Skip to content
Cosmetic Peat
Association

By Cosmetic Peat Editorial Team Updated September 2026

← All substances

Humic Acids

Chemical Compounds
Also: HA, humic acid, humate, sodium humate, potassium humate
CAS: 1415-93-6
Molecular weight: 10,000–100,000+ Da
Solubility: Insoluble at pH < 2, soluble at higher pH
Concentration in peat: 10–40% of dry mass

If peat has a single star ingredient, this is it. Humic acids are large, complex organic molecules — dark brown to black, formed over millennia as plant material decomposes in waterlogged bogs. They make up 10–40% of peat’s dry mass and are responsible for most of the therapeutic effects that European spa medicine has observed for two centuries.

What makes humic acids unusual is their versatility. A single molecule simultaneously exhibits anti-inflammatory, antioxidant, antimicrobial, and chelating properties. Most pharmaceutical compounds do one thing well. Humic acids do several things at once — less potently than a targeted drug, but through multiple pathways that work together.

What humic acids do

Fight inflammation — through the same pathways as ibuprofen. Humic acids suppress the inflammatory signalling molecules TNF-α, IL-1β, and IL-6 (van Rensburg 2015, Klöcking 2005). These are the same signals that NSAIDs and biologic drugs target. In skin cells, humic acids from lignite significantly decreased IL-6 and IL-1β gene expression and protected keratinocytes against urban dust damage (Verrillo 2022). In a mouse model of allergic contact dermatitis, topical peat-derived humic acids suppressed a broad panel of inflammatory cytokines including IFN-γ, IL-4, IL-17, and TNF-α, and reduced serum histamine (Zhernov 2020).

There’s a fascinating dose-dependent twist: at low concentrations (10–80 μg/ml), humic acids actually increase TNF-α production by 3×. Above 100 μg/ml, they flip and decrease it by 10× (Übner 2013, citing Junek et al. 2009). A direct primary study of the same effect confirms it: low-concentration peat-derived humic acid raised TNF-α release roughly 3-fold in stimulated immune cells, reversing to a decrease at higher concentrations — while fulvic acid, tested alongside it, never triggered the pro-inflammatory phase at any concentration (Klöcking 2008). This bimodal behaviour explains why whole-peat applications — which deliver high concentrations — are anti-inflammatory, while very dilute preparations may have the opposite effect.

Kill bacteria and viruses. Of 81 natural humic acid preparations tested, 57 showed antimicrobial activity against a panel of microorganisms (Ansorg 1978). The mechanism involves disrupting bacterial cell membranes and, for viruses, occupying the positively charged glycoprotein regions that viruses need to attach to host cells (Übner 2013). A 2025 review confirms antiviral properties including viral fusion inhibition (Gvozdeva 2025). The strongest antiviral potency data in the whole knowledge graph for this compound class comes from a coal-derived relative rather than peat itself: oxihumate blocked HIV-1 infection of cultured cells at a low concentration (IC50 12.5 µg/ml), with no resistance developing over 12 weeks of exposure (van Rensburg 2002). It’s not peat-specific, but it demonstrates what the humic-acid structure is capable of.

Protect against oxidative damage. The phenolic hydroxyl groups in humic acids donate hydrogen atoms to neutralise free radicals — the same mechanism behind vitamin C and vitamin E, but delivered in a complex organic matrix (van Rensburg 2015). In an ex-vivo model using human placental mitochondria, Tolpa Peat Preparation reduced lipid-peroxidation markers with antioxidant capability comparable to vitamin E itself (Piotrowska 2000).

Filter UV radiation. Humic acids share a structural feature with melanin and absorb ultraviolet light strongly — 60–84% of UV-B and around half of UV-A at moderate concentrations. In cultured skin cells, that translated into real protection: cells shielded by a humic-acid layer before UV-B exposure suffered over 60% less cytotoxic damage, performing comparably to PABA, a reference sunscreen ingredient (Seel 2012). This is preliminary, in-vitro evidence only — no clinical or ex-vivo skin study has tested it — but it points to a possible photoprotective role alongside humic acid’s other effects on skin aging and rosacea, where UV exposure is a known trigger.

Preserve your skin’s hyaluronic acid. Humic acids neutralise hyaluronidase, the enzyme that breaks down hyaluronic acid in skin (Hinn 2026). This is the mechanism behind many expensive anti-aging serums — but instead of adding synthetic hyaluronic acid, humic acids help your skin keep the hyaluronic acid it already produces.

