Ingredient intelligence

L-Ascorbic acid

Antioxidant · Ascorbic Acid · C6H8O6

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L-ascorbic acid is vitamin C: a water-soluble reducing agent and an essential for the prolyl and lysyl hydroxylases that mature .

Repeated (2 studies)Two independent human studies point the same way; more replication would strengthen this.

Any underlined term can be tapped for an everyday-English translation.

Molecular identity

Two-dimensional chemical structure of L-Ascorbic acid
Formula
C6H8O6
Molecular weight
176.12 g/mol
PubChem CID
54670067
ChEBI
CHEBI:29073
Open PubChem record →

Biological targets

  • Prolyl 4-hydroxylase subunit alpha-1 (P4HA1)

    high confidence

    activates · enzyme

    Ascorbate is a required for prolyl hydroxylation.

    UniProt P13674
  • Procollagen-lysine 5-dioxygenase (PLOD1)

    high confidence

    activates · enzyme

    UniProt Q02809
  • Tyrosinase (TYR)

    low confidence

    inhibits · enzyme

    Reduction of intermediates reported ; not established as the dominant in skin.

    UniProt P14679
  • Sodium-dependent vitamin C transporter 2 (SLC23A2)

    medium confidence

    targets · transporter

    UniProt Q9UGH3

Molecules & genes

Molecules

  • L-Ascorbic acidC6H8O6 · 176.12 g/mol
  • Dehydroascorbic acidC6H6O6 · 174.11 g/mol

Genes / proteins

How could this ingredient interact with biology?

Biological network

Ingredient → molecule → target → gene/protein → pathway → process → studied outcome. Relationship strength is drawn from the curated confidence tier; nothing is added to make the chain look complete.

100%
L-Ascorbic acidL-Ascorbic acidDehydroascorbic acidProlyl 4-hydroxylase subu…Procollagen-lysine 5-diox…Sodium-dependent vitamin …P4HA1PLOD1COL1A1Collagen biosynthesis and…Detoxification of reactiv…Collagen biosynthesisOxidative stress responseStudied for photoaging-re…Formulation instability i…

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IngredientMoleculeTargetGenePathwayProcessOutcome

4 lower-confidence relationships are hidden at this filter level. Use “Show more biology” to include them.

Text alternative for this network
  • L-Ascorbic acid is molecule L-Ascorbic acid — high confidence
  • L-Ascorbic acid is molecule Dehydroascorbic acid — high confidence
  • L-Ascorbic acid activates Prolyl 4-hydroxylase subunit alpha-1 (P4HA1) — high confidence
  • L-Ascorbic acid activates Procollagen-lysine 5-dioxygenase (PLOD1) — high confidence
  • L-Ascorbic acid targets Sodium-dependent vitamin C transporter 2 (SLC23A2) — medium confidence
  • Prolyl 4-hydroxylase subunit alpha-1 (P4HA1) encoded by P4HA1 — high confidence
  • Procollagen-lysine 5-dioxygenase (PLOD1) encoded by PLOD1 — high confidence
  • P4HA1 participates in Collagen biosynthesis and modifying enzymes — high confidence
  • PLOD1 participates in Collagen biosynthesis and modifying enzymes — high confidence
  • COL1A1 participates in Collagen biosynthesis and modifying enzymes — medium confidence
  • P4HA1 participates in Detoxification of reactive oxygen species — medium confidence
  • PLOD1 participates in Detoxification of reactive oxygen species — medium confidence
  • COL1A1 participates in Detoxification of reactive oxygen species — medium confidence
  • Collagen biosynthesis and modifying enzymes associated with Collagen biosynthesis — high confidence
  • Detoxification of reactive oxygen species associated with Collagen biosynthesis — medium confidence
  • Collagen biosynthesis and modifying enzymes associated with Oxidative stress response — medium confidence
  • Detoxification of reactive oxygen species associated with Oxidative stress response — medium confidence
  • Collagen biosynthesis studied in Studied for photoaging-related endpoints and pigmentation evenness — medium confidence
  • Oxidative stress response studied in Studied for photoaging-related endpoints and pigmentation evenness — medium confidence
  • Collagen biosynthesis studied in Formulation instability is a frequently reported limitation — high confidence
  • Oxidative stress response studied in Formulation instability is a frequently reported limitation — medium confidence

Biological pathways

Collagen biosynthesis and modifying enzymes

high confidence

Ascorbate-dependent hydroxylation steps required for stable triple-helix formation.

Reactome R-HSA-1650814

Detoxification of reactive oxygen species

medium confidence

Ascorbate participates in cellular redox buffering.

Reactome R-HSA-3299685

Melanin biosynthesis

low confidence

reduction of intermediates; limited translation to skin.

Gene Ontology GO:0042438

Evidence engine

Moderate

Some human evidence exists, but replication or sample sizes are limited.

Skinceptor Evidence Index

58

experimental · of 100

This index is a research-navigation aid describing how much evidence exists and how it was produced. It is not a medical safety score, an efficacy guarantee, or a clinical recommendation.

Study composition

  • Human1
  • Randomised controlled trial1
  • In-vitro3
  • Review2
Total studies
7
Human studies
2
Largest sample
19
Range
1991–2020

Index breakdown

  • Study design quality46% × 28%

    Mean design weight across curated studies (meta-analysis 1.0, RCT 0.9, other human 0.7, review 0.45, animal 0.35, in-vitro 0.25).

