漆黄素 ( 紫铆素) - Names and Identifiers
Name | Butin
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Synonyms | Butin (S)-7,3',4'-Trihydroxyflavanone (2S)-7,3',4'-Trihydroxyflavanone 7, 3', 4'-trihydroxydihydroflavone butin (7, 3′, 4′-trihydroxydihydroflavone) (S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-7-hydroxy-4H-1-benzopyran-4-one (2S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-7-hydroxy-4H-1-benzopyran-4-one 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-, (S)- 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-, (2S)-
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CAS | 492-14-8
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漆黄素 ( 紫铆素) - Physico-chemical Properties
Molecular Formula | C15H12O5
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Molar Mass | 272.25 |
Density | 1.485 |
Melting Point | 224-226℃ |
Boling Point | 582.4±50.0 °C(Predicted) |
Appearance | Powder |
pKa | 7.69±0.40(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Physical and Chemical Properties | Bioactive (-)-Butin is the S enantiomer of Butin. Butin is a major bioactive flavonoid isolated from the heartwood of Dalbergia, which has strong antioxidant, antiplatelet and anti-inflammatory activities. |
漆黄素 ( 紫铆素) - Reference
Reference Show more | 1. Lin Yifan, Zhang zonwei, Liu Jian, Ren Mingcheng, Xu Wen, Zhao Haiyu, Huang Mingqing. Simultaneous determination of 30 phenolic components in Pholidota chinensis from different habitats by UPLC-MS/MS [J]. Pharmaceutical Research, 2021,40(01):16-23. 2. Kedi Liu et al. [IF = 3.24]. "Network pharmacology and molecular docking reveal the effective entities and active mechanisms of Dalbergia." Plos One. 2021 Sep;16(9):e0255736 |
漆黄素 ( 紫铆素) - Introduction
Fizuflavin, also known as Butin or Butin, is an organic compound with the chemical formula C15H10O2. It is a yellow to brown crystalline solid, soluble in organic solvents such as ethanol, ether and benzene.
Urushiflavin has a variety of biological activities, such as antioxidant, anti-inflammatory and antibacterial. Therefore, it is widely used in the pharmaceutical and cosmetic industries. It is often used in skin care products such as skin creams, masks and sunscreens to help maintain healthy and youthful skin with its antioxidant and anti-inflammatory properties.
There are two main methods for the preparation of uricin: natural extraction and chemical synthesis. Natural extraction refers to the extraction of urusin from plants, such as Woody (Styrax) and Taiwanese Galla Chinensis (Galla Chinensis). Chemical synthesis method is through the organic synthesis of chemical reaction to get the uricin.
Regarding safety information, the use of urusin should follow the relevant safety procedures. It may cause irritation to the eyes and skin, so care should be taken to avoid contact with eyes and skin when using it. In addition, the inhalation of dust or gas of the urusflavin should be avoided. If you take it by mistake or accidentally come into contact with urifusin, you should seek medical help immediately and bring the packaging container or label.
Please note that when using and disposing of urusin, it should be operated in accordance with relevant regulations and guidelines to ensure human health and environmental safety.
Last Update:2024-04-09 20:02:46