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CAS RN: 94105-90-5 | Product Number: E0922
(±)-Equol
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Purity: >98.0%(GC)
Synonyms:
- 3-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol
- 7-Hydroxy-3-(4-hydroxyphenyl)chroman
- 4',7-Isoflavandiol
Product Documents:
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 200MG |
₹8,300.00
|
1 | ≥100 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | E0922 |
| Purity / Analysis Method | >98.0%(GC) |
| Molecular Formula / Molecular Weight | C__1__5H__1__4O__3 = 242.27 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Hygroscopic |
| CAS RN | 94105-90-5 |
| Reaxys Registry Number | 87753 |
| PubChem Substance ID | 135727283 |
| MDL Number | MFCD00016662 |
Specifications
| Appearance | White to Light yellow to Light red powder to crystal |
| Purity(GC) | min. 98.0 % |
Properties (reference)
| Melting Point | 175 °C |
| Solubility (soluble in) | Ethanol |
GHS
Related Laws:
Transport Information:
Application
(±)-Equol: A Nonsteroidal Estrogen of the Isoflavonoid Class
(±)-Equol is a metabolite produced in vivo from the soy phytoestrogen daidzein [D2668] by the action of certain gut microflora, and is a nonsteroidal estrogen of the isoflavonoid class. (±)-Equo has been reported to have estrogenic activity and affinity for estrogen receptors. (±)-Equo can exist in two enantiomeric forms, (S)-equol and (R)-equol. In binding assays, (S)-equol has a higher binding affinity for estrogen β receptors.
References
- Equol, a natural estrogenic metabolite from soy isoflavones convenient preparation and resolution of R- and S-equols and their differing binding and biological activity through estrogen receptors alpha and beta
- Isolation and identification of new bacterial stains producing equol from Pueraria lobate extract fermentation
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