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Home > Products >  Tinzaparin Sodium

Tinzaparin Sodium CAS NO.101921-26-0

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T,
  • Product Details

Keywords

  • Heparin sodium
  • Ardeparin sodium
  • Sodium Heparin

Quick Details

  • ProName: Tinzaparin Sodium
  • CasNo: 101921-26-0
  • Molecular Formula: ca. (C12H16NS2Na3)20
  • Appearance: White or grey brown indefiniteness pow...
  • Application: Used to delay and prevent blood clots.
  • DeliveryTime: 7 days after receipt of 30% T/T.
  • PackAge: as per clients' request.
  • Port: China Port
  • ProductionCapacity: 400 Metric Ton/Month
  • Purity: 99% min.
  • Storage: Sealed and store in a cool and dry pla...
  • Transportation: By sea, by air, by courier, by train.
  • LimitNum: 1 Kilogram

Superiority

Heparin sodium

CAS NO. 9041-08-1;101921-26-0;102785-31-9;12656-11-0

Ardeparin sodium; Dalteparin Sodium; Tinzaparin Sodium; Fragmin; Sodium Heparin

Items

Standard

Identification

A. H-NMR Spectrum: Comply with the USP35 specification of heparin about H-NMR requirements

B. Chromatographic identity: The retention time of the major peak from the Sample solution corresponds to that from the Standard solution

C. Anti-Factorxa to Anti-factor IIa Ratio:0.9~1.1

D.Sodium: It meets the requirements of the flame test for sodium

Residue on ignition 

28.0%~41.0%

Nitrogen(calculated on the dried basis)

1.3%~2.5%

Heavy metals

≤30ppm

Limit of galactosamine in total hexosamine

≤1%

Nucleotidic impurities

Absorbance at 260nm:≤0.20

Absence of oversulfated chondroitin  dulfate

A. Proceed as directed in identification test A. No featurcs associated with oversulfated chondroitin sulfate are found between 2.12 and 3.00ppm

Proceed as dired in identification test B.No peaks corresponding to oversulfated chondroiton sulfate shoud be detected eluting after the heparin peak

PH

5.0~7.5

Loss on drying

≤5.0%

Protein impurities

≤1.0%

Bacterial endotoxins test

Not more than 0.03 USPEU/USPU of Heparin

Not more than 0.03 USPEU/USPU of Heparin

≥180USP U/mg

 

Residual solvents

Ethanol: Not more than 5000 ppm

Microbial contamination

A: Total viable aerobic count: max.10CFU/g

B:Molds/yeasts. max  USP35

 

Details

Heparin sodium

CAS NO. 9041-08-1;101921-26-0;102785-31-9;12656-11-0

Ardeparin sodium; Dalteparin Sodium; Tinzaparin Sodium; Fragmin; Sodium Heparin

Items

Standard

Identification

A. H-NMR Spectrum: Comply with the USP35 specification of heparin about H-NMR requirements

B. Chromatographic identity: The retention time of the major peak from the Sample solution corresponds to that from the Standard solution

C. Anti-Factorxa to Anti-factor IIa Ratio:0.9~1.1

D.Sodium: It meets the requirements of the flame test for sodium

Residue on ignition 

28.0%~41.0%

Nitrogen(calculated on the dried basis)

1.3%~2.5%

Heavy metals

≤30ppm

Limit of galactosamine in total hexosamine

≤1%

Nucleotidic impurities

Absorbance at 260nm:≤0.20

Absence of oversulfated chondroitin  dulfate

A. Proceed as directed in identification test A. No featurcs associated with oversulfated chondroitin sulfate are found between 2.12 and 3.00ppm

Proceed as dired in identification test B.No peaks corresponding to oversulfated chondroiton sulfate shoud be detected eluting after the heparin peak

PH

5.0~7.5

Loss on drying

≤5.0%

Protein impurities

≤1.0%

Bacterial endotoxins test

Not more than 0.03 USPEU/USPU of Heparin

Not more than 0.03 USPEU/USPU of Heparin

≥180USP U/mg

 

Residual solvents

Ethanol: Not more than 5000 ppm

Microbial contamination

A: Total viable aerobic count: max.10CFU/g

B:Molds/yeasts. max  USP35

 

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