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Chemodex
Stearyl behenate
116
CHF
CHF 116.00
In stock
CDX-S0371-M250250 mgCHF 116.00
CDX-S0371-G0011 gCHF 348.00
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| Product Details | |
|---|---|
| Synonyms | Octadecyl docosanoate; Stearyl docosanoate; Behenic acid stearyl ester; Purester 40 |
| Product Type | Chemical |
| Properties | |
| Formula | C40H80O2 |
| MW | 593.06 |
| CAS | 24271-12-3 |
| Source/Host Chemicals | Synthetic |
| Purity Chemicals | ≥98% (NMR) |
| Appearance | White to off-white flakes. |
| Solubility | Soluble in chloroform. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | GAQPWOABOQGPKA-UHFFFAOYSA-N |
| Smiles | CCCCCCCCCCCCCCCCCCOC(CCCCCCCCCCCCCCCCCCCCC)=O |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +20°C |
| Long Term Storage | +4°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at +4°C. |
| Documents | |
| MSDS | Inquire |
| Product Specification Sheet | |
| Datasheet |
 Download PDF |
Description
Stearyl behenate is an esterified lipid compound formed by the esterification of stearyl alcohol and behenic acid. In scientific research, it has been extensively used as a model compound for studying the behavior of lipophilic esters in various applications, including cosmetic and industrial formulations. It is known for its lubricating properties and stability, making it a valuable tool in exploring the interactions between lipophilic substances and surfactants. In material science research, stearyl behenate has been employed to understand the self-assembling properties of fatty acid esters and their impact on crystallization, polymorphism, and phase behavior. Its interaction with emulsifiers and surfactants has also provided insights into optimizing the stability and performance of emulsions and oil-in-water systems.
Product References
(1) K. Yase, et al.; Thin Solid Films 219, 231 (1992) | (2) N. Dayan, et al.; Cosmetics & Toiletries 126, 188 (2011) | (3) K. Urbanova, et al.; J. Lipid Res. 53, 204 (2012) | (4) M.M. Fiume, et al.; Int. J. Toxicol. 31, 141S (2012) | (5) P. Horka, et al.; J. Mass Spectrom. 49, 628 (2014) | (6) M.M. Fiume, et al.; Int. J. Toxicol. 34, 5S (2015) | (7) A. Schnapp, et al.; Methods 104, 194 (2016) | (8) L. Wenning, et al.; Biotechnol. Bioeng. 114, 1025 (2017) | (9) D.R. Serrano, et al.; Pharmaceutics 11, 167 (2019)