Skip to Content
MilliporeSigma
All Photos(2)

Documents

M26615

Sigma-Aldrich

4′-Methylacetophenone

95%

Synonym(s):

Methyl p-tolyl ketone

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3C6H4COCH3
CAS Number:
122-00-9
Molecular Weight:
134.18
Beilstein/REAXYS Number:
606053
EC Number:
204-514-8
MDL number:
MFCD00008751
UNSPSC Code:
12352100
PubChem Substance ID:
24896755
NACRES:
NA.22

Quality Level

100

assay

95%

refractive index

n20/D 1.533 (lit.)

bp

226 °C (lit.)

mp

22-24 °C (lit.)

density

1.004 g/mL at 20 °C
1.005 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1ccc(C)cc1

InChI

1S/C9H10O/c1-7-3-5-9(6-4-7)8(2)10/h3-6H,1-2H3

InChI key

GNKZMNRKLCTJAY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H315

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

wgk_germany

WGK 1

flash_point_f

179.6 °F

flash_point_c

82 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

4-METHOXY-4'-METHYLCHALCONE AldrichCPR

S511021

4-METHOXY-4'-METHYLCHALCONE

4′-Bromoacetophenone 98%

Sigma-Aldrich

B56404

4′-Bromoacetophenone

p-Tolualdehyde 97%

Sigma-Aldrich

T35602

p-Tolualdehyde

4′-Nitroacetophenone 98%

Sigma-Aldrich

N9608

4′-Nitroacetophenone

3′-Methoxyacetophenone 97%

Sigma-Aldrich

M9408

3′-Methoxyacetophenone

4′-(Trifluoromethyl)acetophenone 98%

Sigma-Aldrich

233188

4′-(Trifluoromethyl)acetophenone

Koji Uwai et al.
Bioorganic & medicinal chemistry, 16(3), 1084-1089 (2007-11-17)
Stereoselective reductive metabolism of various p-substituted acetophenone derivatives was studied using isolated rat liver 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD). Kinetic experiments were performed and analyzed by measuring the products by HPLC using a chiral column. The results demonstrated that the presence of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service