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Ibandronate sodium monohydrate

Ibandronate sodium monohydrate Structure
CAS No.
138926-19-9
Chemical Name:
Ibandronate sodium monohydrate
Synonyms
Boniva;Bonviva;Ibandrate;BM-21.0955;RPR-102289A;Ibronate Sodium;Ibadronate SodiuM;Ibandronate sodium;Boniva monohydrate;Bondronat monohydrate
CBNumber:
CB4286017
Molecular Formula:
C9H24NNaO8P2
Molecular Weight:
359.23
MOL File:
138926-19-9.mol
MSDS File:
SDS
Modify Date:
2023/9/20 16:43:00

Ibandronate sodium monohydrate Properties

Melting point 840C (dec)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Soluble in DMSO (up to at least 25 mg/ml)
form solid
color White
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
CAS DataBase Reference 138926-19-9(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xn
Risk Statements  40
Safety Statements  22-36-24/25
HS Code  29319090
NFPA 704
0
3 0

Ibandronate sodium monohydrate Chemical Properties,Uses,Production

Description

Ibandronate Sodium Monohydrate is a highly potent nitrogen-containing bisphosphonate used for the treatment of osteoporosis.
Ibandronate Sodium Monohydrate inhibits bone resorption as a sodium salt and complexed with technetium Tc 99m for bone imaging. The monophosphonates are not active and the biphosphonates are used in disorders affecting the skeleton such as metastatic disease, asteoporosis and Paget's. Ibandronate Sodium Monohydrate is an inhibitor of FDPS.

Chemical Properties

[1-Hydroxy-3-(methylpentylamino)-propylidene]bisphosphonic acid sodium salt is White Crystalline Powder

Uses

Inhibits bone resorption as a sodium salt and complexed with technetium Tc 99m for bone imaging. The monophosphonates are not active. Biphosphonates are used in disorders affecting the skeleton such as asteoporosis, metastatic disease, and Paget d

Mechanism of action

The action of ibandronate on bone tissue is based on its affinity for hydroxyapatite, which is part of the mineral matrix of bone. Ibandronate inhibits osteoclast activity and reduces bone resorption and turnover. In postmenopausal women, it reduces the elevated rate of bone turnover, leading to, on average, a net gain in bone mass.

Pharmacokinetics

Absorption
The absorption of oral ibandronate occurs in the upper gastrointestinal tract. Plasma concentrations increase in a dose-linear manner up to 50 mg oral intake and increases nonlinearly above this dose.
Following oral dosing, the time to maximum observed plasma ibandronate concentrations ranged from 0.5 to 2 hours (median 1 hour) in fasted healthy postmenopausal women. The mean oral bioavailability of 2.5 mg ibandronate was about 0.6% compared to intravenous dosing. The extent of absorption is impaired by food or beverages (other than plain water). The oral bioavailability of ibandronate is reduced by about 90% when BONIVA is administered concomitantly with a standard breakfast in comparison with bioavailability observed in fasted subjects. There is no meaningful reduction in bioavailability when ibandronate is taken at least 60 minutes before a meal. However, both bioavailability and the effect on bone mineral density (BMD) are reduced when food or beverages are taken less than 60 minutes following an ibandronate dose.
Distribution
After absorption, ibandronate either rapidly binds to bone or is excreted into urine. In humans, the apparent terminal volume of distribution is at least 90 L, and the amount of dose removed from the circulation via the bone is estimated to be 40% to 50% of the circulating dose. In vitro protein binding in human serum was 99.5% to 90.9% over an ibandronate concentration range of 2 to 10 ng/mL in one study and approximately 85.7% over a concentration range of 0.5 to 10 ng/mL in another study.
Metabolism
There is no evidence that ibandronate is metabolized in humans.
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Ibandronate sodium monohydrate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 329)Suppliers
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Jigs Chemical ltd +919099003427 Gujarat, India 239 58 Inquiry
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NIVEDITA CHEMICALS PVT LTD. +91 22 2832 7321 New Delhi, India 14 58 Inquiry
Rivashaa Agrotech Biopharma Pvt. Ltd. 91-79-26462688 Gujarat, India 987 58 Inquiry
Ibandrate Ibandromate Monosodium Sodium Trihydrogen (1-Hydroxy-3-(methylpenthylamino)propylidene)diphosphonate Monohydrate BM-21.0955 Boniva Bonviva IBANDRONATE SODIUM/1-HYDROXY-3-(METHYLPENTYLAMINO)PROPYLIDENE Ibadronate SodiuM Ibandronate Sodium (100 mg) {1-hydroxy-3-[Methyl(pentyl)aMino]-1-phosphonopropyl}phosphonic acid IBANDRONATE SODIUM MONOHYDRATE 1-Hydroxy-3-(methylpentylamino)propylidenebisphosphonatemonosodiummonohydrate [1-Hydroxy-3-(methylpentylamino)-propylidene]bisphosphonic acid sodium salt Ibandronate sodium IBANDRONATE SODIUM SALT Ibandronate sodiuM salt Monhydrate Phosphonic acid, P,P'-[1-hydroxy-3-(methylpentylamino)propylidene]bis-, sodium salt, hydrate (1:1:1) Ibandronate Sodium (200 mg) Ibandronate Sodium Hydrate Ibandronate sodium monohydrate, >=99% Bondronat monohydrate Boniva monohydrate RPR-102289A Ibronate Sodium [1-Hydroxy-3-(methylpentylamino)propylidene]bisphosphonic acid sodium salt monohydrate Ibandronate Sodium MonohydrateQ: What is Ibandronate Sodium Monohydrate Q: What is the CAS Number of Ibandronate Sodium Monohydrate Q: What is the storage condition of Ibandronate Sodium Monohydrate Q: What are the applications of Ibandronate Sodium Monohydrate Ibandronate Sodium (1335417) 138926-19-9 38926-19-9 C9H23NO7P2NaH2O C9H24NO8NaP2 C9H24NNaO8P2 C9H22NO7P2Na C9H22O7NP2NaH2O C9H22NO7P2NaH2O C9H22NNaO7P2H2O C9H22O7NP2Na C9H22NO7P2H2ONa Inhibitors BONIVA Intermediates & Fine Chemicals Pharmaceuticals API's Ibandronate anti-osteoporosis Bone resorption inhibitor