| Product Name |
Pure NMN Powder (β-Nicotinamide Mononucleotide) |
|---|---|
| CAS No. | 1094-61-7 |
| MF | C11H15N2O8P |
| MW | 334.22 |
| Purity | 99% |
| Appearance | White powder |
| Packing | 1kg/bag,5kg/bag,25kg/drum |
| Apply | Dietary Supplement Raw Materials |
NMN(β-Nicotinamide Mononucleotide) is a naturally occurring nucleotide and a direct precursor to NAD+ (nicotinamide adenine dinucleotide), a vital coenzyme in cellular energy production and DNA repair. Our NMN is produced via advanced enzymatic biosynthesis, ensuring ultra-high purity (≥99.0%, HPLC) and stability. It is vegan, non-GMO, gluten-free, and contains no additives.
NAD+ precursor for energy metabolism and anti-aging
Produced via enzymatic biosynthesis, avoiding chemical residues
High stability and purity, meeting pharmaceutical-grade standards
Suitable for dietary supplements, functional beverages, and cosmetic applications
| Aspect | Common/Ordinary NMN | Our Pure NMN Powder | Impact on Your Product |
|---|---|---|---|
| Production Process |
Chemical Synthesis: Multi-step chemical reactions starting from precursors like nicotinamide. Harsh process prone to generating inactive isomers (e.g., α-NMN).
|
Enzymatic Catalysis: Precise synthesis under mild conditions using specific enzymes. Produces 100% biologically active β-NMN isomer.
|
Foundation of Efficacy & Safety. Our method ensures correct structure, superior safety, and compliance for high-end applications.
|
| Purity & Specifications |
Often only claims “≥98% NMN” without specifying isomer ratio or impurity profile. May contain by-products and solvents.
|
Dual High Standards:
|
Guarantees Predictable Potency. Each percentage point of higher purity means fewer ineffective impurities.
|
| Bioavailability & Stability |
Crude processing can lead to poor crystal morphology, high hygroscopicity, and instability in formulations.
|
Optimized Crystalline Form: Excellent powder flowability and stability. Formulation support for enhanced bioavailability available.
|
Determines End-User Experience. High bioavailability means consumers can feel effects at lower doses.
|
| Quality System |
Often lacks robust traceability and may not consistently pass stringent third-party testing.
|
Pharmaceutical-Grade Quality:
|
Your Passport to Market Access. Essential for entering regulated markets and building a premium brand.
|
| Specification | Qualified Testing Result | Actual Testing Result | Test Method |
|---|---|---|---|
| Part 1. Physical & Chemical Analysis | |||
| Appearance | White to off-white crystalline powder | Complied | Visual |
| Odor | Characteristic | Complied | Organoleptic |
| Assay (HPLC) | ≥99.0% | 99.5% | HPLC |
| Loss on Drying | ≤0.5% | 0.08% | USP <731> |
| Residue on Ignition | ≤0.1% | 0.02% | USP <281> |
| pH (10 mg/mL) | 2.0–4.0 | 3.3 | USP <791> |
| Part 2. Heavy Metal Analysis & Chemical Control | |||
| Total Heavy Metals | ≤10 ppm | Complied | AAS |
| Lead (Pb) | ≤3 ppm | <1 ppm | ICP-MS |
| Arsenic (As) | ≤1 ppm | <0.1 ppm | ICP-MS |
| Cadmium (Cd) | ≤1 ppm | <0.05 ppm | ICP-MS |
| Mercury (Hg) | ≤0.1 ppm | <0.01 ppm | ICP-MS |
| Part 3. Microbiological Analysis & Control | |||
| Total Plate Count (cfu/g) | ≤1,000 | <100 | USP <61> |
| Yeast & Mold (cfu/g) | ≤100 | <10 | USP <61> |
| E. coli | Negative | Negative | USP <62> |
| Salmonella (per 25 g) | Negative | Negative | USP <62> |
1kg/aluminium foil bag, with two plastic bags inside.
Gross Weight: 1.5kg Size: 18cmxH27cm
25kg/fiber drum, with two plastic bags inside.
Gross Weight: 28kg Size: 42cmxH52cm Volume: 0.0625mg/Drum.
DHL / FEDEX / EMS / E-PACKET / BY AIR / BY SEA
1. ≤50kg, Express delivery(DHL /FEDEX) recommended, usually called as DDU service;
2. ≤500kg, Air shipping recommended, usually called as CIF service;
3. >500kg, sea shipping recommended, usually called as FOB, CFR, or CIF service;
4. For high value products, please select air shipping and express delivery for safe.
We will contact you within 1 working day, please pay attention to the email with the suffix “forrest@oriherb.com”.
