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A0881

Sigma-Aldrich

p-Anisidine

crystalline

Sinónimos:

4-Aminoanisole, 4-Methoxyaniline

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About This Item

Fórmula lineal:
CH3OC6H4NH2
Número de CAS:
104-94-9
Peso molecular:
123.15
Beilstein/REAXYS Number:
471556
EC Number:
203-254-2
MDL number:
MFCD00007864
UNSPSC Code:
12352200

form

crystalline

autoignition temp.

959 °F

color

dark gray to brown

bp

240-243 °C (lit.)

mp

56-59 °C (lit.)

storage temp.

2-8°C

SMILES string

COc1ccc(N)cc1

InChI

1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3

InChI key

BHAAPTBBJKJZER-UHFFFAOYSA-N

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Referencia del producto
Descripción
Precios

A88255

p-Anisidine, 99%

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Carc. 1B - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

251.6 °F - closed cup

flash_point_c

122 °C - closed cup

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K Héberger et al.
Lipids, 34(1), 83-92 (1999-04-03)
Decomposition of hydroperoxides in sunflower oil under strictly oxygen-free conditions was followed by measuring peroxide values against time, absorbance values at 232 and 268 nm, para-anisidine values, and by quantitative analyses of volatile products using various additives. The results were
Francesco Caponio et al.
Journal of food science, 74(9), C701-C706 (2010-05-25)
An experimental investigation was carried out to evaluate the influence of processing and storage time on the lipidic fraction of taralli. The data obtained pointed out that the kneading phase caused a significant increase of the oxidized triacylglycerols and triacylglycerol
C Meier et al.
Carcinogenesis, 12(9), 1633-1640 (1991-09-01)
We report here on the conformational analysis of C8-arylamine nucleoside and nucleotide adducts of the borderline carcinogens 4-methylaniline and 4-methoxyaniline. The non-phosphorylated adducts show anti conformation of the glycosidic link, while the corresponding 5'-phosphorylated adducts have a syn conformation. All
James S Harvey et al.
Mutagenesis, 20(1), 51-56 (2005-01-27)
The pH 6.7 Syrian hamster embryo (SHE) cell morphological transformation assay is a short-term in vitro test that has been used to predict rodent carcinogenicity. Previous reports have indicated that the SHE assay has an overall concordance of approximately 80%
Yujiro Hayashi et al.
Nature protocols, 2(1), 113-118 (2007-04-03)
This protocol describes a procedure for the synthesis of syn-beta-amino alpha-substituted aldehydes, versatile intermediates in synthetic organic chemistry, via asymmetric, direct, one-pot, three-component, cross-Mannich reaction of two different aldehydes. The reaction consists of two steps; one is the formation of
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