What is Pure NAD+ Powder?
Pure NAD+ Powder (Nicotinamide Adenine Dinucleotide) is a high-purity, high-quality raw ingredient that is used extensively by functional food manufacturers, cosmetic developers, and dietary supplement manufacturers in their advanced formulations for wellness. This is a critical coenzyme in all living cells, and a basic substrate in cellular energy production, mitochondrial function, and biological repair mechanisms. The addition of fine-grade opens the door for product development for enterprises seeking to enhance their product lines with new formulas that align with current trends in consumer preferences and science. Our industrial-grade product is produced with a high degree of quality control, ensuring a superior solubility and particle size distribution, and is highly stable for easy incorporation into capsules, tablets, topicals, or powdered beverage mixes. With emphasis on biochemical reliability, we supply the client with the analytical documentation, including detailed Certificates of Analysis (COA), heavy metal screening, and purity testing that can satisfy the strict regulations in various countries. The commercial-grade bulk material allows brands to create innovative formulations that activate natural metabolic pathways and cellular resilience to provide a certain level of confidence in their supply chain, thereby giving an edge to businesses seeking a market share in the fast-growing cellular health and premium ingredient market.

COA
| Test Items | Specifications (Standard) | Test Methods | Results |
| Physical & Chemical Analysis | |||
| Appearance | White to off-white powder | Visual | White powder |
| Clarity of Solution | Clear and colorless | Visual | Conforms |
| pH (10 mg/mL in water) | 2.0 – 4.0 | pH Meter | 3.2 |
| Water Content (Loss on Drying) | ≤6.0% | Karl Fischer / Vacuum | 3.20% |
| Purity & Assay | |||
| Assay (NAD+ Content, dry basis) | ≥98.0% | HPLC | 99.40% |
| Absorbance Ratio ($A_{250}/A_{260}$) | 0.81 – 0.85 | UV-Vis Spectrometry | 0.83 |
| Absorbance Ratio ($A_{280}/A_{260}$) | 0.20 – 0.24 | UV-Vis Spectrometry | 0.22 |
| Heavy Metals | |||
| Total Heavy Metals | ≤10 ppm | ICP-MS | < 5 ppm |
| Lead (Pb) | ≤0.5 ppm | ICP-MS | 0.08 ppm |
| Arsenic (As) | ≤0.5 ppm | ICP-MS | 0.05 ppm |
| Mercury (Hg) | ≤0.1 ppm | ICP-MS | Not Detected |
| Cadmium (Cd) | ≤0.2 ppm | ICP-MS | 0.02 ppm |
| Microbiological Control | |||
| Total Plate Count | ≤1,000 cfu/g | USP <61> | < 10 cfu/g |
| Yeast & Mold | ≤100 cfu/g | USP <61> | < 10 cfu/g |
| E. Coli | Negative | USP <62> | Negative |
| Salmonella | Negative | USP <62> | Negative |
| Staphylococcus Aureus | Negative | USP <62> | Negative |
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Main Ingredients
It's a highly purified, biologically active, single essential ingredient for this bulk material, Beta-Nicotinamide Adenine Dinucleotide (NAD+), which is the major active component of this bulk material. It is a fine-grade powder, stable, and formulated strictly for industrial use only. No fillers or synthetic additives have been added to the product for enterprise-level manufacturers to receive a premium, high-purity substrate for various product formulations. The main ingredient is a key natural electron carrier in the metabolic pathways of mitochondria, helping to naturally break down nutrients into cellular energy (ATP), and promoting the endogenous cellular maintenance and repair processes. The unadulterated, professionally verified biochemical compound guarantees a consistent and very potent active base, allowing functional food, supplement, and cosmetic brands to build an active product portfolio based on the scientific information found in the scientific literature.
Manufacturing Pathway
1. Raw Material Preparation
The first step is the purchase of high-purity precursors of the substrate, namely nicotinamide mononucleotide (NMN) or nicotinamide riboside (NR) and adenosine triphosphate (ATP) as the source of phosphate and adenosine.
2. Enzymatic Biocatalysis
The core reaction is done in a temperature and pH-controlled bioreactor. Specific immobilized enzymes, namely the enzymes of the nicotinamide mononucleotide adenylyltransferase (NMNAT) or the special fused NAD synthases, are added to catalyse the coupling of the precursors with ATP in high efficiency mode with the presence of essential mineral cofactors, such as magnesium ions (Mg2+).
3. Ultrafiltration and Enzyme Separation
The liquid of the reaction is then passed through the membrane ultrafiltration after reaching the optimal conversion rate. During this stage, the valuable biocatalytic enzymes are separated and recovered in a physical way, with the result that there are no protein residues left in the product stream.
4. Chromatographic Purification.
The solution of crude NAD+ is allowed to run through the advanced ion exchange chromatography columns. This crucial separation process removes the target nicotinamide adenine dinucleotide molecules from unreacted raw materials, by-products, and residual fragments of the nucleotides, increasing the chemical purity to enterprise standards.
5. Concentration and Crystallization
Eluate is purified and concentrated at low temperature under vacuum conditions in order to maintain the structural stability of the coenzyme. Then it is subjected to a controlled crystallization or precipitation from solvent to produce uniform crystals.
6. Lyophilization and Finishing
The final wet crystals are freeze-dried (lyophilized) to dry the compounds without causing any thermal degradation in the compounds. This leaves a fine white NAD+ Powder, which is then milled, sieved for uniformity of particle size, and vacuum packaged in industrial bulk packaging.

Safety
Thanks to its endogenous coenzyme (naturally synthesized and used by all living cells) and excellent safety profile, NAD+ Bulk Powder is an optimal raw material. Biocatalytic enzymatic process for commercial production results in a compound that closely resembles the body's natural biochemistry, reducing the potential for adverse biological reactions if handled and formulated properly. The bulk material will be extensively tested for its toxicological properties, thereby demonstrating its non-mutagenicity, non-tissue-irritation, and ensuring that it has an exceptionally low toxicological profile even at high manufacturing concentrations, to establish its empirical safety and meet international regulatory requirements. Additionally, enterprise quality NAD+ powder is rigorously tested under a diverse temperature and humidity range to ensure there is no production of degrading by-products which may affect the final product integrity. Safety compliance is regularly tested using standard documentation such as full Material Safety Data Sheets (MSDS), microbiological screening for the presence of toxic metals and pathogens, and third-party analytical testing to assure a stable, non-toxic, and extremely secure active ingredient for worldwide commercialization.
Production Process

Certificate

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