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RETINOL PALMITATE
Chemical structure of RETINOL PALMITATE

RETINOL PALMITATE

CAS — · other

Caution5 citationsNot pregnancy safe

RETINOL PALMITATE. Formula: C36H60O2. MW: 524.9. IUPAC: [(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] hexadecanoate

RETINOL PALMITATE is an other ingredient used in skincare formulations.

⚠️ Data is provided for informational purposes only. It may contain inaccuracies and should be independently verified. This is not medical advice. Consult a healthcare professional before making health decisions.

Quick facts

Description: RETINOL PALMITATE — RETINOL PALMITATE. Formula: C36H60O2. MW: 524.9. IUPAC: [(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] hexadecanoate.

Quick Facts:

  • Category: other
  • Regulatory Note: Restricted in the US

Proven Benefits At A Glance:

  • Retinol palmitate is a form of vitamin A used in eye drops and oral supplements
  • Research shows it may help with dry eyes and certain corneal surface conditions
  • It has antioxidant properties, though evidence for skin benefits is limited in these sources
  • Side effects from oral use can include dry skin and mucous membranes, but are usually mild
  • Most research here focuses on eye health, not skincare

Chemical Overview

All-trans-retinyl palmitate is an all-trans-retinyl ester obtained by formal condensation of the carboxy group of palmitic (hexadecanoic acid) with the hydroxy group of all-trans-retinol. It is used in cosmetic products to treat various skin disorders such as acne, skin aging, wrinkles, dark spots, and also protect against psoriasis. It has a role as an antioxidant, a human xenobiotic metabolite and an Escherichia coli metabolite. It is a retinyl palmitate and an all-trans-retinyl ester. It is functionally related to an all-trans-retinol. retinyl palmitate has been reported in Homo sapiens with data available. Retinyl Palmitate is a naturally-occurring phenyl analogue of retinol (vitamin A) with potential antineoplastic and chemopreventive activities. As the most common form of vitamin A taken for dietary supplementation, retinyl palmitate binds to and activates retinoid receptors, thereby inducing cell differentiation and decreasing cell proliferation. This agent also inhibits carcinogen-induced neoplastic transformation, induces apoptosis in some cancer cell types, and exhibits immunomodulatory properties. (NCI04)

Source(s): LOTUS – the natural products occurrence database, ChEBI, NCI Thesaurus (NCIt), via PubChem

Comedogenicity

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