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|
IUPAC Name |
: Tetradecanoic Acid |
|
Cas Number |
: 544-63-8 |
|
HS Code |
: 2915.90.20 |
|
Formula |
: C14H28O2 |
|
Appearance Name |
: White Flakes |
|
Common Names |
: Tetradecanoic acid |
|
Packaging |
: 25 Kg Polyethylene Laminated Bag |
For more detailed information including pricing, customization, and shipping:
Myristic acid, also known as tetradecanoic acid, is a prevalent fatty acid present in both plant oils and animal fats. It is widely distributed in fats across the plant and animal kingdoms, including commonly consumed human foods like nutmeg. This essential fatty acid plays a crucial role in the body, contributing to the stabilization of various proteins, including those utilized in the immune system.
Myristic acid is industrially produced through the saponification process of fatty oils. This process involves hydrolyzing triglyceride chains to produce chains of fatty acids and glycerine. Subsequently, glycerine is separated, and the fatty acid chains undergo purification via fractionation under vacuum conditions. The final step involves collecting the distillate of myristic acid, ensuring a composition of at least 99%. Achieving a higher concentration of myristic acid content requires a more advanced fractionation design and increased energy input, considering the specific composition of myristic acid.
Myristic acid, also known as tetradecanoic acid, is a prevalent fatty acid present in both plant oils and animal fats. It is widely distributed in fats across the plant and animal kingdoms, including commonly consumed human foods like nutmeg. This essential fatty acid plays a crucial role in the body, contributing to the stabilization of various proteins, including those utilized in the immune system.
Myristic acid is industrially produced through the saponification process of fatty oils. This process involves hydrolyzing triglyceride chains to produce chains of fatty acids and glycerine. Subsequently, glycerine is separated, and the fatty acid chains undergo purification via fractionation under vacuum conditions. The final step involves collecting the distillate of myristic acid, ensuring a composition of at least 99%. Achieving a higher concentration of myristic acid content requires a more advanced fractionation design and increased energy input, considering the specific composition of myristic acid.
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