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Zoledronic acid (CAS No.: 118072-93-8)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Zoledronic acid, 118072-93-8.
We offer the product Zoledronic acid, 118072-93-8 from our manufacturer / supplier / principals for your Research and Development / Evaluation or Commercial requirements, based on the product's availability from our network. We can also offer Zoledronic acid, 118072-93-8 intermediates with the supportive technical package required for evaluation.
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CAS number:

118072-93-8

Chemical Name:

Zoledronic acid; [1-Hydroxy-2-(1H-imidazol-1-yl)-ethylidene]bisphosphonic acid, Zoledronic acid (CAS No.: 118072-93-8)

Pharmacopeia:

EP, IP, In House

Manufacturer Certificate:

GMP, cGMP, WHO GMP, ISO Certified, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

[1-Hydroxy-2-(1H-imidazol-1-yl)-ethylidene]bisphosphonic acid; Zoledronic acid, Zoledronic acid (CAS No.: 118072-93-8)

Molecular Formula

C5H10N2O7P2

Molecular Weight

272.09

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PORPOSE ONLY

Product Name	CAS No.
Ethyl 1H-imidazole-1-acetate	17450-34-9	View \| Inquire
1H-Imidazole-1-acetic acid hydrochloride	87266-37-3	View \| Inquire
Imidazol-1-yl-acetic acid	22884-10-2	View \| Inquire

Description:

Zoledronate or zoledronic acid, is used to prevent skeletal fractures in patients with cancers such as multiple myeloma and prostate cancer. It can also be used to treat hypercalcemia of malignancy and can be helpful for treating pain from bone metastases. An annual dose of zoledrinic acid may also prevent recurring fractures in patients with a previous hip fracture.

Manufacturer Documentation / Approvals :

USDMF	EDMF	DMF (OPEN PART)	DMF (CLOSED PART)	TDP	JDMF

Products protected by valid patents from a manufacturer are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use from a manufacturer in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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