Illustrative chrome-paper vial, not inventory photography. Supplied label claims are not verified analytical results.
Laboratory research material
NAD+ Laboratory Research Material
KCC-NAD-500
500 mg
Cataloged for qualified non-clinical laboratory research; identity and lot documentation are required before release.
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IDENTITY & SPECIFICATIONS
Exact identity first.
- Catalog number
- KCC-NAD-500
- Material identity
- NAD+ Laboratory Research Material
- Nominal amount
- 500 mg
- Material type
- Laboratory research material
- Use classification
- Laboratory research use only
Molecular identity
Published structural information for research review—not measured results, a certificate of analysis, or confirmation of a KCC lot’s identity. Match the exact form to released supplier and lot documentation before use.
β-Nicotinamide adenine dinucleotide (NAD+)
Oxidized NAD, reference form
Not applicable—this compound is not a peptide.
- Reference formula
- C21H27N7O14P2
- Reference molecular weight
- 663.43 g/mol
- Reference CAS
- 53-84-9
Dinucleotide cofactor, not a peptide: an amino-acid sequence does not apply. NADH and NMN are distinct compounds; salt and hydration state require confirmation.
How to read the notation
Sequences run from N to C. Ac = acetyl; -NH2 = C-terminal amide; -OH = free C-terminal acid; D- marks stereochemistry; Aib = α-aminoisobutyric acid; Nle = norleucine; pGlu = pyroglutamate; γ-Glu = gamma-glutamyl linkage; AEEA = 2-[2-(2-aminoethoxy)ethoxy]acetic acid. Lipid linkers and ring closures are described separately. Molecular weights are reference molar masses, not measured MS peaks or per-vial amounts.
Reference review: September 6, 2026 · Research use only
RESEARCH CONTEXT
Research areas & sources.
NAD cofactor biology, mitochondrial transport, and cellular energy metabolism.
These references explain the research classification. They are not evidence of testing, purity, safety, or efficacy for a KCC Labs product or lot, and do not authorize human or veterinary use.
AVAILABLE LOTS
Release-specific status.
Check this material's current availability and documentation status. Documentation-pending purchases require acknowledgment; an approved COA is published only after release review.
ANALYTICAL DOCUMENTS
Evidence tied to the lot.
A generic certificate is not evidence for this material. Published COAs must correspond to the exact released batch.
Review the quality framework →STORAGE & HANDLING
Follow the applicable COA and documentation.
Storage, handling, physical form, and stability conditions may vary by material and lot. Use only the instructions supplied with the released documentation and your institution’s approved laboratory procedures. Do not rely on third-party clinical or administration protocols.
What the lab record should establish
Documentation guide—not a claim that these assays have been performed. Only the approved document for the exact lot can establish results. An absent report means no result is published, not that a test passed.
- Identity & structure
- Mass spectrometry / LC–MS and sequence or structural confirmation, as applicable.
- Purity & content
- Lot-specific chromatogram, method and purity result; net compound content reported separately from chromatographic area percentage.
- Chemical form & impurities
- Counterion, hydration, residual solvents and relevant elemental impurities, where characterized.
- Handling & traceability
- Exact lot, SDS, physical form, storage conditions and supported retest or expiry date. Microbiological or endotoxin results only when applicable and documented.
PROCUREMENT



