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99.59% Raw Furosemide Powder,Furosemide With BP standard

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99.59% Raw Furosemide Powder,Furosemide With BP standard

China 99.59% Raw Furosemide Powder,Furosemide With BP standard supplier
99.59% Raw Furosemide Powder,Furosemide With BP standard supplier 99.59% Raw Furosemide Powder,Furosemide With BP standard supplier

Large Image :  99.59% Raw Furosemide Powder,Furosemide With BP standard

Product Details:

Place of Origin: WUHAN
Brand Name: Yuancheng
Certification: ISO9001
Model Number: 54-31-9

Payment & Shipping Terms:

Minimum Order Quantity: 10G
Price: Negotiable
Packaging Details: Discreet packaging
Delivery Time: About 4-7 working days
Payment Terms: T/T,western union,money gram,bitcoin
Supply Ability: 300KG/Month
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Detailed Product Description
Product Name: Furosemide CAS: 54-31-9
Purity: 99% Appearance: White Powder
Grade: Pharmaceutical Grade Minimum Order Quantity: 10G

99.59% Raw Furosemide Powder,Furosemide With BP standard

 

If you are interested in my products,please contact:
nancypeng@ycphar.com
skype:steroidsbio
whatsApp:86-15372437208

 

Furosemide
MF:C12H11ClN2O5S
MW:330.74
CAS:54-31-9
Appearance:white powder
Purity:99%
Standard:BP standard

 

Furosemide 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. The amount of medication required depends on the person in question. 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.

 

The COA of Furosemide :

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

99.59% Raw Furosemide Powder,Furosemide With BP standard

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