Eburicoic acid3β-Hydroxy-24-methylene-8-lanosten-21-oic acid - Names and Identifiers
Name | Eburicoic acid
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Synonyms | NSC 41969 Eburicoicaci Eburcoic acid Eburicoic acid 3beta-Hydroxy-24-methylene-8-lanosten-21-oic acid Lanost-8-en-21-oic acid, 3-hydroxy-24-methylene-, (3β)- Eburicoic acid3β-Hydroxy-24-methylene-8-lanosten-21-oic acid (2R)-2-[(3S,5S,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3 ,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-m ethyl-5-methylidene-heptanoic acid
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CAS | 560-66-7
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Eburicoic acid3β-Hydroxy-24-methylene-8-lanosten-21-oic acid - Physico-chemical Properties
Molecular Formula | C31H50O3
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Molar Mass | 470.74 |
Density | 1.05±0.1 g/cm3(Predicted) |
Melting Point | 283 °C |
Boling Point | 572.6±50.0 °C(Predicted) |
Appearance | Powder |
pKa | 4.65±0.10(Predicted) |
Storage Condition | 2-8℃ |
Eburicoic acid3β-Hydroxy-24-methylene-8-lanosten-21-oic acid - Introduction
Eburicoic acid(Eburicoic acid) is a naturally occurring triterpenoid, which belongs to the Eburicoic acid class of compounds. The following is an introduction to the nature, use, preparation and safety information of eburicic acid:
Nature:
eburicic acid is a white crystal or crystalline powder, no special odor. Its molecular formula is C30H48O3 and its relative molecular mass is 456.71. Eburicoic acid is solid at room temperature, insoluble in water, soluble in organic solvents such as ethanol, ether, etc. It has a certain stability in organic solvents.
Use:
eburicic acid has some application value in medicine and medical field. Studies have shown that Eburicoic acid has antioxidant, antibacterial and anti-inflammatory activities, and can be used as raw materials or ingredients in drugs for the treatment of diseases. In addition, Eburicoic acid can also be used in cosmetics and skin care products, with a certain whitening, anti-aging and moisturizing effect.
Method:
The preparation method of eburicic acid can be achieved by natural material extraction or chemical synthesis. Natural Eburicoic acid is usually extracted from the roots, stems, leaves, fruits, etc. of certain plants. Chemical synthesis methods require the use of specific synthetic routes and reagents, including catalysts, solvents, etc.
Safety Information:
The toxicity data for eburicic acid is limited, so a detailed toxicity assessment cannot be given. However, according to the study of structure and related compounds, Eburicoic acid may have some toxicity and irritation. When using Eburicoic acid, it is necessary to follow safe operating methods and personal protective measures to avoid contact with eyes, skin and respiratory tract. At the same time, eburicic acid needs to be stored and handled properly to avoid danger when mixed with other chemicals. Before using eburicic acid, it is recommended to consult the relevant safety data and operation guidelines to ensure the safety of use.
Last Update:2024-04-09 21:11:58