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Cosmetic Grade Sodium Hyaluronate Powder / Micro Ingredients Hyaluronic Acid

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Province/State:shanghai
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Cosmetic Grade Sodium Hyaluronate Powder / Micro Ingredients Hyaluronic Acid

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Brand Name :BBP
Model Number :BBP-HA-37
Certification :ISO9001, US FDA Registration
Place of Origin :China
MOQ :Negotiable
Price :Negotiable
Payment Terms :T/T
Supply Ability :500KG / Month
Delivery Time :Depending on your PO Quantity
Packaging Details :1KG/ bag, then 10 bags put in one Fiber Drum.
Product Name :Sodium Hyaluronate Powder
Grade :Cosmetic Grade
Assay of HA :>95%
CAS NO. :9067-32-7
Quality Standard :EP7.0 Standard
Other Name :Micro Ingredients Hyaluronic Acid
DMF :Yes, DMF Available
Application :Ophthalmic surgery drugs
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Cosmetic Grade Sodium Hyaluronate Powder / Micro Ingredients Hyaluronic Acid

beyond biopharma Sodium Hyaluronate Powder Application

Cosmetic grade

Hyaluronic acid is a Natural biological molecule widely existing in skin and other tissues, which has an excellent moisturizing effect. It is known as the ideal Natural moisturizing Factor (NMF) in the world. It is currently found in the nature of cosmetics with the best moisturizing performance of the material. Different molecular weights of hyaluronic acid have different ability to penetrate into the skin and bring different efficacy.

Pharmaceutical Grade

Hyaluronic acid has been widely used in medicine due to its unique physicochemical properties and physiological functions. It can be used as a viscoelastic agent for ophthalmic intraocular lens implantation, as a filler for joint surgery such as osteoarthritis and rheumatoid arthritis, as a medium, widely used in eye drops, and also used to prevent postoperative adhesion and promote the healing of skin wounds.

Food grade

Oral hyaluronic acid to increase the content of the body, the body can supplement the lack of hyaluronic acid. Hyaluronic acid through digestion, absorption, can make the skin moist smooth, soft and elastic; Can delay consenescence, prevent the happening of the disease such as arthritis, arteriosclerosis, pulse mussily and cerebral atrophy.

Quick Deatails of beyond biopharma Sodium Hyaluronate Powder

Material name beyond biopharma Sodium Hyaluronate Powder
Origin of material Bacteria Fermentation
Color and Apperance White powder
Quality Standard EP Pharmaceutical Grade
Purity of the material 95%-105%
Moisture content ≤10% (105°for 2hours)
Molecular weight Around 1000 000 Dalton
Bulk density >0.30g/ml as bulk density
Solubility Perfect solubility into water
Application Pharma Eye Drop, Burn Topical Ointment
GMP Certificate EU GMP Certificate
DMF Documentation Yes, DMF is available
Shelf Life 2 years from production date
Packing Inner packing: Sealed Foil bag,1KG/Bag, 5KG/Bag
Outer packing: 10kg/Fiber drum

The advantage of beyond biopharma Sodium Hyaluronate Powder


1. GMP and DMF: Our manufacturer of pharmaceutical Grade Hyaluronic acid is EU GMP verified, and the DMF is available for Hyaluronic acid.

2. Complete EU Pharmacopoeia compliance: Our Pharma Grade HA complies with EP standard completely.

4. Customized Molecular weight : We provide different molecular weight of HA for your choice.

3. Competitive prices: We have direct factory prices.

Typical Specification sheet of pharma grade Hyaluronic acid / Sodium Hyaluronate

ITEMS

SPECIFICATIONS (TEST METHOD)

RESULT

Appearance White or almost white powder or fibrous aggregate Conforms
Identification
A: Infrared Absorption Complies with Ph. EUR. Reference spectrum of sodium hyaluronate Comply
B: Reaction of sodium Postive Postive
Appearance of solution Clear and the absorbance is NMT 0.01 at 600nm Clear, A600nm=0.002
Molecular weight Report the test value 1.11x 106 Dalton
Assay of sodium hyaluronate 95% -105% 100%
Intrinsic Viscosity Report the test value 1.87 m³/kg
Loss on drying Less than10%(USP731) 8.5%
Nucleic Acid The absorbance is NMT 0.5 at 260nm 0.06
PH (1%H2O solution) 5.0-8.5 (0.5% solution) 6.5
Protein ≤0.1% (on the dried substance) 0.03%
Chlorides ≤0.5% <0.5%
Heavy Metal NMT10 PPM Pass
Iron ≤80 ppm(on the dried substance) 13.6ppm
Residual solvents (Ethanol) ≤0.5% 0.008%
Microbial Contamination <100CFU/g <10CFU/g
Bacterial Endotoxins <0.5IU/mg <0.5IU/mg
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