NAD+ — Certificate of Analysis
Vial Collection
NAD+
NAD+
certificate of analysis.
CAS53-84-9
Latest Purity99.40%
Batches Tested3
Endotoxin< 0.1 EU/mg
Batch history.
3 tests · Vial Collection| Batch | Date | Purity (HPLC) | Impurities | Water | Endotoxin | Microbial | Status | Certificate |
|---|---|---|---|---|---|---|---|---|
| BH-V-101-2026-05-A | 29 May 2026 | 99.40% | 0.30% | 0.45% | < 0.1 EU/mg | < 10 CFU/g | PASSED | REQUEST |
| BH-V-088-2025-10-B | 01 Oct 2025 | 99.38% | 0.33% | 0.48% | < 0.1 EU/mg | < 10 CFU/g | PASSED | REQUEST |
| BH-V-042-2025-06-C | 01 Jun 2025 | 99.42% | 0.28% | 0.44% | < 0.1 EU/mg | < 10 CFU/g | PASSED | REQUEST |
Methodology
How we
How we
test.
Every batch is independently verified at our Lausanne reference lab. Identity by HPLC-MS, purity by HPLC-UV at 220 nm, and endotoxin by USP <85> LAL kinetic chromogenic assay.
Identity
HPLC-MS confirmation against certified reference standard. Molecular mass within ±0.5 Da of theoretical.
Purity
HPLC-UV at 220 nm, gradient elution. Acceptance ≥99.0%. Related impurities sum < 1.0%.
Endotoxin
USP <85> LAL kinetic chromogenic. Acceptance < 0.5 EU/mg per USP General Chapter.
Microbial
USP <61>/<62> — total aerobic count, yeasts and moulds, absence of specified organisms.