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PEPTIDE GUIDE · LONGEVITY · TRENDING 70

NAD+

Nicotinamide Adenine Dinucleotide/NAD

Coenzyme central to redox reactions and energy metabolism in every cell. Levels decline with age, which has driven a research interest in NAD+ supplementation as a longevity intervention.

QUICK ANSWER

NAD+ (nicotinamide adenine dinucleotide) is a coenzyme central to redox reactions and energy metabolism in every cell. Cellular NAD+ levels decline measurably with age, which has motivated longevity-research interest in NAD+ supplementation. NAD+ itself has poor oral bioavailability, so research protocols use subcutaneous or IV administration, or precursors like NMN and NR.

Research notes

How does NAD+ work?

NAD+ (nicotinamide adenine dinucleotide) is a coenzyme involved in hundreds of metabolic reactions, particularly the redox reactions that drive ATP production and the sirtuin enzyme family that's been studied in aging research. Cellular NAD+ levels decline measurably with age, which has motivated interest in supplementation as a longevity-protocol target.

NAD+ itself is a large, polar molecule with poor membrane permeability. Most research-protocol NAD+ administration is subcutaneous or IV because oral bioavailability is low. Precursors like NMN and NR are common alternatives because they cross membranes more efficiently and convert to NAD+ intracellularly.

What doses are used in research?

The published research-protocol literature spans a wide range. Common reference doses:

  • 100–250 mg subcutaneous as a maintenance protocol
  • 500 mg IV as an intensive single-dose research administration
  • NMN / NR oral analogs typically dosed in the 250–1000 mg range

Half-life is short — NAD+ is rapidly partitioned across compartments and converted to downstream metabolites. The clinical question of whether boosting circulating NAD+ produces meaningful increases in tissue NAD+ levels is still being characterized in human trials.

What does the research show about side effects?

Most-reported research-protocol observations are administration-route specific. Subcutaneous NAD+ commonly produces flushing and a transient burning sensation at the injection site — this is mechanistically expected and generally resolves within minutes. IV administration at high doses can produce nausea and chest tightness if infused too quickly; protocols specify slow infusion rates accordingly.

What does this guide cover?

Vendor audits for NAD+ focus on:

  • Identity confirmation — NAD+ is sometimes shipped as the precursor (NMN or NR) labeled as NAD+. Mass-spec identity confirmation is essential.
  • Purity — NAD+ degrades during storage and shipping if not properly handled. Lower-purity batches often reflect storage problems rather than synthesis problems.
  • Bacteriostatic water reconstitution — NAD+ is unstable in solution. Some research protocols specify sodium chloride 0.9% rather than bacteriostatic water; vendor packaging instructions vary.

What it's researched for

  • cellular energy
  • mitochondrial function
  • aging research

Where to source it

ALL 4 VENDORS →
VENDOR
SCORE
PRICE
PER-MG
CODE
BioTech Peptides
Established US-domestic peptide synthesizer with a substantia…
76
$179
500 MG
$0.358/mg
VISIT ↗

RANKED BY COMPOSITE SCORE · PRICES ARE SNAPSHOTS FROM THE PRICE INDEX · PER-MG IS A WITHIN-COMPOUND COMPARATOR

Frequently asked about NAD+

What is NAD+?

NAD+ is nicotinamide adenine dinucleotide, a coenzyme involved in hundreds of metabolic reactions — particularly the redox reactions that drive ATP production and the sirtuin enzyme family that has been extensively studied in aging research.

Why is NAD+ studied for longevity?

Cellular NAD+ levels decline measurably with age, and this decline is correlated with reduced sirtuin and PARP activity in published research. The hypothesis driving longevity-protocol interest is that restoring NAD+ levels may slow age-related metabolic dysfunction. Causal evidence in humans is still developing.

Why isn't NAD+ taken orally?

NAD+ is a large, polar molecule with poor membrane permeability and is rapidly broken down in the gut. Oral bioavailability is low. This is why most research-protocol NAD+ administration is subcutaneous or IV, and why NAD+ precursors like NMN and NR are popular alternatives — they cross membranes more efficiently and convert to NAD+ intracellularly.

What doses are used in NAD+ research?

Published research literature cites 100–500 mg subcutaneous or IV, with protocols ranging from single-dose tolerability studies to weekly maintenance schedules. Doses are highly variable across studies and protocols; this is not a settled dose range.

Is research-grade NAD+ the same as IV NAD+ at clinics?

The molecule is the same. The difference is that clinic-administered NAD+ is typically pharmaceutical-grade with a chain of custody under medical supervision, whereas research-grade NAD+ from peptide vendors is for laboratory research only and is not formulated, tested, or distributed for human use.

PUBLIC JANOSHIK TESTING RECORD

8 tests in our mirror.

Aggregated from Janoshik's public-tests database via our local mirror. Submitters with fewer than three public tests appear as anonymous clients in the detailed table below.

8
public tests indexed
8
submitters
median purity
0/8
identity-flagged

Janoshik public tests

8 TESTS · 8 SUBMITTERS
PUBLIC TESTS INDEXED
8
SUBMITTERS
8
MEDIAN PURITY
IDENTITY FLAGGED
0 / 8

Aggregated from Janoshik's public-tests database via our local mirror. Submitters with fewer than 3 public tests appear below the ranked leaderboard as "limited data." Identity-flagged tests are surfaced on the relevant rows; check our COA verifier to look up a specific test.

Limited data

N < 3 · NOT RANKED
Longevity Pro's · n=1SH Petitde Ltd · n=1support@puruspeptides.com · n=1info@peptidegurus.com · n=1ZLZ peptides · n=1MEI-PEPETIDE · n=1admin@reta-peptide.com · n=1HK Peptide Ltd (hk peptides) · n=1

Catalog COAs by vendor

VENDOR-PUBLISHED
Ascension Peptides
MZ Biolabs (HPLC-UV-MS)
2 RECORDS

Ascension Peptides publishes batch-level COAs (MZ Biolabs (HPLC-UV-MS)) for NAD+. 2 records on file; median purity 98.59%.

BATCH
DATE
PURITY
IDENTITY
COA
25-01260229dose-mismatch
2026-01-26
99.66%
● confirmed
45-03250428
2025-10-06
97.53%
● confirmed
Injectify
Janoshik Analytical (HPLC-UV)
1 RECORDS

Injectify publishes batch-level COAs (Janoshik Analytical (HPLC-UV)) for NAD+. 1 record on file.

BATCH
DATE
PURITY
IDENTITY
COA
PE2401-638
2026-01-12
● confirmed

Sources

2 REFERENCES

Other peptides

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