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.

Standart USP
Country of Origin Çin
Fiziksel Form 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
Son Kullanma Tarihi 2030-02-23

Teknik Özellikler

Chondroitin Sulfate Sodium Specification & COA Results

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

Test Item Şartname Result Test Method
Appearance & Identification
Görünüş 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
Ateşleme Üzerinde Kalıntı 20.0%–30.0% 26.5% USP
Chloride NMT 0.50% <0.50% USP
Sülfat 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
Toplam Bakteri Sayısı NMT 1,000 cfu/g 60 cfu/g USP
Yeasts & Molds NMT 100 cfu/g 30 cfu/g USP
Salmonella Absence Not detected USP
Escherichia coli Absence Not detected USP
Elemental Contaminants
Lead (Pb) NMT 0.5 ppm Geç In House Method
Arsenic (As) NMT 1.5 ppm Geç In House Method
Cadmium (Cd) NMT 0.5 ppm Geç In House Method
Cıva (Hg) NMT 0.3 ppm Geç 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
Kurutma Kaybı NMT 12.0% 11.4% USP
Residue of Solvents NMT 5,000 ppm (Ethanol) 2,410 ppm USP
Parçacık Boyutu NLT 95% through 80 mesh 98.1% USP
Yığın Yoğunluğu 0.60–0.85 g/mL 0.67 g/mL USP
Sıkıştırılmış Yoğunluk 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.

01

Joint-Health Supplements

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

02

Kapsüller ve Tabletler

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.

Paketleme

25 KG Net / Drum

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

25 kg net

Depolama

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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