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Benzil

Benzil Structure
CAS No.
134-81-6
Chemical Name:
Benzil
Synonyms
DIBENZOYL;Diphenylethane-1,2-dione;1,2-DIPHENYLETHANEDIONE;1,2-Diphenylethane-1,2-dione;BENZIL;CHC-12;Wy 20910;wy-20910;BIBENZOYL;Benzil≥98%
CBNumber:
CB8478221
Molecular Formula:
C14H10O2
Molecular Weight:
210.23
MOL File:
134-81-6.mol
MSDS File:
SDS
Modify Date:
2024/5/15 13:45:27

Benzil Properties

Melting point 94-95 °C(lit.)
Boiling point 346 °C
Density 1,521 g/cm3
vapor pressure 1 mm Hg ( 128.4 °C)
refractive index 1.5681 (estimate)
Flash point 346-348°C
storage temp. Store below +30°C.
solubility <0.5g/l
form Crystalline Powder
color White
Water Solubility 0.5 g/L (20 ºC)
Merck 14,1078
BRN 608047
Dielectric constant 13.0(94℃)
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey WURBFLDFSFBTLW-UHFFFAOYSA-N
CAS DataBase Reference 134-81-6(CAS DataBase Reference)
NIST Chemistry Reference Ethanedione, diphenyl-(134-81-6)
EPA Substance Registry System Benzil (134-81-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  2
RTECS  DD1925000
10
Hazard Note  Irritant
TSCA  Yes
HS Code  29143900
Toxicity LD50 orally in Rabbit: 2710 mg/kg
NFPA 704
1
2 0

Benzil price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) B0050 Benzil min. 99.0 % 134-81-6 25G ₹2000 2022-05-26 Buy
TCI Chemicals (India) B0221 Benzil Zone Refined (number of passes:22) 134-81-6 1SAMPLE ₹15600 2022-05-26 Buy
TCI Chemicals (India) B0050 Benzil min. 99.0 % 134-81-6 500G ₹6400 2022-05-26 Buy
ottokemi B 1525 Benzil 99% 134-81-6 250gm ₹198 2022-05-26 Buy
ottokemi B 1525 Benzil 99% 134-81-6 500gm ₹1692 2022-05-26 Buy
Product number Packaging Price Buy
B0050 25G ₹2000 Buy
B0221 1SAMPLE ₹15600 Buy
B0050 500G ₹6400 Buy
B 1525 250gm ₹198 Buy
B 1525 500gm ₹1692 Buy

Benzil Chemical Properties,Uses,Production

Chemical Properties

yellow crystals or powder

Uses

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.

Definition

A reaction in which benzil (1,2- diphenylethan-1,2-dione) is treated with hydroxide and then with acid to give benzilic acid (2-hydroxy-2,2-diphenylethanoic acid):
C6H5.CO.CO.C6H5
(C6H5)2C(OH).COOH
The reaction, which involves migration of a phenyl group (C6H5-) from one carbon atom to another, was the first rearrangement reaction to be described (by Justus von Liebig in 1828).

benefits

Benzil has potential applications in biological metabolism and clinical medicine. Benzil derivates exhibit radical scavenging and antibacterial and hypertensive, antiprotozoal, antiproliferative, and antimitotic activities. Benzil derivatives have versatile applications in the pharmaceutical industry, and various heterocyclic compounds such as triazine, quinoxaline, and imidazole can be synthesized from 1,2-diketones. It is also used as a nanocatalyst in the application of imidazole derivatives. Recently, it is reported that benzil derivatives acted as photosensitive agents and photoinitiators due to its antitumor activity[1].

Safety Profile

Low toxicity by ingestion. An eyeirritant. Combustible. When heated to decomposition itemits acrid smoke and irritating fumes.

Safety

Potential Acute Health Effects: Very hazardous in case of skin contact (irritant), of eye contact (irritant). Hazardous in case of ingestion, of inhalation.
The substance is toxic to lungs, mucous membranes. Repeated or prolonged exposure to the substance can produce target organs damage. Eye Contact: Check for and remove any contact lenses.
Fine dust dispersed in air may ignite. Dust can form an explosive mixture in air. Thermal decomposition can lead to release of irritating gases and vapors. Keep product and empty container away from heat and sources of ignition.

Solubility in organics

Soluble in ethanol (50 mg/ml), chloroform, ether, and ethyl acetate. Insoluble in water.

Purification Methods

Crystallise benzil from *benzene after washing with alkali. (Crystallisation from EtOH did not free benzil from material reacting with alkali.) [Hine & Howarth J Am Chem Soc 80 2274 1958.] It has also been crystallised from CCl4, diethyl ether or EtOH [Inoue et al. J Chem Soc, Faraday Trans 1 82 523 1986]. [Beilstein 7 IV 2502.]

References

[1] N. Kanagathara. “Structural and Vibrational Investigation of Benzil-(1,2-Diphenylethane-1,2-Dione): Experimental and Theoretical Studies.” New Journal of Chemistry 3 1 (2022).

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