Molecular Formula | C6H10O5 |
Molar Mass | 162.14 |
Melting Point | 218-221°C (A)(lit.) |
Boling Point | 331.1°C at 760 mmHg |
Flash Point | 100°C |
Water Solubility | slightly soluble |
Solubility | Sparingly soluble in water, freely soluble in ethanol (96 per cent), practically insoluble in methylene chloride. |
Vapor Presure | 8.27E-05mmHg at 25°C |
Appearance | Crystalline Powder |
Color | Almost white to beige |
Merck | 14,7328 |
BRN | 5109263 |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Stability | Stable. Incompatible with acid chlorides, acid anhydrides, bases, oxidizing agents. Combustible. |
Sensitive | Light Sensitive |
Physical and Chemical Properties | melting point 218-221°C water-soluble easily soluble |
Use | Used as an analytical reagent |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 2 |
RTECS | DC4662500 |
TSCA | Yes |
HS Code | 29072990 |
Downstream Products | Chrysin |
use | used as analytical reagent used as pharmaceutical, biological reagent, dye, can also be used to synthesize 5,7-dihydroxyflavone used as biological reagent, dye, and used to test vanillin, lignin, determination of sugar aldehyde, pentose, etc. |
Production method | 1.? In the presence of a catalyst, benzene is reacted with propylene, and the resulting mixture is rectified to obtain triisopropylbenzene. Then compressed air is introduced into triisopropylbenzene, and the autooxidation reaction is carried out at 60?~ 120 ℃ with azo-diradical initiator as catalyst, and the solution ph = 8~9 is controlled. The alcohol by-products produced by the reaction are oxidized with 2 to 6 times hydrogen peroxide under acidic conditions and converted into the required product 1,3, 5-triisopropylbenzene trihydroperoxide. The peroxide is decomposed into the target product phloroglucinol under the action of a high-activity acidic catalyst, and the reaction heat should be removed in time during the reaction. The main reaction formula of the process is: the obtained acidic phloroglucinol is neutralized with 40% sodium hydroxide, and after extraction separation, adsorption and recrystallization, high-purity phloroglucinol can be obtained. |