474-68-0 - Names and Identifiers
Name | Episterol
|
Synonyms | Episterol episterol 9xi-episterol 24-Methylenelathosterol Ergosta-7,24(28)-dien-3beta-ol 5α-Ergosta-7,24(28)-dien-3β-ol (3S,10S,13R,17R)-17-[(1R)-1,5-Dimethyl-4-methylene-hexyl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
|
CAS | 474-68-0
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474-68-0 - Physico-chemical Properties
Molecular Formula | C28H46O
|
Molar Mass | 398.66424 |
Melting Point | 128-130°C |
Solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) |
Appearance | Solid |
Color | White to Off-White |
Storage Condition | -20°C Freezer |
474-68-0 - Introduction
Episterol(Episterol) is a naturally occurring sterol compound belonging to the class of sterols. Its chemical name is 5β-cholester-6-en-3β-ol. The molecular formula of Episterol is C27H46O and the molecular weight is 390.67.
Episterol is a colorless crystalline solid, stable at room temperature. It is almost insoluble in water, but soluble in organic solvents such as ethanol and dichloromethane. The melting point of Episterol is about 148-150 ° C.
Episterol plays an important role in biology. It is a kind of hormone in plants, which plays a regulatory role in the growth and development of plants. In addition, Episterol is widely used as an intermediate in drug synthesis.
There are many ways to prepare Episterol. A common method is to extract from plants, such as Sphenopsida or some Bryophyta. The biotransformation reaction can produce Episterol. In addition, Episterol can also be prepared by chemical synthesis. These methods generally involve the reaction and conversion of sterol precursors.
About the safety information of Episterol, there is little understanding of its toxicity and harmfulness. However, due to its existence in natural plants, Episterol is generally considered to be a relatively safe compound. However, proper safety precautions must still be taken during use and handling, and appropriate laboratory practices must be followed.
Last Update:2024-04-09 21:54:55