Precision Research ChemicalsThird-Party TestedBatch-Specific CoASame-Day Shipping14 Compounds99%+ Purity
Precision Research ChemicalsThird-Party TestedBatch-Specific CoASame-Day Shipping14 Compounds99%+ Purity
KERN
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NAD+ (1000mg)

NAD+

Nicotinamide adenine dinucleotide. Coenzyme in all living cells. Extensively studied for cellular energy metabolism and longevity.

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$552.75$569.85USD

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Research Use Only. This product is intended for laboratory research purposes only. Not for human or veterinary use. Not for sale to minors.

Certificate of Analysis

Latest

Independent third-party analytical certificates for NAD+. A batch-specific CoA is provided with every purchase.

01At a Glance01 / 08

NAD+ — Key Data

A snapshot of published research on NAD+. Each figure links to the literature summarized below.

Plasma NAD+ Increase
0750 mg IV infusion over 6 hours (Grant et al.)
CD38 vs NAD+
0Near-perfect inverse correlation drives age-related decline
Decline by Age 60
0Human skin tissue measurements
SIRT3 Activity
0When CD38-driven NAD+ consumption is blocked
Oral Bioavailability
0Why subcutaneous delivery matters for NAD+
02Mechanism02 / 08

How NAD+ Works

NAD+ is a coenzyme found in every living cell, serving as an electron carrier in mitochondrial energy production and a required substrate for sirtuins, PARP enzymes, and CD38. Cellular NAD+ levels decline 10-50% across all tissues during aging, driven primarily by a 2-3x increase in CD38 (the main NAD+ consumer). The correlation between CD38 and NAD+ levels is r = -0.99. For research use only.

Discovered 190610,000+ publicationsFirst described by Arthur Harden and William John Young as a cell-free fermentation factor

  1. 01

    Sirtuin Activation

    Primary
    • 3.5x SIRT3 activity when NAD+ levels are preserved
    • SIRT1-7 require NAD+ as a co-substrate for deacetylation
    • Sirtuin activity directly tracks available NAD+ levels
  2. 02

    CD38 / NADase Axis

    Primary
    • 2-3x CD38 protein increase with aging (all tissues)
    • r = -0.99 correlation between CD38 and NAD+ levels
    • CD38 knockout mice show no age-related NAD+ decline
  3. 03

    PARP / DNA Repair

    Secondary
    • PARP1 activation depletes NAD+ during DNA damage repair
    • ~85% NAD+ reduction possible from sustained DNA repair activity
    • PARP inhibition as alternative strategy to supplementation
03Findings03 / 08

What the Studies Show

Peer-reviewed outcomes from published NAD+ research.

0

750 mg infused over 6 hours in 8 subjects. No rise until after 2 hours (initial NAD+ consumed by liver). 538% urinary excretion increase. Liver function markers improved.

Grant et al., 2019

Additional Clinical Outcomes

  1. 0

    Human skin tissue. Subjects aged 61-77 vs 23-30. Brain decline 10-25%. Liver decline ~30%. 10-50% decline across all tissues measured.

    Covarrubias et al., 2021
  2. 0

    250 mg NMN daily for 12 weeks in older men (avg age 71). 1.45 to 1.60 m/s vs placebo decline. p = 0.015. Left grip strength also improved.

    Igarashi et al., 2022

NAD+ Delivery Method Comparison

+398% plasma
IV Infusion (750mg)
Bypasses GI
Subcutaneous
2-10% bioavailable
Oral NAD+

Grant et al., 2019 (8 subjects, 750mg over 6 hours)

04Applications04 / 08

Research Applications

Reported areas of investigation across the NAD+ literature.

  1. 01
    SIRTUIN ACTIVATION

    Sirtuin-Dependent Longevity Pathways

    All 7 sirtuins (SIRT1-7) require NAD+ as a co-substrate. Preserving NAD+ levels enables 3.5x SIRT3 activity for mitochondrial health.

    SIRT3 activity increase
    3.5x
    Sirtuins requiring NAD+
    All 7

    Study finding. Sirtuin activity directly tracks available NAD+ levels, making NAD+ the rate-limiting factor for longevity pathways.

  2. 02
    PHYSICAL FUNCTION

    Gait Speed and Strength

    Older men (avg age 71) showed 10% gait speed improvement and left grip strength gains with 250mg NMN daily for 12 weeks.

    Gait speed increase
    +10%
    Study duration
    12 weeks
    Significance
    p = 0.015

    Study finding. Gait speed: 1.45 to 1.60 m/s vs placebo decline. Left grip strength also improved.

    Igarashi et al., 2022
  3. 03
    METABOLIC HEALTH

    Plasma NAD+ Restoration

    IV infusion of 750mg over 6 hours produced 398% plasma NAD+ increase with improved liver function markers.

    Plasma NAD+ increase
    +398%
    Urinary excretion increase
    +538%

    Study finding. No rise until after 2 hours (initial NAD+ consumed by liver), then dramatic increase at 6 hours.

