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β-Cyclodextrin-Zimtaldehyd is a chemical complex formed by the interaction between β-cyclodextrin, a cyclic oligosaccharide consisting of seven glucose units, and Zimtaldehyd, also known as cinnamaldehyde. This complex is often used in various applications due to its unique properties, such as encapsulation and controlled release of the aldehyde compound. β-Cyclodextrin's hydrophobic cavity can accommodate the aldehyde group, enhancing solubility and stability while potentially reducing the volatility and reactivity of cinnamaldehyde. This complex has potential uses in the food, pharmaceutical, and cosmetic industries, where it can serve as a flavor enhancer, a preservative, or a component in fragrances.

69962-94-3

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69962-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69962-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69962-94:
(7*6)+(6*9)+(5*9)+(4*6)+(3*2)+(2*9)+(1*4)=193
193 % 10 = 3
So 69962-94-3 is a valid CAS Registry Number.

69962-94-3Downstream Products

69962-94-3Relevant academic research and scientific papers

Mechanism and structure studies of cinnamaldehyde/cyclodextrins inclusions by computer simulation and NMR technology

Sun, Qiaomei,Tang, Peixiao,Zhao, Ludan,Pu, Hongyu,Zhai, Yuanming,Li, Hui

, p. 294 - 302 (2018)

This work aims to explore the inclusion mechanism and structure of cinnamaldehyde (CNMA) and cyclodextrins (CDs), and to provide some theoretical information for the application of CNMA and its inclusion. In this study, we prepared three kinds of inclusion and investigated the mechanism and structure by theory and experiment. Molecular docking and dynamical simulations presented a stable 1:1 inclusion complex and the visual structure model. The structural features indicated that the benzene ring of CNMA was enclosed in the hydrophobic cavity of CDs, which were consistent with the results of 1H NMR, 2D-ROESY, Fourier transform infrared spectroscopy. The inclusion mechanism studies showed that the inclusion process was driven mainly by enthalpy with the binding constant following the order of DM (dimethyl) > HP (hydroxypropyl) > β-CD. Moreover, the inclusion complex showed an advantageous water solubility and dissolution rate compared with CNMA.

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