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Ibandronate Sodium Structure

PRODUCT TYPE

Active Pharmaceutical Ingredient (API)

GRADE

USP / BP / EP (as applicable)

CHEMICAL NAME

Ibandronate sodium (monosodium salt, monohydrate)

CHEMICAL FORMULA

Approx. C₉H₂₂N O₇P₂·Na·H₂O (salt monohydrate form)

MOLECULAR WEIGHT

~359.2 g/mol (monohydrate salt form)

CAS NUMBER

138926-19-9 (sodium monohydrate salt)

IUPAC NAME

3-(N methyl-N-pentyl)amino 1 hydroxypropane-1,1-diphosphonic acid, monosodium salt, monohydrate

CHEMICAL CLASS

Nitrogen-containing bisphosphonate derivative

THERAPEUTIC CLASS

Bone resorption inhibitor

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White to off-white crystalline powder
Solubility Freely soluble in water; practically insoluble in most organic solvents.
Melting Point 210–215 °C
pH -

Product Description

Ibandronate sodium is a potent nitrogen containing bisphosphonate widely used for the prevention and treatment of osteoporosis in post menopausal women. It reduces bone resorption by inhibiting osteoclast activity, thereby helping to maintain or increase bone mineral density (BMD) and lowering the risk of fractures. Beyond osteoporosis, ibandronate has also been used to manage hypercalcemia of malignancy and to prevent skeletal complications in cancers with bone metastases.

How Ibandronate Sodium Works

Ibandronate binds strongly to bone mineral (hydroxyapatite) at sites of active bone remodeling. Once osteoclasts attempt to resorb bone containing ibandronate, the bisphosphonate is internalized and inhibits the enzyme Farnesyl diphosphate synthase (FDPS), thereby disrupting the mevalonate pathway — essential for prenylation of small GTPase signaling proteins required for osteoclast function. This inhibition reduces osteoclast activity and promotes their apoptosis, leading to decreased bone resorption, reduced bone turnover, and a net gain (or maintenance) of bone mass.

Use(s)

Adverse Effects

Why choose Salius for Ibandronate Sodium?

  1. Regulatory-Grade Manufacturing Standards
    They maintain WHO GMP compliance, with some facilities FDA certified, and follow stringent internal QC protocols. Every batch is tested in state-of-the-art labs before release.
  2. Enhancing Cost-Effectiveness Through Large Volume API Utilization
    As an exporter and distributor house, Salius aims to deliver high-quality APIs at competitive prices, a key advantage for cost-sensitive markets.
  3. Global Export Experience & Documentation Support
    Salius regularly exports APIs, provides regulatory documents (DMF, impurity profiles), and supports filings for international clients—even in stringent regulated markets.
  4. Documents We Provide
  5. Transparency & Trustworthiness
    They present as a government-recognized star export house with strong quality and delivery ratings.
Attribute Why Salius Pharma Is a Good Choice
Quality Certification WHO GMP, ISO 9001:2015, FDA audited facilities
Affordability & Generic Access Cost competitive generics for global supply
Export Experience Proven track record of supplying globally

What You Receive in Our Package

When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.

Each Shipment Includes:

Product

Expected Delivery Time

We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.

Overall Delivery Time:

7 to 21 business days from dispatch, depending on your location.

FAQs

Bone resorption inhibitor; nitrogen-containing bisphosphonate.

Typically supplied as crystalline monohydrate; amorphous forms are rare.

Primarily via renal excretion; part binds to bone for prolonged effect.

Handle in a dry environment; use moisture-protected packing and avoid dust exposure.

Yes; oral monthly dosing is common, IV used for GI intolerance or compliance issues.

Yes, both CoA and MSDS are provided along with pharmacopeial compliance.

Place an Order or Request a Quote from Salius Pharma

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