| CAS No. | 749181-88-2 |
| Molecular Formula | C6H10N4O |
| Molecular Weight | 154.17 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including trans-4-(1H-1,2,3-Triazol-1-yl)pyrrolidin-3-ol.
CATO supplies trans-4-(1H-1,2,3-Triazol-1-yl)pyrrolidin-3-ol (CAS 749181-88-2), a certified reference material (molecular formula C6H10N4O, MW 154.17 g/mol) for analytical method development and quality control.
The molecular framework of trans-4-(1H-1,2,3-Triazol-1-yl)pyrrolidin-3-ol (C6H10N4O) is characterized by an amide group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
CATO manufactures trans-4-(1H-1,2,3-Triazol-1-yl)pyrrolidin-3-ol 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 | C6H10N4O |
| Molecular Weight | 154.17 g/mol |
| Appearance | Off-white to pale yellow crystalline powder. (faint amine-like odor) |
| Purity | 97%+ |
| 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) | 4.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1986 |
| Nitrogen Atoms | 4 |