Why is Trimyristin insoluble in water?

Why is Trimyristin insoluble 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 an ester with the chemical formula C45H86O6. It is a saturated fat which is the triglyceride of myristic acid. Trimyristin is a white to yellowish-gray solid that is insoluble in water, but soluble in ethanol, benzene, chloroform, dichloromethane, and ether.

What type of functional groups are present in Trimyristin?

Trimyristin is a triglyceride obtained by formal acylation of the three hydroxy groups of glycerol by myristic (tetradecanoic) acid. It is a triglyceride and a tetradecanoate ester.

What is the molecular weight of Trimyristin?

723.16 g/mol

Is Trimyristin soluble in methanol?

Trimyristin is an triester of glycerol with the chemical formula C45H86O6. to soluble in a desired solvent . Also Trimyristin is a polar compound and mostly non polar molecules can be picked up in methanol.

What solvent is Trimyristin more soluble in and why?

Trimyristin was extracted in the ether instead of acetone because it is more soluble in the ether since the molecule is largely nonpolar.

Is Trimyristin soluble in acetone?

Trimyristin is not very soluble in acetone. That is why acetone was used as the crystallization solvent. The trimyristin has to be soluble in the solvent to get extracted from the nutmeg. Trimyristin is more soluble in ether than in acetone.

Why is diethyl ether used as an extraction solvent rather than acetone?

Why is diethyl ether rather than acetone chosen as the extraction solvent? Diethyl ether was chosen as the solvent because it is less polar than acetone. Since like dissolves like, the diethyl ether will dissolve the trimyristin, while the acetone will not.