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6336-63-6

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6336-63-6 Usage

Description

(1E)-1-(hydroxyimino)hexane-2,3,4,5-tetrol (non-preferred name) is a complex organic compound with a six-carbon chain featuring a hydroxyimino group and multiple hydroxyl groups. As a hexane derivative, it possesses the potential to function as a chelating agent, given its capacity to form coordination complexes with metal ions through its hydroxyl groups.

Uses

Used in Pharmaceutical Industry:
(1E)-1-(hydroxyimino)hexane-2,3,4,5-tetrol (non-preferred name) is used as a potential ligand in the development of metal-based drugs, capitalizing on its ability to chelate with metal ions. This unique property allows it to play a crucial role in the design of pharmaceutical compounds with specific therapeutic applications.
Additionally, it may be utilized as a component of chelation therapy:
In chelation therapy, (1E)-1-(hydroxyimino)hexane-2,3,4,5-tetrol (non-preferred name) could serve to bind and remove heavy metals from the body, thus aiding in the treatment of heavy metal poisoning or detoxification processes.
Further research is necessary to fully explore the properties and potential applications of (1E)-1-(hydroxyimino)hexane-2,3,4,5-tetrol (non-preferred name) in various fields, including its efficacy and safety in pharmaceutical uses.

Check Digit Verification of cas no

The CAS Registry Mumber 6336-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6336-63:
(6*6)+(5*3)+(4*3)+(3*6)+(2*6)+(1*3)=96
96 % 10 = 6
So 6336-63-6 is a valid CAS Registry Number.

6336-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1E)-1-hydroxyiminohexane-2,3,4,5-tetrol

1.2 Other means of identification

Product number -
Other names rhamnose oxime

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:6336-63-6 SDS

6336-63-6Relevant articles and documents

Antioxidant activity of a water-soluble polysaccharide purified from Pteridium aquilinum

Xu, Wentao,Zhang, Fangfang,Luo, YunBo,Ma, Liyan,Kou, Xiaohong,Huang, Kunlun

experimental part, p. 217 - 222 (2009/04/11)

A water-soluble crude polysaccharide, obtained from fern Pteridium aquilinum, was fractionated by DEAE-Sepharose Fast-Flow column chromatography, and purified by Sephacryl S-400 HR column chromatography. The average molecular weight (Mw) of the purified polysaccharide (PLP) is 458,000 Da. The monosaccharide components of PLP were characterized by gas chromatography (GC), and the majority of the monosaccharide components was glucose (relative mass 58.1%) with low levels of galactose, mannose, rhamnose, and arabinose (relative mass 18.7%, 6.8%, 10.2%, and 6.1%, respectively). The Fourier-transform infrared spectra (FTIR) of PLP revealed typical characteristics of polysaccharides. On the basis of the ferric-reducing antioxidant power assay (FRAP), DPPH radical-scavenging, the superoxide radical assay, and self-oxidation of 1,2,3-phentriol assay, the antioxidant activities of PLP were investigated. The purified polysaccharide was demonstrated to have strong reductive power (FRAP value: 827.6 μmol/L), moderate scavenging activities against DPPH radicals (83.1%) and superoxide radicals (60.5%), and moderate inhibiting power for self-oxidation of 1,2,3-phentriol (52.4%).

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