| Weight | 403.907 g/mol |
|---|---|
| Formula | C18H30ClN3O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
BAMBUTEROL HYDROCHLORIDE (81732-46-9)
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- Quantification of bambuterol hydrochloride in a formulated product using solid-state NMR (Journal of Pharmaceutical and Biomedical Analysis, 2005)
- Determination of montelukast sodium and bambuterol hydrochloride in tablets using RP HPLC (Indian Journal of Pharmaceutical Sciences, 2009)
- Highly enantioselective synthesis, crystal structure, and circular dichroism spectroscopy of (R)bambuterol hydrochloride (Chirality, 2008)
- Liquid chromatographic methods for the determination of bambuterol hydrochloride and related compounds (Journal of Chromatography A, 1988)
- SIMULTANEOUS DETERMINATION OF MONTELUKAST SODIUM AND BAMBUTEROL HYDROCHLORIDE IN TABLET DOSAGE FORM BY ULTRAVIOLET SPECTROPHOTOMETRY (DUAL WAVELENGTH METHOD) (2010)
- Development and Validation of UV Spectrophotometric Method for Simultaneous Estimation of Montelukast Sodium and Bambuterol Hydrochloride in Bulk and Tablet Dosage Formulation. (Jordan Journal of Pharmaceutical Sciences, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)NCC(C1=CC(=CC(=C1)OC(=O)N(C)C)OC(=O)N(C)C)O.Cl
-
InChIKeyLBARATORRVNNQM-UHFFFAOYSA-N
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Alternate Names
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Synthesis
tert-Butylamine
+
Reactant
(Alkylation of primary amines)
ODGNJEHRJKMKGI-UHFFFAOYSA-N
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
Dimethylamine
(Schotten-Baumann amide from acid)
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