All Photos(1)

Key Documents

COO/COA

View All Documentation

419788

7-Methoxyflavanone

Name: 7-Methoxyflavanone
Brand: ALDRICH

98%

Sign Into View Organizational & Contract Pricing

All Photos(1)

About This Item

Empirical Formula (Hill Notation):

C₁₆H₁₄O₃

CAS Number:

21785-09-1

Molecular Weight:

254.28

MDL number:

MFCD00017486

UNSPSC Code:

12352100

PubChem Substance ID:

24866276

This product is discontinued. Contact Technical Servicefor assistance.

assay

98%

mp

89-91 °C (lit.)

SMILES string

COc1ccc2C(=O)CC(Oc2c1)c3ccccc3

InChI

1S/C16H14O3/c1-18-12-7-8-13-14(17)10-15(19-16(13)9-12)11-5-3-2-4-6-11/h2-9,15H,10H2,1H3

InChI key

VYESEQLQFXUROZ-UHFFFAOYSA-N

Gene Information

human ... CYP19A1(1588)

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P305 + P351 + P338

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

11422HG

05504BC

03815HS

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

7-methoxyflavanone alleviates neuroinflammation in lipopolysaccharide-stimulated microglial cells by inhibiting TLR4/MyD88/MAPK signalling and activating the Nrf2/NQO-1 pathway.

Zhao Qu et al.

The Journal of pharmacy and pharmacology, 72(3), 385-395 (2019-12-24)

Neuroprotective potential of 7-methoxyflavanone (7MF) and its underlying mechanism was investigated. Inhibitory effects of 7MF on microglial activation and neuroinflammation were evaluated by employment of lipopolysaccharide (LPS)-induced BV2 microglial cells. Changes in expression of genes and proteins of interest were

Further study on enantiomer resolving ability of amylose tris(3-chloro-5-methylphenylcarbamate) covalently immobilized onto silica in nano-liquid chromatography and capillary electrochromatography.

Giovanni D'Orazio et al.

Journal of chromatography. A, 1623, 461213-461213 (2020-06-09)

In the present study separation of enantiomers of some chiral neutral, basic and weakly acidic analytes was investigated on the chiral stationary phase (CSP) made by covalent immobilization of amylose tris(3-chloro-5-methylphenylcarbamate) onto aminopropylsilanized (APS) silica in nano-liquid chromatography (nano-LC) in

Ordered mesoporous silica functionalized with β-cyclodextrin derivative for stereoisomer separation of flavanones and flavanone glycosides by nano-liquid chromatography and capillary electrochromatography.

Mariana Silva et al.

Journal of chromatography. A, 1490, 166-176 (2017-02-17)

In this paper a chiral stationary phase (CSP) was prepared by the immobilization of a β-CD derivative (3,5-dimethylphenylcarbamoylated β-CD) onto the surface of amino-functionalized spherical ordered mesoporous silica (denoted as SM) via a urea linkage using the Staudinger reaction. The

Occurrence and distribution of unsubstituted B-ring flavanones in Eucalyptus foliage.

Karen J Marsh et al.

Phytochemistry, 160, 31-39 (2019-01-27)

A group of plant specialised metabolites (PSMs) collectively known as unsubstituted B-ring flavanones (UBFs) have previously been found in the foliage of some species from the genus Eucalyptus L'Hér. (Myrtaceae), specifically from the subgenus Eucalyptus (monocalypts). Captive feeding studies using

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