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Sigma-Aldrich

4′-Methylpropiophenone

90%, technical grade

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About This Item

Linear Formula:
CH3C6H4COC2H5
CAS Number:
5337-93-9
Molecular Weight:
148.20
EC Number:
226-267-5
MDL number:
MFCD00009312
UNSPSC Code:
12352100
PubChem Substance ID:
24873986
NACRES:
NA.22

grade

technical grade

Assay

90%

refractive index

n20/D 1.528 (lit.)

bp

238-239 °C (lit.)

density

0.993 g/mL at 25 °C (lit.)

SMILES string

CCC(=O)c1ccc(C)cc1

InChI

1S/C10H12O/c1-3-10(11)9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3

InChI key

PATYHUUYADUHQS-UHFFFAOYSA-N

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Application

4′-Methylpropiophenone can be used as a building block to synthesize:
  • N





  • -(4-Chlorophenyl)-N′-[1-(4-methylphenyl)propyl]urea as a potential CRAC channel inhibitor.
  • Mono and trinuclear cobaloxime/organocobaloxime complexes, which are used as efficient catalysts for the synthesis of cyclic carbonates.
  • Tolperisone (TOL) via acid-catalyzed reaction with piperidine hydrochloride and 1,2-dioxolane.

Other Notes

Remainder 3′-methylpropiophenone

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ketone synthesized cobaloxime/organocobaloxime catalysts for cyclic carbonate synthesis from CO2 and epoxides: Characterization and electrochemistry
Kilic A, et al.
Journal of Organometallic Chemistry, 767, 150-159 (2014)
TLC-densitometric determination of tolperisone and its impurities 4-methylpropiophenone and piperidine in pharmaceutical preparations
Hubicka U, et al.
Journal of Liquid Chromatography and Related Technologies, 35(10), 1325-1335 (2012)
Paul I Dargan et al.
Drug testing and analysis, 3(7-8), 454-463 (2011-07-15)
Mephedrone (4-methylmethcathinone) is a synthetic cathinone that is used as a recreational drug. It has been available since 2007 but its availability and use increased significantly during 2009 and 2010. In this review article we will summarize the available literature
Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone.
Zhao SF, et al.
Tetrahedron Letters, 52(21), 2702-2705 (2011)
V Karunakaran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 128, 1-14 (2014-03-25)
Combined experimental and theoretical studies have been performed on the structure and vibrational spectra (IR and Raman spectra) of 4'-methylpropiophenone (MPP). The FT-IR and FT-Raman spectra of 4'-methylpropiophenone (MPP) have been recorded in the region 4000-400 cm(-1) and 3500-100 cm(-1)
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