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.

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Product Information

Chondroitin Sulfate Sodium at a Glance

Core product identification and handling information.

قياسي جامعة جنوب المحيط الهادئ
Country of Origin الصين
الشكل المادي White powder
Sterilization Status Non-irradiation / ETO

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

Batch CS202603002
Batch Quantity 3,000 kg
Manufacturing Date 2026-02-24
تاريخ انتهاء الصلاحية 2030-02-23

المواصفات الفنية

Chondroitin Sulfate Sodium Specification & COA Results

Acceptance criteria, reported results and test methods are presented side by side for clear specification review.

Test Item المواصفات Result Test Method
Appearance & Identification
المظهر White or off-white powder White powder In House Method
I.D.-A Infrared Absorption Compare with the CRS Corresponding جامعة جنوب المحيط الهادئ
I.D.-B General Sodium Gives reaction of sodium Positive جامعة جنوب المحيط الهادئ
I.D.-C Disaccharide Composition ΔDi-4S / ΔDi-6S ≥ 1.0 > 1.0 جامعة جنوب المحيط الهادئ
I.D.-D Specific Rotation Between –20.0° and –30.0° Meet requirement جامعة جنوب المحيط الهادئ
Assay & Inorganic Components
Content by CPC Titration 90.0%–105.0% (dried basis) 90.6% جامعة جنوب المحيط الهادئ
البقايا عند الاشتعال 20.0%–30.0% 26.5% جامعة جنوب المحيط الهادئ
كلوريد NMT 0.50% <0.50% جامعة جنوب المحيط الهادئ
كبريتات NMT 0.24% <0.24% جامعة جنوب المحيط الهادئ
Electrophoretic Purity NMT 2% <2% جامعة جنوب المحيط الهادئ
Limit of Protein NMT 6.0% (dried basis) <6.0% جامعة جنوب المحيط الهادئ
Microbiological Quality
إجمالي عدد البكتيريا NMT 1,000 cfu/g 60 cfu/g جامعة جنوب المحيط الهادئ
Yeasts & Molds NMT 100 cfu/g 30 cfu/g جامعة جنوب المحيط الهادئ
السالمونيلا Absence Not detected جامعة جنوب المحيط الهادئ
الإشريكية القولونية Absence Not detected جامعة جنوب المحيط الهادئ
Elemental Contaminants
Lead (Pb) NMT 0.5 ppm تخطي In House Method
Arsenic (As) NMT 1.5 ppm تخطي In House Method
Cadmium (Cd) NMT 0.5 ppm تخطي In House Method
الزئبق (Hg) NMT 0.3 ppm تخطي In House Method
Solution & Physical Properties
Clarity and Color of Solution NMT 0.35 at 420 nm 0.150 جامعة جنوب المحيط الهادئ
Optical Rotation –20.0° to –30.0° –25.3° جامعة جنوب المحيط الهادئ
الرقم الهيدروجيني 5.5–7.5 6.8 جامعة جنوب المحيط الهادئ
الخسارة عند التجفيف NMT 12.0% 11.4% جامعة جنوب المحيط الهادئ
Residue of Solvents NMT 5,000 ppm (Ethanol) 2,410 ppm جامعة جنوب المحيط الهادئ
حجم الجسيمات NLT 95% through 80 mesh 98.1% جامعة جنوب المحيط الهادئ
الكثافة السائبة 0.60–0.85 g/mL 0.67 g/mL جامعة جنوب المحيط الهادئ
الكثافة المضغوطة 0.65–1.20 g/mL 0.96 g/mL جامعة جنوب المحيط الهادئ

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.

01

Joint-Health Supplements

Used as an ingredient in formulations developed for joint and mobility support.

02

الكبسولات والأقراص

Suitable for solid dosage formulations where powder flow, particle size and density are part of formulation review.

03

Powder Formulations

Can be considered for powder-based formulations when the finished product specification requires chondroitin sulfate sodium.

04

Ingredient Qualification

Analytical results support specification review before the material is selected for a formulation.

التعبئة والتغليف

25 KG Net / Drum

Packed at 25 kg net in a polyethylene bag with a cardboard drum.

25 kg net

التخزين

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.
Solvents used for the documented product batch: water and ethanol.
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