Skip to Content
Merck
All Photos(4)

Key Documents

T7004

Sigma-Aldrich

Thymidine 5′-monophosphate disodium salt hydrate

≥99%

Synonym(s):

5′-Thymidylic acid disodium salt, TMP, dTMP

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H13N2Na2O8P · xH2O
CAS Number:
Molecular Weight:
366.17 (anhydrous basis)
Beilstein:
4086927
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.51

Quality Level

Assay

≥99%

storage temp.

−20°C

SMILES string

O.[Na+].[Na+].CC1=CN([C@H]2C[C@H](O)[C@@H](COP([O-])([O-])=O)O2)C(=O)NC1=O

InChI

1S/C10H15N2O8P.2Na.H2O/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(20-8)4-19-21(16,17)18;;;/h3,6-8,13H,2,4H2,1H3,(H,11,14,15)(H2,16,17,18);;;1H2/q;2*+1;/p-2/t6-,7+,8+;;;/m0.../s1

InChI key

KCOPAVKVHIWPKB-SPSULGLQSA-L

Looking for similar products? Visit Product Comparison Guide

General description

Thymidine 5′-monophosphate de novo synthesis from deoxyuridine monophosphate (dUMP) is catalyzed by the enzyme thymidylate synthase.

Application

Thymidine 5′-monophosphate disodium salt hydrate has been used as a standard for the quantification of metabolites from plasma and tumor interstitial fluid using liquid chromatography-mass spectrometry analysis (LC/MS). It has also been used as a single deoxy-mononucleotide to test its effect on the cell growth of human malignant intestinal CaCo-2 cells and normal rat intestinal cell line IEC-6 cells.
Thymidine 5′-monophosphate disodium salt hydrate has been used as a standard solution.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Alexander Cecil et al.
Genome biology, 12(3), R24-R24 (2011-03-23)
Xenobiotics represent an environmental stress and as such are a source for antibiotics, including the isoquinoline (IQ) compound IQ-143. Here, we demonstrate the utility of complementary analysis of both host and pathogen datasets in assessing bacterial adaptation to IQ-143, a
Fixed-gap tunnel junction for reading DNA nucleotides
Pang P, et al.
ACS Nano, 8(12), 11994-12003 (2014)
Gregory F Funston et al.
Anatomical record (Hoboken, N.J. : 2007), 303(4), 918-934 (2019-07-05)
The fossil record of caenagnathid oviraptorosaurs consists mainly of their fused, complexly sculptured dentaries, but little is known about the growth and development of this diagnostic structure. Previous work has suggested that the ridges and grooves on the occlusal surface
Víctor López Del Amo et al.
Nature communications, 11(1), 352-352 (2020-01-19)
CRISPR-based gene drives can spread through wild populations by biasing their own transmission above the 50% value predicted by Mendelian inheritance. These technologies offer population-engineering solutions for combating vector-borne diseases, managing crop pests, and supporting ecosystem conservation efforts. Current technologies raise
Ángeles Ortega et al.
The Journal of nutritional biochemistry, 22(6), 595-604 (2010-10-26)
Dietary nucleotides (NTs) have an important role in cellular and humoral immunity, intestinal growth, differentiation and recovery from tissue damage. Nucleosides (NSs) are the best-absorbed chemical form of NTs in the intestinal epithelium. The aim of this study was to

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service