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46117

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4,4′-Oxydianiline

analytical standard

Synonym(s):

4,4′-Diaminodiphenyl ether, 4-Aminophenyl ether

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About This Item

Linear Formula:
O(C6H4NH2)2
CAS Number:
Molecular Weight:
200.24
Beilstein:
475735
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

vapor pressure

10 mmHg ( 240 °C)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

188-192 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Nc1ccc(Oc2ccc(N)cc2)cc1

InChI

1S/C12H12N2O/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8H,13-14H2

InChI key

HLBLWEWZXPIGSM-UHFFFAOYSA-N

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General description

4,4′-Oxydianiline is a potent carcinogen belonging to the class of aromatic amines. It is commonly used in the production of pesticides, pharmaceuticals, dyes, packaging of food products, etc.

Application

4,4′-Oxydianiline may be used as an analytical reference standard for the quantification of the analyte in water samples and water food simulant using different chromatography techniques.

Caution

Restricted to professional users. Attention − Avoid exposure − obtain special instructions before use.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 1 - Carc. 1B - Muta. 1B - Repr. 2 - Skin Sens. 1 - STOT RE 2 Oral

Target Organs

Thyroid

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

426.2 °F - closed cup

Flash Point(C)

219 °C - closed cup


Certificates of Analysis (COA)

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Analysis of carcinogenic aromatic amines in water samples by solid-phase microextraction coupled with high-performance liquid chromatography
Chang Y-W, et al.
Analytica Chimica Acta, 495(1-2), 109-122 (2003)
Determination of primary aromatic amines in water food simulant using solid-phase analytical derivatization followed by gas chromatography coupled with mass spectrometry
Brede C, et al.
Journal of Chromatography A, 983(1-2), 35-42 (2003)
[Cardiotoxic action of 4,4-diaminodiphenyl ether].
V A Kondratiuk et al.
Gigiena i sanitariia, (6)(6), 31-34 (1986-06-01)
4,4'-Diaminodiphenyl ether.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 29, 203-212 (1982-05-01)
[Functional and morphologic changes in the myocardium caused by chemical damage].
M S Gnatiuk et al.
Gigiena i sanitariia, (2)(2), 54-57 (1990-02-01)

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