structure of Sodium N-dodecanoyl-L-valinate

Sodium N-dodecanoyl-L-valinate

CAS No.: 37869-33-3
M. Wt: 321.43100
M. Fa: C17H32NNaO3
InChI Key: -

Names and Identifiers of Sodium N-dodecanoyl-L-valinate

CAS Number

37869-33-3

IUPAC Name

sodium;(2S)-2-(dodecanoylamino)-3-methyl-butanoate

Canonical SMILES

CCCCCCCCCCCC(=O)N[C@@H](C(C)C)C(=O)[O-].[Na+]

Physical and chemical properties of Sodium N-dodecanoyl-L-valinate

Boiling Point

470.2ºC at 760mmHg

Exact Mass

321.22800

Flash Point

238.2ºC

LogP

3.18890

Molecular Formula

C17H32NNaO3

Molecular Weight

321.43100

PSA

69.23000

Applications of Sodium N-dodecanoyl-L-valinate

Sodium N-dodecanoyl-L-valinate finds applications across various fields:

  • Chemistry: Used as a surfactant in nanoparticle synthesis and stabilization of colloidal systems.
  • Biology: Investigated for its role in studying membrane dynamics and protein interactions within lipid environments.
  • Medicine: Explored for drug delivery systems, particularly for enhancing the solubility of lipophilic drugs.
  • Industry: Utilized in personal care products, detergents, and emulsifiers due to its surfactant properties.

Interaction Studies of Sodium N-dodecanoyl-L-valinate

Studies have shown that Sodium N-dodecanoyl-L-valinate interacts effectively with lipid membranes, facilitating molecular transport across barriers. Its micelle-forming ability allows it to encapsulate hydrophobic substances, enhancing their solubility in aqueous environments. Research has also indicated its potential role in improving drug delivery mechanisms by promoting cellular uptake of therapeutic agents.

Biological Activity of Sodium N-dodecanoyl-L-valinate

Sodium N-dodecanoyl-L-valinate has demonstrated notable biological activities. It functions as a surfactant that can stabilize colloidal dispersions and facilitate drug delivery systems. Its ability to interact with lipid membranes enhances permeability, making it valuable in studies involving membrane proteins and liposomes. Research indicates its potential for improving the solubility of hydrophobic drugs, thus enhancing their bioavailability.