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Salbutamol EP Impurity L
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Stock Locations

  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

* Stock subject to availability.

Documentation

Download MSDS

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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

898542-81-9Salbutamol EP Impurity L

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Catalogue No.:VE0021956
CAS No.:898542-81-9
Mol. Formula:C13H20ClNO3
Mol. Weight:273.76 g/mol

Additional information on CAS 898542-81-9

Parent drug

Salbutamol

IUPAC Name

(1RS)-2-[(1, 1-Dimethylethyl)amino]-1-[3-chloro-4-hydroxy-5- (hydroxymethyl)phenyl]ethanol

Pharmacopoeial Synonyms

Salbutamol BP Impurity L

Other Synonyms

Chloroalbuterol; 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-chloro-6-(hydroxymethyl)phenol; 1, 3-Benzenedimethanol, 5-chloro-alpha1-(((1, 1-dimethylethyl)amino)methyl)-4-hydroxy-

Smiles

O[C@](CNC(C)(C)C)([H])C1=CC(Cl)=C(O)C(CO)=C1

InChI

InChI=1S/C13H20ClNO3/c1-13(2, 3)15-6-11(17)8-4-9(7-16)12(18)10(14)5-8/h4-5, 11, 15-18H, 6-7H2, 1-3H3/t11-/m0/s1

Description

Salbutamol EP Impurity L also known in pharmacopoeias as Salbutamol BP Impurity L is a thoroughly characterized reference standard. It meets strict regulatory standards including those set by USP EMA JP and BP. This product is crucial for use in Abbreviated New Drug Applications (ANDA) New Drug Applications (NDA) and the commercial production of Salbutamol. Additionally it comes with a detailed Structure Elucidation Report (SER) ensuring its precision and dependability for a variety of analytical uses.

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