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33037-46-6

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33037-46-6 Usage

Description

Aloe-eModin-8-O-β-D-glucopyranoside is an anthraquinone glycoside, a type of natural compound derived from plants, particularly from the Aloe species. It is characterized by its unique chemical structure that includes an anthraquinone moiety linked to a glucose molecule through a β-D-glucopyranosidic bond. Aloe-eModin-8-O-β-D-glucopyranoside has been the subject of research due to its potential antioxidant and neuroprotective properties, which can be beneficial for various health and therapeutic applications.

Uses

Used in Pharmaceutical Industry:
Aloe-eModin-8-O-β-D-glucopyranoside is used as a pharmaceutical agent for its antioxidant activities. Aloe-eModin-8-O-β-D-glucopyranoside's ability to neutralize free radicals and reduce oxidative stress makes it a promising candidate for the development of treatments aimed at combating various diseases associated with oxidative damage.
Used in Neuroprotective Applications:
In the field of neuroscience, Aloe-eModin-8-O-β-D-glucopyranoside is used as a neuroprotective agent. Its potential to protect neurons from damage and degeneration, particularly under conditions of oxidative stress, positions it as a valuable component in the development of therapies for neurodegenerative diseases such as Alzheimer's, Parkinson's, and multiple sclerosis.
Used in Cosmetic Industry:
Aloe-eModin-8-O-β-D-glucopyranoside is also used in the cosmetic industry as an ingredient with antioxidant and skin protective properties. Its ability to combat free radicals and protect the skin from environmental stressors makes it a valuable addition to skincare products, promoting skin health and reducing the signs of aging.
Used in Food and Beverage Industry:
In the food and beverage sector, Aloe-eModin-8-O-β-D-glucopyranoside can be used as a natural preservative and antioxidant. Its capacity to extend the shelf life of products and protect them from oxidative spoilage can be beneficial in maintaining the quality and safety of various food and drink items.
Overall, Aloe-eModin-8-O-β-D-glucopyranoside's diverse applications across different industries highlight its potential as a versatile and valuable compound with significant health and therapeutic benefits. Further research and development are necessary to fully harness its potential and integrate it into various products and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 33037-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,3 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33037-46:
(7*3)+(6*3)+(5*0)+(4*3)+(3*7)+(2*4)+(1*6)=86
86 % 10 = 6
So 33037-46-6 is a valid CAS Registry Number.

33037-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name aleo-emodin-8-O-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names ALOE-EMODIN-8-O-BETA-D-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:33037-46-6 SDS

33037-46-6Downstream Products

33037-46-6Relevant articles and documents

Anthraquinones and stilbenes from the roots and rhizomes of Rhubarb

Chen, Wen-Hao,Chen, Juan,Shi, Yan-Ping

, p. 1036 - 1041 (2011)

Two new anthraquinone glucosides [aloe-emodin 8-O-β-D-(6′- galloyl)glucopyranoside (1) and rhein 8-O-β-D-(6′-galloyl) glucopyranoside (2)], together with 16 known compounds (3-18), were isolated from the roots and rhizomes of Rheum hotaoense C.Y. Cheng et C.T. Kao. Their structures were elucidated on the basis of extensive investigation of 1D and 2D NMR, HR-ESI-MS, and chemical evidence. In addition, the free-radical-scavenging activity was tested using the 1,1-diphenyl-2-picrylhydrazyl assay.

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