3',4',5,7-Tetrahydroxyflavone, 97%
3',4',5,7-Tetrahydroxyflavone, 97%
3',4',5,7-Tetrahydroxyflavone, 97%
Thermo Scientific Chemicals

3',4',5,7-Tetrahydroxyflavone, 97%

CAS: 491-70-3 | C15H10O6 | 286.239 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
100 mg
500 mg
Catalog number L14186.ME
also known as L14186-ME
Price (USD)
227.65
Special offer
Online exclusive
Ends: 30-Jun-2026
268.00
Save 40.35 (15%)
Each
Quantity:
500 mg
Request bulk or custom format
Price (USD)
227.65
Special offer
Online exclusive
Ends: 30-Jun-2026
268.00
Save 40.35 (15%)
Each
Chemical Identifiers
CAS491-70-3
IUPAC Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
Molecular FormulaC15H10O6
InChI KeyIQPNAANSBPBGFQ-UHFFFAOYSA-N
SMILESOC1=CC(O)=C2C(=O)C=C(OC2=C1)C1=CC=C(O)C(O)=C1
View more
SpecificationsSpecification SheetSpecification Sheet
FormPowder
Appearance (Color)Cream to yellow to brown
Proton NMRConforms
Assay (HPLC)≥96.0%
3',4',5,7-Tetrahydroxyflavone is used as an apoptosis inducer.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3′,4′,5,7-Tetrahydroxyflavone is used as an apoptosis inducer.

Solubility
Soluble in aqueous alkaline solutions (1.4 mg/ml), ethanol (∼5 mg/ml), dimethyl sulfoxide (7 mg/ml), 1eq. Sodium hydroxide (5 mM), dimethylformamide (∼20 mg/ml), water (1 mg/ml) at 25°C and methanol.

Notes
Incompatible with strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature is 2 - 8°C.
RUO – Research Use Only

General References:

  1. NK Peters.; JW Frost.; SR Long. A plant flavone, luteolin, induces expression of Rhizobium meliloti nodulation genes. Science. 1986, 233 (4767), 977-980.
  2. Seelinger G.; Merfort I.; Schempp CM. Anti-oxidant, anti-inflammatory and anti-allergic activities of luteolin. Planta Medica. 2007, 208 (15), 1694-1706.
  3. Anti-oxidant and radical scavenger in biological systems: Methods Enzymol., 234, 420 (1994).