3590-36-1
5-methylcytidine 5'-(dihydrogen phosphate)
CAS: 117309-80-5;3590-36-1
Molecular Formula: C10H13N2Na2O9P
3590-36-1 - Names and Identifiers
| Name | 5-methylcytidine 5'-(dihydrogen phosphate) |
| Synonyms | Aids187058 Aids-187058 5-Me-UMP.Na2 5-Methyl-Uridine-5'-monophosphate 5-Methylcytidine 5'-monophosphate 5-Methyl-5'-cytidylic acid diammonium salt 5-Methyl-5'-Cytidylic Acid Diammonium Salt 5-methylcytidine 5'-(dihydrogen phosphate) 5-Methyl-Uridine-5'-monophosphate, disodium salt 5-Methyluridine-5'-monophosphate diammonium salt |
| CAS | 117309-80-5 3590-36-1 |
| InChI | InChI=1/C10H16N3O8P/c1-4-2-13(10(16)12-8(4)11)9-7(15)6(14)5(21-9)3-20-22(17,18)19/h2,5-7,9,14-15H,3H2,1H3,(H2,11,12,16)(H2,17,18,19)/t5-,6-,7-,9-/m1/s1 |
3590-36-1 - Physico-chemical Properties
| Molecular Formula | C10H13N2Na2O9P |
| Molar Mass | 382.171521 |
| Density | 2.04g/cm3 |
| Boling Point | 666.5°C at 760 mmHg |
| Flash Point | 356.9°C |
| Vapor Presure | 1.3E-20mmHg at 25°C |
| Refractive Index | 1.745 |
3590-36-1 - Introduction
5-methyl uridine -5 '-monophosphate is a nucleic acid derivative, chemical formula is C11H16N3O11P, belonging to the nucleotide class of compounds.
Nature:
5-Methyluridine-5 '-monophosphate is a white crystalline solid, soluble in water. It is stable under neutral or alkaline conditions, but decomposes under strong acid conditions.
Use:
5-methyluridine-5 '-monophosphate is an important reagent for nucleic acid modification and methylation. It plays multiple biological functions in cellular processes, such as regulating gene expression, maintaining DNA stability and participating in metabolism. In addition, it can also be used as a tool for studying nucleic acids, such as for constructing DNA or RNA sequences, preparing labeled probes, etc.
Preparation Method:
There are many synthesis methods of 5-methyl uridine -5 '-monophosphate, and the commonly used methods are chemical synthesis or enzymatic synthesis. Chemical synthesis methods include the use of compounds to transfer phosphate groups and methylation reactions, while enzymatic synthesis generally relies on nucleic acid methyltransferases for methylation reactions.
Safety Information:
5-methyluridine-5 '-monophosphate is a relatively safe compound under normal circumstances, but appropriate safety measures still need to be taken. It may cause irritation to the eyes, skin and respiratory tract, so appropriate protective equipment should be worn during operation, including laboratory gloves, protective glasses and air vents outside the laboratory. In addition, contact with substances such as strong acids, strong bases and oxidants should be avoided to avoid dangerous reactions. During handling and storage, relevant safety procedures shall be observed. When waste is disposed of, it should be disposed of in accordance with national and regional regulations.
Nature:
5-Methyluridine-5 '-monophosphate is a white crystalline solid, soluble in water. It is stable under neutral or alkaline conditions, but decomposes under strong acid conditions.
Use:
5-methyluridine-5 '-monophosphate is an important reagent for nucleic acid modification and methylation. It plays multiple biological functions in cellular processes, such as regulating gene expression, maintaining DNA stability and participating in metabolism. In addition, it can also be used as a tool for studying nucleic acids, such as for constructing DNA or RNA sequences, preparing labeled probes, etc.
Preparation Method:
There are many synthesis methods of 5-methyl uridine -5 '-monophosphate, and the commonly used methods are chemical synthesis or enzymatic synthesis. Chemical synthesis methods include the use of compounds to transfer phosphate groups and methylation reactions, while enzymatic synthesis generally relies on nucleic acid methyltransferases for methylation reactions.
Safety Information:
5-methyluridine-5 '-monophosphate is a relatively safe compound under normal circumstances, but appropriate safety measures still need to be taken. It may cause irritation to the eyes, skin and respiratory tract, so appropriate protective equipment should be worn during operation, including laboratory gloves, protective glasses and air vents outside the laboratory. In addition, contact with substances such as strong acids, strong bases and oxidants should be avoided to avoid dangerous reactions. During handling and storage, relevant safety procedures shall be observed. When waste is disposed of, it should be disposed of in accordance with national and regional regulations.
Last Update：2024-04-10 22:29:15