  • Human evidence share57% × 22%

    Proportion of curated evidence measured in people rather than cells or animals.

  • Evidence volume95% × 14%

    Log-scaled count of curated studies, so volume alone cannot dominate the score.

  • Largest sample size43% × 12%

    Log-scaled largest reported sample size across curated human studies.

  • Replication67% × 12%

    Independent human studies, capped at three; one study is never treated as replicated.

  • Recency70% × 7%

    Linear decay over a twenty-year window from the most recent curated publication.

  • Source traceability14% × 5%

    Share of curated studies with a verified PMID or DOI in this dataset.

How is this determined? →

Insufficient comparable evidence for quantitative synthesis.

Research timeline

How the evidence accumulated

  1. 1991

    Ascorbate requirement for hydroxylation and secretion of procollagen

    Reviewsample size unavailable · American Journal of Clinical Nutrition (review)

  2. 2002

    Topical vitamin C and photoaging: a double-blind half-face study

    Randomised controlled trialn = 19 · Dermatologic Surgery

  3. 2005

    Ferulic acid stabilises a solution of vitamins C and E and doubles its photoprotection

    Humann = 9 · Journal of Investigative Dermatology

  4. 2007

    Ascorbyl glucoside stability and enzymatic release of ascorbic acid in skin models

    In-vitrosample size unavailable · International Journal of Cosmetic Science

  5. 2012

    Stability and skin delivery of ascorbyl phosphate derivatives

    In-vitrosample size unavailable · International Journal of Cosmetic Science

  6. 2013

    Stability of L-ascorbic acid in topical formulations

    In-vitrosample size unavailable · International Journal of Cosmetic Science

  7. 2020

    Vitamin C derivatives for facial hyperpigmentation: a narrative review

    Reviewsample size unavailable · Journal of Cosmetic Dermatology (review)

Ingredient fingerprint

19 nodes · 37 relationships · seed "l-ascorbic-acid"

The fingerprint is a deterministic visual signature: ridge amplitude comes from the number of entities in each tier, node placement from identifier hashes, and opacity from confidence. Two ingredients can never produce the same figure unless their networks are identical.

Open in Biology as Art →

Research

7 curated studies

ReviewJournal of Cosmetic Dermatology (review) · 2020

Vitamin C derivatives for facial hyperpigmentation: a narrative review

Concludes that derivative-specific human evidence is thinner than for L-ascorbic acid, with conversion efficiency the main open question.

Limitations — Review of heterogeneous small studies; identifier not verified during curation.

Identifier not curated — search Europe PMCAscorbyl glucoside · Magnesium ascorbyl phosphate · L-Ascorbic acid
In-vitroInternational Journal of Cosmetic Science · 2013

Stability of L-ascorbic acid in topical formulations

Reported rapid oxidative degradation of L-ascorbic acid at neutral pH, mitigated by low pH and antioxidant co-formulation.

Limitations — Formulation chemistry only; no biological endpoints.

Identifier not curated — search Europe PMCL-Ascorbic acid · Ferulic acid · Tocopherol
In-vitroInternational Journal of Cosmetic Science · 2012

Stability and skin delivery of ascorbyl phosphate derivatives

Reported improved formulation stability for magnesium ascorbyl phosphate but slower and variable conversion to free ascorbate in skin models.

Limitations — Formulation and ex-vivo delivery only; no clinical endpoints.

Identifier not curated — search Europe PMCMagnesium ascorbyl phosphate · L-Ascorbic acid
In-vitroInternational Journal of Cosmetic Science · 2007

Ascorbyl glucoside stability and enzymatic release of ascorbic acid in skin models

Reported greater aqueous stability than L-ascorbic acid and glucosidase-dependent release of free ascorbate in skin homogenates.

Limitations — Homogenate model may overstate in-vivo conversion; identifier not verified during curation.

Identifier not curated — search Europe PMCAscorbyl glucoside · L-Ascorbic acid
HumanJournal of Investigative Dermatology · 2005n = 9

Ferulic acid stabilises a solution of vitamins C and E and doubles its photoprotection

Reported improved formulation stability and increased measured photoprotection for a C/E/ferulic combination on human skin.

Limitations — Very small sample; surrogate photoprotection endpoints; industry-affiliated.

PMID 16297196Ferulic acid · L-Ascorbic acid · Tocopherol
Randomised controlled trialDermatologic Surgery · 2002n = 19

Topical vitamin C and photoaging: a double-blind half-face study

Reported improvement in investigator-assessed photoaging scores on the vitamin C treated side.

Limitations — Very small sample; identifier not verified during curation; formulation stability not reported.

ReviewAmerican Journal of Clinical Nutrition (review) · 1991

Ascorbate requirement for hydroxylation and secretion of procollagen

Establishes ascorbate as an obligatory cofactor for prolyl and lysyl hydroxylases in collagen maturation.

Limitations — Nutritional/biochemical focus rather than topical cosmetic use.

Identifier not curated — search Europe PMCL-Ascorbic acid · Magnesium ascorbyl phosphate

Community evidence

Submitted by readers

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Reader submissions appear here only after review. They are not part of the curated dataset and do not affect the Skinceptor Evidence Index.

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Sources