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HomeProduct name listGlycitin

Glycitin

Synonym(s):4′,7-Dihydroxy 6-methoxyisoflavone 7-O-glucoside;4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-;Glycitein 7-O-β-glucoside

Glycitin Structural

What is Glycitin?

Chemical properties

White Solid

The Uses of Glycitin

A derivative of Glycitein. Inhibitor

The Uses of Glycitin

A metabolite of isoflavone derivatives. A derivative of Glycitein. Inhibitor.

What are the applications of Application

Glycitin is a soy isoflavone

Definition

ChEBI: A glycosyloxyisoflavone that is isoflavone substituted by a methoxy group at position 6, a hydroxy group at position 4' and a beta-D-glucopyranosyloxy group at position 7.

General Description

Glycitin is an isoflavonoid recently found in flowers of Pueraria thunbergianaI. Glycitin can be modified into the metabolite glycitein which has anti-inflammatory properties.

Biochem/physiol Actions

Glycitin is a soy isoflavone in the glucoside form. A rat model study demonstrated glycitin to be effective in preventing bone loss and reversing the unfavorable changes of lipid metabolism in this model.

Properties of Glycitin

Melting point: 2100C
Boiling point: 751.1±60.0 °C(Predicted)
Density  1.545
storage temp.  room temp
solubility  DMSO (Slightly, Sonicated), Methanol (Slightly, Heated)
form  Solid
pka 9.62±0.30(Predicted)
color  White to Off-White
Stability: Hygroscopic
CAS DataBase Reference 40246-10-4(CAS DataBase Reference)

Safety information for Glycitin

Signal word Warning
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H302:Acute toxicity,oral
H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for Glycitin

Related products of tetrahydrofuran

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