Sample / demo verification record
This public sample record demonstrates how PeptideSource presents lot identity, analytical criteria, and QA release review for B2B procurement files. Live customer batches remain controlled and must be confirmed by PeptideSource QA before internal file use.
Batch summary
Purity
98.35 %
Analytical review
Values below are part of this public demo record and show the format used for batch identity, purity, residual solvent, and release-control review. Current order lots require QA matching by SKU and lot ID.
| Test item | Acceptance criteria | Result | Status |
|---|---|---|---|
| Appearance | White to off-white lyophilized powder | White to off-white lyophilized powder | Pass |
| Identification (LC-MS) | Consistent with reference standard or controlled identity file | Conforms | Pass |
| Peptide Purity (RP-HPLC) | NLT 98.0% | 98.35% | Pass |
| Related Impurities (HPLC) | Each impurity NMT 1.0%; total NMT 2.0% | Each <= 0.80%; total 1.77% | Pass |
| Mass Spectrum (ESI-MS) | 232.3 Da theoretical | 232.3 Da | Pass |
| Peptide Content (Assay) | NLT 90.0% on dry basis |
Batch documents
Use the full report and method overview when your procurement team needs a document packet for batch identity and release review.
Public Sources & References
| 96.1% |
| Pass |
| Water Content (Karl Fischer) | NMT 7.0% | 2.5% | Pass |
|---|
| Residual Solvents (GC) | ACN NMT 410 ppm; DCM NMT 600 ppm; MTBE NMT 5000 ppm | ACN 136 ppm; others N.D. | Pass |
|---|
| Heavy Metals (as Pb) | NMT 10 ppm | < 2 ppm | Pass |
|---|
| Bacterial Endotoxins | NMT 1 EU/mg | < 0.10 EU/mg | Pass |
|---|
| Microbial Limits | TAMC NMT 100 cfu/g; TYMC NMT 100 cfu/g | TAMC < 20; TYMC < 20 cfu/g | Pass |
|---|
| Fill Content | Catalog fill +/-10% | 10 mg / vial | Pass |
|---|