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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:
122-80-5
Molecular Weight:
150.18
Beilstein:
742888
EC Number:
204-576-6
MDL number:
MFCD00007853
UNSPSC Code:
12352100
PubChem Substance ID:
24846417
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

mp

164-167 °C (lit.)

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

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

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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Certificates of Analysis (COA)

Lot/Batch Number
STBK8422
STBK0101
STBJ3710
STBH3987
STBH2951

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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
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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