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Certificate of Analysis

NAD+ (1000mg)

Report No: NML-NADP-260608-001 Analysis Date: 2026-06-21 Report Issued: 2026-06-25
Sample Identification
Compound NAD+ (1000mg) Client Numira Peptides  ·  numira.cc
CAS Number53-84-9Date Received2026-06-17
Molecular FormulaC21H27N7O14P2Date Tested2026-06-21
Molecular Weight 663.43 g/mol PubChem CID5893
Lot Number NML-NADP-260608 Test Methods HPLC-UV · ICP-MS · Kinetic LAL
Appearance White lyophilised powder Date Reported 2026-06-25
HPLC-UV Purity & Content Analysis
1000mg
Ordered Amount
992mg
Measured Amount
99.18%
Purity (HPLC-UV)
99.2%
Recovery
Fig. 1 — HPLC-UV Chromatogram (214 nm)  ·  Run: NML_NADPLUS_NADP-260608_1.d
mAU 0 300 600 900 1200 0 2 4 6 8 10 12 Time [min] NAD+ 3.18 min
NAD+ (1000mg) vial
APPEARANCE
#Retention Time (min)Area% AreaAssignment
11.551.1E+020.30Unknown impurity
23.184.010E+0499.18NAD+
35.021.1E+020.26Unknown impurity
Bacterial Endotoxin Test (USP <85>)
MethodResultSpecificationVerdict
Kinetic LAL (USP <85>)< 0.125 EU/mL≤ 0.125 EU/mLPASS
Elemental Impurities (USP <233> / ICH Q3D)
ElementMethodResult (ppm)Limit (ppm)Verdict
Arsenic (As)ICP-MS< 0.0012.1PASS
Cadmium (Cd)ICP-MS< 0.0010.5PASS
Lead (Pb)ICP-MS< 0.0010.5PASS
Mercury (Hg)ICP-MS< 0.0013.0PASS

Note: Peptide samples may contain counter-ions (TFA, acetate) and excipients (mannitol, sucrose) used as lyoprotectants and pH buffers. These are not detected by UV and are not classified as impurities under USP <233>.

Analysis Performed by
Dr. M. Chen, Ph.D. (Analytical Chemistry)
Senior Analytical Chemist · Nexus Molecular Labs
info@nexusmolecularlabs.com
2026-06-25