CHA.35664
5-Fluoro-2′-deoxyuridine 5′-monophosphate sodium salt
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Ordering
Available Variants5 mg
CHA.35664-5mg
Price
€192.00
Available – Dispatch in 14 days
25 mg
CHA.35664-25mg
Price
€768.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.35664-5mg | €192.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mg | CHA.35664-25mg | €768.80 |
~85%, solid
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C9H12FN2O8P |
|---|---|
| CAS Number | 103226-10-4 |
| Molecular Weight | 326.17 |
| UNSPSC Code | 41106305 |
| PubChem Substance ID | 24894845 |
| NACRES | NA.51 |
| MDL number | MFCD00057409 |
| Assay | ~85% |
| Form | solid |
| Solubility | water: 50 mg/mL, clear, colorless to faint yellow or tan |
| Storage temp. | −20°C |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
 GHS08,GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 + H312 + H332,H351 |
| pcodes | P202 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P308 + P313 |
| Hazard Classifications | Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
5-Fluoro-2′-deoxyuridine 5′-monophosphate sodium salt, with a CAS number of 103226-10-4, is a nucleotide analog that has garnered significant attention in the realm of biochemical research. This compound is a derivative of deoxyuridine, wherein a fluorine atom is substituted at the 5-position, and it exists as a sodium salt to enhance its solubility. The incorporation of this fluorinated nucleotide into DNA can lead to the inhibition of thymidylate synthase, an enzyme crucial for DNA synthesis. As a result, 5-Fluoro-2′-deoxyuridine 5′-monophosphate sodium salt has been explored for its potential applications in cancer therapy and as a tool for studying nucleic acid metabolism. Its unique properties make it a valuable reagent in various biochemical and pharmacological investigations, particularly those focused on the mechanisms of nucleotide metabolism and the development of novel therapeutic agents.
