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Semax

Analytical report

Batch 1665 – Semax 99.39% 10.23mg

Research Use Only (RUO) — In-Vitro Laboratory Use Only

This research-grade analytical standard is produced for controlled laboratory environments and supplied exclusively for in-vitro research. Each lot is manufactured with batch-level traceability and released only after structured, multi-point quality verification. Not for human or veterinary use.

  • Intended solely for laboratory research (RUO / in-vitro only)
  • Lot-specific Certificate of Analysis (CoA) with batch traceability
  • ≥99% purity reported per lot (see CoA)
  • 7-point testing program (analytical identity/purity plus additional quality verification per lot)
  • Endotoxin and elemental impurity screening reported per lot (see CoA)
  • Independent third-party verification, including two-lab microbial contamination testing (documentation available)
  • Sealed, tamper-evident packaging to help maintain compound integrity during storage and handling

Testing metrics and documentation are provided for analytical characterization and research reproducibility only and do not imply safety or suitability for any other use.

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Structure & Specification

Semax Peptide Summary

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Money Back Guarantee

Return or exchange your unopened product within 30 days no questions asked.
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Satisfaction Guarantee

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Always quality-tested, verified with third party COA’s

At every step, we prioritize quality by conducting rigorous third-party testing on all our products. These tests focus on four key characteristics—identity, purity, sterility, and endotoxicity—ensuring that each batch meets the highest standards for safety and performance, with independent third-party Certificates of Analysis (COAs) to verify our commitment to excellence.

1

Identity Test

Identity testing ensures that the product contains the correct ingredient as labeled, verifying its authenticity and matching it to established reference standards.

2

Purity Test

Purity and concentration testing verifies that the ingredient is present in the correct amount, with a purity of 98% or higher to meet stringent quality standards.

3

Sterility Test

Sterility testing ensures that the product is completely free from bacteria, fungi, and other microorganisms.

4

Endotoxicity

Endotoxicity testing specifically detects and quantifies lipopolysaccharides (LPS), components of bacterial cell walls, to ensure the product is free from harmful endotoxins.

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