Benzil, 98%
Benzil, 98%
Benzil, 98%
Thermo Scientific Chemicals

Benzil, 98%

CAS: 134-81-6 | C14H10O2 | 210.23 g/mol
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Catalog number A12579.22
also known as A12579-22
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Chemical Identifiers
CAS134-81-6
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Yellow
Assay (GC)≥97.5%
Melting Point (clear melt)92-98?C
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Benzil is used as a pharmaceutical intermediate and uv curing resin photosensitizer. In polymer chemistry, it is used as a photoinitiator. Further, it serves as a potent inhibitor of human carboxylesterases. It is used in the preparation of diketimines by reacting with amines. It is also involved in the famous benil-benzilic acid rearrangement. In addition this, it reacts with 1,3-diphenylacetone to get tetraphenylcyclopentadienone.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Benzil is used as a pharmaceutical intermediate and uv curing resin photosensitizer. In polymer chemistry, it is used as a photoinitiator. Further, it serves as a potent inhibitor of human carboxylesterases. It is used in the preparation of diketimines by reacting with amines. It is also involved in the famous benil-benzilic acid rearrangement. In addition this, it reacts with 1,3-diphenylacetone to get tetraphenylcyclopentadienone.

Solubility
Soluble in ethanol and ethyl ether. Insoluble in water.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Kayadibi, F.; Sagdinc, S. G.; Kara, Y. S. Density functional theory studies on the corrosion inhibition of benzoin, benzil, benzoin-(4-phenylthiosemicarbazone) and benzil-(4-phenylthiosemicarbazone) of mild steel in hydrochloric acid. Prot. Met. Phys. Chem. Surf. 2015, 51 (1), 143-154.
  2. Zarnegar, Z.; Safari, J. Green chemistry-mediated synthesis of benzil by using nano-MgO. J. Exp. Nanosci. 2015, 10 (9), 651-661.