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223034

Sigma-Aldrich

1-Phenyl-1,2-propanedione

99%

Synonym(s):

Acetyl benzoyl

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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

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)

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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’.

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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
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
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
Atsushi Kameyama et al.
Lasers in medical science, 26(3), 279-283 (2011-02-24)
The purpose of this study was to evaluate whether a Gallium Nitride (GaN) -based violet laser diode (VLM500) could be used as a light source for light-cured dental resins. Three experimental unfilled resins containing different photoinitiators (camphorquinone, CQ; phenyl propanedione
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