L-ALPHA-PHOSPHATIDYL-DL-GLYCEROL, DIPALMITOYL SODIUM SALT - Names and Identifiers
L-ALPHA-PHOSPHATIDYL-DL-GLYCEROL, DIPALMITOYL SODIUM SALT - Physico-chemical Properties
Molecular Formula | C38H74NaO10P
|
Molar Mass | 744.95 |
Melting Point | 185-189oC |
Solubility | Chloroform:Methanol:Water = 2:1:0.1 (Slightly) |
Appearance | Solid |
Color | White |
Storage Condition | −20°C |
L-ALPHA-PHOSPHATIDYL-DL-GLYCEROL, DIPALMITOYL SODIUM SALT - Risk and Safety
L-ALPHA-PHOSPHATIDYL-DL-GLYCEROL, DIPALMITOYL SODIUM SALT - Introduction
1,2-Dimyristoyl-sn-glyceryl-3-phosphate-rac-(1-glycerol) (sodium salt)(DPPG-NA) is a phosphatidylcholine compound. It is formed from 1,2-dimyristoyl-sn-glycerol and phosphoric acid, which also has a phosphate group and a glycerol group attached to it. The sodium ion maintains a negative charge and combines with the phosphate to form the sodium salt.
DPPG-NA is a surface-active substance and is often used as a model for studying cell membranes and lipid molecules. It has a wide range of applications in the fields of drug delivery, drug delivery and biomedicine. As a tool for studying lipid interactions and cell membrane dynamics, DPPG-NA play an important role in the fields of biophysics and biochemistry.
The preparation method of DPPG-NA is usually to react 1,2-dimyristoyl-sn-glycerol with phosphoric acid to obtain 1,2-dimyristoyl-sn-glycerol -3-phosphate, and then react with alkali to form sodium salt.
Regarding safety, DPPG-NA is a relatively safe compound, but it still needs to follow the laboratory's safe operation regulations. It is soluble in water and organic solvents, but may undergo thermal decomposition in solution. When using, you need to pay attention to avoid contact with strong oxidants, avoid inhalation of dust and skin contact. If accidental contact causes discomfort, seek medical attention immediately. When using or handling this compound in the laboratory, it is recommended that proper laboratory safety practices be followed.
Last Update:2024-04-09 21:54:55