Skip to Content
Merck
All Photos(1)

Documents

223034

Sigma-Aldrich

1-Phenyl-1,2-propanedione

99%

Synonym(s):

Acetyl benzoyl

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5COCOCH3
CAS Number:
579-07-7
Molecular Weight:
148.16
EC Number:
209-435-2
MDL number:
MFCD00008755
UNSPSC Code:
12352100
PubChem Substance ID:
24853362
NACRES:
NA.22

Quality Level

200

Assay

99%

form

liquid

impurities

1% methyl benzoate

refractive index

n20/D 1.532 (lit.)

bp

103-105 °C/14 mmHg (lit.)

density

1.101 g/mL at 25 °C (lit.)

SMILES string

CC(=O)C(=O)c1ccccc1

InChI

1S/C9H8O2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6H,1H3

InChI key

BVQVLAIMHVDZEL-UHFFFAOYSA-N

Gene Information

human ... ACHE(43) , BCHE(590) , CES1(1066)

Looking for similar products? Visit Product Comparison Guide

General description

The enantioselective hydrogenation of 1-phenyl-1,2-propanedione over Pt colloids was studied.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

183.2 °F - closed cup

Flash Point(C)

84 °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’.

Already Own This Product?

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

Visit the Document Library

Igor Busygin et al.
The Journal of organic chemistry, 73(17), 6559-6569 (2008-08-08)
Structures and conformational behavior of several cinchona alkaloid O-ethers in the solid state (X-ray), in solution (NMR and DFT), and in the gas phase (DFT) were investigated. In the crystal, O-phenylcinchonidine adopts the Open(3) conformation similar to cinchonidine, whereas the
Miguel G Neumann et al.
Dental materials : official publication of the Academy of Dental Materials, 22(6), 576-584 (2005-11-18)
To evaluate the efficiency of the photopolymerization of dental resins it is necessary to know to what extent the light emitted by the light curing units is absorbed by the photoinitiators. On the other hand, the efficiency of the absorbed
Luis Felipe J Schneider et al.
Dental materials : official publication of the Academy of Dental Materials, 25(5), 566-572 (2008-12-30)
Stress development during the polymerization process continues to be a major factor that limits predictability and longevity of resin composite restorations. This study evaluated the effect of the photoinitiator type on the maximum rate of polymerization (R(p)(max)), stress development (final
Luis Felipe J Schneider et al.
Dental materials : official publication of the Academy of Dental Materials, 24(9), 1169-1177 (2008-03-08)
To evaluate the degree of conversion (DC), maximum rate of polymerization (Rpmax), Knoop hardness (KHN) and yellowing (b-value) of resin composites formulated with phenylpropanedione (PPD), camphorquinone (CQ), or CQ/PPD at different concentrations. The hypotheses tested were (i) PPD or CQ/PPD
William Cunha Brandt et al.
Journal of dentistry, 39(6), 438-447 (2011-04-23)
The aim of this study was to evaluate the degree of conversion (DC), rate of polymerization (R(p)(max)), Knoop hardness (KHN) and bond strength between tooth/restoration of composite resins containing different photo-initiators photo-activated by different light-curing units (LCUs). A mixture of
View All Related Papers

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