Sodium Hyaluronate USP NF BP Ph Eur Suppliers & Manufacturers |
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SDS MSDS of Sodium Hyaluronate USP NF BP Ph Eur Manufacturers
Sodium Hyaluronate
CAS Number 9067-32-7, USP NF BP Ph Eur & Pure
We supply as under:
Sodium hyaluronate is the sodium salt of hyaluronic acid, a glycosaminoglycan found in various connective tissue of humans. Sodium hyaluronate is similar to the fluid that surrounds the joints in your body. This fluid acts as a lubricant and shock absorber for the joints. Sodium hyaluronate is used to treat knee pain caused by osteoarthritis. As an anti-aging treatment, dermatologists inject it into the dermis of the skin to restore facial fullness in areas where volume is lost.
Sodium Hyaluronate BP Ph Eur Grade:
(C14H20NNaO11) --- CAS 9067-32-7
Action and use: High viscosity mucopolysaccharide.
DEFINITION
Sodium salt of hyaluronic acid, a glycosaminoglycan consisting of D-glucuronic acid and N-acetyl-D-glucosamine disaccharide units. It is extracted from cocks' combs or obtained by fermentation from Streptococci, Lancefield Groups A and C.
Content: 95.0 per cent to 105.0 per cent (dried substance).
Intrinsic viscosity: 90 per cent to 120 per cent of the value stated on the label.
PRODUCTION
Where applicable, the animals from which sodium hyaluronate is derived must fulfil the requirements for the health of animals suitable for human consumption.
When produced by fermentation of gram-positive bacteria, the process must be shown to reduce or eliminate pyrogenic or inflammatory components of the cell wall.
CHARACTERS
Appearance: White or almost white, very hygroscopic powder or fibrous aggregate.
Solubility: Sparingly soluble or soluble in water, practically insoluble in acetone and in anhydrous ethanol.
IDENTIFICATION
A. Infrared absorption spectrophotometry.
Comparison Ph. Eur. reference spectrum of sodium hyaluronate.
B. It gives reaction (a) of sodium.
TESTS
Solution S: Weigh a quantity of the substance to be examined equivalent to 0.10 g of the dried substance and add 30.0 mL of a 9 g/L solution of sodium chloride. Mix gently on a shaker until dissolved (about 12 h).
Appearance of solution: Solution S is clear and its absorbance at 600 nm is not greater than 0.01.
pH: 5.0 to 8.5.Dissolve the substance to be examined in carbon dioxide-free water to obtain a solution containing a quantity equivalent to 5 mg of the dried substance per millilitre.
Intrinsic viscosity: To pass the test.
Sulfated glycosaminoglycans: Maximum 1 per cent, i the product is extracted from cocks' combs. To pass the test.
Nucleic acids: To pass the test.
Protein: To pass the test.
Chlorides: Maximum 0.5 per cent.
Iron: Maximum 80 ppm.
Atomic absorption spectrometry: To pass the test.
Loss on drying: Maximum 20.0 per cent, determined on 0.500 g by drying at 100-110C.over diphosphorus pentoxide for 6 h.
Microbial contamination:
TAMC: acceptance criterion 100 CFU/g.
Bacterial endotoxins:
Less than 0.5 IU/mg, if intended for use in the manufacture of parenteral preparations without a further appropriate procedure for the removal of bacterial endotoxins; less than 0.05 IU/mg, if intended for use in the manufacture of intra-ocular preparations or intra-articular preparations without a further appropriate procedure for the removal of bacterial endotoxins.
Sodium Hyaluronate is also supplied as USP NF Grade.
Sodium Hyaluronate USP NF BP Ph Eur Manufacturers:
Muby Chem Ltd.
Toll manufacturing & Warehouse at Houston & Midland, Texas, USA and India
USA, Canada, Mexico Customers may e-mail: usa@mubygroup.com
Call 1-844-682-9243
Europe Africa Asia India Mumbai e-mail: info@mubygroup.com
Call +91-22-23774610
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Suppliers Manufacturers Exporters Importers between USA Canada UAE Europe Russia South Africa Tanzania Kenya Uganda Egypt Nigeria Turkey Mexico Brazil Argentina Chile Dubai China India etc.
Copyright and Usual Disclaimer is Applicable.
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