logo
Send Message
Hefei Home Sunshine Pharmaceutical Technology Co.,Ltd
products
products
Home > products > API Active Pharmaceutical Ingredient > Strontium Ranelate CAS NO:135459-87-9

Strontium Ranelate CAS NO:135459-87-9

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 135459-87-9

Payment & Shipping Terms

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

Get Best Price
Highlight:
CAS NO::
135459-87-9
Appearance ::
White To Beige Powder
Molecular Formula::
C12H6N2O8SSr2
Molecular Weight::
513.49
EINECS NO::
690-882-9
MDL NO::
MFCD09038742
CAS NO::
135459-87-9
Appearance ::
White To Beige Powder
Molecular Formula::
C12H6N2O8SSr2
Molecular Weight::
513.49
EINECS NO::
690-882-9
MDL NO::
MFCD09038742
Strontium Ranelate CAS NO:135459-87-9

Product Description:

Product Name: strontium ranelate CAS NO:135459-87-9

 

 

 

 

 

 

 

 

Synonyms:

2,2'-((5-Carboxy-4-(carboxymethyl)-3-cyanothiophen-2-yl)azanediyl)diacetic acid, distrontium salt;

Ranelic Acid Strontium Salt;

 

 

 

 

 

 

 

 

Chemical & Physical Properties:

Appearance : white to beige powder

Assay :≥99.0%

Density:1.8g/cm3

Boiling Point: 778.8℃ at 760 mmHg

Melting Point: >310℃

Flash Point:424.8℃

 

 

 

 

 

 

 

 

Strontium ranelate, a strontium(II) salt of ranelic acid, is a medication for osteoporosis marketed as Protelos or Protos by Servier. Studies indicate it can also slow the course of osteoarthritis of the knee. The drug is unusual in that it both increases deposition of new bone by osteoblasts and reduces the resorption of bone by osteoclasts. It is therefore promoted as a "dual action bone agent" (DABA).

 

 


On 13 May 2013, Servier released a Direct Healthcare Professional Communication which stated that new restrictions for the use of strontium ranelate are now in place, as randomised trials have shown an increased risk of myocardial infarction. Servier states that the use is now restricted to treatment of severe osteoporosis in postmenopausal women at high risk for fracture. The European Pharmacovigilance Risk Assessment Committee (PRAC) recommends restriction in the use of strontium ranelate, based on a routine benefit-risk assessment of the medicine, which included data showing an increased risk of heart problems, including heart attacks. On 21 February 2014 the European Medicine Agency recommended that strontium ranelate remain available with restrictions relative to patients with existing heart disease.

 

 

 

 

 

 

 

If you are interested in our products or have any questions, please feel free to contact us !

 

 

 

 

Products under patent are offered for R & D purpose only. However, the final responsibility lies exclusively with the buyer.