What is Benfotiamine Bulk Powder?
Benfotiamine Bulk Powder is a high-volume, industrial-grade, lipid-soluble vitamin B1 derivative for bulk production, suitable for dietary supplements and functional ingredients. It is specially packed and processed for procurement, usually on a kilogram or drum-scale basis, to meet the needs of contract manufacturers, private label brands, and raw material distributors who have a need for consistent and economical vitamin delivery. The bulk format is designed for ease of logistics, uniform blending, and quality control, enabling the material to be used in a continuous production setting where the uniformity and reliability of ingredients are crucial. It is highly appreciated for its suitability to high-throughput manufacturing systems and its scalability. It is often used in large batch premix systems where a high level of accuracy in weighing, mixing, and consistent formulation results is essential. The bulk supply form can also help manufacturers reduce the number of handling steps required per unit, minimize costs of handling, and ensure materials are available for long production runs. It is suitable for flexible downstream processing, down to high-speed blending, granulation, and encapsulation processes in the industrial-scale benfotiamine supplement production. It offers good physical stability and a uniform particle size, enabling it to have a consistent flow behaviour through automated filling systems, which is crucial for minimising production interruptions.

COA
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| Item | Specification | Result | Test Method |
| Product Name | Benfotiamine Bulk Powder | Complies | Internal Specification |
| Botanical/Source | Synthetic Vitamin B1 Derivative | Complies | Internal Specification |
| Appearance | White to Off-White Crystalline Powder | Complies | Visual Inspection |
| Identification | Positive | Positive | HPLC |
| Assay (Benfotiamine) | ≥99.0% | 99.35% | HPLC |
| Loss on Drying | ≤1.0% | 0.42% | USP <731> |
| Residue on Ignition | ≤0.5% | 0.12% | USP <281> |
| Melting Point | 124°C–128°C | 126.3°C | USP |
| Particle Size | 95% Pass 80 Mesh | Complies | USP <786> |
| Bulk Density | 0.35–0.65 g/mL | 0.48 g/mL | USP |
| Heavy Metals | ≤10 ppm | <10 ppm | ICP-MS |
| Lead (Pb) | ≤2.0 ppm | <0.10 ppm | ICP-MS |
| Arsenic (As) | ≤1.0 ppm | <0.05 ppm | ICP-MS |
| Cadmium (Cd) | ≤1.0 ppm | <0.05 ppm | ICP-MS |
| Mercury (Hg) | ≤0.1 ppm | <0.01 ppm | ICP-MS |
| Total Plate Count | ≤1,000 CFU/g | <100 CFU/g | USP <2021> |
| Yeast & Mold | ≤100 CFU/g | <10 CFU/g | USP <2021> |
| Escherichia coli | Negative/10g | Negative | USP <2022> |
| Salmonella | Negative/25g | Negative | USP <2022> |
| Staphylococcus aureus | Negative/10g | Negative | USP <2022> |
| Residual Solvents | Meets USP Requirements | Complies | USP <467> |
| Conclusion | Conforms to Enterprise Specification | Complies | - |
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Industry Background
Benfotiamine Powder industry background is tightly coupled with the world's development of the vitamin derivatives and functional nutrition ingredients industry, which saw the demand gradually transferred from the traditional single-form vitamins to more application-oriented nutrient compounds. The dietary supplement, fortified food, and nutraceutical manufacturing industries grow steadily by the day around the world, and the selection of ingredients is now more targeted to processing stability, formulation compatibility, and efficiency in the supply chain. In this context, the lipid-soluble form of vitamin B1 (benfotiamine) has emerged as a significant raw material in the eyes of the suppliers and the raw material manufacturers because it is suitable for modern industrial production systems and can be used in a variety of formulation types. Its bulk supply business is also linked closely to the globalization of contract manufacturing and private label production models – brands and formulators want standardized and high-volume raw materials which are available for continuous production cycles, are less "sourced," and which are able to perform in a consistent way from batch to batch. Meanwhile, international quality expectations and regulations have tightened, increasing the significance of certified production systems (GMP, ISO, and HACCP) and making traceability and documentation key aspects of the selection of raw materials. This further solidifies bulk benfotiamine's place as a specification-driven controlled substance with application to cross-border trade.
Development History
Its development is closely associated with the evolution of vitamin B1 derivatives and their increasing usage in the food sector for the formulation of more stable and ready-for-formulation dietary components. The early applications involved the use of traditional thiamine, but thiamine was limited due to processing stability and compatibility issues, which led to the development of lipid-soluble thiamine derivatives. As a result of the developments in organic synthesis and purification techniques, it slowly began to leave the lab and become available as a commercial product, with enhanced quality control methods such as HPLC testing and standardised specification systems. The global nutraceutical market grew-and large-scale manufacturing grew more popular-so that the use of bulk, consistent raw materials increased. Benfotiamine Powder is manufactured under GMP and ISO Certified systems following the international requirements of traceability, safety documentation, and batch consistency in the modern stage. Today, it is extensively utilized in vitamin premixes and OEM formulations as part of the industry's trends towards high-purity, scalable, and application-oriented ingredient solutions.

Application
1. Dietary Supplement Manufacturing
Benfotiamine Bulk Powder is a highly functional ingredient in vitamin premixes and multi-nutrient formulations and can be used in capsules, tablets, and powder blends used in general nutrition product development.
2. Functional Food & Beverage Industry
Used to fortify foods and beverage systems that demand stability of the fortified vitamin in the product, such as fortified ready-to-mix powders, nutrition bars, and other engineered food products.
3. Nutritional Premix Production
Often added to a specially formulated vitamin premix to create standard nutrient formulations, help large-scale industrial clients with easier mixing, and provide the flexibility to create custom vitamin mixes.
4. Pharmaceutical Ingredient Supply Chain (Non-prescription Use)
Is used as an intermediate raw material in controlled formulation conditions where high-purity vitamin derivatives are needed when the product development workflow needs to be standardized.
5. OEM/ODM Contract Manufacturing
Often used by Private Label and Contract Manufacturers in customized formulation projects for flexible product design and scalable production according to various market needs.
6. Nutraceutical R&D and Product Development
To test compatibility, stability, and performance in multi-component formulations, supporting innovation of next-generation nutritional products in formulation research settings.
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