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Merck

T7004

Thymidine 5′-monophosphate disodium salt hydrate

≥99%

Synonym(s):

5′-Thymidylic acid disodium salt, TMP, dTMP

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About This Item

Empirical Formula (Hill Notation):
C10H13N2Na2O8P · xH2O
CAS Number:
33430-62-5
Molecular Weight:
366.17 (anhydrous basis)
UNSPSC Code:
41106305
NACRES:
NA.51
PubChem Substance ID:
329826857
EC Number:
251-518-0
Beilstein/REAXYS Number:
4086927
MDL number:
MFCD09039259

Product Name

Thymidine 5′-monophosphate disodium salt hydrate, ≥99%

InChI key

KCOPAVKVHIWPKB-SPSULGLQSA-L

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

SMILES string

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

biological source

synthetic (organic)

assay

≥99%

form

powder

solubility

H2O: 100 mg/mL to clear, colorless

storage temp.

−20°C

Quality Level

200

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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.

General description

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000523305
0000523305
0000400076
0000375851
0000375851

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Medical Biochemistry null
Tiina Virtanen et al.
Scientific reports, 10(1), 3427-3427 (2020-02-27)
Membrane fouling is the major factor limiting the wider applicability of the membrane-based technologies in water treatment and in separation and purification processes of biorefineries, pulp and paper industry, food industry and other sectors. Endeavors to prevent and minimize fouling
Wenruo Bai et al.
IEEE/ACM transactions on computational biology and bioinformatics, 16(4), 1168-1181 (2018-07-12)
Identification of spectra produced by a shotgun proteomics mass spectrometry experiment is commonly performed by searching the observed spectra against a peptide database. The heart of this search procedure is a score function that evaluates the quality of a hypothesized
Koji Takada et al.
ACS applied materials & interfaces, 11(39), 35770-35776 (2019-09-10)
Concentrated electrolytes of LiN(SO2F)2 (LiFSA) and organic phosphates (e.g., trimethyl phosphate, TMP) are receiving intense attention for safe and long-lasting lithium-ion batteries, because of their nonflammable character and unusual passivation ability toward negative electrodes. However, their high viscosity and low
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
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