C1131

Cytidine 5′-monophosphate

≥99% (HPLC), synthetic, powder

• Synonym(s): 5′-CMP, 5′-Cytidylic acid, C-5′-P
• Empirical Formula (Hill Notation): C₉H₁₄N₃O₈P
• CAS Number: 63-37-6
• Molecular Weight: 323.20
• NACRES: NA.51
• PubChem Substance ID: 24892358
• UNSPSC Code: 41106305
• EC Number: 200-556-6
• MDL number: MFCD00006544
• Beilstein/REAXYS Number: 46982
• Assay: ≥99% (HPLC)
• Biological source: synthetic
• Form: powder
• Solubility: 1 M NH4OH: 50 mg/mL, clear, colorless
• Storage temp.: 2-8°C

Properties

• Product Name: Cytidine 5′-monophosphate, Sigma Grade, ≥99% (HPLC), synthetic, powder
• biological source: synthetic
• Quality Level: 200
• grade: Sigma Grade
• assay: ≥99% (HPLC)
• form: powder
• solubility: 1 M NH4OH: 50 mg/mL, clear, colorless
• storage temp.: 2-8°C
• SMILES string: NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O
• InChI: 1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
• InChI key: IERHLVCPSMICTF-XVFCMESISA-N

Description

Application

Cytidine 5′-monophosphate has been used in Raman spectroscopy studies.

Biochem/physiol Actions

Cytidine 5′-monophosphate (CMP) is used as a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) to form CDP which upon phosphorylation to CTP supports DNA and RNA biosynthesis.

The nucleoside diphosphates cytidine diphosphate (CDP) and uridine diphosphate (UDP) are essential for pyrimidine synthesis[1] Cytidine 5′-monophosphate (CMP) nucleotide is useful in adsorption studies on biomimetic apatite for mimicking bone mineral. It also serves an immunity supplement in pediatric formulas.

Safety Information

• Storage Class: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)