| Identification | More | [Name]
Disodium uridine-5'-monophosphate | [CAS]
3387-36-8 | [Synonyms]
5'-UMP-NA2
5'-URIDYLIC ACID
5'-URIDYLIC ACID DISODIUM SALT
U 5'-P DISODIUM SALT
UMP
UMP 2NA
UMP DISODIUM
UMP DISODIUM SALT
UMP, NA2
URIDINE-5'-MONOPHOSPHATE DISODIUM
URIDINE-5'-MONOPHOSPHATE DISODIUM SALT
URIDINE-5'-MONOPHOSPHORIC ACID, DISODIUM
URIDINE 5'-MONOPHOSPHORIC ACID DISODIUM SALT
5’-umpdisodium
disodium5’-ump
disodium5’-uridylate
disodiumump
disodiumuridine5’-phosphate
uridine,5’-dihydrogenphosphate,disodiumsalt
5`-UMP,2Na | [EINECS(EC#)]
222-211-9 | [Molecular Formula]
C9H11N2Na2O9P | [MDL Number]
MFCD00006525 | [Molecular Weight]
368.14 | [MOL File]
3387-36-8.mol |
| Chemical Properties | Back Directory | [Appearance]
Crystalline | [Melting point ]
208-210 °C
| [refractive index ]
-14 ° (C=1, H2O) | [storage temp. ]
−20°C
| [solubility ]
Water (Slightly) | [form ]
Crystalline Powder | [pka]
6.4, 9.5(at 25℃) | [color ]
White | [Water Solubility ]
40 g/100 mL (20 ºC) | [BRN ]
3582885 | [Stability:]
Very Hygroscopic | [InChI]
InChI=1/C9H13N2O9P.Na.H/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18);;/t4-,6-,7-,8-;;/s3 | [InChIKey]
KURVIXMFFSNONZ-WFIJOQBCSA-L | [SMILES]
O[C@@H]1[C@@H]([C@@H](COP(O)(O)=O)O[C@H]1N1C=CC(=O)NC1=O)O.[NaH] |&1:1,2,3,11,r| | [CAS DataBase Reference]
3387-36-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
2
| [RTECS ]
YU7975000
| [F ]
10-21 | [HS Code ]
29389090 |
| Hazard Information | Back Directory | [Chemical Properties]
Crystalline | [Uses]
A nucleotide that is a major component of ribonucleic acid. It is found in dietary supplements as well as natural RNA rich foods and has been shown to increase cognitive function in animals. | [General Description]
Uridine 5′-monophosphate is a pyrimidine mononucleotide. It is formed by decarboxylation of orotidine 5′-monophosphate. UMP is further converted to UTP (uridine 5′-triphosphate) using kinases. |
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