特殊成分
β-NMN Manufacturer & Bulk NMN Powder Supplier
Gensei supplies β-Nicotinamide Mononucleotide (NMN) as a fine powder for ingredient evaluation and supplement formulation. The product is supported by batch-level analytical data, specification review, sample coordination and commercial packaging information.
Product Information
β-NMN at a Glance
A clear product definition for material review before sample approval or commercial sourcing.
Product Overview
What Matters When Reviewing β-NMN
For ingredient qualification, the useful comparison is not purity alone. Identity, assay basis, impurity controls, physical properties and microbiological results should be reviewed together.
Identity & Assay
The supplied material is identified as β-Nicotinamide Mononucleotide (NMN). The COA separates assay reported on an anhydrous basis from chromatographic area purity, so the two values can be reviewed for different analytical purposes.
Contaminant & Microbial Control
The batch record includes heavy metals, individual elemental contaminants, sodium residue, pesticide residues, ethanol and microbiological parameters, allowing a more complete review of the material than a single purity number.
Product Batch
β-NMN Batch Information
技術仕様
β-NMN Specification & COA Results
The following results are taken from the supplied Certificate of Analysis for the batch shown above.
| Test Item | 仕様 | Test Method | Result |
|---|---|---|---|
| 説明 | |||
| 外観 | Pure white fine powder | ビジュアル | Complies |
| 臭気 | 特徴 | Sensory | Complies |
| 味覚 | 特徴 | Sensory | Complies |
| 乾燥減量 | ≤ 1.0% | 2g/105℃/5hrs | 0.12% |
| かさ密度 | / | W/V | 0.64 g/ml |
| pH (1mg/1ml water) | 2.0 - 4.0 | pH meter | 3.4 |
| アッセイ | |||
| Assay (on the anhydrous basis) | ≥ 98% | HPLC | 99.20% |
| Purity (area%) | ≥ 99.5% | HPLC | 99.90% |
| 汚染物質 | |||
| 重金属 | ≤ 10 ppm | Colorimetric method | Complies |
| Arsenic (As) | ≤ 0.5 ppm | AFS | Complies |
| Lead (Pb) | ≤ 0.5 ppm | AFS | Complies |
| Cadmium (Cd) | ≤ 0.1 ppm | AFS | Complies |
| 水銀（Hg） | ≤ 0.1 ppm | AFS | Complies |
| Na+ Residue | ≤ 1.0% | IC | Complies |
| Pesticides Residues | Meet USP | LC-MSMS/GC-MS | Complies |
| Ethanol | ≤ 5000 ppm | GC | Complies |
| Microbiological | |||
| Total microbacterial count | ≤ 1000 CFU/g | GB 4789.2 | Complies |
| Yeast | ≤ 100 CFU/g | GB 4789.15 | Complies |
| Mold | ≤ 100 CFU/g | GB 4789.15 | Complies |
| E. Coli | 否定 | GB 4789.38 | 否定 |
| サルモネラ菌 | 否定 | GB 4789.4 | 否定 |
Application Areas
Where β-NMN Fits in Product Development
The ingredient is commonly evaluated as a NAD+ precursor for supplement formats. Final formulation, dosage and market use should follow the applicable product requirements.
カプセル
Powder handling and bulk density are relevant when assessing capsule fill performance and finished-product manufacturing requirements.
タブレット
The ingredient can be reviewed as part of tablet development where the material specification and processing requirements are defined in advance.
Powder Formats
Powder blends and stick-style formats can be evaluated against material properties, stability needs and the intended finished-product process.
カスタムプレミックス
For multi-ingredient formulations, specification matching can be reviewed before a sample or pilot blend is prepared.
Ingredient Review
How to Evaluate a β-NMN Material
A useful material review starts with the intended finished product and then works backward to the raw-material specification.
Key Review Points
Use the points below to structure a first-pass ingredient review before moving into sample testing or a commercial order.
Research Context
NMN is an NAD+ precursor that has been evaluated in randomized human studies. Published trials have reported increases in blood NAD+ measures, while findings for functional and metabolic outcomes vary by study, population and endpoint.
パッケージング
25 kg / Drum
The supplied COA specifies paper drums with two food-grade poly bags inside. Net weight is 25 kg per drum.
ストレージ
Cool & Dry Conditions
- Seal the package and keep the material in a cool, dry place.
- Avoid direct sunlight during storage.
- Shelf life is 24 months under the stated conditions and original packaging.
ドキュメント
Information for Material Qualification
The supplied batch record gives a practical starting point for technical review, while project-specific document requirements can be confirmed with the quotation.
Certificate of Analysis
Batch-level analytical results covering physical properties, assay, contaminants and microbiological parameters.
仕様書の検討
Review the target assay, impurity controls, physical parameters and finished-product requirements before ordering.
Sample Coordination
Share the intended application, target quantity and specification so sample and document requirements can be reviewed together.
Request β-NMN Pricing & Product Information
Send your required quantity, target specification, finished-product format and destination market. We can review the material requirements and align the quotation with the requested documents and packaging.