    Grant et al., 2019
05Safety05 / 08

Reported Observations

  • IV administration: flushing, nausea, chest tightness, mild GI discomfort (transient, dose-dependent)
  • Subcutaneous: injection-site reactions reported
  • No serious adverse events attributed to NAD+ in published clinical studies

This summary reflects observations from published peer-reviewed research. It is not a comprehensive safety assessment. Researchers should review primary literature before designing protocols. For Research Use Only.

06Compound06 / 08

Compound Profile

Molecular Profile

What Is NAD+?

TypeCoenzyme / Dinucleotide
CAS Number53-84-9
Molecular Weight663.43 g/mol
FormulaC21H27N7O14P2
View on PubChem
Storage & Handling

Stability Information

  • Protect from light and moisture
  • Hygroscopic -- keep sealed
  • Avoid repeated freeze-thaw cycles

Lyophilized

Up to 2 years

-20C

Reconstituted

Up to 7 days

2-8C

Working solution

Use within 8 hours

Room temp
07Questions07 / 08

NAD+ (nicotinamide adenine dinucleotide) is a coenzyme found in every living cell. It plays a central role in cellular energy metabolism, serving as an electron carrier in the mitochondrial electron transport chain. NAD+ is also a required substrate for sirtuins (SIRT1-7), PARP enzymes involved in DNA repair, and CD38, which regulates immune function. Cellular NAD+ levels decline significantly with age, a finding that has made it one of the most researched molecules in the longevity field.

NAD+ is the active coenzyme itself. NMN (nicotinamide mononucleotide) and NR (nicotinamide riboside) are precursors that the body converts into NAD+ through different enzymatic pathways. Oral NMN and NR supplements are widely available, but their conversion efficiency is debated. Research-grade NAD+ in lyophilized form is the direct molecule, bypassing the conversion step entirely. Dr. Eric Verdin of the Buck Institute has noted that NAD+ itself is too large to enter cells directly and is likely broken down into nicotinamide before being resynthesized intracellularly.

Reconstitute lyophilized NAD+ with bacteriostatic water. For a 500mg vial, 5mL of bacteriostatic water yields a concentration of 100mg/mL. Introduce water slowly along the vial wall and allow the powder to dissolve without shaking. Store reconstituted NAD+ refrigerated at 2-8C and use within 30 days. NAD+ has a relatively short plasma half-life (approximately 14 minutes), which is relevant for research protocol design.

Published clinical research on IV NAD+ administration has reported flushing, nausea, chest tightness, and mild gastrointestinal discomfort as the most common observations. These effects are generally described as transient and dose-dependent in the literature. Subcutaneous administration research has reported injection-site reactions. No serious adverse events have been attributed to NAD+ in published clinical studies.

Research-grade NAD+ undergoes rigorous synthesis, purification, and third-party testing (HPLC and mass spectrometry) to confirm identity, purity, and sterility. Oral NMN supplements are manufactured to dietary supplement standards, which are significantly less stringent. The cost difference reflects the difference in manufacturing standards, testing requirements, and purity verification.

Look for 99%+ purity confirmed by HPLC analysis with mass spectrometry identity verification. A proper CoA should show purity, identity, sterility, and endotoxin testing results. NAD+ is sensitive to degradation, so the CoA should correspond to a recent lot. Every Kern NAD+ vial comes with a third-party Certificate of Analysis provided with every purchase.

Every batch undergoes third-party HPLC and mass spectrometry testing. HPLC confirms purity (99%+ standard). Mass spectrometry confirms molecular identity. A batch-specific Certificate of Analysis is provided with every purchase and available for download directly on this page.

All Kern products ship same-day (orders placed before 1pm EST). Lyophilized peptides are shipped at ambient temperature and are stable during transit. Upon receipt, store at -20C for long-term stability or 2-8C for near-term use. If the product arrives damaged, contact us within 7 days with photos for a free replacement.

Price differences usually reflect differences in purity, testing standards, and manufacturing quality. Low-cost vendors may skip mass spectrometry verification (which confirms you actually have the right molecule), use lower-grade raw materials, or skip sterility and endotoxin testing. Kern tests every batch with both HPLC and mass spec, and our CoAs are available before you buy.

08References08 / 08

References

These references are provided for informational purposes. Kern is not affiliated with the authors or institutions listed above.

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The statements made within this website have not been evaluated by the US Food and Drug Administration. The products we offer are not intended to diagnose, treat, cure, or prevent any disease. The peptides sold on this website are intended for research use only. The buyer is responsible for adhering to all local laws and regulations. Kern is not a pharmacy and does not provide medical advice or prescriptions. They are not for human consumption, are not FDA approved, and are not supplements or pharmaceutical drugs. The information provided on this website is for informational purposes and not a substitute for professional medical advice, diagnosis, or treatment. If you have questions or concerns about your health, please talk to your doctor. This site is an advertisement for education, research peptides, and not any specific medication. By purchasing from Kern, you confirm that you are a qualified researcher purchasing these compounds for legitimate in vitro or laboratory research purposes only. You must be 21 years of age or older to purchase.