| CAS No. | 1638241-89-0 |
| Molecular Formula | C20H24N10O10P2S2 |
| Molecular Weight | 690.54 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 Adenosine, [P(R)]-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thioadenylyl-(2′→5′)-, cyclic nucleotide.
CATO supplies Adenosine, [P(R)]-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thioadenylyl-(2′→5′)-, cyclic nucleotide (CAS 1638241-89-0), a certified reference material (molecular formula C20H24N10O10P2S2, MW 690.54 g/mol) for analytical method development and quality control.
Adenosine, [P(R)]-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thioadenylyl-(2′→5′)-, cyclic nucleotide (C20H24N10O10P2S2) contains a flavonoid core, an amide group, a sulfone group, a phosphate ester group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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 Adenosine, [P(R)]-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thioadenylyl-(2′→5′)-, cyclic nucleotide 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 | C20H24N10O10P2S2 |
| Molecular Weight | 690.54 g/mol |
| 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) | 14.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1993 |
| Nitrogen Atoms | 10 |
| Sulfur Atoms | 2 |