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Certificate of Analysis

NAD+

Batch H2326074 · Tested August 6, 2026

Third-Party Lab Tested

Independent laboratory testing confirms purity, composition, and endotoxin safety per USP <85> standards. Results apply only to this specific batch; for research use only.

Sample Summary

Identification and intake details for this tested batch.

Product
NAD+
Batch / Lot
H2326074
Accession #
2608060654
Test Date
August 6, 2026
Appearance
White Lyophilized Powder
Identity
Confirmed via LC-MS

Purity Analysis

HPLC with UV detection coupled with mass spectrometry (LC-MS)

Purity (HPLC-UV)
99.84%
Identity (LC-MS)
NAD+
Net Peptide Content
123.73 mg
Test Method
HPLC with UV detection coupled with mass spectrometry (LC-MS)
What this test measures

High-performance liquid chromatography with UV detection separates the peptide from related impurities and quantifies each fraction. Mass spectrometry confirms molecular identity by measuring the exact mass-to-charge ratio.

Endotoxin Analysis

Limulus Amebocyte Lysate assay in accordance with USP <85>.

Result
✓ Cleared (below threshold)
Sensitivity
≤0.05 EU/mL
What this test measures

The LAL assay detects bacterial endotoxin at the reporting threshold shown. Both replicates must be below the threshold established by USP Chapter <85> to clear. For research-grade material handling only.

Freedom Diagnostics
Issued08/06/2026

Full Certificate PDF

Signed laboratory-issued PDF with chromatogram and mass confirmation plots.

Test History for NAD+

24 independent lab tests on file for this product.

99.76%
Avg Purity · 23 batches
99.38% – 99.97%
Range
9 on file
Endotoxin Tests
99.84%
Batch H2326074
Aug 6, 2026 · Purity + Endotoxin
Current
99.70%
Batch H2126074
Aug 6, 2026 · Purity + Endotoxin
View →
99.89%
Batch A2926057 · 1000mg
Jul 31, 2026 · Purity + Endotoxin
View →
99.38%
Batch A2926015 · 500mg
Jul 29, 2026 · Purity
View →
99.84%
Batch B0526 · 500mg
Jul 9, 2026 · Purity
View →
99.97%
Batch A1226 · 1000mg
Jul 9, 2026 · Purity
View →
99.56%
Batch F2426074 · 100mg
Jul 8, 2026 · Purity + Endotoxin
View →
99.57%
Batch F2426015 · 500mg
Jul 3, 2026 · Purity + Endotoxin
View →
99.66%
Batch A1226 · 500mg
Jul 1, 2026 · Purity
View →
99.82%
Batch D1526015 · 500mg
Jun 26, 2026 · Purity + Endotoxin
View →
99.82%
Batch D1526057 · 1000mg
Jun 26, 2026 · Purity + Endotoxin
View →
99.78%
Batch D1526057 · 1000mg
Jun 24, 2026 · Purity + Endotoxin
View →
99.97%
Batch F2426057 · 1000mg
Jun 23, 2026 · Purity
View →
99.70%
Batch A1226 · 100mg
Jun 10, 2026 · Purity
View →
99.83%
Batch A1226 · 1000mg
Jun 4, 2026 · Purity
View →
Cleared
Batch B1326015 · 500mg
Apr 27, 2026 · Endotoxin
View →
99.64%
Batch B1326015 · 500mg
Apr 27, 2026 · Purity
View →
99.79%
Batch B0526 · 500mg
Mar 24, 2026 · Purity
View →
99.77%
Batch 57ABF · 1000mg
Jan 16, 2026 · Purity
View →
99.76%
Batch 15ABF · 500mg
Jan 16, 2026 · Purity
View →
99.78%
Batch 64CBF · 700mg
Jan 12, 2026 · Purity
View →
99.89%
Batch 63CBF · 300mg
Jan 12, 2026 · Purity
View →
99.71%
Batch 15CBF · 500mg
Jan 7, 2026 · Purity
View →
99.75%
Batch 15HBE · 500mg
Aug 25, 2025 · Purity
View →

Frequently Asked Questions

Quick references for what each test means.

What is HPLC-UV purity testing?
High-Performance Liquid Chromatography (HPLC) separates the peptide from related impurities based on how strongly each molecule interacts with a chromatographic column. A UV detector quantifies each separated fraction, and the total peptide peak area divided by all peaks yields the purity percentage.
What does LC-MS confirm?
Liquid Chromatography–Mass Spectrometry (LC-MS) confirms the peptide's molecular identity by measuring its exact mass-to-charge ratio. This verifies the peptide is what it claims to be — not a related molecule with a similar chromatographic profile.
Why are endotoxin tests run in duplicate?
USP <85> requires duplicate analysis to rule out measurement error. Both replicates must be below the sensitivity threshold (typically ≤0.05 EU/mL) for the batch to pass. Disagreement between replicates triggers a re-test.
Does "Cleared" mean safe for human use?
No. "Cleared" here means the batch meets the USP <85> endotoxin reporting threshold — a standard relevant to laboratory research materials. All products from Oath Research are strictly for research use only and are not approved for human, veterinary, diagnostic, or therapeutic applications.
Are all my orders from this exact batch?
Not necessarily — batches are rotated as inventory moves. Check the batch code on your vial against the test history above to find the matching certificate. Every batch we sell has been independently tested.
Research Use Only The peptides tested are intended for research use only and are not approved for human or veterinary use, diagnostic, therapeutic, or clinical applications. Results apply only to the specific sample provided and should be interpreted by qualified professionals within the scope of the intended research.
NAD+
NAD+
99.84% · Endo Cleared
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