JIAXING HENGJIE BIOPHARMACEUTICAL CO., LTD.

chondroitin sulfate DC garde

• Category :

  Intermediates/Pharmaceutical intermediates

• Synonyms :

  Chondroitin Sulfate Sodium;chondroitin 4-sulfate sodium salt from bovine trachea;[(2R,3R,4R,5R,6R)-5-acetamido-4-[(2S,3S,4R,5R,6R)-6-carboxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxy-6-hydroxy-2-(hydroxymethyl)tetrahydropyran-3-yl]oxysulfonylperoxysodium;CSA;Chondroitin Sulphate Sodium;Chondroitin sulfate A sodium salt;Chondroitin 6-sulfate sodium salt;Chondroitin Sulfate C Sodium Salt;Csc-Na;Shark Chondroitin Sulfate;Shark Chondroitin;Chondroitin-6-Sulfate Sodium Sult;

• CAS NO :

  9082-07-9

• EC NO :

• Molecular Formula :

  C₁₄H₂₂NNaO₁₆S

• Molecular Weight :

  515.3763

• Main Specifications :

  DE grade USP34

• InChI :

  InChI=1/C14H23NO16S.Na/c1-3(17)15-5-10(9(30-32(25,26)31-24)4(2-16)27-13(5)23)28-14-8(20)6(18)7(19)11(29-14)12(21)22;/h4-11,13-14,16,18-20,23-24H,2H2,1H3,(H,15,17)(H,21,22);/q;+1/p-1/t4-,5-,6-,7-,8+,9+,10-,11-,13-,14+;/m1./s1/rC14H22NNaO16S/c1-3(18)15-5-10(28-14-8(21)6(19)7(20)11(29-14)12(22)23)9(4(2-17)27-13(5)24)30-33(25,26)32-31-16/h4-11,13-14,17,19-21,24H,2H2,1H3,(H,15,18)(H,22,23)/t4-,5-,6-,7-,8+,9+,10-,11-,13-,14+/m1/s1

• Packing :

  25kg/drum

• Product description :

  JIA XING HENGJIE BIOPHARMACEUTICAL CO., LTD

   CERTIFICATE OF ANALYSIS

                                                                              COA NO.: HS1104082

  Product: CHONDROITIN SULFATE SODIUM

  Origin:      Bovine(Terrestrial)                                        Report Date:  2011/04/20

  Batch No.: HS1104082                                                  Quantity:  1000KGS

  Net Weight: 25KG/DRUM                                               Gross weight:  27.5KG/DRUM

  Manufacturing Date: 2011/04/11                                  Expiry Date: 2013/04/10

                                                                                                                                                            

                 ITEMS                                      SPECIFICATIONS(TEST METHOD)                    RESULT

  Apperance	white to off-white powder	pass
  Identification	Infra Red confirmed (USP197K), Sodium reaction(USP191)	Pass, Positive
  Assay	90%-105%(CPC)	91.0%
  Loss on drying	Less than 10% (USP731)	8.7%
  Protein	NMT 6.0% (USP32)	4.6%
  Heavy Metal	NMT20PPM(Method II USP231)	<20 PPM
  PH(1%H2O solution)	5.5-7.5(USP791)	6.8
  Specific Rotation	minus 20°-minus30°(USP981S)	-26.8°
  Chloride	NMT0.5% (USP221)	<0.5%
  Sulfate	NMT0.24% (USP221)	<0.24%
  Residue on Ignition	20%-30% (dry base) (USP281)	25.6%
  Clarity (5% H2O solution)	<0.35@420nm	0.22
  Organic Volatile Impuritues	Meet Requirements(USP467)	Pass
  Electrophoretic purity	NMT2.0% (USP726)	Pass
  Total Bacteria Count	<1000 Col/g	<1000 Col/g
  Yeast and Mold	<100 Col/g	<100 Col/g
  Salmonella	Negative(USP2022)	Pass
  E.Coli	Negative(USP2022)	Pass
  Particle size	100% through 60 mesh	Pass

• Uses :

  Pharmaceutical raw material used to produce tablet, capsule,cream and etc.

• Molecular Structure :