Joint Health Ingredient
Chondroitin Sulfate Sodium CPC 90% | Bulk Powder
Chondroitin Sulfate Sodium CPC 90% is a white powder with a 90.6% CPC assay, USP test methods, controlled impurity and microbiological specifications, and defined particle size and density characteristics for formulation review.
Product Information
Chondroitin Sulfate Sodium at a Glance
Core product identification and handling information.
Product Overview
Chondroitin Sulfate Sodium for Ingredient Qualification
Chondroitin Sulfate Sodium is the sodium salt of a sulfated glycosaminoglycan. In ingredient qualification, buyers typically review identity, assay, impurity profile, microbiological quality and physical properties together, rather than relying on assay alone.
Identity and Composition
The supplied COA uses infrared absorption, sodium reaction, disaccharide composition and specific rotation as identification controls, with the applicable tests listed against USP methods.
Batch-Level Quality Data
Identity, assay, impurity, microbiological and physical-property controls are presented together so the ingredient specification can be reviewed in one place.
Batch Traceability
Supplied COA Batch Information
技術仕様
Chondroitin Sulfate Sodium Specification & COA Results
Acceptance criteria, reported results and test methods are presented side by side for clear specification review.
| Test Item | 仕様 | Result | Test Method |
|---|---|---|---|
| Appearance & Identification | |||
| 外観 | White or off-white powder | White powder | In House Method |
| I.D.-A Infrared Absorption | Compare with the CRS | Corresponding | USP |
| I.D.-B General Sodium | Gives reaction of sodium | Positive | USP |
| I.D.-C Disaccharide Composition | ΔDi-4S / ΔDi-6S ≥ 1.0 | > 1.0 | USP |
| I.D.-D Specific Rotation | Between –20.0° and –30.0° | Meet requirement | USP |
| Assay & Inorganic Components | |||
| Content by CPC Titration | 90.0%–105.0% (dried basis) | 90.6% | USP |
| 点火時の残留物 | 20.0%–30.0% | 26.5% | USP |
| Chloride | NMT 0.50% | <0.50% | USP |
| 硫酸塩 | NMT 0.24% | <0.24% | USP |
| Electrophoretic Purity | NMT 2% | <2% | USP |
| Limit of Protein | NMT 6.0% (dried basis) | <6.0% | USP |
| Microbiological Quality | |||
| 総細菌数 | NMT 1,000 cfu/g | 60 cfu/g | USP |
| Yeasts & Molds | NMT 100 cfu/g | 30 cfu/g | USP |
| サルモネラ菌 | Absence | Not detected | USP |
| 大腸菌 | Absence | Not detected | USP |
| Elemental Contaminants | |||
| Lead (Pb) | NMT 0.5 ppm | パス | In House Method |
| Arsenic (As) | NMT 1.5 ppm | パス | In House Method |
| Cadmium (Cd) | NMT 0.5 ppm | パス | In House Method |
| 水銀（Hg） | NMT 0.3 ppm | パス | In House Method |
| Solution & Physical Properties | |||
| Clarity and Color of Solution | NMT 0.35 at 420 nm | 0.150 | USP |
| Optical Rotation | –20.0° to –30.0° | –25.3° | USP |
| pH | 5.5–7.5 | 6.8 | USP |
| 乾燥減量 | NMT 12.0% | 11.4% | USP |
| Residue of Solvents | NMT 5,000 ppm (Ethanol) | 2,410 ppm | USP |
| 粒子径 | NLT 95% through 80 mesh | 98.1% | USP |
| かさ密度 | 0.60–0.85 g/mL | 0.67 g/mL | USP |
| タップ密度 | 0.65–1.20 g/mL | 0.96 g/mL | USP |
The values shown apply to batch CS202603002.
Application Context
Formulation Uses
Chondroitin sulfate is widely used in joint-health formulations, where the finished product format and target market determine the appropriate ingredient specification.
Joint-Health Supplements
Used as an ingredient in formulations developed for joint and mobility support.
カプセルと錠剤
Suitable for solid dosage formulations where powder flow, particle size and density are part of formulation review.
Powder Formulations
Can be considered for powder-based formulations when the finished product specification requires chondroitin sulfate sodium.
Ingredient Qualification
Analytical results support specification review before the material is selected for a formulation.
パッケージング
25 KG Net / Drum
Packed at 25 kg net in a polyethylene bag with a cardboard drum.
ストレージ
Storage & Shelf Life
Preserve in tight containers. Shelf life is 48 months when stored under the stated conditions in the original packaging.
- Store in tight containers.
- Keep the product in its original packaging.
- Follow the documented storage conditions throughout the stated shelf-life period.
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