The N-acetyl Epithalon Amidate Analysis is a targeted laboratory test designed to confirm the identity, determine the amount, and assess the peptide purity of N-acetyl Epithalon Amidate 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 Epithalon Amidate
N-acetyl Epithalon Amidate is a modified analogue of Epithalon, a short synthetic peptide studied primarily in relation to cellular aging, telomere biology, and neuroendocrine regulation.
This form is used primarily as a research compound, and scientific data specifically focused on N-acetyl Epithalon Amidate remain limited.
Key Features
- Targeted identification and quantification of N-acetyl Epithalon Amidate
- 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 Epithalon Amidate
- Other names: NA Epithalon Amidate, NA Epitalon Amidate
- 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 prevent the sample from absorbing moisture
- Average turnaround time: 7 business days
Important Notice
- This analysis is specifically intended for N-acetyl Epithalon Amidate. Before ordering, please make sure that the sample contains this specific modified form and not another version of Epithalon.
- The analysis does not automatically screen the sample for standard Epithalon, other Epithalon analogues, 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 minimise moisture absorption.
- 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
