CAS: 37869-33-3; N-Dodecanoyl-Valinemonosodiumsalt

该化合物是一种表面活性剂和两栖化合物,其结构特征包括一种与氨氨酸valine相连的多德诺基(脂肪酸链),该化合物通常具有水溶性等特性,同时具有长期碳氢化合物链的疏水特性,并经常用于多种用途,包括药品,化妆品和食品工业,因为它能够提高溶性,并稳定制剂.钠盐形式表明它能够分解溶解,有助于其表面活性特性,可以降低表面的紧张性,改善乳化.此外,N-dodecanoyl-Valine单体钠盐可能展示生物活动,使其对生物化学研究和潜在的治疗应用感兴趣.其稳定性,与其他成分的兼容性以及形成小鼠的能力也是提高其在各种配方中的效用的显著特征.

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      专利号:US-6090250-A
      优先权日:1993-09-20
      标题 :Chiral surfactants and methods for their use in chiral separations
      发明人:MAZZEO JEFFREY R; GROVER EDWARD R; SWARTZ MICHAEL E; MERION MICHAEL; PETERSEN JOHN S
      权利人:WATERS INVESTMENTS LTD
      摘要:PCT No. PCT/US94/10655 Sec. 371 Date Mar. 20, 1996 Sec. 102(e) Date Mar. 20, 1996 PCT Filed Sep. 20, 1994 PCT Pub. No. WO95/08529 PCT Pub. Date Mar. 30, 1995Chiral surfactants, methods for their synthesis and use, and apparatus designed to facilitate chiral separations using nucellar capillary electrophoresis is disclosed. A chiral surfactant having the general formula: is described, R1 is the hydrophobic tail, Y-A-X is the linker, the brackets define a chiral center, and the hydrophilic head group is Z. All the various components may potentiate the enantioselectivity of the chiral surfactant. The capillary electrophoresis (CE) system includes a narrow diameter capillary, a high voltage power supply, an electrolyte reservoir at each end of the capillary, a means for injecting a sample, and a detector. Chiral surfactants are dissolved in the electrolyte above their critical micelle concentration (cmc), resulting in the formation of chiral micelles. The electrolyte reservoirs and capillary tube are filled with the electrolyte. A sample containing a mixture of enantiomers is then injected into the capillary, and a high voltage potential is applied across the capillary. The sample components migrate through the capillary due to the influence of the applied electric field. An example separation of the four sereoisomers of aspartame is shown.

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      合成参考文献


      参考文献:10.1007/s11743-998-0001-y
      摘要:Zhu Y, Rosen MJ, Morrall SW. Chemical structure/property relationships in surfactants. 17. N‐substituted‐N‐acyl glycinates in pure and synthetic hard river water. J Surfact & Detergents. 1998 Jan;1(1):1–9. doi: 10.1007/s11743-998-0001-y.
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