Chelate minerals. The carboxyl and phenolic groups in humic acids bind metal ions — iron, zinc, magnesium — keeping them bioavailable while controlling their reactivity (Stevenson 1994). Isolated humic acid shows this directly: extracted from whole peat, it had over twice the ion-exchange capacity and 120% more total sorption capacity than the raw material it came from, confirming that humic acid — not the peat matrix generally — carries most of peat’s mineral-binding capacity (Gierlach-Hladon 2008). In balneotherapy, this chelation enables mineral delivery through the skin during treatment.

In peat

Humic acids typically make up 10–40% of peat’s dry mass, depending on the source. Estonian peat reaches up to 39.3% in some deposits — among the highest measured (Orrù 2011). Finnish peat averages 24.8–26.8% across sphagnum and sedge types (Korhonen 2008). The quality threshold for balneological peat is generally set at >20% humic acid by dry weight.

Concentration increases with depth and humification — the more decomposed the peat, the more humic acid it contains. This is why cosmetic peat is sourced from deep, highly humified layers (H6–H8+ on the von Post scale), not from the surface.

How it’s studied

Humic acids are extracted from peat using alkaline solutions (sodium or potassium hydroxide), then separated by acidification below pH 2 — the humic acid precipitates while fulvic acids remain in solution. This extraction method matters: water-extractable fractions have different properties than alkali-extracted ones, and the biological activity of any humic acid preparation depends on how it was prepared.

In Poland, a standardised humic acid preparation from peat (Tolpa Peat Preparation, TPP) was registered as an immunomodulatory drug — one of the few cases where a peat-derived compound has achieved pharmaceutical registration (Übner 2013). The primary human-cell data behind that registration: TPP induced dose-dependent interferon and TNF production in human peripheral blood leukocytes at the same 10–100 μg/ml range (Inglot 1993). A small trial in human volunteers taking oral TPP for two weeks found dose-dependent shifts in T-lymphocyte subsets and inflammatory markers — a real signal, though the authors themselves flagged it as preliminary given the small group size and lack of a placebo arm (Baj 1993).

Where it matters

Humic acids are the primary active compound in virtually all peat-based treatments. They’re most relevant for:

Every face mask, bath, cream, and scalp treatment that uses whole peat or peat extract delivers humic acids as its primary bioactive component.

Evidence & Claims

exhibits anti-inflammatory (strong)

Inhibits pro-inflammatory cytokines TNF-α, IL-1β, IL-6; dose-dependent bimodal effect; suppresses allergic contact dermatitis

van-rensburg-2015 — Section 3.2 — cytokine inhibition in vitro
klocking-2005 — Review of anti-inflammatory activity of humic substances
cheleschi-2020 — In-vitro evidence of anti-inflammatory pathways in balneotherapy
flaig-1992 — Links humic substance chemistry to therapeutic effects
blonska-sikora-2024 — Anti-inflammatory properties in cosmetological context
ubner-2013 — HA dose-dependent: 10–80 μg/ml increases TNF-α 3× (pro-inflammatory), >100 μg/ml decreases TNF-α 10× (anti-inflammatory) — Junek et al. 2009 via review
klocking-2008 — Direct primary evidence for the same bimodal effect: low-concentration BLP-HA significantly increased TNF-α release (~3-fold) in LPS-stimulated U937 cells, reversing to a decrease at higher concentrations; fulvic acid (BRW-HS) did not activate the pro-inflammatory phase at any concentration tested — likely the conference precursor to Junek et al. 2009 (same research group, same cell line/endpoint)
verrillo-2022 — Lignite-derived HA significantly decreased IL-6 and IL-1β gene expression in HaCaT keratinocytes; protective against Urban Dust damage
zhernov-2020 — Topical peloid-derived HA suppressed IFN-γ, IL-4, IL-10, IL-13, IL-17, TNF-α in DNCB-induced ACD mice; reduced serum histamine
gvozdeva-2025 — 2025 review confirms HA anti-inflammatory properties via cytokine modulation and ROS scavenging
exhibits antioxidant (moderate)

Free radical scavenging via phenolic hydroxyl groups

van-rensburg-2015 — Section 3.4 — antioxidant capacity measurements
piotrowska-2000 — TPP and its fractions reduced malondialdehyde production in human placental mitochondria (ex vivo lipid-peroxidation model), antioxidant capability comparable to vitamin E
exhibits antimicrobial (moderate)

