Certificate PL-26-00247 · NAD+ 1000 mg · lot PL-2610-133
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PrymaLab
PrymaLab
PrymaLab Analytical · In-house laboratory
3705 Music Branch Rd, Ashland, KY 41102 · +1 (606) 465-9063 · prymalab.net
Certificate no.
PL-26-00247
Verification key
EX7MSTY4
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Certificate of Analysis · Lot release

NAD+ 1000 mg

Lot PL-2610-133 · Lyophilized powder · Label claim 1000 mg per vial
Tested in-house by PrymaLab
In-house analytical result,
not an independent third-party test
Lot / batch number
PL-2610-133
Date made
2026-10-05
Date of analysis
2026-10-06
Date issued
2026-10-20
Retest / expiry
2028-10-05
Units in lot / sampled
180 / 2
Storage
−20 °C, tightly sealed, dry, dark
Certificate type
Lot COA, 2 pages
Compound
NAD+
β-Nicotinamide adenine dinucleotide, oxidized (free acid); coenzyme, not a peptide
CAS number
53-84-9
Molecular formula
C21H27N7O14P2
Theoretical mass (avg.)
663.43 Da
Structure
Purity · RP-HPLC, area %
99.60%
Specification ≥ 99.0% • main peak at 6.80 min
Identity · Observed Mass
663.44 Da
Theoretical 663.43 Da • +0.01 Da (15 ppm)
Overall conclusion
PASS
Meets every specification for the tests performed
TestMethodSpecificationResultConclusion
Identity (mass)LC-MS, ESI positiveTheoretical ± 1.0 Da663.44 DaPASS
PurityRP-HPLC, UV 254–306 nm, area%≥ 99.0%99.60%PASS
Largest impurityRP-HPLC, area%≤ 1.0%0.27% (RT 7.60)PASS
Water contentKarl Fischer≤ 5.0%1.62%PASS
Bacterial endotoxinLAL, kinetic≤ 5.0 EU/mg0.294 EU/mgPASS
SterilityUSP <71>, 14-dayNo growthNo growthPASS

1HPLC chromatogram

Data file: PL-2610-133-HPLC.raw · Column C18, 150 × 4.6 mm · UV 254–306 nm
0.01%0.1%1%10%100%45678910Retention time (min) · stick height = area % (log scale)99.60% · 6.80 min0.07% †0.27% †0.06% †
Peak plot drawn from the integrated peak table (area %, log scale); it is not the instrument trace, which is retained in PL-2610-133-HPLC.raw. † Nominal reference retention time for the assigned impurity; the main-peak RT is observed in this lot.
PrymaLab
PrymaLab
Certificate of Analysis · continued
NAD+ 1000 mg · Lot PL-2610-133 · Certificate PL-26-00247
Lot PL-2610-133
Method, peak table and approval

2HPLC method · PL-2610-133-HPLC.raw

Instrument
Waters Alliance e2695
Data System
Empower 3
Detector
UV absorbance
Detection Wavelength
254–306 nm
Column
C18, 150 × 4.6 mm, 3.5 µm
Mobile Phase A
0.1% TFA in water
Mobile Phase B
0.1% TFA in MeCN
Gradient
5–95% B over 25 min (linear)
Flow Rate
1.0 mL/min
Column Temperature
40 °C
Injection Volume
10 µL

3Gradient program

Time (min)% A% B
0.0955
25.0595

4Peak table

PeakRT (min)AreaArea %
15.70 †—0.07
26.80—99.60
37.60 †—0.27
48.40 †—0.06
Total—100.00
Peaks: 1 nadh; 2 main peak (NAD+); 3 adp-ribose; 4 unidentified impurity · Area % from the integrated peak table (absolute areas are not part of the lot-release export) · † nominal reference RT for the assigned impurity · Purity = main peak area ÷ total integrated area × 100, to two decimals; main peak shaded.

5Identity by mass spectrometry

Instrument
Waters SQD
Ionization / Mode
ESI, positive
Reference m/z (ion)
664.44 [M+H]+
Deconvoluted Mass
663.44 Da
Theoretical Mass
663.43 Da
Difference
+0.01 Da (15 ppm)
Data File
PL-2610-133-MS.d
Acceptance
Within ± 1.0 Da

6Additional tests

TestPerformed byDateReport / file
Water content (Karl Fischer)PrymaLab Analytical2026-10-06—
Endotoxin (LAL, kinetic)PrymaLab Analytical2026-10-06—
Sterility (USP <71>, day-14 read-out)PrymaLab Analytical2026-10-20—
A test with no row here was not performed on this lot. Outside-laboratory reports, when used, are attached and named below.

7Review and approval

D. Reynolds
Analyst · performed the testing
Date: 2026-10-20
S. Calloway
Reviewer · checked against raw data
Date: 2026-10-20
M. Phelps
Lab Director · approved for release
Date: 2026-10-20