- Cytidylic acid
-
- $0.00 / 1Kg/Bag
-
2026-04-08
- CAS:63-37-6
- Min. Order: 1KG
- Purity: 98%min HPLC
- Supply Ability: 1000KG
|
| | Cytidine 5’-monophosphate Basic information |
| | Cytidine 5’-monophosphate Chemical Properties |
| Melting point | ~222 °C (dec.) | | Boiling point | 678.1±65.0 °C(Predicted) | | density | 2.15±0.1 g/cm3(Predicted) | | refractive index | 9.8 ° (C=1, 0.5mol/L Na2HPO4) | | storage temp. | 2-8°C | | solubility | Water (Slightly, Heated) | | pka | pK2:4.39(0);pK3:6.62(+1) (25°C) | | form | crystalline | | color | White | | biological source | synthetic | | Water Solubility | soluble | | BRN | 46982 | | InChI | 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 | | InChIKey | IERHLVCPSMICTF-JDNPWWSISA-N | | SMILES | P(OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](O)[C@@H]1O)(O)(O)=O | | CAS DataBase Reference | 63-37-6(CAS DataBase Reference) | | EPA Substance Registry System | 5'-Cytidylic acid (63-37-6) |
| Hazard Codes | Xn,Xi | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 24/25-37/39-36-26 | | WGK Germany | 3 | | RTECS | HA3980000 | | F | 10-21 | | TSCA | TSCA listed | | HS Code | 29349990 | | Storage Class | 11 - Combustible Solids | | Toxicity | LD50 intraperitoneal in mouse: > 1gm/kg |
| | Cytidine 5’-monophosphate Usage And Synthesis |
| Description | Cytidine 5'-monophosphate, also known as 5'-CMP, is a nucleotide that is used as a monomer in RNA. 5'-CMP is a key intermediate in the preparation of several nucleotide derivatives and is widely used in food and pharmaceutical industries. | | Chemical Properties | white crystalline powder | | Uses | Cytidine 5′-monophosphate has been used in Raman spectroscopy studies. | | Uses | Cytidine 5'-monophosphate (5'-CMP) is a key intermediate in the production of nucleotide derivatives and has been widely used in the food, agriculture and pharmaceutical industries. | | Definition |
ChEBI: Cytidine 5'-monophosphate is a pyrimidine ribonucleoside 5'-monophosphate having cytosine as the nucleobase. It has a role as a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a pyrimidine ribonucleoside 5'-monophosphate and a cytidine 5'-phosphate. It is a conjugate acid of a cytidine 5'-monophosphate(2-).
| | Production Methods | As a key intermediate in preparing several nucleotide derivatives, cytidine 5′-monophosphate (5′-CMP) is widely applied in food and pharmaceutical industries. Enzymatic synthesis of 5′-CMP is catalyzed by cytidine kinase (CK, EC 2.7.1.213), a type of nucleoside kinase that belongs to the PfkB family. Li et al. constructed a highly efficient biosynthesis system for manufacturing 5′-CMP in vitro. CK was used for the biotransformation of cytidine to 5′-CMP, while polyphosphate kinase (PPK) was coupled for adenosine triphosphate regeneration. Both CK and PPK were selected from extremophiles, possessing great potential for biocatalytic synthesis. After optimization, 96 mM 5′-CMP was produced within 6 h, and the yield reached nearly 100%[1]. | | benefits | Cytidine 5’-monophosphate (CMP) is a nucleotide supplement with potential benefits such as improved muscle function, immune support, and enhanced neuronal growth. CMP is a component of RNA and phospholipids and sometimes pairs with uridine and other nutrients to produce synergistic effects, particularly in brain health. Studies have shown that adding CMP as a supplement to fish feed can contribute to their growth, health performance, and immune response. | | 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. | | Side effects | Cytidine 5’-monophosphate (CMP) is a naturally occurring substance and is considered relatively safe, with no adverse health effects or respiratory irritation. No serious adverse reactions have been reported when CMP is used as a supplement; the most common side effects are gastrointestinal reactions, including nausea, vomiting, diarrhea, abdominal pain, and decreased appetite. Headaches may occur with long-term use. | | References | [1] Zonglin Li. “Efficient One-Pot Synthesis of Cytidine 5′-Monophosphate Using an Extremophilic Enzyme Cascade System.” Journal of Agricultural and Food Chemistry 68 34 (2020): 9188–9194.
|
| | Cytidine 5’-monophosphate Preparation Products And Raw materials |
|