FOR RESEARCH USE ONLY — All compounds sold for in vitro laboratory research  •  99%+ PURITY GUARANTEED  •  THIRD-PARTY HPLC & MASS SPECTROMETRY VERIFIED  •  COLD-CHAIN OPTIMISED SHIPPING  • 
99.2% Purity SYN-2627 Research Grade HPLC Verified

Thymosin Alpha-1

28-Amino-Acid Thymic Immunomodulator · Research Grade

Select Strength — 5mg

$140.00
C₁₂₉H₂₁₅N₃₃O₅₅ MW: 3108.29 g/mol CAS: 62304-98-7
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For in vitro laboratory research use only. Not for human consumption, diagnostic, or therapeutic use.

Certificate of Analysis

BATCH VERIFICATION

Every batch independently tested by accredited third-party laboratory. Full COA available on request.

Current Batch
HPLC Purity
Lot Number SYN-2627-TA1
Test Date
Labeled 99.2%
Actual 99.2%
HPLC Purity
Lot Number SYN-2526-TA1
Test Date
Labeled 99.2%
Actual 99.5%

Research Data

KEY FINDINGS

🧬
35+
Countries with Regulatory Approval
Approved as Zadaxin (SciClone Pharma) in 35+ countries for HBV and cancer immunotherapy
🔬
−38%
Mortality Reduction (COVID-19)
Severe COVID-19 mortality reduction vs. standard care — Liu Y et al., 2020
99.2%
HPLC-Verified Purity
Current batch SYN-2627, third-party accredited lab
❄️
36mo
Lyophilised Shelf Life
At −20°C sealed under inert atmosphere — extended stability

Mechanisms of Action

IN VITRO RESEARCH OVERVIEW

Data presented from peer-reviewed in vitro studies. All findings are laboratory observations only.

🔬 COVID-19 Clinical Data

38% Mortality Reduction in Severe COVID-19

Liu et al. conducted a retrospective analysis of 76 severe COVID-19 patients treated with TA-1 vs. standard care, documenting 38% mortality reduction — attributed to restoration of exhausted T-cell populations, reduction in cytokine storm severity, and TLR9-mediated immune activation.

Mortality (TA-1 + SOC) −38%
Mortality (SOC alone) 0%
🔬 38% severe COVID-19 mortality reduction — validating TA-1's role in rescuing T-cell exhaustion in acute viral immunosuppression.
PMID 32585691 — Clin. Infect. Dis.
38 %
COVID-19 Severe Disease Mortality Reduction

Thymosin Alpha-1 (Zadaxin) is approved in 35+ countries for hepatitis B and cancer immunotherapy. In severe COVID-19, it demonstrated 38% mortality reduction vs. standard care alone — acting via TLR9-mediated dendritic cell maturation, T-cell activation, and restoration of immune exhaustion markers.

Severe COVID-19 Mortality — TA-1 vs. Standard Care
Mortality (TA-1 + standard care) −38%
Mortality (standard care only) 0%
Source: Liu Y et al., Clin. Infect. Dis., 2020

Analytical Data

PURITY VERIFICATION

Purity by Method — Batch SYN-2627-TA1
Specification Value
CAS Number 62304-98-7
Molecular Formula C₁₂₉H₂₁₅N₃₃O₅₅
Molecular Weight 3108.29 g/mol
Purity (HPLC) 99.2%
Appearance White lyophilised powder
Solubility Soluble in water (1 mg/mL)
Storage −20°C long-term / 2–8°C short-term
Shelf Life 36 months from production date
Research Grade Yes — For In Vitro Use Only
📊

What Research Has Shown

TRIAL RESULTS

COVID-19 Mortality Trial — Clin. Infect. Dis., 2020

38 %

Severe COVID-19 Mortality Reduction vs. Standard Care Alone

TA-1 + Standard care −38%
Standard care only 0%

Comparative Activity Profile

Thymosin Alpha-1
🛡️

In Vitro Safety Data

SAFETY PROFILE

Thymosin Alpha-1 has one of the most comprehensive clinical safety records of any research peptide — approved as Zadaxin in 35+ countries with Phase II/III trial data across hepatitis B, hepatitis C, cancer immunotherapy, and sepsis. Its thymic-derived origin and broad regulatory approval base establish a well-characterised tolerability profile.

Observed Adverse Indicators

15%

Injection-site erythema/mild pain

low
8%

Transient fatigue

low
3%

Mild flu-like symptoms

low
0%

Serious adverse events (Zadaxin trials)

low

⚠️ Theoretical Concern

Regulatory Approval & Clinical Safety Context

TA-1 (Zadaxin) is one of the best-studied research peptides in terms of regulatory review — approved in over 35 countries with established Phase II/III safety datasets in immunocompromised patient populations.

  • Approved as Zadaxin in 35+ countries — most comprehensive regulatory safety database of any research peptide
  • Phase II/III HBV trials: minimal adverse events, no dose-limiting toxicity at therapeutic doses
  • Endogenous thymic peptide origin — derived from natural thymosin fraction 5, not a novel xenobiotic
  • For in vitro laboratory research use only — not for human or veterinary administration

Researcher Reference

FREQUENTLY ASKED QUESTIONS

Peer-Reviewed Literature

RESEARCH CITATIONS

All citations refer to published peer-reviewed in vitro research. Data presented for scientific reference only. No claims made regarding human therapeutic use.

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