Furosemide (Lasix) Polvere (CAS 54-31-9) | Materie prime farmaceutiche

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Furosemide (Lasix) Polvere (CAS 54-31-9) | Materie prime farmaceutiche

CATEGORY AND TAGS:
altre API , , , , , , , ,

MF:C12H11ClN2O5S
MW:330.74
CAS:54-31-9
Aspetto:white powder
Purezza:99.56%
Standard:USP standard

richiesta
  • Specifications

Buy USP Standard China Pharmaceutical Raw Materials Furosemide (Lasix) Polvere (CAS 54-31-9)

 

Furosemide (Lasix) Application

Furosemide is a potent diuretic (water pill) that is used to eliminate water and salt from the body.

Furosemide is used to treat fluid retention (edema) in people with congestive heart failure, liver disease, or a kidney disorder such as nephrotic syndrome.

Furosemide is also used to treat high blood pressure (hypertension).

 

Furosemide (Lasix) Certifiate of Analysis

Nome del prodotto furosemide
CAS. 54-31-9 Imballaggio esterno 25KG/DRUM
Data di produzione JAN.2019 Data di scadenza JAN.2023
Standard adottato USP37
Elementi di analisi Specifica: Risultati
description white or almost white crystalline powder white crystalline powder
solubility practically insoluble in water and methylene chloride,soluble in acetone,sparingly soluble in ethanol(96%),slightly soluble in ether,it dissolves in dlute solution of alkali hydroxide. complies
identification    
UN Infrared absorption spectrum should be concordant with IR spectrum of Furosemide CRS complies
B ultra violate and visible absorption spectrophotometer(ratio 0.52-0.57) complies
melting point 210℃ 210℃
residue on ignition NMT 0.10% W/W 0.06% W/W
heavy metals NMT 20 ppm less than 20 ppm
chloride NMT 200ppm less than 200ppm
sulphates NMT 300 ppm less than 300ppm
loss on drying(hot air oven at 105℃ for 3 hrs) NMT 0.50% W/W 0.24%
Related substance by HPLC    
impurity A NMT 0.25% less than 0.25%
impurity B NMT 0.25% less than 0.25%
impurity C NMT 0.25% less than 0.25%
impurity D NMT 0.25% less than 0.25%
impurity E NMT 0.25% less than 0.25%
total impurity NMT 0.50% 0.12%
any individual impurity NMT 0.10% 0.05%
assay 98%-101% on dry basis 99.56%
residual solvent iso propyl alcohol:not more than 5000ppm 263 ppm
Conclusione Qualificato

 

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