The N-Acetyl Selank Analysis is a targeted laboratory test designed to confirm the identity, determine the amount, and assess the peptide purity of N-Acetyl Selank in lyophilised vials and raw active pharmaceutical ingredient (API) powders.
For lyophilised samples, results are reported in milligrams per vial together with peptide purity. Raw API powders can be evaluated using purity in % (m/m) together with peptide purity.
About N-Acetyl Selank
N-Acetyl Selank is a modified form of Selank, a synthetic peptide studied primarily in relation to anxiety, stress responses, and neurochemical signalling.
This form is used primarily as a research compound, and scientific data specifically focused on N-Acetyl Selank remain limited. Research on the parent peptide Selank has examined its anxiolytic and neuroactive properties.
Key Features
- Targeted identification and quantification of N-Acetyl Selank
- Determination of peptide purity
- Suitable for lyophilised vials and raw API powders
- Analysis by HPLC
- Results for lyophilised samples reported in mg per vial and peptide purity
- Alternative result format for raw API powders includes purity in % (m/m) and peptide purity
- Minimum sample amount of one whole unopened vial with lyophilisate
- Minimum sample amount of 30 mg for raw API powders
- Average turnaround time of 7 business days
Analysis Parameters
- Target compound: N-Acetyl Selank
- Other name: NA Selank
- Testing method: HPLC
- Minimum amount of target compound for evaluation: Less than 1/20 of the usual dosage per vial
- Result format for lyophilised samples: mg per vial and peptide purity
- Result format for raw API powders: Purity in % (m/m) and peptide purity
- Minimum sample amount for lyophilised samples: One whole unopened vial with lyophilisate
- Minimum sample amount for raw API powders: 30 mg in a sealed glass vial to protect the sample from moisture
- Average turnaround time: 7 business days
Important Notice
- This analysis is specifically intended for N-Acetyl Selank. Before ordering, please make sure that the sample contains this specific form and not another version of Selank.
- The analysis does not automatically screen the sample for standard Selank, N-Acetyl Selank Amidate, other Selank variants, related peptides, degradation products, contaminants, or undeclared substances.
- For lyophilised samples, one whole unopened vial containing lyophilisate is required.
- Raw API powder should be supplied as at least 30 mg in a sealed glass vial to protect the sample from moisture.
- The alternative result format for raw API powders includes both purity in % (m/m) and peptide purity.
Optional Additional Analyses
The following optional laboratory services are available:
- TFA Analysis
- Complete Raw Analytical Data
- Fentanyl Screening
- Alternative Result Format: Purity in % (m/m)
- Batch Variance Testing
- pH Measurement
- Endotoxin Analysis
- CHNS Mass Report
- LCMS Screening for Peptide Contamination
- Sterility Testing (TAMC + TYMC)
- Heavy Metals Analysis (As, Cd, Pb, Hg)
- Additional Laboratory Report
