Pharmaceutical Intermediate Powder CAS No.128270-60-0 Bivali

Brand Name: SGONEK

Price: $100 -$150/Gram

Place of Origin: Shaanxi, China

Certification: ISO FDA SG COA MSDS

Grade: Food Grade Pharmaceutical Grade

Payment Terms: T/T, Western Union, MoneyGram

Product Name:  Bivalirudin Cas No.:  128270-60-0
Molecular Formula:  C98H138N24O33 Purity:  99%min
Brand Name:  SGONEK Certification:  ISO FDA SG COA MSDS

Pharmaceutical Intermediate Powder CAS No.128270-60-0 Bivali


Product Name  Bivalirudin
CAS No.  128270-60-0
Purity  99%
Appearance  White Crystalline Powder
Molecular Formula  C98H138N24O33
EINECS No.  /

Description:

Bivalirudin is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). Bivalirudin with provisional use of glycoprotein IIb/IIIa inhibitor (GPI) is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI). Bivalirudin is indicated for patients with, or at risk of HIT/HITTS undergoing PCI. Bivalirudin is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin. 


Product Name

Bivalirudin Trifluoroacetate

Cas No.

128270-60-0

Molecular Formula

C98H138N24O33

Molecular Weight

2180.33

Purity (HPLC)

99.0%min.

Appearance 

White powder

Single Impurity (HPLC) 

0.5%max

Amino Acid Composition 

±10% of theoretical

Peptide Content (N%)

≥80.0%

Water Content (Karl Fischer) 

≤8.0%

Acetate Content (HPIC)

≤12.0%

MS (ESI)

Consistent

Mass Balance 

95.0~105.0%

Bivalirudin is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). Bivalirudin with provisional use of glycoprotein IIb/IIIa inhibitor (GPI) is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI). Bivalirudin is indicated for patients with, or at risk of HIT/HITTS undergoing PCI. Bivalirudin is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin.


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