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Glucosamine Sulphate Potassium Chloride – USP/EP

Product Description

Glucosamine Sulphate Potassium Chloride is probably the most commonly used Glucosamine salt. We offer this product as a white crystalline powder free from any black particles. Our product & manufacturing process comply to the highest quality standard and is offered at a competitive price.

 

Nutraceutical Grade
Basic Information
Product name Glucosamine Sulphate Potassium Chloride USP
Chemical name Bis (D-Glucose,2-amino-2-deoxy-), sulfate potassium chloride complex
Ingredients Chitin, Hydrochloricacid, Activated carbon, Hyflosupercel, Methanol, Potassium Sulphate
Specification data sheet
Formula C12H28Cl2K2N2O14S
Molecular weight 606
CAS 38899-05-07
Einecs
FEMA
Tariff number
Version USP-39
Date of version August-1,2016
Certification Drug License from Govt. of India, cGMP Certificate, WHO-GMP Certificate, MPEDA Certificate, Halal Certificate, Halal Trust Certificate, ISO 22000:2005(Covering HACCP). EU Approval (Traces) (Regulation (EC) No. 852/2004 & 853/2004 Compliance) ,Written Confirmation(API)(Article (a) b of Directive 2001/83/EC).
Specifications
Appearance White crystalline powder
Colour White
Odour Odourless
Solubility Soluble in water
Assay (% gc) 98-102%w/w
Stability and storage 5Years and Ambient
Packaging 25Kg HDPE Drums
Key application areas/industry Fibromylgia, Osteoarthritis and Rheumatoid Arthritis.
Pharmaceutical Grade
Basic Information
Product name Glucosamine Sulphate Potassium Chloride Ph.Eur
Chemical name Bis(2-amino-2-deoxy-D-glucopyranose) sulfate bis(potassium chloride).
Ingredients Chitin, Hydrochloricacid, Activated carbon, Hyflosupercel, Methanol, Potassium Sulphate
Specification data sheet
Formula C12H28Cl2K2N2O14S
Molecular weight 606
CAS 38899-05-07
Einecs
FEMA
Tariff number
Version Ph.Eur-9.0
Date of version January-16,2017
Certification Drug License from Govt. of India, cGMP Certificate, WHO-GMP Certificate, MPEDA Certificate, Halal Certificate, Halal Trust Certificate, ISO 22000:2005(Covering HACCP). EU Approval (Traces) (Regulation (EC) No. 852/2004 & 853/2004 Compliance) ,Written Confirmation(API)(Article (a) b of Directive 2001/83/EC).
Specifications
Appearance White or almost white crystalline powder
Colour White
Odour Odourless
Solubility Freely Soluble in water, Sparingly soluble in methanol and Practically insoluble in acetone
Assay (% gc) 98-102%w/w
Stability and storage 4Years and Ambient
Packaging 25Kg HDPE Drums
Key application areas/industry Fibromylgia, Osteoarthritis and Rheumatoid Arthritis.

Product Details

Manufacturer AMPIL
Industry Nutraceuticals, Pharmaceuticals