All Photos(1)

Key Documents

COO/COA

View All Documentation

H4155

7-Hydroxyflavanone

Name: 7-Hydroxyflavanone
Brand: SIGMA

Synonym(s):

7-Hydroxy-2-phenylchroman-4-one

Sign Into View Organizational & Contract Pricing

All Photos(1)

About This Item

Empirical Formula (Hill Notation):

C₁₅H₁₂O₃

CAS Number:

6515-36-2

Molecular Weight:

240.25

MDL number:

MFCD00017487

UNSPSC Code:

12352100

mp

188-190 °C (lit.)

SMILES string

Oc1ccc2C(=O)CC(Oc2c1)c3ccccc3

InChI

1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2

InChI key

SWAJPHCXKPCPQZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

In vitro analysis of iron chelating activity of flavonoids.

Přemysl Mladěnka et al.

Journal of inorganic biochemistry, 105(5), 693-701 (2011-04-01)

Flavonoids have been demonstrated to possess miscellaneous health benefits which are, at least partly, associated with iron chelation. In this in vitro study, 26 flavonoids from different subclasses were analyzed for their iron chelating activity and stability of the formed

[Microbial kinetics: experiences with Staphylococcus aureus ATCC 25 293 and bacteriostatic drugs].

N B Pappano et al.

Revista latinoamericana de microbiologia, 29(4), 367-372 (1987-10-01)

New 7,8-benzoflavanones as potent aromatase inhibitors: synthesis and biological evaluation.

Samir Yahiaoui et al.

Bioorganic & medicinal chemistry, 16(3), 1474-1480 (2007-11-29)

Some natural compounds such as flavonoids are known to possess a moderate inhibitory activity against aromatase, this enzyme being an interesting target for hormone-dependent breast cancer treatment. It has been demonstrated that the modulation of flavonoid skeleton could increase anti-aromatase

Microbial transformations of 7-hydroxyflavanone.

Edyta Kostrzewa-Susłow et al.

TheScientificWorldJournal, 2012, 254929-254929 (2012-06-02)

Microbial transformations of racemic 7-hydroxyflavanone using strains of genus Aspergillus (A. niger KB, A. niger 13/5, A. ochraceus 456) and the species Penicillium chermesinum 113 were studied. The products of O-methylation, O-methylation along with hydroxylation at C-3' and C-4', reduction

Bioconversion of 7-hydroxyflavanone: isolation, characterization and bioactivity evaluation of twenty-one phase I and phase II microbial metabolites.

Julie Rakel Mikell et al.

Chemical & pharmaceutical bulletin, 60(9), 1139-1145 (2012-09-15)

Microbial metabolism of 7-hydroxyflavanone (1) with fungal culture Cunninghamella blakesleeana (ATCC 8688a), yielded flavanone 7-sulfate (2), 7,4'-dihydroxyflavanone (3), 6,7-dihydroxyflavanone (4), 6-hydroxyflavanone 7-sulfate (5), and 7-hydroxyflavanone 6-sulfate (6). Mortierella zonata (ATCC 13309) also transformed 1 to metabolites 2 and 3 as

View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service