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Astragalin 7-O-β-D-glucopyranoside is a flavonoid glycoside derivative of astragalin, characterized by its antioxidant and anti-inflammatory properties. It is commonly found in plant sources such as Persian walnuts and Korean mulberries and has been studied for its potential health benefits, including anti-cancer, anti-diabetic, and neuroprotective effects. Additionally, it has been reported to possess anti-inflammatory and anti-aging properties, making it a promising natural remedy for various health conditions.

25615-14-9

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25615-14-9 Usage

Uses

Used in Pharmaceutical Industry:
Astragalin 7-O-β-D-glucopyranoside is used as a pharmaceutical agent for its potential health benefits, including its anti-cancer, anti-diabetic, and neuroprotective effects. Its antioxidant and anti-inflammatory properties contribute to its therapeutic potential in treating various health conditions.
Used in Nutraceutical Industry:
Astragalin 7-O-β-D-glucopyranoside is used as a nutraceutical ingredient for its health-promoting properties, such as its anti-inflammatory and anti-aging effects. It can be incorporated into dietary supplements and functional foods to support overall health and well-being.
Used in Cosmetic Industry:
Astragalin 7-O-β-D-glucopyranoside is used as an active ingredient in cosmetic products for its antioxidant and anti-aging properties. It can help protect the skin from environmental stressors and promote a youthful appearance by reducing the signs of aging.
Used in Agricultural Industry:
Astragalin 7-O-β-D-glucopyranoside can be used in agricultural applications as a natural pesticide or growth promoter due to its antioxidant and anti-inflammatory properties. It may help protect plants from stress and promote healthy growth.
Overall, Astragalin 7-O-β-D-glucopyranoside has shown promise in various industries, and ongoing research aims to explore its full potential and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 25615-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,1 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25615-14:
(7*2)+(6*5)+(5*6)+(4*1)+(3*5)+(2*1)+(1*4)=99
99 % 10 = 9
So 25615-14-9 is a valid CAS Registry Number.

25615-14-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name kaempferol-3-O-β-D-glucopyranosyl-7-O-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names kaempferol 7-O-β-glucopyranosyl 3-O-β-glucopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25615-14-9 SDS

25615-14-9Relevant articles and documents

Synthetic method of kaempferol-3,7-β-D-bisglucoside and use thereof

-

, (2020/03/31)

The purpose of the present invention is to provide a method for chemically synthesizing Kaempferol-3,7-β-D-bisglucoside which has effects of antioxidant, anticancer, etc to be industrially utilized. The present invention relates to a method for chemically synthesizing Kaempferol-3,7-β-D-bisglucoside in quantity, and uses thereof.

Flavonoid glycosides from the leaves of Allium victorialis var. platyphyllum and their anti-neuroinflammatory effects

Woo, Kyeong Wan,Moon, Eunjung,Park, So Young,Kim, Sun Yeou,Lee, Kang Ro

supporting information, p. 7465 - 7470 (2013/02/22)

Eight new flavonoid glycosides, named allivictoside A-H (1-8), together with twelve known flavonoids (9-20) were isolated from the leaves of Allium victorialis var. platyphyllum. The structures of 1-8 were determined by chemical and spectroscopic methods,

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