Traceability. The analytical report behind this certificate carries no lot identifier. It covers this material at this fill weight and it names no production run, so this certificate cannot be matched to one by number. Vantage publishes it on that basis rather than implying a link the document does not print.
Results
| Test | Specification | Result | Status |
|---|---|---|---|
| Appearance Visual inspection (Vantage Aminos) | White lyophilized powder | Conforms | PASS |
| Identity HPLC-UV-MS, positive polarity (+MS) | NAD+ confirmed | 332.38 [M+4H]4+ · 663.93 [M+3H]3+ | PASS |
| Purity HPLC-UV, area % | ≥ 98.0 % | 99.955 % | PASS |
| Net content As reported by the laboratory | Report (label 500 mg) | 518.09 mg (103.6 % of label) | REPORT |
| Bacterial endotoxin LAL, USP <85> | Pass | Pass (duplicate, USP <85>) | PASS |
No chromatogram is reproduced. Vantage plots a figure only from the instrument's own exported data or one reissued by the laboratory; neither is held for this lot. Results above are transcribed from the laboratory report retained unaltered on file.
Open the certificate (PDF, opens in a new tab) Go to NAD+ All batch records
Identity and handling
Specimen readout VA-NAD-500MG
- CAS
- 53-84-9
- FORMULA
- C21H27N7O14P2
- MOL. WEIGHT
- 663.4
- FORM
- White lyophilized powder
- FILL
- 500 mg
- CONTAINER
- 3 mL vial
- MANUFACTURED
- 2026-01-07
- FILLED
- 2026-01-15
- ANALYSED
- 2026-02-16
- RETEST BY
- 2028-01-07
- STORAGE
- Refrigerated, 2-8 °C, protected from light
- DOCUMENT
- COA-VA-2602-9762 rev 1.0
Method
- Technique HPLC-UV, area %
- MS technique HPLC-UV-MS (as printed on the report)
- Ionisation Positive polarity (+MS)
- Observed mass 332.38 [M+4H]4+ · 663.93 [M+3H]3+