D-Fructose phenylosazone
D-arabino-hexosulose bis(phenylhydrazone)
CAS: 534-97-4
Molecular Formula: C18H22N4O4
D-Fructose phenylosazone - Names and Identifiers
D-Fructose phenylosazone - Physico-chemical Properties
| Molecular Formula | C18H22N4O4 |
| Molar Mass | 358.4 |
D-Fructose phenylosazone - Introduction
D-arabino-hexosulose bis(phenylhydrazone) is an organic compound with the following properties:
1. Appearance: D-arabino-hexosulose bis(phenylhydrazone) exists as a white crystalline solid.
2. Solubility: insoluble in water, but soluble in organic solvents such as ethanol, benzene and dichloromethane.
3. Stability: The compound is relatively stable at room temperature, but may decompose when exposed to high temperature, sunlight or oxygen.
The main uses of D-arabino-hexosulose bis(phenylhydrazone) are as follows:
1. Chemical reagent: It can be used as a commonly used reagent for analysis and detection of aldehyde saccharides in carbohydrates.
2. Surfactant: Due to its special structure, D-arabino-hexosulose bis(phenylhydrazone) can be used as a surfactant to change wettability, reduce surface tension, etc.
A common method for preparing D-arabino-hexosulose bis(phenylhydrazone) is as follows:
D-arabinosketo furfural (D-arabino-hexosululose) reacts with phenylhydrazine (phenylhydrazine) under alkaline conditions to generate the D-arabino-hexosulose bis(phenylhydrazone).
Regarding safety information, there are relatively few toxicological and safety studies on D-arabino-hexosulose bis(phenylhydrazone). Therefore, the use and handling of the compound need to comply with regular laboratory safety practices, such as wearing appropriate protective equipment, avoiding skin contact and inhalation. At the same time, the compound should be stored properly and away from open flames and oxidants to prevent fire and violent reactions.
1. Appearance: D-arabino-hexosulose bis(phenylhydrazone) exists as a white crystalline solid.
2. Solubility: insoluble in water, but soluble in organic solvents such as ethanol, benzene and dichloromethane.
3. Stability: The compound is relatively stable at room temperature, but may decompose when exposed to high temperature, sunlight or oxygen.
The main uses of D-arabino-hexosulose bis(phenylhydrazone) are as follows:
1. Chemical reagent: It can be used as a commonly used reagent for analysis and detection of aldehyde saccharides in carbohydrates.
2. Surfactant: Due to its special structure, D-arabino-hexosulose bis(phenylhydrazone) can be used as a surfactant to change wettability, reduce surface tension, etc.
A common method for preparing D-arabino-hexosulose bis(phenylhydrazone) is as follows:
D-arabinosketo furfural (D-arabino-hexosululose) reacts with phenylhydrazine (phenylhydrazine) under alkaline conditions to generate the D-arabino-hexosulose bis(phenylhydrazone).
Regarding safety information, there are relatively few toxicological and safety studies on D-arabino-hexosulose bis(phenylhydrazone). Therefore, the use and handling of the compound need to comply with regular laboratory safety practices, such as wearing appropriate protective equipment, avoiding skin contact and inhalation. At the same time, the compound should be stored properly and away from open flames and oxidants to prevent fire and violent reactions.
Last Update：2024-04-09 21:11:58
