Nmn Nicotinamide Mononucleotide Powder
Description
High-Purity NMN Nicotinamide Mononucleotide Powder - Factory Direct B2B Supplier for Anti-Aging Formulations
Xi'an Le-Nutra Ingredients Inc specialises in manufacturing pharmaceutical quality Nmn Nicotinamide Mononucleotide Powder with purity >99%. We have a GMP-certified plant with 60,000㎡ and an annual capacity of 3,000 tonnes. Our enzymatic synthesis process is free from toxic organic solvents and has excellent bioavailability shown by HPLC and NMR studies. We have over 14 years experience in the production of nucleotide ingredients and can provide a stable bulk supply with 98% on-time delivery performance, full batch traceability and complete compliance documentation including FDA, ISO and Kosher certifications for nutraceutical and functional food manufacturers around the world.

What is NMN Nicotinamide Mononucleotide Powder?
The product is a direct precursor of NAD+ addressing age-related loss of coenzyme in cellular metabolism. This nucleotide derivative has greater oral absorption than standard NAD+ supplementation.
The chemical penetrates cellular membranes easily and is converted to NAD+ in mitochondria. Clinical investigations show that oral doses of 1,000mg raise blood NAD levels within hours. Unlike indirect processes, this direct precursor skips metabolic bottlenecks limiting traditional vitamin B3 derivatives.
The chemical, an endogenous molecule present in human tissues, had very good safety characteristics. We use enzymatic synthesis in our production process for purity and molecular integrity . No worries about synthetic byproducts or residual pollutants .
Technical Specifications
| Item | Specification |
|---|---|
| Product Name | Nicotinamide Mononucleotide Powder (β-NMN) |
| CAS Number | 1094-61-7 |
| Appearance | White to off-white crystalline powder |
| Assay (HPLC) | ≥99.0% |
| Beta-Form Purity | ≥99.5% (Chiral HPLC) |
| Nicotinamide (NAM) | ≤0.1% |
| Loss on Drying | ≤1.0% |
| Heavy Metals (ICP-MS) | ≤10 ppm (Pb/As/Hg/Cd <0.5ppm each) |
| Total Plate Count | ≤1,000 cfu/g |
| Yeast & Mold | ≤100 cfu/g |
| E. Coli | Negative |
| Salmonella | Negative |
| Residual Solvents (GC) | Meets USP <467> limits |
| Storage Conditions | Cool, dry place, sealed container |
| Shelf Life | 24 months under proper conditions |
Manufacturing Excellence and Quality Control
Our manufacturing site is run under stringent GMP standards, and has specialised clean rooms for nucleotide synthesis. The enzymatic production process removes the use of harmful organic solvents and produces pharmaceutical-grade material suited for nutritional supplements and functional foods.
Each production lot is subjected to extensive multi-step testing. Purity is determined by HPLC, NMR Spectroscopy is used for structure verification and chiral analysis to ensure 100% beta-form content. The alpha-form is physiologically inert and must be totally excluded.
ICP-MS for heavy metal analysis to meet California Prop 65 and EU requirements. Microbiological testing techniques are above industry norms with levels of endotoxins kept below 10 EU/g for sensitive applications. Residual solvents are below detection limits as determined by gas chromatography.
We have full batch traceability from raw material purchase to final packing. Third-party verification testing is available on request. Our quality management system delivers COA, TDS, MSDS and stability data for regulatory filings globally.
Core Benefits for Product Development
Enhanced NAD+ Synthesis
The substance is a direct NAD+ precursor, avoiding rate-limiting enzymatic steps. This direct mechanism supports cellular energy production and metabolic efficiency in different tissue types.
Enhanced Bioavailability Profile
Rapid absorption and systemic dispersion after oral administration. Clinical pharmacokinetics show measurable rise of NAD+ within 2-3 hours of dosing, excellent for fast-acting formulations.
Support Mitochondrial Function
substance restores NAD+ reserves, supporting mitochondrial respiration and ATP production. This system counteracts age-related loss in energy and metabolic dysfunction at the cellular level.
Cellular Resilience and DNA Repair
NAD+ is a substrate for a PARP enzyme that is involved in DNA repair. NAD+ levels need to be sufficient to maintain genomic integrity and cellular stress response pathways important for healthy ageing.
Antioxidant Defense Activation
It activates sirtuin, a family of NAD+-dependent enzymes that regulate oxidative stress response. This system helps protect cells from free radical damage and inflammation.

