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Bambuterol hydrochloride

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Bambuterol hydrochloride Basic information

Product Name:
Bambuterol hydrochloride
Synonyms:
  • KWD-2183
  • BAMBUTEROL HCL
  • BAMBUTEROL HYDROCHLORIDE
  • BAMBEC
  • Bambuterol monohydrochloride
  • dimethylcarbamic acid 5-[2[(1,1-dimethyl)amino]1-hydroxyethyl]-1,3-phenylene ester hydrochloride
  • DIMETHYLCARBAMIC ACID 5-[2-[(1,1-DIMETHYLETHYL)AMINO]-1-HYDROXYETHYL]-1,3-PHENYLENE ESTER HYDROCHLORIDE
  • Bambuterol hydrochloride, 98%, a long acting beta-adrenoceptor agonist (LABA)
CAS:
81732-46-9
MF:
C18H30ClN3O5
MW:
403.9
EINECS:
643-060-9
Product Categories:
  • BAMBEC
  • Bambuterol
  • Amines
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Active Pharmaceutical Ingredients
Mol File:
81732-46-9.mol
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Bambuterol hydrochloride Chemical Properties

Melting point:
222-224°C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
H2O: ~33 mg/mL, soluble
form 
powder
color 
off-white
Merck 
14,953
InChIKey
LBARATORRVNNQM-UHFFFAOYSA-N
CAS DataBase Reference
81732-46-9(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29242990

MSDS

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Bambuterol hydrochloride Usage And Synthesis

Description

Bambuterol is an inactive prodrug of terbutaline. It has a prolonged duration of action when administered orally.

Chemical Properties

White Solid

Uses

Ester prodrug of the ?-adrenergic agonist terbutaline

Uses

Ester prodrug of the ?2-adrenergic agonist terbutaline.

Uses

beta adrenergic agonist, bronchodilator, cholinesterase inhibitor

Definition

ChEBI: The hydrochloride salt of bambuterol. A long acting beta-adrenoceptor agonist used in the treatment of asthma, it is a prodrug for terbutaline.

Synthesis

Conventionally, as a method for preparing bambuterol hydrochloride, bis-3,5- (N, N-dimethylcarba) is subjected to an acylation process from 3 ′, 5′-dihydroxyacetophenone represented by the following reaction formula in US Pat. No. 4419364. Preparing moyloxy) -acetophenone (step 1); Preparing a bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2-bromo-acetophenone therefrom (step 2); Preparing an bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2- (N-benzyl tert-butyl) amino-acetophenone from the alkylation process therefrom (step 3); From this step to prepare a 1- [bis- (3 ', 5'-N, N-dimethylcarbamoyloxy) phenyl] -2-N-3 tert-butylaminoethanol hydrochloride, ie bambuterol hydrochloride.

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