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20-30 Mesh Granulated Chondroitin Sulfate Sodium DC Grade For Tablet Compressing
  • 20-30 Mesh Granulated Chondroitin Sulfate Sodium DC Grade For Tablet Compressing

20-30 Mesh Granulated Chondroitin Sulfate Sodium DC Grade For Tablet Compressing

Place of Origin Zhejiang Province, China
Brand Name HS
Certification NSF-GMP,ISO9001/22000,DMF,HALAL
Model Number 90%
Product Details
Product Name:
Bovine Chondrotin Sulfate Sodium USP36 CPC 90%
Application:
Joint Health Tablet Compressing
Origin:
Bovine Cartilages
Quality Standard:
USP38
Identification:
Infra Red Confirmed
DMF:
Available
Particle Size:
20-30 Mesh
Bulk Density:
About 0.70g/ml
Highlight: 

sodium chondroitin sulfate

,

chondroitin sulfate USP

Payment & Shipping Terms
Minimum Order Quantity
Negotiation
Price
negotiation
Packaging Details
Packed into double PE bags ,put into a volume of 25KGS Fiber drums
Delivery Time
Negotiation, CIQ 7days
Payment Terms
T/T, L/C,DP,negotiation
Supply Ability
15 MTper month
Product Description

20-30 Mesh Granulated Chondroitin Sulfate Sodium DC Grade For Tablet Compressing

 

 

Description:

 

This is the DC grade granulated bovine chondroitin sulfate sodium. Compared with normal granulated chondroitin sulfate, the most significant difference of ou

r granulated Chondroitin sulfate is that we didn't adding any excipients during the granulation. We granulated the chondroitin sulfate sodium with what we called "Drying Granulation". By doing this, we are able to maintain the purity of the chondroitin sulfate to be 90% or even 95% after granulation.

 

 

Specifications:

 

 

ITEMS

SPECIFICATIONS

TEST METHOD

Appearance

White to off-white powder

Visual checking

Identification

Infra Red Confirmed

(USP197K)

 

Sodium reaction

(USP191)

Assay(ODB)

NLT90% (Granulated without adding any excipients)

(CPC Titration)

Loss on drying

Less than10%

(USP731)

Protein

NMT6.0%

(USP36)

Heavy Metal

NMT20PPM

(Method I USP231)

PH (1%H2O solution)

5.5-7.5

(USP791)

Specific Rotation

- 20°~ -30°

(USP781S)

Residue on Ignition

20%-30%

(dry base)(USP281)

Organic Volatile Residual

NMT0.5%

(USP467)

Clarity (5%H2O solution)

<0.35@420nm

USP36

Electrophoretic purity

NMT2.0%

(USP726)

Total Bacteria Count

<1000CFU/g

(USP2021)

Yeast & Mold

<100CFU/g

(USP2021)

Salmonella

Negative

(USP2022)

E.Coli

Negative

(USP2022)

Staphylococcus Aureus

Negative

(USP2022)

Particle size

20-30mesh

In-house

Bulk Density NLT 0.65g/ml In-House

 

 

What is the function of DC grade bovine chondroitin sulfate sodium ?

 

Glucosamine and chondroitin are the unique "building blocks" of cartilage and joint tissues. Cartilage provides cushioning in the joints, like a spring, softening the damaging, harsh jolts to each joint with exercise or just everyday activities. Glucosamine and chondroitin sulfate are also building blocks of synovial fluid, which lubricates the joint like oil.

 

Applications:

 

Tablets

Bovine chondroitin sulfate sodium is widely used in combination with Glucosamine and MSM(Methyl-Sulfonyl-Methane) in Tablets as dietary supplements intended for joint health

Capsules

Bovine chondroitin sulfate sodium could also be served in capsules form together with glucosamine and MSM.

Powder form

 Bovine chondroitin sulfate could also be produced into powder form in sachets

 

 

Quality Management System

 

  • 2010 May----Received the Drug Manufacturing License issued by State FDA, Renewed in October 2014.
  • 2010 October---ISO9001& ISO22000 Verified
  • 2012 August---NSF-GMP Verified
  • 2012 September---Registered as animal by products manufacturer in EU, Approval number is 3300DZ0091.
  • 2012 December---  DMF # for chondroitin sulfate: 26474. DMF documents are available.
  • 2014 March--- MSC Verified for shark chondroitin and shark cartilage powder
  • 2016 March---HALAL Verified

 

The packing of DC Bovine chondroitin sulfate sodium USP38 CPC 90%

 

20-30 Mesh Granulated Chondroitin Sulfate Sodium DC Grade For Tablet Compressing 0

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