Diphenyl carbonate (Diphenyl carbonate)

Bargaining 10-21 09:11 Update

Inquiry

Whatsapp:
+86 19117288062

Contact person： Chemwin

Phone： +86 19117288062

Diphenyl carbonate

Warehouse

Services Merchant Delivery

Payment Method T/T ; L/C ;

Shipping Fee Place of delivery： Need to ask for quotation with the seller

Specification weight

Total Selected{{ form.amount }}Pieces {{ form.amount }} Total￥{{ form.price * form.amount }}

phenyl phenoxyformate
EINECS 203-005-8
Carbonic acid,diphenyl ester
Carbonic Acid Diphenyl Ester
Diphenyl carbonate
Phenyl carbonate
Carbonic acid, diphenyl ester
Diphenylcarbonate
bisphenyl carbonate
Phenyl carbonate ((PhO)2CO)

+Expand -Stow

102-09-0

C13H10O3

214.217

2920909090

Information View:

Chinese

English

Nature Description

White crystalline solid. Melting point 83 ℃, boiling point 302 ℃,168 ℃(2.0kPa), relative density of liquid 1.1215(87/4 ℃). Insoluble in water, soluble in hot ethanol, benzene, ether, carbon tetrachloride, glacial acetic acid and other organic solvents. Can be decomposed by hot alkali and ammonolysis. It can be halogenated and nitrified.

301-302℃

78-81℃

168℃

不溶

Product Applications

Important environmental protection chemical products can be used to synthesize many important medicines, pesticides, other organic compounds and polymer materials, such as aliphatic monoisocyanate and p-Hydroxybenzoic acid polyester. It can also be used as plasticizer and solvent for polyamides and polyesters.

Production method

1. The phosgene method is obtained by the reaction of phenol and phosgene. The dissolved phenol is added to the sodium hydroxide solution of 16-20 to prepare the sodium phenol solution. Stirring and cooling, start to introduce phosgene at about 10℃, and control the phosgenation reaction to proceed at 20-30℃. The reaction tail gas contains hydrogen chloride and unreacted phosgene is introduced into the absorption tower, it is discharged from high altitude after being destroyed by dilute alkali solution. At the later stage of the reaction, take the reaction solution to test the pH to neutral stop light. Remove the phosgene and hydrochloric acid gas in the pot, filter, wash with water, melt and dehydrate under decompression to obtain the crude product. The crude product is distilled under reduced pressure, and narrow fraction is collected. After condensation, the liquid product is processed through Flaker tablets to obtain refined diphenyl carbonate. Polymerization grade products have high requirements on purity, and the melting point should be ≥78℃. Raw material consumption quota: phenol 963kg/t; Sodium hydroxide (30)577kg/t; Phosgene (≥ 98)592kg/t. 2. Transesterification synthesis of diphenyl carbonate by exchange of phenol and dimethyl carbonate is usually carried out in two steps: the first step is to convert phenol into methyl phenyl carbonate, and the second step is to further interact with phenol to obtain diphenyl carbonate. This route has a low yield and needs to develop efficient catalysts and improve the process flow. 3. Phenol oxidative carbonylation method directly synthesize diphenyl carbonate in the presence of phenol, carbon monoxide and oxygen in the next step. This method has the characteristics of simple process, cheap and easily available raw materials and no pollution. However, it has not realized industrialization and is in the process of research and development.