4',5,7-Trihydroxyflavanone, 97%, Thermo Scientific Chemicals
4',5,7-Trihydroxyflavanone, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4',5,7-Trihydroxyflavanone, 97%, Thermo Scientific Chemicals

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Quantity:
10 g
2 g
Catalog number L09834.09
also known as L09834-09
Price (USD)/ Each
85.65
Online exclusive
94.90 
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Quantity:
10 g
Request bulk or custom format
Price (USD)/ Each
85.65
Online exclusive
94.90 
Save 9.25 (10%)
Add to cart
4',5,7-Trihydroxyflavanone, 97%, Thermo Scientific Chemicals
Catalog numberL09834.09
Price (USD)/ Each
85.65
Online exclusive
94.90 
Save 9.25 (10%)
-
Add to cart
Chemical Identifiers
CAS67604-48-2
IUPAC Name5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one
Molecular FormulaC15H12O5
InChI KeyFTVWIRXFELQLPI-UHFFFAOYNA-N
SMILESOC1=CC=C(C=C1)C1CC(=O)C2=C(O)C=C(O)C=C2O1
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SpecificationsSpecification SheetSpecification Sheet
FormPowder
Appearance (Color)White to cream to brown
Identification (FTIR)Conforms
Assay (HPLC)≥96.0%
Melting Point (clear melt)246-252?C
(±)-Naringenin is an antioxidant flavonoid. It has anti-inflammatory and antitumor properties. (±)-Naringenin induces apoptosis. It stimulates DNA repair following oxidative damage. (±)-Naringenin inhibits the activity of PI 3-kinase (PI(3)K).

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
(±)-Naringenin is an antioxidant flavonoid. It has anti-inflammatory and antitumor properties. (±)-Naringenin induces apoptosis. It stimulates DNA repair following oxidative damage. (±)-Naringenin inhibits the activity of PI 3-kinase (PI(3)K).

Solubility
Soluble in ethanol (50 mg/ml), DMSO, methanol, and ammonium hydroxide (50 mg/ml). Insoluble in water (almost)

Notes
Store at room temperature. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. J. Foyere Ayafor.; Joseph D. Connolly. 2R,3R-(+)-3-acetoxy-4',5-dihydroxy-7-methoxyflavanone and 2R,3R-(+)-3-acetoxy-4',5,7-trihydroxyflavanone: two new 3-acetylated dihydroflavonols from Aframomum pruinosum Gagnepain (Zingiberaceae).J. Chem. Soc., Perkin Trans. 1. 1981, ,2563-2565 .