β-Nicotinamide Mononucleotide (NMN) Grade I · NAD+ Precursor Ingredient for Nutrition Formulations

β-Nicotinamide mononucleotide (NMN) is a nucleotide-derived compound used in nutrition formulations as an NAD+ precursor ingredient. Manufacturers typically select NMN grades based on purity, identity testing, moisture control and contaminant limits, and then apply it in capsules, tablets and powdered blends. Atlas Global Trading Co. supplies NMN Grade I to agreed specification targets with COA, documentation and export logistics coordinated from Ankara, Türkiye.

Function: NAD+ precursor ingredient for nutrition and supplement formulations
Typical format: Fine powder; purity and moisture targets as agreed
Key feature: Documentation-ready supply for regulated supplement workflows

Regulatory status and permitted uses for NMN may differ significantly by country and product type. Atlas can support documentation and supply coordination; customers remain responsible for confirming local compliance, claims and labeling.

Product overview

NMN Grade I: specification focus for industrial and brand use

NMN is typically sourced and qualified using identity and purity testing, supported by batch documentation. In production, key quality considerations include consistent assay, controlled moisture, low impurities and clear traceability. Atlas helps customers align NMN Grade I specifications with their finished-product format and QA requirements, including export documentation where needed.

Key characteristics

  • Ingredient name: β-Nicotinamide mononucleotide (NMN).
  • Use case: nutrition and supplement formulations as an NAD+ precursor ingredient.
  • Typical formats:
    • Capsules and tablets,
    • Powder blends and premixes for downstream dosing.
  • Handling considerations:
    • Use appropriate humidity control to protect stability and flowability,
    • Accurate low-dose blending requires validated mixing and segregation control.
  • Quality priorities:
    • Confirmed identity and purity,
    • Controlled moisture and impurity profile,
    • Batch traceability and documentation readiness.

Atlas can support grade matching and documentation requests for brand and contract manufacturing workflows.

Indicative specification points

Specifications are agreed per grade and destination requirements. Typical control points include:

  • Assay / purity: defined by agreed analytical method.
  • Identity: supported by suitable identity testing per supplier and customer QA requirements.
  • Moisture: controlled for stability and handling.
  • Impurities: defined limits based on method and product requirements.
  • Contaminants: heavy metals and other parameters within required limits for supplement workflows.
  • Microbiology: targets suitable for intended use and market requirements.

Each lot is supplied with a Certificate of Analysis (COA) and specification sheet. Additional documentation can include allergen statements, GMO status (where applicable), origin declarations and compliance documentation requested for destination markets.

Applications

NMN Grade I applications in capsules, tablets and powder blends

NMN is most commonly used in supplement formats. The correct grade and processing approach depends on dose target, excipient system and the chosen manufacturing route. Pilot and stability trials are recommended to confirm blend uniformity, finished-product assay stability and packaging suitability.

Capsules

  • Hard capsules: used with suitable excipients to support flow and fill weight control.
  • Blend uniformity: premixing strategies support accurate dosing at low inclusion levels.
  • Moisture management: helps protect stability and prevent caking during storage.

Tablets

  • Direct compression or granulation: route depends on excipients and compression behavior.
  • Flow and compressibility: excipient selection supports weight control and tablet strength.
  • Stability: validate assay and impurity profile through shelf life under target packaging.

Powder blends and premixes

  • Functional blends: combined with vitamins, minerals and other actives (manage segregation control).
  • Sachets: used in powder concepts where regulatory frameworks allow and stability is validated.

Usage and manufacturing guidance

  • Dosing:
    • Set the target dose per serving and confirm regulatory suitability in destination markets,
    • Use calibrated weighing and validated mixing to ensure dose accuracy.
  • Stability and packaging:
    • Use low-moisture excipients and consider desiccants where appropriate,
    • Validate stability in final packaging (bottles, blisters, sachets) under expected conditions.
  • Quality control:
    • Confirm identity and assay through incoming QC and finished-product testing,
    • Monitor impurities and moisture as part of shelf-life programs.
  • Compliance:
    • NMN regulatory status varies; confirm permitted uses, labeling and claims for each market,
    • Align documentation and traceability with your GMP workflow.

Need NMN Grade I for your supplement project?

Share your target purity specification, intended format (capsule/tablet/powder), target dosage, destination markets, annual volume and documentation needs (COA, heavy metals, microbiology targets, stability expectations, origin statements). Atlas will propose NMN Grade I supply options and coordinate QA/export documentation.

Discuss NMN supply
Quality & supply

Quality documentation and global supply support for NMN Grade I

Atlas Global Trading Co. coordinates NMN supply through qualified partners and manages documentation and export logistics from Ankara, Türkiye, supporting supplement brands, contract manufacturers and ingredient blenders worldwide.

Quality and documentation

  • Supplied as β-Nicotinamide mononucleotide (NMN) Grade I with agreed specification targets for assay, moisture, impurities, microbiology and contaminants.
  • Each lot includes a Certificate of Analysis (COA) and specification sheet.
  • Documentation can include allergen statements, GMO status (where applicable), origin declarations, heavy metals data and other compliance documents according to destination needs.
  • Quality certificates can be shared on request depending on supplier and market requirements.
  • Customers remain responsible for confirming regulatory status, permitted uses and labeling in destination markets.

Packaging, storage and logistics

  • Standard packaging: sealed foil bags with inner liners inside cartons or fiber drums depending on batch size and supplier pack system.
  • Storage: keep tightly closed in a cool, dry place; protect from humidity and heat to support stability.
  • Handling: use good hygiene and dust control; reseal promptly after opening to limit moisture uptake.
  • Shelf life: stated on COA/specification; validate in your storage and distribution conditions.
  • Shipments: arranged under FOB, CFR, CIF or other agreed Incoterms with export documentation support coordinated from Ankara.

For a quotation, please share target purity/specification, packaging preference, annual volume and destination markets.

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