Gadoteridol Impurity 10 CAS CATO-C4X-225710
| CAS No. | CATO-C4X-225710 |
| Molecular Formula | C17H29N4O7 |
| 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 Gadoteridol Impurity 10.
CATO supplies Gadoteridol Impurity 10 (CAS CATO-C4X-225710), a pharmacopoeial impurity reference standard (molecular formula C17H29N4O7Gd, MW 558.69 g/mol) used for the identification and quantification of trace impurities in APIs.
Based on its molecular formula C17H29N4O7Gd, Gadoteridol Impurity 10 contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 558.69 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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), Gadoteridol Impurity 10 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 | C17H29N4O7 Gd |
| Molecular Weight | 558.69 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | >90% |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 5.5 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| Nitrogen Atoms | 4 |
Related Gadoteridol Standards
- Gadoteridol Impurity 14 HCl (CAS 114873-37-9(free))
- Gadoteridol (CAS 120066-54-8)
- Gadoteridol impurity 40 (CAS 137145-75-6)
- Gadoteridol Impurity 3 (CAS 138884-13-6)
- Gadoteridol Impurity 5 (CAS 148407-91-4)
- Gadoteridol Impurity 13 (CAS 192329-72-9)
- Gadoteridol impurity 29 (CAS 213312-49-3)
- Gadoteridol Impurity 6 (CAS 214195-92-3)
Recommended Standards
- Clenbuterol EP impurity A (CAS 62909-66-4)
- N-Nitroso Verapamil Impurity-1 (CAS CATO-C4X-177840)
- Zolmitriptan Impurity 41 (CAS CATO-C4X-135141)
- (5R)-2,7-diazaspiro[4.4]nonan-1-one;hydrochloride (CAS 2198170-42-0)
- n-(2-Chloro-4-iodophenyl)cyclobutanecarboxamide (CAS 1181526-39-5)
- 2,6-DIbromo-[1,2,4]triazolo[1,5-a]pyrazine (CAS 1823624-52-7)
- 1H-pyrazolo[4,3-c]pyridine-7-carboxylic acid (CAS 1363383-10-1)
- BYS10 (CAS CATO-C4X-30232)
- 6-Chloro-2,3-dihydrobenzofuran-5-amine (CAS 1173434-87-1)
- Liraglutide-d8 Tritrifluoroacetate (CAS CATO-C4X-199223)
Why CATO?
- ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
- 130,000+ catalog items in stock, COA supplied with every batch
- Worldwide shipping with full export documentation (HS code guidance available)
- Technical support: +86 18665070610 / Nicole.chen@cato-chem.com