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641-90-7

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641-90-7 Usage

Description

2-hydroxyemodin, also known as emodin-2-ol, is a naturally occurring anthraquinone derivative found in several plant species, such as rhubarb and knotweed. This chemical compound is known for its various biological activities, including anti-inflammatory, antioxidant, and anticancer properties. It has been studied for its potential therapeutic effects, such as inhibiting cell proliferation, inducing apoptosis, and suppressing tumor growth. Additionally, 2-hydroxyemodin has been investigated for its role in regulating immune responses and reducing inflammation. It has also been explored as a potential treatment for skin diseases and microbial infections due to its antimicrobial and antifungal properties. Overall, research on this chemical compound suggests it has promising medicinal applications and warrants further investigation for its potential health benefits.

Uses

Used in Pharmaceutical Industry:
2-hydroxyemodin is used as a therapeutic agent for its anti-inflammatory, antioxidant, and anticancer properties. It is being studied for its potential to inhibit cell proliferation, induce apoptosis, and suppress tumor growth, making it a promising candidate for the development of new cancer treatments.
Used in Skincare Industry:
2-hydroxyemodin is used as a treatment for skin diseases due to its antimicrobial and antifungal properties. It can help in the management and treatment of various skin conditions, such as acne, eczema, and fungal infections.
Used in Nutraceutical Industry:
2-hydroxyemodin is used as a dietary supplement for its potential health benefits, including its anti-inflammatory and antioxidant properties. It can be incorporated into health products to support immune function and overall well-being.
Used in Cosmetic Industry:
2-hydroxyemodin is used as an ingredient in cosmetic products for its potential skin health benefits, such as reducing inflammation and promoting skin regeneration. It can be used in formulations for skincare products, such as creams, lotions, and serums, to improve skin health and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 641-90-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 641-90:
(5*6)+(4*4)+(3*1)+(2*9)+(1*0)=67
67 % 10 = 7
So 641-90-7 is a valid CAS Registry Number.

641-90-7SDS

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 2-hydroxyemodin

1.2 Other means of identification

Product number -
Other names 1,2,6,8-tetrahydroxy-3-methyl-anthraquinone

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:641-90-7 SDS

641-90-7Downstream Products

641-90-7Relevant articles and documents

The Chemical Structure and the Mutagenicity of Emodin Metabolites

Morooka, Nobuhisa,Nakano, Sonoko,Itoi, Noriko,Ueno, Yoshio

, p. 1247 - 1252 (2007/10/02)

Emodin (1,3,8-trihydroxy-6-methyl-9,10-anthraquinone) is a natural occuring anthraquinone formed in rhubarb and fungal metabolites.Emodin was transformed into 6 major metabolites by rat hepatic microsomes.The metabolites were identified as 2-hydroxyemodin, 4-hydroxyemodin, 5-hydroxyemodin, 7-hydroxyemodin, ω-hydroxyemodin, and emodic acid by comparison with the synthetic compounds using thin-layer chromatography.It was clear that 2-hydroxyemodin is a proximate mutagen as a synthetic compound by the Salmonella assay.Other metabolites, such as 5-hydroxyemodin and ω-hydroxyemodin, became active after metabolic activation, but 4-hydroxyemodin and emodic acid were inactive either in the presence or in the absence of the metabolic activation system.

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