Search Results for " Chlorhexidine "
Chlorhexidine EP Impurity L
| SZ CAT No: | SZ-C068012 |
| CAS No | 2518301-34-1 |
| Mol.F. | C13H15ClN2O6 |
| Mol.Wt. | 330.7 |
| Inv. Status | Synthesis on demand |
Chemical Name: (5R,6S)-2-(4-chloroanilino)-5-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-5,6-dihydro-4H-1,3-oxazin-4-one (as per EP) ; (5R,6S)-2-[(4-Chlorophenyl)amino]-5-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-5,6-dihydro-4H-1,3-oxazin-4-one (as per USP)
Synonym: Chlorhexidine Oxazinone Analog (USP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: O=C1[C@H](O)[C@@]([C@H](O)[C@H](O)CO)([H])OC(NC2=CC=C(Cl)C=C2)=N1
Chlorhexidine EP Impurity L is chemically (5R,6S)-2-(4-chloroanilino)-5-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-5,6-dihydro-4H-1,3-oxazin-4-one (as per EP) ; (5R,6S)-2-[(4-Chlorophenyl)amino]-5-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-5,6-dihydro-4H-1,3-oxazin-4-one (as per USP). It is also known as Chlorhexidine Oxazinone Analog (USP). Chlorhexidine EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Chlorhexidine EP Impurity L can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Chlorhexidine.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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