Ubenimex Impurity 10 HCl CAS CATO-C4X-182510
| CAS No. | CATO-C4X-182510 |
| Molecular Formula | C16H30N2O4 |
| 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 Ubenimex Impurity 10 HCl.
Ubenimex Impurity 10 HCl (CAS CATO-C4X-182510) is a certified pharmaceutical impurity reference standard with the molecular formula C16H30N2O4HCl and a molecular weight of 350.88 g/mol.
Based on its molecular formula C16H30N2O4HCl, Ubenimex Impurity 10 HCl contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 350.88 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
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.
As a certified reference material (CRM), Ubenimex Impurity 10 HCl meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
Physical & Chemical Properties
| Molecular Formula | C16H30N2O4 HCl |
| Molecular Weight | 350.88 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 2.0 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 2 |
Related Ubenimex Standards
- Ubenimex Impurity 4 (CAS 118943-09-2)
- Ubenimex Impurity 5 (CAS 118943-10-5)
- Ubenimex Impurity 2 (CAS 1654771-89-7)
- Ubenimex-d7 HCl (CAS 65391-42-6)
- Ubenimex Impurity 10 (CAS CATO-C4X-185210)
- Ubenimex Impurity 11 (CAS CATO-C4X-185211)
- Ubenimex Impurity 12 (CAS CATO-C4X-185212)
- Ubenimex Impurity 13 (CAS CATO-C4X-185213)
Recommended Standards
- Vilanterol Impurity 25 L-Tartrate (CAS CATO-C4X-193525)
- Naphazoline EP Impurity A (CAS 36321-43-4)
- N-Nitroso Revefenacin impurity 102 (CAS 11348-65-3)
- 2-Ethylhexanal (CAS 123-05-7)
- 3,5-Dimethyl-1-(4-methylbenzenesulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-Dioxaborolan-2-yl)-1H-indazole (CAS 1421252-90-5)
- Ethyl 4-bromo-5-chloro-1H-pyrazole-3-carboxylate (CAS 1872370-56-3)
- 3,5-Dimethyl-1-((1-methyl-1h-pyrazol-4-yl)methyl)-1h-pyrazol-4-amine (CAS 1248803-82-8)
- Mephedrone HCl (CAS 1189726-22-4)
- 1-(2-Chloro-7,8-dimethylquinolin-3-yl)ethanol (CAS 1017403-18-7)
- Des-[Gly]31-Semaglutide (CAS CATO-C4X-2226156)
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