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Indacaterol Maleate

Base Information Edit
  • Chemical Name:Indacaterol Maleate
  • CAS No.:753498-25-8
  • Deprecated CAS:435273-74-8
  • Molecular Formula:C4H4O4*C24H28N2O3
  • Molecular Weight:508.571
  • Hs Code.:29339900
  • European Community (EC) Number:610-125-8
  • UNII:2JEC1ITX7R
  • Wikidata:Q27137018
  • NCI Thesaurus Code:C81640
  • ChEMBL ID:CHEMBL1789842
  • Mol file:753498-25-8.mol
Indacaterol Maleate

Synonyms:Indacaterol maleate

Suppliers and Price of Indacaterol Maleate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • IndacaterolMaleicAcidSalt
  • 5mg
  • $ 275.00
  • TRC
  • IndacaterolMaleicAcidSalt
  • 1mg
  • $ 120.00
  • TCI Chemical
  • Indacaterol Maleate >98.0%(HPLC)
  • 20mg
  • $ 119.00
  • TCI Chemical
  • Indacaterol Maleate >98.0%(HPLC)
  • 100mg
  • $ 412.00
  • Medical Isotopes, Inc.
  • IndacaterolMaleicAcidSalt
  • 5 mg
  • $ 890.00
  • Matrix Scientific
  • Indacaterol Maleate 95+%
  • 1g
  • $ 3036.00
  • DC Chemicals
  • Indacaterol Maleate 99%
  • 1 g
  • $ 1200.00
  • DC Chemicals
  • Indacaterol Maleate 99%
  • 250 mg
  • $ 600.00
  • Crysdot
  • Indacaterol Maleate 98+%
  • 50mg
  • $ 59.00
  • Crysdot
  • Indacaterol Maleate 98+%
  • 25mg
  • $ 40.00
Total 78 raw suppliers
Chemical Property of Indacaterol Maleate Edit
Chemical Property:
  • Appearance/Colour:White Solid 
  • Melting Point:195-197°C (dec.) 
  • PSA:160.21000 
  • LogP:3.66390 
  • Storage Temp.:Refrigerator 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:8
  • Exact Mass:508.22095136
  • Heavy Atom Count:37
  • Complexity:708
Purity/Quality:

98%,99%, *data from raw suppliers

IndacaterolMaleicAcidSalt *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=C(C=C2CC(CC2=C1)NCC(C3=C4C=CC(=O)NC4=C(C=C3)O)O)CC.C(=CC(=O)O)C(=O)O
  • Isomeric SMILES:CCC1=C(C=C2CC(CC2=C1)NC[C@@H](C3=C4C=CC(=O)NC4=C(C=C3)O)O)CC.C(=C\C(=O)O)\C(=O)O
  • Recent ClinicalTrials:Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of Two Orally Inhaled Indacaterol Salts in Adult Subjects With Asthma.
  • Recent EU Clinical Trials:Comparison of 1-year treatment with inhaled long acting bronchodilators (LABD) plus inhaled glucocorticosteroids (ICS) versus LABD without ICS on re-hospitalizations and/or death in elderly patients with chronic obstructive pulmonary disease (COPD) recently hospitalized because of an acute exacerbation of COPD (ICS-Life study).
  • Recent NIPH Clinical Trials:Safety of LAMA/LABA combination therapy in the COPD patients
  • Uses A long-acting β2 adrenoreceptor agonist and bronchodilator, for the treatment of asthma and chronic obstructive pulmonary disease.
  • Clinical Use Indacaterol is a b-adrenoceptor agonist currently approved in Europe as Onbrez, and is marketed by Novartis. It needs to be taken only once a day, unlike competitors formoterol and salmeterol. These drugs are used in the treatment of chronic obstructive pulmonary disease (COPD) and asthma. Onbrez is administered via an aerosol formulation through a dry powder inhaler. A Phase III trial published in July 2010 suggested that indacaterol is significantly more effective than twice-daily formoterol in improving FEV1 and reduces the need for rescue medication.
Technology Process of Indacaterol Maleate

There total 42 articles about Indacaterol Maleate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In isopropyl alcohol; for 1h; Reflux;
Guidance literature:
In methanol; dichloromethane; at 25 - 30 ℃; for 1h;
Refernces Edit
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