Ingrediente especial
Fabricante y proveedor de β-NMN en polvo
El β-NMN (mononucleótido de β-nicotinamida) se suministra como polvo fino de NMN para la formulación de complementos y el suministro comercial de ingredientes. Las especificaciones técnicas, los datos de lote representativos y la información de envasado y almacenamiento respaldan la evaluación del material y las decisiones de compra.
Información del producto
Mononucleótido de β-nicotinamida en polvo
Características clave de identidad y suministro del β-NMN en polvo utilizado en el desarrollo de complementos.
Descripción general del producto
Consideraciones técnicas del NMN en polvo
El NMN en polvo debe evaluarse como una materia prima completa y no por un único valor destacado. La base analítica, el comportamiento físico y los parámetros de control influyen por separado en la cualificación para una formulación final.
Base analítica
El contenido sobre sustancia anhidra y la pureza por área cromatográfica describen características analíticas distintas. Mantener estas medidas separadas ofrece a los formuladores y a los equipos de calidad una base más clara para comparar especificaciones de materia prima de NMN.
Alcance de la cualificación
La revisión de la materia prima también considera sustancias residuales, contaminantes elementales y controles microbiológicos. Estos parámetros ayudan a los equipos de calidad a valorar si una especificación de material es adecuada para la forma de dosificación y el mercado de destino previstos.
Lote del producto
Lote de producción representativo
Especificación técnica
β-NMN Specification & COA Results
Representative batch results are presented alongside the corresponding specification and test method for technical review.
| Parámetro de ensayo | Especificación | Método de ensayo | Resultado |
|---|---|---|---|
| Descripción | |||
| Aspecto | Pure white fine powder | Visual | Cumple |
| Olor | Característico | Sensory | Cumple |
| Sabor | Característico | Sensory | Cumple |
| Pérdida por desecación | ≤ 1.0% | 2g/105℃/5hrs | 0.12% |
| Densidad aparente | / | W/V | 0.64 g/ml |
| pH (1mg/1ml water) | 2.0 - 4.0 | pHmetro | 3.4 |
| Contenido | |||
| Assay (on the anhydrous basis) | ≥ 98% | HPLC | 99.20% |
| Purity (area%) | ≥ 99.5% | HPLC | 99.90% |
| Contaminantes | |||
| Metales pesados | ≤ 10 ppm | Colorimetric method | Cumple |
| Arsénico (As) | ≤ 0.5 ppm | AFS | Cumple |
| Plomo (Pb) | ≤ 0.5 ppm | AFS | Cumple |
| Cadmio (Cd) | ≤ 0.1 ppm | AFS | Cumple |
| Mercurio (Hg) | ≤ 0.1 ppm | AFS | Cumple |
| Na+ Residue | ≤ 1.0% | IC | Cumple |
| Pesticides Residues | Meet USP | LC-MSMS/GC-MS | Cumple |
| Etanol | ≤ 5000 ppm | GC | Cumple |
| Microbiológico | |||
| Total microbacterial count | ≤ 1000 CFU/g | GB 4789.2 | Cumple |
| Yeast | ≤ 100 CFU/g | GB 4789.15 | Cumple |
| Mold | ≤ 100 CFU/g | GB 4789.15 | Cumple |
| E. coli | Negativo | GB 4789.38 | Negativo |
| Salmonella | Negativo | GB 4789.4 | Negativo |
Áreas de aplicación
Where β-NMN Fits in Product Development
As a fine powder, β-NMN can be considered across several solid supplement formats. Processing behavior, excipient system, stability strategy and market requirements should be assessed during formulation development.
Cápsulas
Powder handling and bulk density are relevant when assessing capsule fill performance and finished-product manufacturing requirements.
Comprimidos
Tablet development should account for the complete formulation system, including flow, compression behavior, excipient compatibility and the processing conditions selected for the finished product.
Formatos en polvo
Powder blends and stick-style formats can be evaluated against material properties, stability needs and the intended finished-product process.
Mezclas personalizadas
For multi-ingredient systems, compatibility, blend uniformity and the contribution of each component to the finished dosage form can be considered before pilot-scale work.
Ingredient Review
From Sample Review to Commercial Supply
Moving from initial evaluation to commercial purchasing requires alignment between the formulation, quality documentation, packaging configuration and order requirements.
Commercial Qualification Path
A practical qualification process connects laboratory evaluation with the information needed for purchasing and production planning.
Research Context
NMN has been investigated in randomized human studies in relation to NAD+ metabolism. Reported findings differ across study populations, intervention designs and measured endpoints, so published research should be interpreted in its specific study context.
Envasado
25 kg / bidón
The supplied COA specifies paper drums with two food-grade poly bags inside. Net weight is 25 kg per drum.
Almacenamiento
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.
Documentación
Information for Material Qualification
Documentation requirements can vary by customer, application and destination market. Available project information can be aligned with the material review before commercial ordering.
Certificado de análisis
Representative batch testing provides a reference for comparing the ordered material with the agreed technical specification.
Revisión de la especificación
Use the agreed specification as the technical reference for raw-material approval, incoming quality review and purchasing alignment.
Sample Coordination
Coordinate evaluation material with the intended dosage form and development stage so testing can focus on the requirements relevant to the project.
Consulta de suministro de ingredientes
Discuss Your β-NMN Powder Requirements
Share the key details of your project so technical and commercial information can be matched to your evaluation and purchasing requirements.
Cantidad y destino
Provide the expected order quantity and destination market so commercial supply requirements can be reviewed.
Application & Development Stage
Share the intended dosage form and whether the project is in evaluation, pilot development or commercial purchasing.
Documents & Quotation
Identify the technical documents, packaging information and quotation details needed for your procurement process.