Toluene diisocyanate manufacturer Knowledge Preparation method of diphenylthiocarbazine_Kain Industrial Additive

Preparation method of diphenylthiocarbazine_Kain Industrial Additive

Background and overview[1]

Diphenylthiocarbazine is a hydrazine derivative, which can be used as a pharmaceutical synthesis intermediate. For example, dithizone (dithizone), whose scientific name is diphenylcarbazone, is a blue-black crystalline powder. It is mixed with an aqueous solution of metal and shaken to generate a metal complex salt in the aqueous phase, which is then transferred to the organic The solvent layer undergoes significant color changes. According to the color and depth of the metal complex salt, it can be used for the determination of certain trace metals, such as mercury, lead, zinc, cadmium, etc., especially for trace amounts of lead, it has extremely high sensitivity, good stability and sharpness. Color change is an important analytical reagent in analytical chemistry science.

Structure

Preparation method[1]

The preparation of diphenylthiocarbazine is as follows:

The operation method of step 1) is as follows: add carbon disulfide dropwise to the ethanol solution of phenylhydrazine under constant stirring. The weight ratio of phenylhydrazine to ethanol is 1:4~4.5, and the molar ratio of phenylhydrazine to carbon disulfide is 1 ∶0.55~0.70, reaction temperature 20~25℃, dropwise addition time of carbon disulfide is 3~3.5 hours, continue stirring for 25~35 minutes after the dropwise addition, the generated β-phenyl-dithiocarbazinic acid phenylhydrazine salt remains In the container.

The operation method of step 2) is: reflux and heat the β-phenyl-dithiocarbazinic acid phenylhydrazine salt obtained in step 1) to release hydrogen sulfide gas and finally ammonia gas. The reaction temperature is 75-78°C. Control the end point in the middle, cool, discharge, and centrifuge to dryness to obtain the intermediate diphenylthiocarbazine.

Main reference materials

[1] (CN1970537) Manufacturing method of dithizone

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/2334

author:

Previous article
Next article
Contact Us

Contact us

+86 - 152 2121 6908

Online consultation: QQ交谈

E-mail: sales@newtopchem.com

Working hours: Monday to Friday, 9:00-17:30, closed on holidays
Follow wechat
Scan wechat and follow us

Scan wechat and follow us

Follow Weibo
Back to top
Home
E-mail
Products
Search