Buy Furosemide (Lasix) Powder Pharmaceutical Raw Materials Online CAS 54-31-9
Furosemide Specification
Product Name: Furosemide
CAS: 54-31-9
Standard: BP
Level: Medical grade
Content: 99%
Appearance: white powder
Packing: 25 kg / cardboard drum detachable
Ingredients: For direct export only
Physical and chemical properties: White or off-white crystalline powder. The temperature of 206 ° C. Soluble in acetone, methanol, dimethylformamide, slightly soluble in ethanol, insoluble in water. Odorless, almost tasteless.
Category: Pharmaceutical raw materials
Deferred product: diuretic
Application: This product has strong and short diuretic effect. It is a powerful diuretic for the treatment of edema caused by diseases such as heart, liver and kidney, especially in cases of ineffective statin. It can be used to treat acute pulmonary edema and brain. Edema, acute renal failure and high blood pressure diseases; with the rehydration of the product can promote non-toxic toxic substances.
What is Furosemide?
Furosemide (Lasix), is a medication used to treat fluid build-up due to heart failure, liver scarring, or kidney disease. It may also be used for the treatment of high blood pressure. It can be taken intravenously or by mouth. When taken by mouth it typically begins working within an hour while intravenously it typically begins working within five minutes.
Furosemide Certificate of Analysis
| Product name |
furosemide |
| CAS No. |
54-31-9 |
Outer Packing |
25kg/drum |
| Production date |
JUNE 2017 |
Shelf life |
MAY,2022 |
| Standard adopted |
BP |
| Items of analysis |
Specification |
Results |
| Appearance |
a white or almost white crystalline powder |
almost white crystallilne powder |
| solubility |
practically insoluble in water and methylene chloride,soluble in acetone,sparingly soluble in ethanol(96%),slightly soluble in ether,it dissolves in dilute solution of alkali hydroxide. |
complies |
| identification |
|
|
| A.By UV |
ultra violate and visible absorption spectrophotometer(ratio 0.52 to 0.57) |
complies |
| B.By IR |
the infrared absorption spectrum of the sample should be concordant with the spectrum of Furosemide WS |
complies |
| C.By color test |
formation a red to red-violet color should be produced |
red-violet color formation |
| appearance of solution |
the solution is clear and not more intensely colors than reference soluiton BY5 |
complies |
| 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 substances by HPLC |
|
|
| Impurity C |
NMT 0.20% |
0.11% |
| Impurity D |
NMT 0.15% |
0.09% |
| Any individual impurity |
NMT 0.10% |
0.05% |
| Total impurity |
NMT 0.50% |
0.26% |
| Assay |
98-101%on dry basis |
99.59% |
| Conclusion |
Qualified |
