67232-80-8 Usage
Description
1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT, also known as 1,2-Dimyristoyl-rac-glycero-3-phospho-rac-(1-glycerol) Sodium Salt, is a racemic form of phospholipids that play a crucial role in the formation of lipid bilayers. 1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT is derived from the combination of two tetradecanoyl chains with a glycerol backbone and a phosphorylated glycerol group. It is widely utilized in the creation of phospholipid membranes and phospholipid vesicles due to its ability to form stable lipid bilayers.
Uses
Used in Pharmaceutical Applications:
1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT is used as a key component in the development of phospholipid membranes for various pharmaceutical applications. The formation of lipid bilayers is essential for the structure and function of cell membranes, making this compound a vital ingredient in the creation of drug delivery systems and models for studying membrane-related processes.
Used in Cosmetic Applications:
In the cosmetic industry, 1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT is used as an ingredient in the formulation of liposomes and other delivery systems. These systems are designed to enhance the penetration and absorption of active ingredients, providing improved efficacy and targeted delivery to the skin.
Used in Research and Development:
1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT is also utilized in research and development for the study of membrane biophysics, protein-lipid interactions, and the development of novel drug delivery systems. Its ability to form lipid bilayers makes it an essential tool for creating model membranes and studying their properties.
Used in Diagnostic Applications:
In the field of diagnostics, 1,2-DITETRADECANOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(1-GLYCEROL)] SODIUM SALT is employed in the development of biosensors and diagnostic tools that rely on the properties of lipid bilayers. These tools can be used to detect and analyze various biological molecules, providing valuable information for medical and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 67232-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,3 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67232-80:
(7*6)+(6*7)+(5*2)+(4*3)+(3*2)+(2*8)+(1*0)=128
128 % 10 = 8
So 67232-80-8 is a valid CAS Registry Number.
InChI:InChI=1/C34H67O10P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-33(37)41-29-32(30-43-45(39,40)42-28-31(36)27-35)44-34(38)26-24-22-20-18-16-14-12-10-8-6-4-2;/h31-32,35-36H,3-30H2,1-2H3,(H,39,40);