Active against gram-positive bacteria and some fungi via membrane disruption; antiviral by blocking virus attachment to cells

ansorg-1978 — MIC values against S. aureus and E. coli
ubner-2013 — HA blocks virus replication by occupying positively charged glycoprotein regions needed for cell attachment; most HA showed antibacterial activity in vitro (Ansorg, Rochus 1978)
gvozdeva-2025 — Review confirms HA antimicrobial and antiviral properties including viral fusion inhibition; references HS-Zn/Se complexes inhibiting SARS-CoV-2
van-rensburg-2002 — Not peat-specific (coal-derived oxihumate, same treatment as verrillo-2022's lignite HA): inhibited HIV-1 infection of MT-2 cells, IC50=12.5 µg/ml, via CD4/V3-loop entry blockade; no resistance over 12 weeks — strongest antiviral potency data in the graph for the humic-substance class
exhibits immunomodulatory (moderate)

TPP (Tolpa Peat Preparation) from peat HA registered as immunomodulator in Poland; stimulates interferon-α, interferon-γ, TNF-α synthesis

ubner-2013 — TPP registered as immunomodulator drug in Poland; optimal cytokine stimulation at 10–100 μg/ml; stimulates neutrophils and macrophages
inglot-1993 — Primary human-cell evidence: TPP induced dose-dependent interferon and TNF production in human peripheral blood leukocytes, optimal at 10-100 µg/ml — direct source behind the ubner-2013 review claim
baj-1993 — Human volunteers, oral TPP 50-600 mg/day x14 days: dose-dependent shifts in T-lymphocyte subsets, IL-1/IL-2, TNF-alpha, granulocyte superoxide — authors' own caveat: preliminary (n=4/dose, no placebo)
exhibits hyaluronidase-inhibition (preliminary)

Neutralizes hyaluronidase enzymes, extending natural hyaluronic acid lifespan in skin

hinn-2026 — Humic acid neutralizes hyaluronidase — citing Efert 2018 via Estonian literature
exhibits keratolytic (preliminary)

Mild softening and removal of dead skin cells

wollina-2009 — Review: peat application helps with scaling and plaque reduction in psoriasis — keratolytic component
exhibits chelation (strong)

Binds heavy metals and mineral ions via carboxyl and phenolic groups

stevenson-1994 — Chapter 9 — metal-humic complexation
gierlach-hladon-2008 — Isolated HA from Polish raised-bog peat showed 202% higher ion-exchange capacity and 120% higher total sorption capacity than whole peat, confirming HA as the primary carrier of peat's cation-binding capacity
exhibits photoprotective (preliminary)

Strongly absorbs UV-B and UV-A radiation; protects cultured human cells from UV-induced cytotoxicity in a dose-dependent manner

seel-2012 — Altteich peat HA and brown-coal HA (Humin Feed) absorbed 60-84% UV-B and ~50% UVA at 100 µg/ml; protected U937 cells from UV-B damage by >60% at 100-1000 µg/ml, comparable to PABA reference

