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00401

Sigma-Aldrich

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
Beilstein:
606468
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39031308
PubChem Substance ID:
NACRES:
NA.22

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 (lit.)
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

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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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

321.8 °F - closed cup

Flash Point(C)

161 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Yan Ma et al.
Journal of chromatography. A, 1383, 47-57 (2015-02-05)
Prototype small-size (1.0mm I.D., 5cm long) columns for reversed-phase HPLC were evaluated in relation to instrument requirements. The performance of three types of columns, monolithic silica and particulate silica (2μm, totally porous and 2.6μm, core-shell particles) was studied in the
Thomas Hahne et al.
Journal of bioscience and bioengineering, 118(3), 311-314 (2014-04-04)
Human papillomavirus 6b L1 virus-like particles (VLPs) were successfully expressed using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid expression system and rapidly purified using size exclusion chromatography after ultracentrifugation procedure and characterized by capillary zone electrophoresis (CZE). The average capillary electrophoresis migration

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