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N-Acetyl Selank

Third-party tested · every batch

All tests passed Purity Quantity Identity Sterility Endo Metals Conformity TFA Solvents Solubility CCI

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Please check the product images for an attached COA, or visit our Certificate of Analysis documentation

This research-grade analytical compound 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. 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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Lot 1700 quality scorecard

Lot conforms to all release specifications. Released 2026-06-23 · by Tori Johnson, Operations Manager
25
vials consumed (estimated minimum)
2
independent ISO-17025 labs
10
analytical procedures

Testing performed at Vanguard Laboratory (Olympia, WA) · Eagle Analytical Services Inc. (Houston, TX).

Purity
3 of 3 vials pass
>99.80% · Vanguard Laboratory
HPLC-UV/VIS
Assay
11.12 mg avg
Range 10.92–11.38 mg · 3 samples · Vanguard Laboratory
HPLC-UV/VIS
Heavy metals
All non-detect
Vanguard Laboratory
ICP-MS
Residual solvents
All non-detect
Vanguard Laboratory
GC-MS
Trifluoroacetic acid
All non-detect
Vanguard Laboratory
Ion Chromatography
Endotoxins
3 of 3 vials pass
<5.00 EU/mg · Vanguard Laboratory
LAL
Container closure
3 of 3 vials pass
3 samples · Vanguard Laboratory
Dye Ingress Method
Solubility
3 of 3 vials pass
Fully Soluble in 2 mL Water · Vanguard Laboratory
Fully Soluble in 2 mL Water

Lot 1700 quality scorecard

Lot conforms to all release specifications. Released 2026-06-23 · by Tori Johnson, Operations Manager
25
vials consumed (estimated minimum)
2
independent ISO-17025 labs
10
analytical procedures

Testing performed at Vanguard Laboratory (Olympia, WA) · Eagle Analytical Services Inc. (Houston, TX).

Purity
3 of 3 vials pass
>99.80% · Vanguard Laboratory
HPLC-UV/VIS
Assay
11.12 mg avg
Range 10.92–11.38 mg · 3 samples · Vanguard Laboratory
HPLC-UV/VIS
Heavy metals
All non-detect
Vanguard Laboratory
ICP-MS
Residual solvents
All non-detect
Vanguard Laboratory
GC-MS
Trifluoroacetic acid
All non-detect
Vanguard Laboratory
Ion Chromatography
Endotoxins
3 of 3 vials pass
<5.00 EU/mg · Vanguard Laboratory
LAL
Container closure
3 of 3 vials pass
3 samples · Vanguard Laboratory
Dye Ingress Method
Solubility
3 of 3 vials pass
Fully Soluble in 2 mL Water · Vanguard Laboratory
Fully Soluble in 2 mL Water

Structure & Specification

N-Acetyl Selank Peptide Summary

Product Specifications: Lyophilized Powder (>99% purity) in 3ml vial.

*Requires Reconstitution with solvent such as BAC Water (Sold Here)

Appearance: Solid, white powder in 3mL glass ampule

Chemical Formula: C35H59N11O10

CAS Number: NA

Molecular Weight: 793.9 g/mol

Storage: Store at ≤25°C, sealed, away from heat, light, and moisture.

Disclaimer: This product is intended solely for laboratory research purposes. It is not suitable for consumption by humans, nor for medical, veterinary, or household purposes. Researchers should handle N-Acetyl Selank with care and adhere to strict safety guidelines during experiments. Kindly review our Terms & Conditions before making a purchase. *

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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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