Welcome to LookChem.com Sign In|Join Free

CAS

  • or

24808-04-6

Post Buying Request

24808-04-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24808-04-6 Usage

Description

(-)-Epiafzelechin is a flavonoid lipid molecule belonging to the flavan-3-ols class of compounds. It is found in high concentrations in tea and various fruits, such as kiwis. This bioactive compound is known for its antioxidant and anti-inflammatory properties, making it a valuable component in the pharmaceutical and food industries.

Uses

Used in Pharmaceutical Applications:
(-)-Epiafzelechin is used as a therapeutic agent for its antioxidant and anti-inflammatory properties. It helps in the treatment and prevention of various diseases, including cardiovascular diseases, neurodegenerative disorders, and certain types of cancer, by neutralizing free radicals and reducing inflammation.
Used in Food Industry:
(-)-Epiafzelechin is used as a natural additive in the food industry to enhance the nutritional value and health benefits of products. Its antioxidant properties help in preserving the freshness and quality of food items, while its anti-inflammatory effects contribute to the overall health benefits of consuming these products.
Used in Antioxidant Supplements:
(-)-Epiafzelechin is used as an ingredient in antioxidant supplements due to its potent antioxidant properties. These supplements are designed to support overall health and well-being by combating oxidative stress and promoting a healthy immune system.
Used in Cosmetics:
(-)-Epiafzelechin is used as an active ingredient in cosmetics, particularly in anti-aging and skin care products. Its antioxidant and anti-inflammatory properties help in reducing the signs of aging, promoting skin health, and protecting the skin from environmental stressors.

Check Digit Verification of cas no

The CAS Registry Mumber 24808-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24808-04:
(7*2)+(6*4)+(5*8)+(4*0)+(3*8)+(2*0)+(1*4)=106
106 % 10 = 6
So 24808-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-6,13,15-19H,7H2/t13-,15-/m1/s1

24808-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-2-(4-Hydroxyphenyl)-3,5,7-chromanetriol

1.2 Other means of identification

Product number -
Other names 3,5,7,4'-Tetrahydroxyflavan

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:24808-04-6 SDS

24808-04-6Relevant articles and documents

General synthesis of epi-series catechins and their 3-gallates: Reverse polarity strategy

Ohmori, Ken,Yano, Takahisa,Suzuki, Keisuke

supporting information; experimental part, p. 2693 - 2696 (2010/08/21)

A general synthetic route to the epi-series catechins was developed based on the reverse polarity strategy. Aromatic nucleophilic substitution reaction followed by the sulfinyl-metal exchange and cyclization enabled stereo-controlled access to various members of epi-series catechins and their 3-gallates.

New oligomeric proanthocyanidine from Ziziphus jujuba

Malik, Aibek,Kuliev,Akhmedov,Vdovin,Abdullaev

, p. 40 - 42 (2007/10/03)

Chemical and spectral data establish the structure of an oligomeric proanthocyanidine PZ-5 isolated from Ziziphus jujuba.

(+)-AFZELECHIN 3-RHAMNOSIDE FROM CASSIPOUREA GERRARDII

Drewes, Siegfried E.,Taylor, Craig W.,Cunningham, Anthony B.

, p. 1073 - 1075 (2007/10/02)

A new flavanol glycoside has been isolated from the bark of Cassipourea gerrardii.Its structure has been established from spectroscopic and hydrolytic studies as (+)-afzelechin 3-O-α-L-rhamnopyranoside.Delayed homonuclear COSY studies show up interesting long-range couplings between specific protons. Key words: Cassipourea gerrardii; Rhizophoraceae; bark; (+)-afzelechin 3-O-α-L-rhamnopyranoside.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 24808-04-6