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W322601

Sigma-Aldrich

1-Phenyl-1,2-propanedione

98%, FG

Synonyme(s) :

Acetyl benzoyl

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About This Item

Formule linéaire :
C6H5COCOCH3
Numéro CAS:
Poids moléculaire :
148.16
Numéro FEMA:
3226
Numéro CE :
Conseil de l'Europe Nº :
2275
Numéro MDL:
Code UNSPSC :
12164502
ID de substance PubChem :
Numéro Flavis :
7.079
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

Qualité

FG
Fragrance grade
Halal
Kosher

Agence

follows IFRA guidelines
meets purity specifications of JECFA

Conformité réglementaire

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

Pureté

98%

Indice de réfraction

n20/D 1.532 (lit.)

Point d'ébullition

103-105 °C/14 mmHg (lit.)

Densité

1.101 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Allergène de parfum

no known allergens

Propriétés organoleptiques

honey; buttery; plastic

Chaîne SMILES 

CC(=O)C(=O)c1ccccc1

InChI

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

Clé InChI

BVQVLAIMHVDZEL-UHFFFAOYSA-N

Informations sur le gène

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Description générale

1-Phenyl-1,2-propanedione is a volatile flavor compound found in khat leaves and cambará honey.

Application


  • A Simplified Kinetic Model for the Enantioselective Hydrogenation of 1-Phenyl-1,2-Propanedione over Ir/TiO(2) in the Presence of a Chiral Additive.: This study presents a simplified kinetic model for the enantioselective hydrogenation of 1-Phenyl-1,2-propanedione, emphasizing its potential in synthetic organic chemistry and catalysis, which could have significant implications for pharmaceutical synthesis and industrial applications (Melián-Cabrera et al., 2022).

  • Moving Towards a Finer Way of Light-Cured Resin-Based Restorative Dental Materials: Recent Advances in Photoinitiating Systems Based on Iodonium Salts.: Although primarily focused on photoinitiating systems for dental materials, this review could indirectly encompass applications of 1-Phenyl-1,2-propanedione in dental photopolymerization processes, suggesting potential for further exploration in dental material enhancements (Topa and Ortyl, 2020).

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

183.2 °F - closed cup

Point d'éclair (°C)

84 °C - closed cup

Équipement de protection individuelle

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


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Investigation of the aroma compounds from headspace and aqueous solution from the cambara (Gochnatia Velutina) honey
Moreira RFA & De Maria CAB.
Flavour and Fragrance Journal, 20(1), 13-17 (2005)
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

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