Application Solutions Across Industries
Nutraceuticals and Dietary Supplements
Our Nmn Nicotinamide Mononucleotide Powder is easy to add to capsule, tablet and powder formulations. The excellent solubility profile offers for variable dosage options ranging from 125mg to 500mg per dose. Compatible with conventional excipients and suited for vegetarian capsule systems.
Health Drinks and Functional Beverages
This chemical is fully soluble in aqueous solutions without changing flavour characteristics. Ideal for use in ready-to-drink products, effervescent pills and powdered beverage mixes targeted to the active lifestyle market. Stability testing has confirmed a 24-month shelf life in correctly prepared systems.
Longevity and Anti-Aging Formulations
Resveratrol, pterostilbene and coenzyme Q10 are particularly suited to premium positioning of age-management products. Our pharmaceutical grade purity is what advanced wellness markets anticipate in North America, Europe and the Asia-Pacific.
Sports Nutrition and Performance
Supports energy metabolism and recuperation routines for athletes. Compatible with pre-workout, intra-workout and recovery stack formulations . Performance nutrition needs fit well with the fast absorption profile.
Why Professional Buyers Choose Le-Nutra?
Pharmaceutical Grade Manufacturing Standards
We operate a 60,000㎡ facility with environmental controls that are better than food grade standards. Six discrete production lines with specific equipment to prevent cross-contamination. Third party annual GMP audits ensure conformity with international quality systems.
Factory Direct Pricing – Competitive
We take control from enzymatic synthesis all the way through to final packaging, removing the middle men’s markups. Bulk discounts apply on orders above 100kg. Transparent pricing system without hidden costs and without minimum order increases.
Flexibility Customisation
We can meet unique parameters including particle size distribution, bulk density targets, and particular packaging needs. We offer private labelling services with affordable minimums starting at 25kg for white label partners.
Trustworthy Supply Chain Worldwide
Strategic inventory management maintains a safety supply of over 30 days to be able to ship immediately. Flexible delivery terms such as EXW, FOB, CIF and DDP are provided by major goods forwarders partnerships. Customs clearance documentation support in 40+ countries.
Technical Support During the Product Life Cycle
Our R&D team can assist you with formulation guidance, stability testing consultancy and regulatory documentation. Multilingual technical service in English, Spanish and Chinese. Technical questions answered within 12 hours.

Packaging and Logistics
Standard Packaging: 25kg fibre drums with double-layer food-grade polyethylene liner bags for moisture protection in overseas delivery. Or for smaller purchases or for sampling purposes we have alternate packaging of 1kg, 5kg and 10kg vacuum sealed aluminium foil bags.
All shipments are nitrogen flushed to guarantee shelf stability in transit. Temperature sensitive logistics for tropical destination markets. The documentation bundle contains commercial invoice, packing list, certificate of analysis and needed certificates for customs clearance.
We offer a variety of shipping options, from sea freight for bulk orders to air freight for urgent deliveries and express courier for sample shipments. For stocked items, the average lead time is 7-10 business days from order confirmation to port of departure.

FAQ
Q: How do you make your products?
A: Our product is produced by advanced enzymatic synthesis, avoiding the use of hazardous organic solvents used in the old chemical approach. This biotechnological process yields a crystalline powder of great purity, which is more bioavailable and stable. The whole procedure is performed in pharmaceutical-grade clean room settings with in-process quality monitoring. Several purification stages ensure a final purity greater than 99% with little degradation products. The green chemistry-based approach to manufacture is environmentally friendly and produces pharmaceutical quality products.
Q: How does the active ingredient work in the body?
A: NMN functions as a direct biosynthetic precursor to NAD+, the essential coenzyme present in every living cell. The chemical is rapidly absorbed by oral administration via specific transporters in the small intestine. NMN is efficiently transformed to NAD+ inside cells by the salvage pathway enzyme NMNAT. The regenerated NAD+ pool serves as a substrate for approximately 500 enzymatic processes in energy metabolism, DNA repair through PARP activation, and sirtuin-mediated cellular defence. This approach directly tackles the age-dependent reduction of NAD+, which is a contributor to metabolic inefficiency and diminished cellular resilience.
Q: What is your lead time and competitive advantage?
A: For bulk orders, our standard MOQ is 25kg with lead times of 7-10 business days for in-stock material. Custom Synthesis Projects 15-20 business days, based on specs We supply free samples of 20-100g for qualification testing. Competitive advantages: guarantyd >99% purity by HPLC and NMR, superior bioavailability by dissolution testing, 14+ years of nucleotide production experience, factory-direct pricing on average 15-20% below market rates. Payment terms: T/T, Alibaba Trade Assurance, Western Union etc. Quality guarantee: If the specification is different from the third-party test, it can be replaced or refunded.
Q: What are your quality certificates and testing?
A: For every batch we provide a full Certificate of Analysis which covers HPLC purity, chiral purity, heavy metals analysis, microbiology reports and residual solvent testing. Our facility is FDA registered, ISO 9001 and 22000 certified, Kosher and Halal certified. Full regulatory support including allergen statements, GMO free statements, BSE / TSE certificates and country specific compliance documents. ICH condition stability data available on request. We may organise a third party verification via SGS, Eurofins or the lab chosen by the customer.

Partner With a Trusted Manufacturer
For quotations, technical specifications, or sample requests for Nmn Nicotinamide Mononucleotide Powder, contact our international sales team at enquiry@lenutra.com.
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