(2S)-2-(3,5-Dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-4H-c hromen-4-one - Names and Identifiers
Name | Blumeatin
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Synonyms | Blumeatin blumeatin Bluemeatin 5,3',5'-trihydroxymethoxylflavanone 5,3',5'-Trihydroxy-7-methoxyflavanone (2S)-2-(3,5-Dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-4H-c hromen-4-one 4H-1-Benzopyran-4-one, 2-(3,5-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (2S)-
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CAS | 118024-26-3
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(2S)-2-(3,5-Dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-4H-c hromen-4-one - Physico-chemical Properties
Molecular Formula | C16H14O6
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Molar Mass | 302.28 |
Density | 1.458±0.06 g/cm3(Predicted) |
Melting Point | 218-220 °C |
Boling Point | 603.3±55.0 °C(Predicted) |
Appearance | Powder |
pKa | 7.39±0.40(Predicted) |
Storage Condition | 2-8℃ |
Physical and Chemical Properties | Light yellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from Aina incense, desert ga. |
(2S)-2-(3,5-Dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydro-4H-c hromen-4-one - Introduction
Blumeatin is a chemical compound whose molecular formula is C14H12O5, and the common chemical name is umbleserone. The following is a description of the nature, use, preparation and safety information of Blumeatin:
Nature:
-Appearance: Blumeatin is a yellow crystalline solid.
-Solubility: Blumeatin is soluble in ethanol, dimethyl sulfoxide and chloroform, slightly soluble in water.
-Melting point: The melting point of Blumeatin is about 220-230°C.
Use:
-Pharmacological effects: Blumeatin has certain pharmacological activities, it is considered to have anti-inflammatory, antioxidant and antibacterial properties. Therefore, Blumeatin is often used in the field of drug research.
-Spices: Blumeatin is also widely used in the spice industry to enhance the aroma in food and beverages.
-Antioxidant: Due to its antioxidant properties, Blumeatin is used as a protective agent in cosmetics and skin care products.
Preparation Method:
Blumeatin is usually prepared by synthetic methods, the main steps include:
1. Hydrogenation: the appropriate amount of celery ketone and hydrogen are reacted under the action of a catalyst to obtain the corresponding phenol compound.
2. Reaction: The phenol compound is reacted with an appropriate amount of acid chloride or acid anhydride to generate Blumeatin.
Safety Information:
- Blumeatin has certain toxicity to human body, so relevant safety operation regulations should be followed during use.
-Avoid direct contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
-Storage should be sealed to avoid contact with oxygen and fire.
-During use, ventilation measures should be taken to avoid inhaling Blumeatin dust or gas.
-in the use and storage process, to comply with the relevant laws and regulations and safety practices.
Last Update:2024-04-09 20:49:11