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Home > products > Chemical Intermediates > Fondaparinux Sodium CAS 114870-03-0

Fondaparinux Sodium CAS 114870-03-0

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 114870-03-0

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Packaging Details: Aluminum Foil Bag, Drum

Delivery Time: 7-15DAY

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Highlight:
CAS NO::
114870-03-0
Appearance::
White Powder
Molecular Formula::
C31H43N3Na10O49S8
Molecular Weight::
1728.08000
EINECS NO::
686-283-7
MDL NO::
MFCD06794972
CAS NO::
114870-03-0
Appearance::
White Powder
Molecular Formula::
C31H43N3Na10O49S8
Molecular Weight::
1728.08000
EINECS NO::
686-283-7
MDL NO::
MFCD06794972
Fondaparinux Sodium CAS 114870-03-0

Product Description:

Product Name: Fondaparinux sodium CAS NO: 114870-03-0


Synonyms:

MethylO-2-Deoxy-6-O-sulfo-2-(sulfoaMino)-α-D-glucopyranosyl-(14)-O-β-D-glucopyranuronosyl-(14)-O-2-deoxy-3,6-di-O-sulfo-2-(sulfoaMino)-α-D-glucopyranosyl-(14)-O-2-O-sulfo-α-L-idopyranuronosyl-(14)-2-deoxy-2-(sulfoaMino)-α-D-glucopyranoside 6-(Hydrogen Sulfate) DecasodiuM Salt;


Chemical & Physical Properties:

Appearance: White powder

Assay :≥99.00%


Safety Information:

HS Code: 3822000002


Fondaparinux sodium was first introduced in the US for prophylaxis of deep vein thrombosis which may lead to pulmonary embolism following major orthopaedic surgery. Fondaparinux is the first of a new class of antithrombic agents distinct from low molecular weight heparin (LMWH) and heparin. This entirely synthetic molecule is a copy of the heparin pentasaccharide sequence, the shortest fragment able to catalyze antithrombin lllmediated inhibition of factor Xa thereby inhibiting thrombin generation without antithrombin action. Fondaparinux does not display significant effects on coagulation tests (such as activated partial thromboplastin time and prothrombin time), does not bind to platelet factor 4 or promote heparin-induced thrombocytopenia. In phase III studies, fondaparinux significantly reduced the incidence of thromboembolism following orthopedic surgery, with an overall risk reduction of 50% in comparison to the LMWH, enoxaparin. Following subcutaneous administration, fondaparinux has a nearly complete bioavailability, a rapid onset of action, a prolonged half-life (17.2 h) enabling once daily dosing and is not metabolized preceeding renal excretion. The drug appears to be generally safe, with haemoragic complications either comparable to or higher than those for LMWH.


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