Joint Health Ingredient
Vegan Glucosamine Ingredient Supplier
A defined glucosamine hydrochloride ingredient supplied for product development and specification review. The page below presents the product identity, tested batch record and complete analytical results without mixing batch data into the application or purchasing sections.
Product Identity
素食葡萄糖胺 HCl
The fixed product details below come from the supplied Certificate of Analysis or the product identity documented with it.
Batch Record
Certificate of Analysis Batch Record
This section identifies the tested lot. The detailed release results follow in the technical table.
技術規格
Vegan Glucosamine HCl Specification & COA Results
Release limits, recorded results and analytical methods listed on the supplied certificate.
| Test Item | 規格 | Result | Analytical Method |
|---|---|---|---|
| Identity & Physical Properties | |||
| 外觀 | Crystalline powder | Complied | 視覺 |
| 顏色 | 白色 | 特徵 | 視覺 |
| 分析法 | 98.0% – 102.0% | 99.5% | USP40-HPLC |
| 識別 |
A: Infrared absorption B: Chloride test C: Retention time D: Vegan Source |
Complied |
USP40 <197K> USP40 <191> HPLC In House Standard |
| 特定旋轉 | +70.0° – +73.0° | +71.5° | USP40 <781S> |
| 點火殘留物 | NMT 0.1% | 0.04% | USP40 <281> |
| 乾燥損失 | NMT 1.0% | 0.05% | USP40 <731> |
| pH | 3.0 – 5.0 | 4.1 | USP40 <791> |
| Contaminants & Inorganic Components | |||
| 重金屬 | NMT 10 ppm | Complied | USP40 <231> method II |
| 砷 | NMT 3 ppm | Complied | USP40 |
| Content of Sulfate | NMT 0.24% | Complied | USP40 |
| 微生物學 | |||
| Total Plate Count | NMT 1000 cfu/g | <10 cfu/g | USP40 |
| 酵母與黴菌 | NMT 100 cfu/g | <10 cfu/g | USP40 |
| 沙門氏菌 | 否 | 否 | USP40 |
| 大腸桿菌 | 否 | 否 | USP40 |
| 總結 | |||
| COA Conclusion | Conforms to USP40 | 符合 | Certificate of Analysis |
應用
Formulation Formats
The ingredient can be evaluated for joint-health supplement products where glucosamine HCl matches the finished product requirement.
膠囊
Used in capsule formulas where the selected glucosamine form and powder characteristics fit the target serving and manufacturing process.
錠劑
Used in tablet formulas subject to the compression, excipient and processing requirements of the finished product.
Powder Products
Considered for powder-based supplements and blends when the material's physical and analytical requirements match the process.
Qualification
What to Confirm for Your Formula
These checks help determine whether the documented material fits the finished product before a commercial order is placed.
Product Specification
Compare your required ingredient identity and release limits with the applicable product specification and current lot documentation.
Processing Requirements
Confirm that the selected material fits your dosage form, blending process, handling conditions and intended market requirements.
Request Pricing & Product Information
Send your required quantity, application, specification and destination so the product information can be matched to your project.