References

van Rensburg, Constance E.J. (2015). The anti-inflammatory properties of humic substances: A mini review — University of Pretoria repository (review article)
Section 3.2 — cytokine inhibition in vitro
Klöcking, R., Helbig, B. (2005). Medical aspects and applications of humic substances — Biopolymers for Medical and Pharmaceutical Applications (Wiley-VCH)
Review of anti-inflammatory activity of humic substances
Flaig, W. (1992). Humic substances and associated small molecules from peats in balneology — Science of The Total Environment
Links humic substance chemistry to therapeutic effects
Błońska-Sikora, Ewelina, Klimek-Szczykutowicz, M. (2024). Potential Possibilities of Using Peat, Humic Substances, and Sulfurous Waters in Cosmetology — Applied Sciences
Anti-inflammatory properties in cosmetological context
Übner, Monika (2013). Ülevaade raviturbast ja turbaravist (Review of therapeutic peat and peat therapy) — University of Tartu, Pärnu College — Health Resort Laboratory
HA dose-dependent: 10–80 μg/ml increases TNF-α 3× (pro-inflammatory), >100 μg/ml decreases TNF-α 10× (anti-inflammatory) — Junek et al. 2009 via review
Klöcking, R., Junek, R., Kleiner, C., Schubert, R., Schoenherr, J.I. (2008). In vitro investigations on the effect of peat humic substances on inflammation — Proceedings of the 13th International Peat Congress (Peat Balneology section)
Direct primary evidence for the same bimodal effect: low-concentration BLP-HA significantly increased TNF-α release (~3-fold) in LPS-stimulated U937 cells, reversing to a decrease at higher concentrations; fulvic acid (BRW-HS) did not activate the pro-inflammatory phase at any concentration tested — likely the conference precursor to Junek et al. 2009 (same research group, same cell line/endpoint)
Verrillo, M., Parisi, M., Savy, D., Caiazzo, G., Di Caprio, R., Luciano, M.A., Cacciapuoti, S., Fabbrocini, G., Piccolo, A. (2022). Anti-inflammatory activity and potential dermatological applications of characterized humic acids from a lignite and a green compost — Scientific Reports
Lignite-derived HA significantly decreased IL-6 and IL-1β gene expression in HaCaT keratinocytes; protective against Urban Dust damage
Zhernov, Y.V. (2020). Application of topical peloid-derived humic acid suppresses allergic contact dermatitis — World Allergy Organization Journal
Topical peloid-derived HA suppressed IFN-γ, IL-4, IL-10, IL-13, IL-17, TNF-α in DNCB-induced ACD mice; reduced serum histamine
Gvozdeva, Y., Peneva, P., Katsarov, P. (2025). Biomedical Applications of Humic Substances: From Natural Biopolymers to Therapeutic Agents — Antioxidants
2025 review confirms HA anti-inflammatory properties via cytokine modulation and ROS scavenging
Piotrowska, D., Długosz, A., Witkiewicz, K., Pajak, J. (2000). The Research on Antioxidative Properties of TOŁPA Peat Preparation and Its Fractions — Acta Poloniae Pharmaceutica
TPP and its fractions reduced malondialdehyde production in human placental mitochondria (ex vivo lipid-peroxidation model), antioxidant capability comparable to vitamin E
Ansorg, R., Rochus, W. (1978). Studies on the antimicrobial effect of natural and synthetic humic acids — Arzneimittel-Forschung
MIC values against S. aureus and E. coli
van Rensburg, C.E.J., Dekker, J., Weis, R., Smith, T.-L., Janse van Rensburg, E., Schneider, J. (2002). Investigation of the Anti-HIV Properties of Oxihumate — Chemotherapy
Not peat-specific (coal-derived oxihumate, same treatment as verrillo-2022's lignite HA): inhibited HIV-1 infection of MT-2 cells, IC50=12.5 µg/ml, via CD4/V3-loop entry blockade; no resistance over 12 weeks — strongest antiviral potency data in the graph for the humic-substance class
Inglot, A.D., Zielińska-Jenczylik, J., Piasecki, E. (1993). Tołpa Torf Preparation (TTP) Induces Interferon and Tumor Necrosis Factor Production in Human Peripheral Blood Leukocytes — Archivum Immunologiae et Therapiae Experimentalis
Primary human-cell evidence: TPP induced dose-dependent interferon and TNF production in human peripheral blood leukocytes, optimal at 10-100 µg/ml — direct source behind the ubner-2013 review claim
Baj, Z., Zeman, K., Sułowska, Z., Majewska, E., Pokoca, L., Kocur, E. (1993). Effect of Tołpa Peat Preparation on Some Immune Parameters in Healthy Volunteers. Preliminary Data — Acta Poloniae Pharmaceutica
Human volunteers, oral TPP 50-600 mg/day x14 days: dose-dependent shifts in T-lymphocyte subsets, IL-1/IL-2, TNF-alpha, granulocyte superoxide — authors' own caveat: preliminary (n=4/dose, no placebo)
Hinn, Helena (2026). Turba väärindamine meditsiini, taastusravi ja kosmeetikatööstuse toormena (Valorization of peat as raw material for medicine, rehabilitation, and cosmetics industry) — Rae Gümnaasium (supervised by Anneli Kontson and Mall Orru, Tallinn University of Technology)
Humic acid neutralizes hyaluronidase — citing Efert 2018 via Estonian literature
Uwe Wollina (2009). Peat: A Natural Source for Dermatocosmetics and Dermatotherapeutics — Journal of Cutaneous and Aesthetic Surgery
Review: peat application helps with scaling and plaque reduction in psoriasis — keratolytic component
Stevenson, F.J. (1994). Humus Chemistry: Genesis, Composition, Reactions — Wiley (book, 2nd edition)
Chapter 9 — metal-humic complexation
Gierlach-Hładoń, T., Szajdak, L. (2008). Chemical character of humic acids isolated from raised bog — Proceedings of the 13th International Peat Congress (Peat Balneology section)
Isolated HA from Polish raised-bog peat showed 202% higher ion-exchange capacity and 120% higher total sorption capacity than whole peat, confirming HA as the primary carrier of peat's cation-binding capacity
Seel, Y., Guhr, M., Klöcking, R., Schubert, R., Schoenherr, J.I. (2012). The UV-B protective effect of humic substances provide the basis for the development of a peat lipstick — 14th International Peat Congress — Extended Abstract No. 344
Altteich peat HA and brown-coal HA (Humin Feed) absorbed 60-84% UV-B and ~50% UVA at 100 µg/ml; protected U937 cells from UV-B damage by >60% at 100-1000 µg/ml, comparable to PABA reference