Gadoteridol Impurity 51 CAS CATO-C4X-225751
| CAS No. | CATO-C4X-225751 |
| Molecular Formula | C19H34N4O7 |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
Structurally, Gadoteridol Impurity 51 (C19H34N4O7Ca) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 470.58 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
Gadoteridol Impurity 51 (CAS CATO-C4X-225751) is a certified pharmaceutical impurity reference standard with the molecular formula C19H34N4O7Ca and a molecular weight of 470.58 g/mol.
This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.
CATO manufactures Gadoteridol Impurity 51 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.
Physical & Chemical Properties
| Molecular Formula | C19H34N4O7 Ca |
| Molecular Weight | 470.58 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 97%+ |
| 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) | 5.0 |
| 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
- Lusutrombopag Impurity 54 (CAS CATO-C4X-208454)
- Paliperidone Impurity 107 HCl (CAS CATO-C4X-1724107)
- Entacapone EP Impurity F (CAS 160391-70-8)
- 1-(2-Methyl-2H-indazol-5-yl)thiourea (CAS 691872-01-2)
- H-Leu-βNA (CAS 732-85-4)
- (1-(6-Methylpyridazin-3-yl)piperidin-4-yl)methanamine (CAS 1250271-86-3)
- 1,4-dibromo-3-(chloromethyl)-2,5-difluorobenzene (CAS 1804883-76-8)
- (6-Amino-2-oxo-benzooxazol-3-yl)-acetic acidmethyl ester 883545-12-8 (CAS 883545-12-8)
- 1-(3-(Pyrimidin-5-yl)phenyl)ethan-1-one (CAS 893737-14-9)
- α Bag Cell Peptide (1-9) (CAS 87549-52-8)
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