Salbutamol EP Impurity H(HCl) CAS 2252153-95-8
| CAS No. | 2252153-95-8 |
| Molecular Formula | C13H21NO |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Salbutamol EP Impurity H(HCl).
As a process- or degradation-related impurity, Salbutamol EP Impurity H(HCl) (CAS 2252153-95-8, C13H21NOHCl) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Salbutamol EP Impurity H(HCl) (C13H21NOHCl) contains an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.
CATO manufactures Salbutamol EP Impurity H(HCl) under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
Physical & Chemical Properties
| Molecular Formula | C13H21NO HCl |
| Molecular Weight | 243.78 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep tightly closed to prevent evaporation |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 3.0 |
| UV Absorption | UV-absorbing |
| CAS Registry Year (est.) | 1998 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 1 |
Related Salbutamol Standards
- Salbutamol Impurity 130 (CAS 115061-55-7)
- Salbutamol Impurity 134 (CAS 115787-50-3)
- Salbutamol Impurity 55 (CAS 115787-52-5)
- Salbutamol Impurity 85 (CAS 115787-52-5（free base）)
- Salbutamol Impurity 87 (CAS 115787-53-6)
- Salbutamol-d3 (CAS 1219798-60-3)
- Salbutamol Impurity 75 (CAS 1221726-71-1)
- Salbutamol Impurity 146 (CAS 124658-76-0)
Recommended Standards
- Lopinavir EP Impurity L (CAS CATO-C4X-168212)
- Avanafil Impurity 1 (CAS 1638497-26-3)
- Adrenaline Impurity 22 (CAS 575-81-5)
- 1-(3-O-Acetyl-2-deoxy-ß-D-erythro-pentofuranosyl)-4-amino-1,3,5-triazin-2(1H)-one (CAS 1254186-97-4)
- 1-(Cyclopropylmethyl)cyclopropanecarboxylic Acid (CAS 1261269-26-4)
- (2S,4S)-1-(tert-Butoxycarbonyl)-4-[2-nitro-4-(tri-fluoromethyl)phenoxy]-2-pyrrolidinecarboxylic acid (CAS 1354484-53-9)
- 3-(3-Fluoro-4-methoxyphenyl)acrylamide (CAS 1000568-53-5)
- 5-Hydrazono-4-methyl-4,5-dihydro-1h-1,2,4-triazole (CAS 551930-25-7)
- Gallium(III) acetylacetonate (CAS 14405-43-7)
- Semaglutide Impurity 192 (CAS CATO-C4X-2226192)
Why CATO?
- ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
- 130,000+ catalog items in stock, COA supplied with every batch
- Worldwide shipping with full export documentation (HS code guidance available)
- Technical support: +86 18665070610 / Nicole.chen@cato-chem.com