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Merck

00401

Acetanilide

puriss. p.a., ≥99.5% (CHN)

Synonym(s):

N-Phenylacetamide

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About This Item

Linear Formula:
CH3CONHC6H5
CAS Number:
Molecular Weight:
135.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39031308
UNSPSC Code:
12352100
EC Number:
203-150-7
MDL number:
Beilstein/REAXYS Number:
606468
Assay:
≥99.5% (CHN)
Form:
solid
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vapor density

4.65 (vs air)

Quality Level

vapor pressure

1 mmHg ( 114 °C)

grade

puriss. p.a.

assay

≥99.5% (CHN)

form

solid

autoignition temp.

1004 °F

bp

304 °C (lit.)

mp

113-115 °C

functional group

amide

SMILES string

CC(=O)Nc1ccccc1

InChI

1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)

InChI key

FZERHIULMFGESH-UHFFFAOYSA-N

General description

Acetanilide is a member of acetamides. It is used as a precursor compound in the synthesis of dyes, varnishes, and rubber accelerators. It is also used as a key intermediate for many pharmaceutical compounds.

Application

Acetanilide can be used as a reactant to synthesize:      
  • Oxindole derivatives via Ir-catalyzed intermolecular C-H functionalization with diazotized Meldrum′s acid.     
  • Ortho-Haloacetanilides via regioselective C-H functionalization/halogenation reaction in the presence of Pd(OAc)2 and Cu(OAc)2 catalyst.      
  • Chlorosubstituted acetanilides via oxidative chlorination with HCI and m-chloroperbenzoic acid in DMF.



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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

321.8 °F - closed cup

flash_point_c

161 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

00401-5G:4.548173388861E12

jan



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Fabrice Gritti et al.
Journal of chromatography. A, 1355, 179-192 (2014-07-09)
The mass transfer mechanism in four prototype columns (2.1 and 3.0×50mm, 2.1 and 3.0×100mm) packed with 1.9μm fully porous Titan-C18 particles was investigated by using two previously reported home-made protocols. The first one was used to measure the eddy dispersion
Naoki Aizawa et al.
Neurourology and urodynamics, 34(4), 368-374 (2014-02-18)
We measured single-unit mechanosensitive afferent activities (SAAs) during reflexic, rhythmic bladder contractions (RBCs), and examined whether L-arginine, an NO substrate, and mirabegron, a β3-adrenoceptor agonist, and oxybutynin, an antimuscarinic agent, can affect the SAAs in such condition. Twenty-nine female Sprague-Dawley
Hassan A Alhazmi et al.
Journal of pharmaceutical and biomedical analysis, 107, 311-317 (2015-02-02)
In this work, the behavior of several metal ions with different globular proteins was investigated by affinity capillary electrophoresis. Screening was conducted by applying a proper rinsing protocol developed by our group. The use of 0.1M EDTA in the rinsing