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Febuxostat CAS 144060-53-7

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 144060-53-7

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Aluminum Foil Bag, Drum

Delivery Time: 7-15 days

Payment Terms: T/T, L/C, D/A, Western Union

Supply Ability: TON

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Highlight:
CAS NO::
144060-53-7
Appearance ::
White Crystalline Powder
Molecular Formula::
C16H16N2O3S
Molecular Weight::
316.375
EINECS NO::
682-158-6
MDL NO::
MFCD00871598
CAS NO::
144060-53-7
Appearance ::
White Crystalline Powder
Molecular Formula::
C16H16N2O3S
Molecular Weight::
316.375
EINECS NO::
682-158-6
MDL NO::
MFCD00871598
Febuxostat CAS 144060-53-7

Product Description:

Product Name: Febuxostat CAS NO:144060-53-7

 

 

 

 

 

 

 

Synonyms:

2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylic acid;

2-(3-Cyano-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylic Acid;

Uloric; Adenuric;

 

 

 

 

 

 

Chemical & Physical Properties:

Appearance : White crystalline powder

Assay :≥99.0%

Density:1.3 1g/cm3

Boiling Point:536.6℃ at 760 mmHg

Flash Point:278.3℃

Melting Point:238-239℃

 

 

 

 

 

 

 

Febuxostat (INN; trade names Adenuric in Europe and New Zealand, Uloric in the US, Goturic in Latin America, Feburic in Japan) is a drug that inhibits xanthine oxidase, thus reducing production of uric acid in the body. It is used in the treatment of chronic gout and hyperuricemia.

 

 

 

 

Febuxostat was discovered by scientists at the Japanese pharmaceutical company Teijin in 1998. Teijin partnered the drug with TAP Pharmaceuticals in the US and Ipsen in Europe. Ipsen obtained marketing approval for febuxostat from the European Medicines Agency in April 2008, Takeda obtained FDA approval in February 2009, and Teijin obtained approval from the Japanese "Pharmaceuticals and Medical Devices Agency" in 2011.

 

 

 

 

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