QS-21-Api

Synthetic Saponin Vaccine Adjuvant – Apiose Isomer

The major isomeric constituent of the QS-21 fraction. Now fully synthetic. Exceptional potency for humoral and cell-mediated immune responses.

Purity ≥95% (HPLC)
Mol. Weight ~1989 Da
Grade Research / GMP
Formula C₁₂₃H₁₉₄O₇₀
QS-21-Api Molecular Structure
Catalog # STR-QS21A-001
CAS 1450904-00-5
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Synthetic Purity

≥95% purity via HPLC. Zero plant-derived impurities. Eliminate biological contaminants from your research.

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Batch Consistency

Identical molecular structure every time. Ensure reproducible results in clinical trials with zero biological variation.

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Secure Supply

Not dependent on natural harvest. Scalable GMP production ensures reliable supply for global demand.

Product Details

Catalog Number STR-QS21A-001
CAS Number 1450904-00-5
Molecular Formula C123H194O70
Molecular Weight ~1989 Da
Purity ≥95% (HPLC)
Primary Function Potent Immunostimulant
Solubility Water-soluble (rec. PBS pH 7.4)
Storage -20°C, protect from light/moisture
Appearance White to off-white lyophilized powder
Grade Research / GMP available
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Synthetic Provenance: Produced via controlled semi-synthesis, ensuring molecular homogeneity and zero plant-derived impurities.
Consistent composition for reproducible research.

Available Grades

verified Research Grade verified GMP Grade

GMP-grade material is produced under cGMP conditions and is accompanied by full documentation including a Drug Master File (DMF) submission. Contact us for GMP pricing and documentation.

Synthetic vs. Natural QS-21

Natural QS-21 is extracted from the bark of the Quillaja saponaria tree, a process subject to seasonal variability, supply chain fragility, and batch-to-batch inconsistency. Our synthetic QS-21-Api eliminates all of these risks.

Attribute Natural Extract Synthetic (STR)
Purity 70–85% ≥95%
Batch consistency Variable Identical
Supply security Seasonal / fragile Year-round
Contaminants Possible None
Regulatory risk Higher Lower
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Sustainability: Synthetic production eliminates the need for bark harvesting, preserving Quillaja saponaria populations and reducing environmental impact.
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Supply Guarantee: Our synthetic process is not subject to seasonal fluctuations, natural disasters, or geopolitical disruption. Scalable to tonnes.

Structural Features

  • Apiose terminal sugar — distinguishes the Api isomer from the Xyl isomer
  • Quillaic acid triterpene core — essential pharmacophore
  • Acyl chain domain — mediates immune cell membrane interaction
  • Branched trisaccharide — contributes to water solubility
  • Fucose-containing sugar chain — modulates immune receptor binding
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[Detailed Annotated Molecular Diagram]

Full structural data available in the Technical Data Sheet

Quality Control Data

Each batch undergoes comprehensive analytical characterization. Representative data packages include HPLC chromatograms, mass spectrometry, and NMR spectra.

Batch-Specific Documentation

Certificates of Analysis (CoA) are provided with every shipment. To request a CoA for a specific batch prior to ordering, use the button below.

TRUSTED GLOBALLY

Proven in Vaccine Development

Our adjuvants support research programs aligned with the most impactful vaccines in development.

≥98%
Product Purity
3
Adjuvant Platforms
GMP
Manufacturing Standard

STR Technologies adjuvants are used in research programs worldwide, including the development of vaccines aligned with Shingrix® (herpes zoster), Mosquirix® (malaria), and Covovax® (COVID-19) — all of which rely on QS-21-based adjuvant systems.

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