22554-66-1 Usage
Main properties
1. Derivative of trehalose
2. Chemically modified with eight acetate groups
3. More stable form of trehalose
4. Improves stability, solubility, and protection against degradation
Specific content
1. Alpha,beta-trehalose octaacetate is a derivative of the disaccharide sugar trehalose.
2. It has been chemically modified with eight acetate groups.
3. Trehalose is a naturally occurring sugar found in plants, insects, and microorganisms.
4. Trehalose has biological functions, including as a stress protectant and supplement for preserving stability and activity of proteins, cells, and tissues.
5. The octaacetate derivative is a more stable form of trehalose.
6. It is utilized in various applications, including pharmaceuticals, cosmetics, and food products.
7. It improves stability, solubility, and protection against degradation.
8. Alpha,beta-trehalose octaacetate has potential as an ingredient in drug delivery systems.
9. It enhances the properties of various materials and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 22554-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,5 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22554-66:
(7*2)+(6*2)+(5*5)+(4*5)+(3*4)+(2*6)+(1*6)=101
101 % 10 = 1
So 22554-66-1 is a valid CAS Registry Number.
22554-66-1Relevant articles and documents
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Chittenden
, p. 323 (1969)
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Vogel,Debowska-Kurnicka
, p. 910,914 (1928)
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A trehalose ester from Lancea tibetica
Liu, Shi-Jun,Liao, Zhi-Xin,Liu, Chao,Qu, Yan-Bo
, p. 1613 - 1618 (2015/11/09)
A phytochemical study of the 95% ethanolic extract of the whole plant of Lancea tibetica Hook. f. et Thoms. led to the isolation of a new trehalose ester, 6-O-undecanoyl-α,β-trehalose (1), along with 23 known compounds (2-24), of which compounds 2-17 were isolated from this plant for the first time. The structures of these compounds were established on the basis of spectroscopic methods. Compound 1 was evaluated for their in vitro anti-proliferative activities against MCF-7, NCI-H460 and Hep-G2 tumour cell lines. Compound 1 exhibited potent inhibitory activity against NCI-H460 cell growth, in contrast to moderate cytotoxic activity against MCF-7 and Hep-G2 cells.
Stereoselektive Synthese von Acetal-β,β-diglucosiden, einer neuen Klasse von Glycosiden und chiraler Acetale
Tietze, Lutz F.,Beller, Matthias
, p. 878 - 880 (2007/10/02)
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