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Home / Encyclopedia / Recovery & Healing / Thymosin Alpha-1
MONOGRAPH No. 097
EVIDENCE BASEStrong
SEQUENCE
28 amino acids
MW
3108 g/mol
CAS
62304-98-7
APPROVED AS
Zadaxin (30+ countries)
EU STATUS
Research only
MIN PURITY
≥98% HPLC
View prices →
🧬 Recovery & Healing

Thymosin Alpha-1 — the immune modulator.

Thymosin Alpha-1 (Tα1) is a 28-amino acid peptide naturally produced by the thymus gland. It is an approved drug in over 30 countries (as Zadaxin) for immune-related conditions, making it one of the better-validated peptides in this category.

Last reviewed:

What is Thymosin Alpha-1?

Thymosin Alpha-1 is a naturally occurring thymic peptide central to T-cell maturation and immune regulation. It enhances the function of immune cells (T-cells, dendritic cells, NK cells) and modulates inflammatory responses. It is approved as Zadaxin in many countries for hepatitis B/C, as a vaccine adjuvant, and as an immune support agent — though not approved in the EU or US.

What does the research show?

EVIDENCE SUMMARY
STRONG
Immune modulation — Extensive clinical data supporting its approval in 30+ countries. Enhances T-cell and NK-cell function.
MODERATE
Antiviral adjunct — Clinical use as adjunct in hepatitis B/C and as a vaccine adjuvant in approved markets.
MODERATE
Sepsis & critical illness — Studied during COVID-19 and in sepsis with mixed-to-encouraging results.
Approved as a pharmaceutical (Zadaxin) in many countries but not in the EU. Research-grade product sold in Europe is for laboratory research only and is not the approved drug. This is a research compound, not a medication.

What to look for when buying in Europe

Among the better-validated peptides clinically. Research-grade Tα1 should be ≥98% HPLC with mass-spec confirmation. PeptideCompare tracks several EU vendors.

✓ PeptideCompare tracks Thymosin Alpha-1 from 7 COA-verified EU vendors, starting from €30.19. Prices move month to month and differ by vendor; compare before ordering.

Molecular information

Molecular formula
C129H215N33O55
Molecular weight
3108 g/mol
CAS number
62304-98-7

Pharmacokinetics

Half-life (t½)
≈ 2 h
Source: Rost KL, et al. Int J Clin Pharmacol Ther 1999 — SC pharmacokinetics in healthy volunteers

Potency retained over time

Each line is one storage condition: it starts at 100% and falls as potency is lost. Above the dashed 80% line the material is considered reliable — hover for exact values.

Freezer −20 °C
36+ mo
Stable · >95% potency
Fridge 4 °C
3-4 mo
In use · after recon
Room 20 °C
10-13 days
Limited · moderate loss
Warm 37 °C+
2-3 days
Critical · rapid degradation

⚠ Modelled per compound from molecular structure — chain length, cyclisation, oxidation- and deamidation-prone residues and light sensitivity. Indicative only, not lab-measured per batch.

Compare Thymosin Alpha-1 across EU suppliers

7 EU vendors · COA-verified · from €30.19 · Updated monthly

References

  1. ETASS, a multicentre randomised controlled trial of thymosin alpha-1 in severe sepsis across six Chinese teaching hospitals, with 28-day all-cause mortality as the primary outcome. The largest single trial behind the sepsis claims. Wu J, et al. Crit Care. 2013;17(1):R8. (ETASS trial) PMC4056079
  2. Systematic review of 19 randomised trials. Mortality was reported in 10 of them, covering 530 patients, with a pooled risk ratio of 0.59 (95% CI 0.45–0.77). The authors themselves flag small sample sizes and weak study design as the limiting factor. Li C, et al. BMC Infect Dis. 2016;16:488. PMC5025565
  3. More recent meta-analysis restricted to monotherapy and excluding the COVID-19 period: 11 trials, 967 versus 960 patients, 28-day mortality odds ratio 0.73 (95% CI 0.59–0.90). A smaller effect than the 2016 review — the usual direction of travel as trial quality improves. Zhang Y, et al. Front Cell Infect Microbiol. 2025;15:1673959. PMC12440967
  4. Pharmacokinetics after subcutaneous injection of three formulations in healthy volunteers — the human study behind the half-life shown above, rather than a literature estimate. Rost KL, et al. Int J Clin Pharmacol Ther. 1999;37(1):51–57.

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