Cas no 238413-60-0 (Cholesteryl Heneicosanoate)
Cholesteryl Heneicosanoate Chemical and Physical Properties
Names and Identifiers
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- CHOLESTERYL HENEICOSANOATE
- (3β)-Cholest-5-en-3-yl heneicosanoate
- Cholesteryl Heneicosanoate
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- Inchi: 1S/C48H86O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-28-46(49)50-41-33-35-47(5)40(37-41)29-30-42-44-32-31-43(39(4)27-25-26-38(2)3)48(44,6)36-34-45(42)47/h29,38-39,41-45H,7-28,30-37H2,1-6H3/t39-,41?,42?,43-,44?,45?,47+,48-/m1/s1
- InChI Key: VKIWHVZSAQORAL-ZAORTALQSA-N
- SMILES: C(OC1CC2[C@](C)(CC1)C1C(C3[C@@](CC1)(C)[C@@H]([C@H](C)CCCC(C)C)CC3)CC=2)(=O)CCCCCCCCCCCCCCCCCCCC
Cholesteryl Heneicosanoate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Larodan | 64-2100-9-100mg |
Cholesteryl Heneicosanoate |
238413-60-0 | >99% | 100mg |
€92.00 | 2025-03-07 |
Cholesteryl Heneicosanoate Related Literature
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Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327
Additional information on Cholesteryl Heneicosanoate
Cholesteryl Heneicosanoate: A Comprehensive Overview
Cholesteryl Heneicosanoate, with the CAS number 238413-60-0, is a compound of significant interest in various scientific and industrial applications. This compound, also known as cholesterol heneicosanoate, belongs to the class of sterol esters, which are derivatives of cholesterol combined with fatty acids. The molecule consists of a cholesterol backbone esterified with a heneicosanoic acid, resulting in a structure that exhibits unique physical and chemical properties.
The synthesis of Cholesteryl Heneicosanoate typically involves the esterification of cholesterol with heneicosanoic acid. This process can be achieved through various methods, including acid-catalyzed esterification, enzymatic catalysis, or even microwave-assisted synthesis. Recent advancements in catalytic techniques have enabled more efficient and environmentally friendly production methods, making this compound more accessible for large-scale applications.
Cholesteryl Heneicosanoate has been extensively studied for its potential applications in the fields of cosmetics, pharmaceuticals, and food science. In cosmetics, it is valued for its ability to act as an emulsifier and stabilizer in formulations such as creams, lotions, and makeup products. Its high melting point and excellent compatibility with skin make it an ideal ingredient for creating products that provide long-lasting hydration and protection.
In the pharmaceutical industry, Cholesteryl Heneicosanoate has shown promise as a carrier for drug delivery systems. Its ability to form stable micelles and vesicles makes it a potential candidate for encapsulating hydrophobic drugs, enhancing their bioavailability and reducing side effects. Recent studies have explored its use in targeted drug delivery systems, where it can be modified with targeting ligands to deliver therapeutic agents directly to specific tissues or cells.
The food industry has also benefited from the unique properties of Cholesteryl Heneicosanoate. It is used as a stabilizer and emulsifier in food products such as margarine, spreads, and confectionery items. Its ability to improve the texture and shelf life of these products makes it a valuable additive in the food manufacturing sector.
Recent research has focused on understanding the molecular mechanisms underlying the properties of Cholesteryl Heneicosanoate. Scientists have investigated its interactions with biological membranes, revealing insights into its role in cellular processes such as signal transduction and membrane fluidity regulation. These studies have implications for understanding diseases associated with lipid metabolism disorders and could pave the way for new therapeutic strategies.
In addition to its practical applications, Cholesteryl Heneicosanoate has become a subject of interest in materials science. Researchers have explored its potential as a precursor for synthesizing novel materials with unique mechanical and optical properties. For instance, it has been used to create biodegradable polymers that are suitable for packaging and biomedical applications.
The environmental impact of Cholesteryl Heneicosanoate has also been a topic of recent studies. Scientists are investigating its biodegradability under various environmental conditions to assess its suitability as an eco-friendly alternative to traditional synthetic additives. Preliminary results suggest that it can degrade under microbial action, making it a promising candidate for sustainable industrial practices.
In conclusion, Cholesteryl Heneicosanoate (CAS No. 238413-60-0) is a versatile compound with a wide range of applications across multiple industries. Its unique chemical properties make it an invaluable ingredient in cosmetics, pharmaceuticals, food products, and materials science. As research continues to uncover new insights into its molecular behavior and potential uses, this compound is poised to play an even greater role in advancing technological innovations while addressing environmental concerns.
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