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Key Documents

100528

Sigma-Aldrich

4′-Aminoacetanilide

99%

Synonym(s):

N-(4-Aminophenyl)acetamide, N-Acetyl-p-phenylenediamine

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About This Item

Linear Formula:
CH3CONHC6H4NH2
CAS Number:
Molecular Weight:
150.18
Beilstein:
742888
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

mp

164-167 °C (lit.)

functional group

amide

SMILES string

CC(=O)Nc1ccc(N)cc1

InChI

1S/C8H10N2O/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,9H2,1H3,(H,10,11)

InChI key

CHMBIJAOCISYEW-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

383.0 °F - DIN 51758

Flash Point(C)

195 °C - DIN 51758

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Jennifer Hennen et al.
ALTEX, 34(2), 279-288 (2016-10-22)
In vitro approaches to address key steps of chemical-induced skin sensitization have been developed, but there is uncertainty how keratinocytes, which play a crucial role not only regarding xenobiotic metabolism but also skin inflammation, impact on a chemical's potential and
Joan Eilstein et al.
Journal of applied toxicology : JAT, 40(3), 416-433 (2020-01-09)
The abundance of xenobiotic metabolizing enzymes (XMEs) is different in the skin and liver; therefore, it is important to differentiate between liver and skin metabolism when applying the information to safety assessment of topically applied ingredients in cosmetics. Here, we
Chad D Iverson et al.
Journal of chromatography. A, 1422, 186-193 (2015-10-28)
Porous graphitic carbon (PGC) is an increasingly popular and attractive phase for HPLC on account of its chemical and thermal stability, and its unique separation mechanism. However, native PGC is strongly hydrophobic and in some instances excessively retentive. As part

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