Sample Available

NMN

NMN Powder (β-Nicotinamide Mononucleotide)

Bulk NMN powder for NAD+ precursor and healthy-aging formulation development

PathGene supplies bulk NMN powder (CAS 1094-61-7) with a specified purity of ≥99.5% for capsule, tablet and powder-blend development. Request a batch COA, sample, packaging details and lead time. NAD+ ingredients

Confirm beta-form identity, assay basis and moisture controls.

NMN Powder (β-Nicotinamide Mononucleotide) (CAS 1094-61-7) bulk active ingredient

Key Specifications

Product PositioningBulk NMN powder for NAD+ precursor and healthy-aging formulation development
Application Scenarioscapsule and tablet formulation · NAD+ pathway research · water-soluble powder development
CAS Number1094-61-7
Purity≥99.5%
Molecular FormulaC₁₁H₁₅N₂O₈P
Molecular Weight334.22 g/mol
AppearanceWhite to off-white crystalline powder
SolubilityFreely soluble in water
StorageSealed packaging, stored at cool, dry and away from light
Shelf Life24 months

Procurement & delivery

Supply details confirmed by intended use, volume and target market

Purity ≥99.5%CAS 1094-61-7
MOQ1 kg
Lead Time3–5 business days
Packaging1 kg / 5 kg / 25 kg
Free sample available
View quality documents ↓

What Is NMN?

PathGene is an NMN manufacturer and bulk ingredient supplier in China, offering beta-NMN raw material (CAS 1094-61-7) for wholesale sourcing and formulation development. Free samples, batch COAs and third-party test reports are available for buyer evaluation. β-Nicotinamide mononucleotide (NMN, CAS 1094-61-7, C11H15N2O8P, MW 334.22 g/mol) is a naturally occurring nucleotide formed from nicotinamide, ribose, and a phosphate group. It occurs in trace amounts in foods such as broccoli, edamame, cabbage, and cucumber, and serves as a direct biosynthetic precursor of NAD+ (nicotinamide adenine dinucleotide), a coenzyme central to cellular energy metabolism and redox signaling. Because natural abundance is far too low for commercial extraction, bulk NMN used in supplements, cosmetic actives, and pharmaceutical-grade materials is manufactured through enzymatic/biocatalytic conversion: engineered microbial enzymes (e.g., nicotinamide riboside kinase or nicotinamide phosphoribosyltransferase), paired with an ATP-regeneration system, convert precursor substrates into NMN, which is then purified and crystallized to achieve high-purity powder form. For private label and OEM projects, contact PathGene about capsule or tablet development and packaging. Finished-product minimum orders and schedules are quoted separately from bulk raw material orders.

Other Names

NMNβ-NMNbeta-Nicotinamide mononucleotideNicotinamide mononucleotideNicotinamide ribonucleotideNAD+ precursor (NMN)CAS 1094-61-7β-NMN powder

Key Features

🧪

Purity Tested up to 99.9%

NMN purity reaches 99.9% in batch testing and third-party testing. Request the corresponding batch COA and independent report to review the result and test method.

⚗️

Immobilized Enzyme Production, No Chloride Contamination

Produced via a controlled immobilized-enzyme biocatalytic process rather than chlorinated chemical routes, minimizing chloride ion residues and other process-related impurities.

❄️

Consistent Crystalline Powder

Uniform white to off-white crystalline powder with controlled particle size, freely soluble in water for easy handling in downstream formulation.

🛡️

Full Contaminant & Microbial Screening

Every batch is screened for heavy metals (Pb, Hg, Cd, As), residual solvents, and microbial limits (total plate count, yeast/mold, E. coli, Salmonella) before release.

📦

Flexible Bulk & OEM Supply

Available in flexible bulk quantities with OEM/private-label support, plus formulation guidance for capsules, sublingual tablets, sachets, and topical serums.

Recent batch test data

Test items, specifications and batch results are shown here; request the formal COA through the card below.

Batch No.

PGNMN-260522

Test date

2026-05-23

Specification

Q/PGNMN-2025

Pack size

25 kg/drum

Storage

Sealed packaging, stored at cool, dry and away from light

Conclusion

Conforms

Test ItemSpecificationResult
AppearanceWhite to off-white powderWhite powder
IdentificationHPLC main peak retention time consistent with reference productComplies
Purity≥99.0%99.9%
Assay (calculated on dry basis)≥99.0%100.0%
Loss on Drying≤2.0%0.19%
pH3.0–4.03.67
Ethanol Residue≤500 ppmComplies
Lead (Pb)≤0.1 ppmComplies
Mercury (Hg)≤0.1 ppmComplies
Cadmium (Cd)≤0.2 ppmComplies
Arsenic (As)≤0.1 ppmComplies
Total Microbial Count≤500 CFU/g<10 CFU/g
Coliforms≤0.92 MPN/g<0.3 MPN/g
Mold and Yeast≤50 CFU/g<10 CFU/g
Staphylococcus aureus0/25 gNot detected
Salmonella0/25 gNot detected
Bulk Density0.60 g/mL

This page shows a batch-data summary only. No direct COA file link is provided; request the signed document through the form below.

Why Choose PathGene

  • Direct China manufacturer supply — factory pricing, no middleman
  • Recent-batch COA & batch traceability
  • In-house R&D + synthetic biology / enzymatic production platform
  • Free sample for qualified B2B buyers before commercial order
  • Flexible MOQ — from lab-scale trial to ton-scale commercial supply
  • One-stop OEM/private-label support for finished dosage forms
  • Worldwide shipping by courier, air freight, and sea freight

OEM & Private-Label Services

  • ·Custom capsule manufacturing
  • ·Custom tablet manufacturing
  • ·Powder blending & custom formulation
  • ·Private-label bottles, pouches & labels
  • ·Small trial orders
  • ·Bulk commercial production
  • ·Export documentation
  • ·Third-party testing support available on request

Documents Available

  • ·Product specification sheet — request from sales
  • ·Recent-batch COA — confirm by product and batch
  • ·Other quality documents — confirm by product and batch

Documents are subject to product and batch availability; third-party reports are provided only when applicable.

Quality documents

Review specifications first, then batch data at shipment

The specification sheet defines acceptance limits. The COA shows actual batch results, which may vary by batch. Third-party reports are provided only for products or batches that have been independently tested.

Product specification

Stable acceptance criteria · Available on request

Recent-batch COA

Actual test data · Issued with each shipment

Third-party test report

Independent test record · Available by product/batch

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