| CAS No. | 3813-27-2 |
| Molecular Formula | C7H16N2O |
| Molecular Weight | 144.21 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Metoclopramide Impurity 9 is closely related to an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
Metoclopramide Impurity 9 (CAS 3813-27-2) is a certified pharmaceutical impurity reference standard with the molecular formula C7H16N2O and a molecular weight of 144.21 g/mol.
Owing to an amide group, a hydroxyl group, an ether linkage, Metoclopramide Impurity 9 is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 144.21 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
CATO manufactures Metoclopramide Impurity 9 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.
| Molecular Formula | C7H16N2O |
| Molecular Weight | 144.21 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 1.0 |
| CAS Registry Year (est.) | 1958 |
| Nitrogen Atoms | 2 |