1510-20-9 Usage
Uses
Used in Pharmaceutical Industry:
Cholesteryl hydrogen succinate is used as a surfactant for its ability to lower surface tension and improve the solubility of drugs, which can enhance the bioavailability and effectiveness of pharmaceutical formulations.
Used in Cosmetic Industry:
In cosmetics, cholesteryl hydrogen succinate serves as a surfactant, helping to stabilize emulsions and improve the texture and feel of cosmetic products, thereby contributing to their performance and consumer appeal.
Used in Drug Delivery Systems:
Cholesteryl hydrogen succinate is utilized in the preparation of liposomal formulations, which are advanced drug delivery systems that can encapsulate drugs and deliver them to specific target sites within the body, improving the therapeutic index of the drug.
Used in Biomaterials for Tissue Engineering and Regenerative Medicine:
It is also used as a component in the development of novel biomaterials, where its properties can contribute to the creation of scaffolds and other structures that support tissue growth and regeneration.
Used in Targeted Drug Delivery Systems:
Cholesteryl hydrogen succinate has been studied for its potential in targeted drug delivery, where it may be used to direct drugs specifically to disease sites, minimizing side effects and increasing treatment efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 1510-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1510-20:
(6*1)+(5*5)+(4*1)+(3*0)+(2*2)+(1*0)=39
39 % 10 = 9
So 1510-20-9 is a valid CAS Registry Number.
1510-20-9Relevant academic research and scientific papers
Marcelis, Antonius T. M.,Koudijs, Arie,Sudhoelter, Ernst J. R.
, p. 1469 - 1472 (1996)
The thermal and optical properties of a series of bis(cholesteryl) alkanedioates were investigated. The melting points, the cholesteric to isotropic transition temperatures, the entropy changes at this temperature and the selective reflection wavelengths of the cholesteric phase all exhibit an odd-even effect as a function of spacer length. This is attributed to a difference in the ordering of the cholesteric phase as a function of the parity of the spacer. Because the properties of the members of the series with a short spacer could not be measured for several reasons, their properties were also determined as a 5 wt% solution in a cholesteric host. A similar odd-even influence on the cholesteric to isotropic transition temperatures and the optical properties of the host was observed as for the pure compounds. The influence on the properties of the host is stronger for compounds with a short spacer than for compounds with a longer spacer.
Conjugates of hirudin and lipophilic compounds
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, (2008/06/13)
The invention relates to novel hirudin conjugates formed from a hirudin and one or more lipophilic compounds, where the lipophilic compound has an octanol/water partition coefficient of more than 1.8 and is chemically linked to the hirudin, to the preparation thereof and to the use thereof.
