| CAS No. | 924643-01-6 |
| Molecular Formula | C11H12INO2 |
| Molecular Weight | 317.12 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 317.12 g/mol gives (R)-(3-hydroxypyrrolidin-1-yl)(4-iodophenyl)methanone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
(R)-(3-hydroxypyrrolidin-1-yl)(4-iodophenyl)methanone (CAS 924643-01-6), molecular formula C11H12INO2 and molecular weight 317.12 g/mol, is a CATO reference standard with documented purity and traceability.
Based on its molecular formula C11H12INO2, (R)-(3-hydroxypyrrolidin-1-yl)(4-iodophenyl)methanone contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 317.12 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
CATO manufactures (R)-(3-hydroxypyrrolidin-1-yl)(4-iodophenyl)methanone 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 | C11H12INO2 |
| Molecular Weight | 317.12 g/mol |
| Appearance | Off-white to pale yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 6.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
| Halogen Content | I-containing |
| Nitrogen Atoms | 1 |