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112933

Sigma-Aldrich

Acetanilide

99%

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Synonym(s):
N-Phenylacetamide
Linear Formula:
CH3CONHC6H5
CAS Number:
Molecular Weight:
135.16
Beilstein:
606468
EC Number:
MDL number:
eCl@ss:
39031308
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.65 (vs air)

Quality Level

vapor pressure

1 mmHg ( 114 °C)

Assay

99%

form

solid

autoignition temp.

1004 °F

bp

304 °C (lit.)

mp

113-115 °C (lit.)

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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1 of 4

This Item
39722910030421004001
Acetanilide 99%

112933

Acetanilide

Acetanilide purified by sublimation, ≥99.9%

397229

Acetanilide

Acetaminophen Related Compound D United States Pharmacopeia (USP) Reference Standard

1003042

Acetaminophen Related Compound D

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

-

mp

113-115 °C (lit.)

mp

113-115 °C (lit.)

mp

113-115 °C (lit.)

mp

113-115 °C (lit.)

form

solid

form

solid

form

-

form

-

bp

304 °C (lit.)

bp

304 °C (lit.)

bp

304 °C (lit.)

bp

304 °C (lit.)

vapor density

4.65 (vs air)

vapor density

4.65 (vs air)

vapor density

4.65 (vs air)

vapor density

4.65 (vs air)

General description

Acetanilide undergoes palladium-catalyzed cross-coupling reaction to form ortho-acylacetanilide.

Application

Acetanilide is used as a EOF (electroosmotic flow) marker in the studies of affinity capillary electrophoresis for drug–protein binding.

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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Yinuo Wu et al.
Chemical communications (Cambridge, England), 49(7), 689-691 (2012-12-12)
A palladium-catalyzed cascade cross-coupling of acetanilide and toluene for the synthesis of ortho-acylacetanilide is described. Toluene derivatives can act as effective acyl precursors (upon sp(3)-C-H bond oxidation by a Pd/TBHP system) in the oxidative coupling between two C-H bonds. This
Zetty Azalea Sutirman et al.
International journal of biological macromolecules, 133, 1260-1267 (2019-05-03)
Grafting of crosslinked chitosan with monomer, N-vinyl-2-pyrrolidone, has been carried out to investigate its adsorption capacity toward Orange G (OG) from aqueous solutions. The adsorption performance of modified chitosan (cts(x)-g-PNVP) was examined and compared with that of the unmodified chitosan.
Gea H van der Lee et al.
Ecology, 102(3), e03275-e03275 (2020-12-23)
Changes in the ecological stoichiometry of primary producers may have considerable implications for energy and matter transfer in food webs. We hypothesized that nutrient enrichment shifts the trophic position of omnivores towards herbivory, as the nutritional quality of primary producers
Deia El-Hady et al.
Journal of pharmaceutical and biomedical analysis, 52(2), 232-241 (2010-01-19)
In order to achieve excellent precision in the estimation of binding constants by affinity capillary electrophoresis (ACE), electroosmotic flow (EOF) stability is the key parameter, especially when using proteins in binding assays. Appropriate rinsing protocols are mandatory. In our study
Weiwei Qin et al.
Journal of chromatography. A, 1432, 84-91 (2016-01-21)
Metal-organic framework (MOF) MIL-100(Fe) with well-defined thickness was homogenously coated onto the outer surface of magnetic microparticles via a liquid-phase epitaxy method. The as-synthesized MIL-100(Fe) was used as stationary phase for high-performance liquid chromatography (HPLC) and separations of two groups

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