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5,7-Dihydroxy-2-[4-hydroxy-3-(4-hydroxy-3-methylbutyl)phenyl]-3,6-dimethoxy-4H-1-benzopyran-4-one, also known as Di-hydroxy-mono-methylbutylflavone, is a flavonoid compound with antioxidant and anti-inflammatory properties. It is found in various plant sources, including fruits, vegetables, and herbs, and has potential health benefits due to its ability to protect against oxidative stress and inflammation.

84294-77-9

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84294-77-9 Usage

Uses

Used in Pharmaceutical Industry:
5,7-Dihydroxy-2-[4-hydroxy-3-(4-hydroxy-3-methylbutyl)phenyl]-3,6-dimethoxy-4H-1-benzopyran-4-one is used as a therapeutic agent for its potential health benefits, including protection against oxidative stress and inflammation. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of new treatments for chronic diseases such as cancer, heart disease, and diabetes.
Used in Nutraceutical Industry:
5,7-Dihydroxy-2-[4-hydroxy-3-(4-hydroxy-3-methylbutyl)phenyl]-3,6-dimethoxy-4H-1-benzopyran-4-one is used as a dietary supplement for its potential health benefits, including protection against oxidative stress and inflammation. Its antioxidant and anti-inflammatory properties make it a valuable ingredient in nutraceutical products aimed at promoting overall health and well-being.
Used in Cosmetic Industry:
5,7-Dihydroxy-2-[4-hydroxy-3-(4-hydroxy-3-methylbutyl)phenyl]-3,6-dimethoxy-4H-1-benzopyran-4-one is used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. Its potential health benefits make it a valuable component in skincare products aimed at promoting skin health and reducing the signs of aging.
Used in Food and Beverage Industry:
5,7-Dihydroxy-2-[4-hydroxy-3-(4-hydroxy-3-methylbutyl)phenyl]-3,6-dimethoxy-4H-1-benzopyran-4-one is used as a natural preservative and antioxidant in the food and beverage industry. Its ability to protect against oxidative stress and inflammation makes it a valuable ingredient in products aimed at promoting health and extending shelf life.

Check Digit Verification of cas no

The CAS Registry Mumber 84294-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84294-77:
(7*8)+(6*4)+(5*2)+(4*9)+(3*4)+(2*7)+(1*7)=159
159 % 10 = 9
So 84294-77-9 is a valid CAS Registry Number.

84294-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Aliarin

1.2 Other means of identification

Product number -
Other names -

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:84294-77-9 SDS

84294-77-9Upstream product

84294-77-9Downstream Products

84294-77-9Relevant academic research and scientific papers

Visconata: A rare flavonol having long chain fatty acid from Dodonaea viscosa which inhibits Human neutrophil elastase (HNE)

Uddin, Zia,Li, Zuopeng,Song, Yeong Hun,Kim, Jeong Yoon,Park, Ki Hun

, p. 2507 - 2511 (2017)

A series of flavonoids were isolated from Dodonaea Viscosa and tested for inhibition of human neutrophil elastase (HNE), enzyme involved in inflammatory disorders. Isolated compounds were identified as a novel flavonol (1) along with eight known flavonoids (2–9). Novel flavonol, visconata (1) has a very rare skeleton having odd numbered long chain (C19) fatty acid, which was completely identified by mass fragmentation and 2D NMR analysis. All compounds (1–9) inhibited HNE in dose dependent manner with IC50s ranging between 2.4 and 150?μM. Visconata (1) emerged to be the most potent compound with 2.4?μM of IC50. In kinetic studies, compound (1) was observed to be reversible, noncompetitive inhibitor having Ki?=?1.8?μM, whereas other flavonoids (2–9) displayed mixed type inhibition.

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