenetidine and N-hydroxyphenacetin to direct-acting mutagens, i.e., N-hydroxyphenetidine and p-nitrosophenetole. Five different molecular species of cytochrome P-450 have been purified from liver microsomes of drug-pretreated Wistar rats or Syrian hamsters
Annabel Kuek et al.
Postgraduate medical journal, 83(978), 251-260 (2007-04-04)
Targeted biologic therapies have revolutionised treatment of immune-mediated inflammatory diseases (IMIDs) due to their efficacy, speed of onset and tolerability. The discovery that clinically unrelated conditions, such as rheumatoid arthritis and Crohn's disease, share similar immune dysregulation has led to
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