NAD+ COA

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  • Create Date June 26, 2026
  • Last Updated June 26, 2026

NAD+ COA

Certificate of Analysis (COA) – NAD+ – Batch 202605

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Overview

This Certificate of Analysis (COA) provides batch-specific analytical documentation for NAD+ Batch 202605. The report includes HPLC purity analysis, LC-MS identity confirmation, UPLC chromatographic profiling, and optional third-party validation by SENO Test Center. The document supports laboratory quality control, batch traceability, and research-grade material verification.


Batch Information

FieldSpecification
Product NameNAD+ (Nicotinamide Adenine Dinucleotide)
Batch ID202605
BrandRPL Peptide
CategoryResearch Compound / Metabolic Research Reagent
Production StatusReleased for Laboratory Distribution
Quality StatusInternal QC Passed + Third-Party Validation (if applicable)
Third-Party LaboratorySENO Test Center
COA IDCOA-NAD-202605
Intended UseLaboratory Research Use Only

Analytical Verification Summary

Each batch undergoes standardized analytical testing to confirm identity, purity, and structural consistency prior to release.

TestMethodInstrument / LabResultStatus
Purity AnalysisHPLCInternal QC Laboratory≥98.0%Pass
Identity ConfirmationLC-MSInternal QC LaboratoryConsistent with Reference StandardPass
Chromatographic ProfileUPLCInternal QC LaboratoryWithin SpecificationPass
Optional Third-Party ValidationCross VerificationSENO Test CenterConfirmed Analytical ConsistencyPass
Final QC ReviewBatch Release AuditRPL QC SystemApprovedReleased

Certificate of Analysis Documentation

A Certificate of Analysis (COA) is a controlled laboratory document used to verify the identity, purity, and batch quality of research-grade materials.

For NAD+ Batch 202605, the COA includes:

  • Batch-specific identification and production records
  • HPLC chromatographic purity assessment
  • LC-MS molecular identity confirmation
  • UPLC chromatographic profiling (where applicable)
  • Internal quality control review
  • Optional third-party validation by SENO Test Center
  • Full batch traceability linkage

Batch Traceability System

Each NAD+ batch is assigned a unique identifier that links all production and analytical records.

This system ensures traceability across:

  • Manufacturing documentation
  • Analytical testing results
  • Internal QC approval records
  • Third-party validation reports
  • COA issuance logs

Batch traceability supports laboratory documentation integrity and quality management compliance.


Download COA

📄 Download Certificate of Analysis (COA PDF – NAD+ Batch 202605)
File Size: 2.53 MB
Last Updated: June 26, 2026


Frequently Asked Questions (FAQ)

What is a Certificate of Analysis (COA)?

A COA is a batch-specific laboratory document containing analytical test results, identity verification, and quality control approval for research materials.


What is NAD+?

NAD+ (Nicotinamide Adenine Dinucleotide) is a research-grade metabolic coenzyme involved in cellular energy transfer and redox reactions. It is not intended for human or veterinary use.


Which analytical methods are used?

Analytical testing includes HPLC for purity assessment, LC-MS for molecular identity confirmation, and UPLC for chromatographic profiling.


What is HPLC used for?

HPLC (High Performance Liquid Chromatography) is used to determine compound purity by separating and quantifying peptide or compound components.


What is LC-MS used for?

LC-MS (Liquid Chromatography–Mass Spectrometry) confirms molecular identity by comparing observed mass spectra with reference standards.


What is batch traceability?

Batch traceability is the system linking manufacturing data, analytical results, and QC documentation to ensure full lifecycle tracking of each batch.


What is SENO Test Center?

SENO Test Center is a third-party analytical laboratory used for independent validation of batch consistency and analytical results.


Is this product for human use?

No. NAD+ is supplied strictly as a research-grade laboratory reagent for scientific research use only.