What is the chemical structure of trimyristin?

Trimyristin

PubChem CID 11148
Structure Find Similar Structures
Molecular Formula C45H86O6
Synonyms TRIMYRISTIN 555-45-3 propane-1,2,3-triyl tritetradecanoate Glycerol trimyristate Glyceryl trimyristate More…
Molecular Weight 723.2

What is trimyristin made of?

What is it? Trimyristin, C45H86O6, is a saturated fat with a white to yellow-gray appearance. Trimyristin can be extracted from nutmeg seeds. There are three major other natural sources of trimyristin — coconut oil, palm kernel oil, and babassu oil.

What is trimyristin melting point?

56°C to 57°C
Specifications

Quantity 25g
Melting Point 56°C to 57°C
Linear Formula [CH3(CH2)12COOCH2]2CHOCO(CH2)12CH3
Beilstein 1718242
Merck Index 14,9724

Why is trimyristin soluble in water?

Trimyristin in insoluble in water because it has a long chain of C-H groups which takes this compound nonpolar. Instead we will be using dichloromethane because trimyristin is soluble in that liquid. What is the structural difference between saturated, monounsaturated and polyunsaturated fats?

Is trimyristin soluble in water?

Trimyristin is a white to yellowish-gray solid that is insoluble in water, but soluble in ethanol, benzene, chloroform, dichloromethane, and ether.

Why is Trimyristin soluble in water?

Is Trimyristin soluble in water?

What is the Colour of trimyristin?

Why is trimyristin not soluble in water?

Trimyristin would not dissolve because it is a non-polar molecule. It also does not have a carboxylic acid group like myristic acid.

Can acetone dissolve trimyristin?

Trimyristin was extracted in the ether instead of acetone because it is more soluble in the ether since the molecule is largely nonpolar. The Trimyristin was recrystallized in acetone because the acetone is more polar which means the trimyristin will be not as soluble in the acetone as it would be in the ether.

Is water a good solvent for trimyristin?

Terms in this set (10) Would water be a suitable solvent for extracting trimyristin from nutmeg? Trimyristin in insoluble in water because it has a long chain of C-H groups which takes this compound nonpolar. Instead we will be using dichloromethane because trimyristin is soluble in that liquid.