Palmitic Acid

Ingredient

Palmitic Acid

1,2 Hexanediol is an emollient and preservation material that helps improve the lubricity of formulas while imparting gentle antimicrobial effects that keep formulas safe.

Common Name

Palmitic Acid

Category

Emollient

Benefits
  • Moisturizing
  • Softening
  • Barrier-supporting
  • Cleansing
Performance Rating

Very Good

Chemical Structure

Image of palmitic acid chemical structure: CH₃(CH₂)₁₄COOH

Quick Summary Benefits

  • Improves skin softness and smoothness
  • Enhances skin barrier function
  • Helps retain moisture in the skin
  • Acts as an effective cleansing agent
  • Provides a stable base for formulations

Use & Background in Skincare

Palmitic acid is a long-chain saturated fatty acid commonly used in skincare formulations as an emollient and thickening agent. It occurs naturally in many plants and animals, including human skin, where it plays a crucial role in maintaining the skin's barrier function and hydration levels.

Detailed Description

Palmitic acid, a 16-carbon saturated fatty acid, is one of the most common fatty acids found in nature. In skincare, it serves multiple functions, primarily as an emollient and skin-conditioning agent. Its molecular structure allows it to integrate seamlessly with the skin's natural lipids, enhancing the skin's barrier function and preventing transepidermal water loss (TEWL) [1].

Historically, palmitic acid has been used in soap making due to its cleansing properties. In modern skincare, it's valued for its ability to soften and smooth the skin without causing irritation. Research has shown that palmitic acid, along with other fatty acids, plays a crucial role in maintaining skin homeostasis and protecting against external stressors [2].

Clinical studies have demonstrated the efficacy of palmitic acid in improving skin hydration and barrier function. A study published in the Journal of Investigative Dermatology found that topical application of palmitic acid and other fatty acids could accelerate skin barrier recovery after disruption [3]. This makes it particularly beneficial for dry, sensitive, or compromised skin.

While palmitic acid offers numerous benefits, it's important to note that its effectiveness can vary depending on the formulation and concentration. Some concerns have been raised about its potential to be comedogenic in high concentrations, although this is generally not an issue in well-formulated products [4].

Comedogenicity

3 out of 5 on the comedogenicity scale. While palmitic acid can be comedogenic in high concentrations, its effects are generally minimal in properly formulated skincare products [5].

Sustainability Notes

Palmitic acid can be derived from both plant and animal sources. When sourced from palm oil, sustainability concerns arise due to deforestation issues associated with palm cultivation. However, sustainable palm oil sources are available, and many companies are moving towards more environmentally friendly alternatives.

How It's Made

Palmitic acid is primarily obtained through the fractionation of palm oil or by hydrogenation of oleic acid. It can also be synthesized from other fatty acids or derived from animal fats

References

[1] Feingold KR, Elias PM. Role of lipids in the formation and maintenance of the cutaneous permeability barrier. Biochim Biophys Acta. 2014;1841(3):280-294. https://doi.org/10.1016/j.bbalip.2013.11.007

[2] Kendall AC, Nicolaou A. Bioactive lipid mediators in skin inflammation and immunity. Prog Lipid Res. 2013;52(1):141-164. https://doi.org/10.1016/j.plipres.2012.10.003

[3] Man MQ, Feingold KR, Elias PM. Exogenous lipids influence permeability barrier recovery in acetone-treated murine skin. Arch Dermatol. 1993;129(6):728-738. https://doi.org/10.1001/archderm.1993.01680270066008

[4] Draelos ZD, DiNardo JC. A re-evaluation of the comedogenicity concept. J Am Acad Dermatol. 2006;54(3):507-512. https://doi.org/10.1016/j.jaad.2005.11.1058

[5] Fulton JE Jr. Comedogenicity and irritancy of commonly used ingredients in skin care products. J Soc Cosmet Chem. 1989;40:321-333.