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Myricetin

D
lead outcome
Topical antioxidant / anti-aging appearance…
grades vary by outcome ↓
Small molecule (non-peptide)
also called — Myricetin · flavonol (3,5,7,3',4',5'-hexahydroxyflavone) · INCI: Myricetin
skin appearance (cosmetic)antioxidant(in-vitro:) UV-protective / anti-glycation
In brief

Myricetin is a plant flavonol — a close relative of quercetin — with a strong in-vitro antioxidant profile: radical scavenging, anti-glycation and reported UV-protective activity in cell and model systems. That laboratory pharmacology is why it appears in some antioxidant cosmetic formulations. But the honest picture for skin is thin: there is little or no controlled human topical data, and myricetin has poor stability and limited penetration, plus the usual flavonol tendency to oxidise and discolour. It is also widely sold as an ingestible supplement, which is outside this register's topical scope. A genuinely potent antioxidant molecule with almost no cosmetic clinical evidence behind the skincare framing.

Legal standing, by region
European Union
Lawful cosmetic ingredient

Myricetin (INCI) can be used as a cosmetic ingredient; claims must remain appearance-based. Also widely sold as an ingestible supplement — outside this register's topical scope.

International
Lawful cosmetic ingredient

Used as a plant-flavonoid antioxidant in some cosmetic formulations; rules vary by region.

Evidence, by outcome
How we grade →

An honest grade per outcome — drawn from the evidence, not any catalogue. Hype and undemonstrated marketing claims grade low.

OutcomeEvidence base · effectGrade
Topical antioxidant / anti-aging appearance (human)
The gap between a potent antioxidant in a dish and a visible cosmetic outcome is the whole story here — and for myricetin that gap is almost entirely unbridged.
Little to no controlled human topical data. Cosmetic interest rests on in-vitro and mechanistic work, not clinical trials on skin. · Not established on human skin.
D
Antioxidant / anti-glycation / UV-protective (mechanism)
Grades the MECHANISM only. Myricetin also has poor stability and limited skin penetration, and — like many flavonols — is prone to oxidation and discolouration in formulation.
A polyphenol flavonol with strong in-vitro antioxidant, radical-scavenging, anti-glycation and reported UV-protective activity in cell and model systems. · Consistent antioxidant activity in the lab.
C
Tyrosinase / pigmentation effects (mechanism)
Not a demonstrated pigment outcome on skin.
Some in-vitro reports of effects on melanin pathways, but inconsistent and not established as a cosmetic brightening outcome. · Suggestive in vitro only.
D
Tolerability / formulation
Stability and colour (flavonols can impart yellow tints and oxidise) are practical formulation challenges; independent safety data for cosmetic use is limited.
Limited cosmetic-use data · Unclear
Disclosure

Vallydia sells its own cosmetic serums, and some ingredients graded here belong to the same categories as those products. Grades are drawn from the published evidence by the method we publish, and applied to our own ingredients on the same terms — our copper-peptide serum is graded no more kindly than the peptides it competes with. We disclose the interest so you can weigh it.

Trade names shown here (for example Matrixyl, Argireline, Syn-Ake) are the property of their respective owners and are used only to identify the ingredient under discussion. Their appearance implies no affiliation with, or endorsement by, the proprietor.

Evidence changes

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Cosmetic claims boundary
✓ Allowed (appearance / feel)
  • antioxidant support for the look of protected skin
  • a plant-flavonoid antioxidant within a routine
✕ Not allowed (medicinal)
  • treats aging
  • reverses wrinkles
  • prevents skin cancer
  • anti-glycation treatment
  • sunscreen replacement

The medicinal-sounding science stays in the reference section; product copy speaks only to appearance/feel (Reg 655/2013). Different fields, never merged.

The honest part

Myricetin is a cosmetic ingredient framed around antioxidant support. Its in-vitro antioxidant activity is real and strong, but there is almost no controlled human topical evidence, and stability, penetration and discolouration are genuine formulation limits. Much of the interest around myricetin concerns ingestible supplement use, which is outside this register's topical scope. Claims should stay modest and appearance-based, and it complements — never replaces — sunscreen.

Identity

Myricetin is a plant flavonol — a polyphenol in the same family as quercetin and kaempferol, found in berries, tea, grapes and many vegetables. Its chemical name, hexahydroxyflavone, flags what makes it a strong antioxidant: six hydroxyl groups, plenty of sites to donate electrons and quench free radicals. In cosmetics it is used under the INCI name Myricetin as a plant-flavonoid antioxidant. (It is also heavily marketed as an ingestible supplement — that use sits outside this register's topical scope.)

Mechanism (as proposed)

As an antioxidant, myricetin scavenges reactive oxygen species generated by UV and pollution, and in the lab it also shows anti-glycation activity (interfering with the sugar-protein cross-linking implicated in skin ageing) and some UV-protective effects in cell and model systems. The in-vitro pharmacology is genuinely strong — which is exactly the trap this register watches for. Two physical limits temper it on skin: myricetin has poor stability and limited penetration, and like other flavonols it is prone to oxidising and discolouring in a formula, which constrains both delivery and shelf life.

Reading the evidence honestly

The decisive fact is the absence of the right kind of study: there is little to no controlled human topical data on myricetin for any skin outcome. The cosmetic case is built almost entirely on in-vitro antioxidant and anti-glycation results, and "potent antioxidant in a dish" has a long, well-documented record of not translating to visible human benefit. That is why the grade sits at D despite a legitimately impressive laboratory profile. Where myricetin does have a larger literature — metabolic and other effects — it concerns ingestible use, which this topical register does not cover.

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Chemical identifiers

Cross-reference identifiers for the authoritative external databases — not a recipe, and nothing about how to use it.

PubChem CID5281672
InChIKeyIKMDFBPHZNJCSN-UHFFFAOYSA-N

via PubChem CID 5281672 — InChIKey and formula (C15H10O8) verified. · verified confidence

Sources — 3 cited
01In-vitro and mechanistic literature on myricetin's antioxidant, anti-glycation and UV-protective activity.
02Reviews of flavonol antioxidants in cosmetic formulation and their stability /penetration limitations.
03resolve:required — verify any topical human citation before publishing; current evidence appears in-vitro-dominant.
Updated 2026-08-07

Grades reflect the published evidence, not our interest. No dosing, reconstitution, or administration is published for research compounds — that restraint is deliberate.

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Explore by goal
Skin & aesthetic
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This site provides neutral scientific reference and sells only products lawful in your region. Nothing here is medical advice, a recommendation, or an offer to supply unapproved medicines. No dosing or administration is published for research compounds. Cosmetic peptides per Regulation (EC) 1223/2009. Unapproved injectable peptides are neither sold nor advertised in the EU (Directive 2001/83/EC, Title VIII). © 2026 Vallydia.