Ordering
Available Variants1 mL
CHA.30989-1mL
Price
€102.40
Available – Dispatch in 14 days
5 mL
CHA.30989-5mL
Price
€330.40
Available – Dispatch in 14 days
1 g
CHA.30989-1g
Price
€173.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 mL | CHA.30989-1mL | €102.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mL | CHA.30989-5mL | €330.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.30989-1g | €173.60 |
analytical standard
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) | C10H14O |
|---|---|
| CAS Number | 17957-94-7 |
| Molecular Weight | 150.22 |
| UNSPSC Code | 85151701 |
| NACRES | NA.24 |
| PubChem Substance ID | 329759886 |
| MDL number | MFCD00142332 |
| Beilstein/REAXYS Number | 2729 |
Safety Information Handling visibility
| pictograms |
GHS07
GHS09
  GHS07,GHS09
|
|---|---|
| signalword | Warning |
| hcodes | H302,H315,H319,H411 |
| pcodes | P264 - P270 - P273 - P301 + P312 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 |
| Storage Class | 10 - Combustible liquids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves |
Technical Overview & Applications Use-case context
DMT-2′Fluoro-dU Phosphoramidite, with a CAS number of 146954-75-8, is a nucleoside phosphoramidite used in the synthesis of modified oligonucleotides. This compound is a derivative of deoxyuridine, where a fluorine atom is introduced at the 2′ position of the sugar moiety. The presence of the fluorine atom confers unique properties to the resulting oligonucleotides, including enhanced stability and resistance to degradation by nucleases. DMT-2′Fluoro-dU Phosphoramidite is commonly used in the preparation of therapeutic oligonucleotides, such as antisense and siRNA molecules, where the introduction of fluorine atoms can improve the efficacy and duration of action of these molecules. The incorporation of this modified nucleoside into oligonucleotides can be achieved through standard solid-phase synthesis protocols, allowing for the efficient preparation of a wide range of fluorinated oligonucleotides.
