Basic Description

Synonyms	3387-36-8 \| Disodium UMP \| Disodium 5'-uridylate \| 5'-Uridylic Acid Disodium Salt \| Disodium uridine-5'-monophosphate \| Uridine 5'-monophosphate disodium salt \| 5'-URIDYLIC ACID, DISODIUM SALT \| Uridine monophosphate disodium \| 5'-UMP Disodium Salt \| Uridine 5'-monophospha
Specifications & Purity	10mM in Water
Biochemical and Physiological Mechanisms	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.
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Pyrimidine nucleotides
    - Subclass Pyrimidine ribonucleotides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Pyrimidine nucleotides
Subclass	Pyrimidine ribonucleotides
Intermediate Tree Nodes	Not available
Direct Parent	Pyrimidine ribonucleoside monophosphates
Alternative Parents	Pentose phosphates Glycosylamines Monosaccharide phosphates Pyrimidones Hydropyrimidines Alkyl phosphates Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Ureas Secondary alcohols Lactams 1,2-diols Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Pyrimidine ribonucleoside monophosphate - Pentose-5-phosphate - Pentose phosphate - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Pyrimidone - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - Monosaccharide - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Urea - Secondary alcohol - Lactam - 1,2-diol - Oxacycle - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside monophosphates. These are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	disodium;[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
INCHI	InChI=1S/C9H13N2O9P.2Na/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);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1
InChIKey	KURVIXMFFSNONZ-WFIJOQBCSA-L
Smiles	C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
Isomeric SMILES	C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
WGK Germany	2
RTECS	YU7975000
PubChem CID	169020
Molecular Weight	368.15
Beilstein	3582885
Reaxy-Rn	3582885

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Sensitivity	Heat Sensitive
Specific Rotation[α]	-14 ° (C=1, H2O)
Melt Point(°C)	208-210°C
Molecular Weight	368.140 g/mol
XLogP3
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	9
Rotatable Bond Count	3
Exact Mass	368 Da
Monoisotopic Mass	368 Da
Topological Polar Surface Area	172.000 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	506.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	3

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Chujing Yang, Zhiwei Zhang, Jingqi Chen, Xinying Zhang, Yankai Dai, Xuyi Li, Yingying Chen, Jiaqiang Xu, Lingyan Feng. (2023) Multiple switchable circularly polarized luminescence from nucleotide/terbium(III) complexes. NEW JOURNAL OF CHEMISTRY, 47 (9): (4472-4477).
2. Quan Li, Zhile Bai, Xingjun Xi, Zhiwei Guo, Cong Liu, Xuerui Liu, Xiaoyan Zhao, Zhiyue Li, Yong Cheng, Yun Wei. (2021) Rapid microwave-assisted green synthesis of guanine-derived carbon dots for highly selective detection of Ag+ in aqueous solution. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 248 (119208).
3. Zhihong Guan, Ruobo Chen, Kaixin Liu, Li Fu, Ling Li, Li Jia. (2025) Copper ion as a peroxidase mimic for fluorescent detection of casein phosphopeptide by a 3D-printed portable device. MICROCHEMICAL JOURNAL, 208 (112501).

Solution Calculators

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5′-UMP-Na2 - 10mM in Water, high purity , CAS No.3387-36-8