PHR1786

Chondroitin Sulfate Sodium

Pharmaceutical Secondary Standard; Certified Reference Material

• Synonym(s): Chondroitin sulfate sodium salt
• CAS Number: 9082-07-9
• UNSPSC Code: 41116107
• NACRES: NA.24

Properties

• grade: certified reference material; pharmaceutical secondary standard
• Quality Level: 300
• agency: traceable to BP 28; traceable to Ph. Eur. Y0000280; traceable to USP 1133570
• API family: chondroitin sulfate
• form: solid
• CofA: current certificate can be downloaded
• packaging: pkg of 500 mg
• technique(s): HPLC: suitable; gas chromatography (GC): suitable
• application(s): pharmaceutical (small molecule)
• storage temp.: 2-30°C
• InChI: 1S/C13H21NO15S/c1-2(15)14-3-8(7(19)13(28-11(3)22)29-30(23,24)25)26-12-6(18)4(16)5(17)9(27-12)10(20)21/h3-9,11-13,16-19,22H,1H3,(H,14,15)(H,20,21)(H,23,24,25)/t3-,4+,5+,6-,7-,8-,9+,11-,12-,13-/m1/s1
• InChI key: KXKPYJOVDUMHGS-OSRGNVMNSA-N

Description

General description

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Chondroitin Sulfate Sodium is the sodium salt of the sulfated linear glycosaminoglycan obtained from bovine, porcine, or avian cartilages of healthy and domestic animals used for food by humans. It consists mostly of the sodium salt of the sulfate ester of N-acetylchondrosamine (2-acetamido-2-deoxy-β-d-galactopyranose) and D-glucuronic acid copolymer.

Application

Chondroitin Sulfate Sodium may be used as a pharmaceutical secondary reference standard for the determination of the analyte in pharmaceutical formulations by size-exclusion high-performance liquid chromatography(HPLC) method.

Chondroitin Sulfate Sodium may be used as a pharmaceutical secondary reference standard for the determination of the analyte in pharmaceutical formulations by size-exclusion and ion-pair high-performance liquid chromatography(HPLC) method.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAC0285 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable