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Carbuterol

Base Information
  • Chemical Name:Carbuterol
  • CAS No.:34866-47-2
  • Molecular Formula:C13H21 N3 O3
  • Molecular Weight:267.328
  • Hs Code.:
  • European Community (EC) Number:252-257-5
  • UNII:0N12JR32MR
  • DSSTox Substance ID:DTXSID00865737
  • Nikkaji Number:J19.430A
  • Wikipedia:Carbuterol
  • Wikidata:Q5038111
  • NCI Thesaurus Code:C79709
  • Metabolomics Workbench ID:154417
  • ChEMBL ID:CHEMBL2110780
  • Mol file:34866-47-2.mol
Carbuterol

Synonyms:(5-(2-(tert-butylamino)-1-hydroxyethyl)-2-hydroxyphenyl)urea;carbuterol;carbuterol monohydrochloride;carbuterol monohydrochloride, (+)-isomer;carbuterol monohydrochloride, (-)-isomer;SK and F 40,383-A;SK and F 40383;SK and F-40,383-A;SK and F-40383;SKF 40383-A

Suppliers and Price of Carbuterol
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • CARBUTEROL 95.00%
  • 5MG
  • $ 495.47
Total 9 raw suppliers
Chemical Property of Carbuterol
Chemical Property:
  • Vapor Pressure:8.68E-09mmHg at 25°C 
  • Melting Point:174-176° 
  • Boiling Point:447.4°Cat760mmHg 
  • Flash Point:224.4°C 
  • PSA:108.60000 
  • Density:1.248g/cm3 
  • LogP:2.28200 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:267.15829154
  • Heavy Atom Count:19
  • Complexity:304
Purity/Quality:

99% *data from raw suppliers

CARBUTEROL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)NCC(C1=CC(=C(C=C1)O)NC(=O)N)O
  • Uses Bronchodilator. Carbuterol is a beta-adrenoceptor binding drug.
  • Therapeutic Function Bronchodilator
Technology Process of Carbuterol

There total 1 articles about Carbuterol 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:

Reference yield:

Guidance literature:
Racemat 41 (Base), (-)-Weinsaeure;
DOI:10.1021/jm00247a011
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