- Min.Order :1 Kilogram
- Purity: 99% min.
- Payment Terms : L/C,T/T,
Keywords
Heparin sodium Ardeparin sodium Sodium Heparin
Quick Details
- Appearance:White or grey brown indefiniteness powder.
- Application:Used to delay and prevent blood clots.
- PackAge:as per clients' request.
- ProductionCapacity:400|Metric Ton|Month
- Storage:Sealed and store in a cool and dry place.
- Transportation:By sea, by air, by courier, by train.
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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