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UTP Trisodium salt Solution - Pharmaceutical grade，≥99%，100mM, high purity , CAS No.19817-92-6

1 Citations COA COA
In stock
Item Number
U427287
Grouped product items
SKU Size
Availability
 Price Qty
U427287-250μl
250μl
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90
U427287-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$206.90
U427287-10ml
10ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,545.90
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Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Class A GPCR (4138) Metabolite (5307) nucleotide (15)

Basic Description

Synonyms AS-80622 | Q27279174 | UNII-GM3E161I3C | Uridine-5'-triphosphate trisodium | UTIPINA | NSC-20260 | UTP, Trisodium Salt | uridine-5'-triphosphoricacidtrisodiumsalt | 6-(Trifluoromethyl)-1H-benzo[d][1,2,3]triazol-1-ol | Uridine 5'-triphosphate sodium salt |
Specifications & Purity pharmaceutical grade, PharmPure™, ≥99%, 100mM
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.
Grade pharmaceutical grade, PharmPure™
Product Description

UTP is Uridine-5'-triphosphate, Chinese name is uridine-5'-triphosphate, which can be used in various related applications in molecular biology, such as in vitro transcription, siRNA synthesis, etc. UTP is also involved in galactose metabolism, in which the activated form of UDP-galactose is converted to UDP-glucose, which enters the glycogen synthesis pathway. This product is an aqueous solution of UTP sodium salt with a purity of ≥ 99% (HPLC) at a concentration of 100mM±5mM, and is free of endonuclease, exonuclease and ribonuclease contamination.

This product is produced with raw and auxiliary materials of pharmaceutical specifications, and all kinds of pollution in the production process are strictly controlled. Product production and quality management procedures in line with GMP standards ensure the traceability of the production process and all raw and auxiliary materials.


Quality requirements

project  standard
appearance  Clear liquid
Visible foreign matter  Compliance with regulations
purity  ≥ 99%
Endonuclease residues  Degradation of substrate shall not exceed 10%
Exonuclease residues  Degradation of substrate shall not exceed 10%
RNase residue  Degradation of substrate shall not exceed 10%
Bacterial endotoxin content  ≤1EU/mg
Mycoplasma detection  negative
Heavy metal residues  ≤10ppm


Produced according to the following specifications

1. ISO 9001:2015, certified facility.

2. "GMP Appendix - Cell Therapy Products" State Drug Administration.

3. "General Introduction to Human Gene Therapy - Chinese Pharmacopoeia 2020" National Pharmacopoeia Commission.

4. USP Chapter <1043>, Ancillary Materials for Cell, Gene, and Tissue-Engineered Products

5. USP Chapter <92>, Growth Factors and Cytokines Used in Cell Therapy Manufacturing

6. Ph. Eur. General Chapter 5.2.12, Raw Materials of Biological Origin for the Production of Cell-based and Gene Therapy Medicinal Products


Storage temperature

The product can be stored or transported at -20±5℃ for a short period of time, and it can be stored at -70±5℃ for a long time, and the product is valid for 1 years;

Avoid multiple freeze-thaw cycles and frequent temperature changes;

Concentration gradients may form after the product is frozen and should be thoroughly mixed before use.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Nucleosides, nucleotides, and analogues
Class Pyrimidine nucleotides
Subclass Pyrimidine ribonucleotides
Intermediate Tree Nodes Not available
Direct Parent Pyrimidine ribonucleoside triphosphates
Alternative Parents Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Pyrimidones  Alkyl phosphates  Hydropyrimidines  Vinylogous amides  Tetrahydrofurans  Heteroaromatic compounds  Ureas  Secondary alcohols  1,2-diols  Lactams  Oxacyclic compounds  Azacyclic compounds  Hydrocarbon derivatives  Organic oxides  Organic sodium salts  Organonitrogen compounds  Organopnictogen compounds  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Pyrimidine ribonucleoside triphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Tetrahydrofuran - Vinylogous amide - Heteroaromatic compound - Urea - Secondary alcohol - 1,2-diol - Lactam - Organic alkali metal salt - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Alcohol - Organopnictogen compound - Organic sodium salt - Organic oxygen compound - Organic salt - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside triphosphates. These are pyrimidine ribobucleotides with triphosphate group linked to the ribose moiety.
External Descriptors Not available

Associated Targets(Human)

ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
S1PR1 Tclin Sphingosine 1-phosphate receptor Edg-1 (5806 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
C5AR1 Tclin C5a anaphylatoxin chemotactic receptor (2677 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
U2OS (164939 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CX3CR1 Tchem C-X3-C chemokine receptor 1 (1686 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FPR2 Tchem Lipoxin A4 receptor (3472 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GPR35 Tchem G-protein coupled receptor 35 (2643 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRPF1 Tchem Peregrin (2217 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HEK-293T (167025 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Aplnr Apelin receptor (201 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gpr119 Glucose-dependent insulinotropic receptor (270 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name trisodium;[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
INCHI InChI=1S/C9H15N2O15P3.3Na/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18;;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H,10,12,15)(H2,16,17,18);;;/q;3*+1/p-3/t4-,6-,7-,8-;;;/m1.../s1
InChIKey MMJGIWFJVDOPJF-LLWADOMFSA-K
Smiles [Na+].[Na+].[Na+].O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP([O-])(=O)OP([O-])(=O)OP(O)([O-])=O)N2C=CC(=O)NC2=O
Isomeric SMILES C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O)O.[Na+].[Na+].[Na+]
WGK Germany 3
Alternate CAS 63-39-8
Molecular Weight 550.09 (anhydrous basis)
Beilstein 3585234
Reaxy-Rn 5373891

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

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

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
F2523644 Certificate of Analysis May 23, 2025 U427287
L2424217 Certificate of Analysis Dec 31, 2024 U427287
K2223049 Certificate of Analysis Sep 20, 2024 U427287
K2223059 Certificate of Analysis Sep 20, 2024 U427287
K2223062 Certificate of Analysis Sep 20, 2024 U427287

Chemical and Physical Properties

Melt Point(°C) >140°C
Molecular Weight 550.090 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 15
Rotatable Bond Count 8
Exact Mass 549.914 Da
Monoisotopic Mass 549.914 Da
Topological Polar Surface Area 267.000 Ų
Heavy Atom Count 32
Formal Charge 0
Complexity 820.000
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 4

Alternative Products

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  2. Uridine 5′-triphosphate trisodium salt hydrate
    Uridine 5′-triphosphate trisodium salt hydrate
    • 10mM in Water

    Starting at $69.90

  3. Uridine 5′-triphosphate trisodium salt hydrate
    Uridine 5′-triphosphate trisodium salt hydrate
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Citations of This Product

How to Cite Aladdin Scientific Products?
1. Ying Ding, Qingyan Jia, Yongmei Wen, Weimin Liu, Jiechao Ge, Jiasheng Wu, Hongyan Zhang, Pengfei Wang.  (2018)  New detection method for nucleoside triphosphates based on carbon dots: The distance-dependent singlet oxygen trapping.  ANALYTICA CHIMICA ACTA,  1031  (145). 

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