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

CAS: 3387-36-8 Cat. No.: U423467 Formule: C9H11N2Na2O9P Poids moléculaire: 368.15 Beilstein Registry Number: 3582885 Numéro CE: 222-211-9 PubChem CID: 169020
DISPONIBLE À COMMANDE
GRADE & PURITY 10mM in Water
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
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Allemagne (EU)
USA*
Price
Qty
1ml
U423467-1ml
—
2 En stock

51,11€

60,65€
Enregistrer 9,55 € (15.74%)
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Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
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
Spécifications et pureté
10mM in Water
Mécanismes biochimiques et physiologiques
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.
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Pubchem Sid528762066
Sourires canoniquesC1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
IUPAC Namedisodium;[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
InChIKeyKURVIXMFFSNONZ-WFIJOQBCSA-L
INCHI1S/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
Isomères 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 Allemagne 2
RTECS YU7975000
PubChem CID 169020
Poids moléculaire 368.15
Beilstein 3582885
Reaxy-Rn 3582885

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClassePyrimidine nucleotides
SubclassPyrimidine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPyrimidine 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 FrameworkAromatic 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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
SensibilitéHeat Sensitive
Rotation spécifique [α]-14 ° (C=1, H2O)
Point de fusion (°C)208-210°C
Poids moléculaire368.140 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count9
Rotatable Bond Count3
Exact Mass368 Da
Monoisotopic Mass368 Da
Topological Polar Surface Area172.000 Ų
Heavy Atom Count23
Formal Charge0
Complexity506.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
FAQ et articles
Citations of This Product
Références
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).  [PMID:] [10.1039/D2NJ06145G]
2. Quan Li, Zhile Bai, Xingjun Xi, Zhiwei Guo, Cong Liu, Xuerui Liu, Xiaoyan Zhao, Zhiyue Li, Yong Cheng, Yun Wei.  (2020)  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,      [PMID:33257251] [10.1016/j.saa.2020.119208]
3. Zhihong Guan, Ruobo Chen, Kaixin Liu, Li Fu, Ling Li, Li Jia.  (2024)  Copper ion as a peroxidase mimic for fluorescent detection of casein phosphopeptide by a 3D-printed portable device.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112501]
4. Xuetao Yan, Lifei Chen, Yuze Ren, Kaixuan Cui, Tianliang Li, Lixing Lin, Zeyu Li, Yingying Chen, Zhenzhen Li, Lingyan Feng.  (2026)  Nucleotide-Based White Circularly Polarized Luminescence Materials in Lanthanide Deep Eutectic Solvents.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.5c08455]
5. Liying Cui, Yong Wang, Qin Zhang, Xin Liu.  (2026)  Closed-loop recyclable and robust underwater adhesive featuring real-time detectable adhesion interface.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.175232]
Calculateurs de solution
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