Phloretin
INCI · Phloretin · also Apple polyphenol, Dihydrochalcone
How it works
Phloretin is a dihydrochalcone — a polyphenol found in the leaves, bark and skin of apples. It neutralises free radicals directly, the way most antioxidants do, and it crosses the stratum corneum comparatively well for a molecule of its class. That second property is the reason formulators reach for it: an antioxidant that stays on the surface does very little, and the useful ones are the ones that get in.
It is almost never used alone. The place it occupies in skincare is as the third component of a fixed antioxidant combination alongside L-ascorbic acid and ferulic acid, formulated at a low pH so the vitamin C stays in its active form.
The evidence
Published work on that combination applied it to skin before exposure to solar-simulated ultraviolet light and reported less redness and lower levels of ultraviolet damage markers than in untreated skin. That is a controlled human endpoint rather than a cell assay, which puts it ahead of most botanical antioxidants.
What it does not establish is what phloretin contributes on its own. The mixture was tested; its components were not separated out in the same setting, so any claim about phloretin specifically is an inference. Separately, phloretin inhibits tyrosinase in enzyme and cell assays, which is where its appearance in brightening copy comes from — laboratory work, not a demonstrated effect on pigment in skin.
Suitability
- Morning routines, as an antioxidant layer under sunscreen
- Anyone whose vitamin C serum already contains it — there is little sense in stacking two
- Sensitive skin, with care: the usual cause of stinging is the acidic vehicle rather than the phloretin
Concentration
No standalone effective concentration is established, and quoting one would be misleading — phloretin is neither sold nor studied on its own. What can be judged from the outside is the formula's design: whether all three components are actually named, and whether the packaging is opaque and air-restricting, because these serums oxidise. A serum that has gone deep amber has lost its vitamin C whatever the phloretin is still doing.
Conflicts & combinations
No documented conflicts with common actives. Its natural partners are the two it ships with: ferulic acid stabilises the system, vitamin C carries most of the antioxidant load, and phloretin adds a differently soluble one. Putting it on the same morning as an exfoliating acid stacks acidity on acidity and usually adds sting without evidence of added benefit. It is not a sunscreen, and nothing in the evidence justifies using less sun protection because it is in the routine.
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Is phloretin the same thing as phlorizin?
No. Phlorizin is the glycoside — phloretin with a sugar attached. Phloretin is what remains once that sugar is removed, and it is the form cosmetic formulas use.
Does phloretin fade dark spots?
It inhibits tyrosinase in laboratory assays, which is where the claim comes from. That has not been shown to translate into measurable lightening on skin, so treat it as a possible bonus rather than a reason to buy.
Do I need it if I already use vitamin C?
Not necessarily. It is a component of certain vitamin C serums rather than a separate step, and there is no evidence that adding a second phloretin product on top does anything.
Why has my serum turned brown?
That is the vitamin C oxidising, and it is the clearest signal these formulas give. An oxidised serum is not dangerous, but it has lost the component doing most of the work.
Can I use it with retinol?
Yes, and the simplest arrangement is the usual one: antioxidants in the morning under sunscreen, retinoid at night. Using both at once is not harmful but adds irritation for no documented gain.