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343315-27-5

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343315-27-5 Usage

Description

Tetraethylenepentamine β-cyclodextrin is a complex chemical compound that combines the properties of tetraethylenepentamine, a compound used in the production of adhesives and coatings, with β-cyclodextrin, a cyclic oligosaccharide that is commonly used to encapsulate and stabilize various molecules. This combined compound has potential applications in a variety of industries, including pharmaceuticals, agriculture, and material science.

Uses

Used in Pharmaceutical Industry:
Tetraethylenepentamine β-cyclodextrin is used as a chelating agent for enhancing the solubility and stability of various pharmaceutical substances. Its ability to form inclusion complexes with guest molecules allows for improved encapsulation and delivery of active ingredients.
Used in Agriculture:
In the agricultural industry, tetraethylenepentamine β-cyclodextrin is used as a carrier for encapsulating and delivering agrochemicals, such as pesticides and fertilizers. This helps in improving the efficiency and reducing the environmental impact of these substances.
Used in Material Science:
Tetraethylenepentamine β-cyclodextrin is used in material science as a component in the development of advanced materials with improved properties. Its ability to form inclusion complexes can be utilized to create materials with enhanced stability and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 343315-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,3,1 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 343315-27:
(8*3)+(7*4)+(6*3)+(5*3)+(4*1)+(3*5)+(2*2)+(1*7)=115
115 % 10 = 5
So 343315-27-5 is a valid CAS Registry Number.

343315-27-5Downstream Products

343315-27-5Relevant articles and documents

Host-guest inclusion system of glycyrrhetic acid with polyamine-β-cyclodextrin: Preparation, characterization, and anticancer activity

Shen, Zhi,Qin, Qi,Liao, Xiali,Yang, Bo

, p. 155 - 161 (2017)

The inclusion complexation behaviors of glycyrrhetic acid (CTA) with four polyamine-modified β-cyclodextrins (CDs) have been investigated by 1H and 2D NMR, thermal gravimetric analysis, X-ray power diffraction and scanning electron microscopy. The results showed that Glycyrrhetic acid was encapsulated into the cavity of cyclodextrin to form the complexes with 1:1 stoichiometry. The water solubility of GTA was significantly enhanced by inclusion complexation with polyamine-modified β-cyclodextrins. The calculated IC50 values indicated that the antitumor activities of inclusion complexes were better than that of GTA. Satisfactory aqueous solubility, along with high thermal stability of inclusion complexes will be potentially useful for their application on the formulation design of natural medicine.

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