Ordering
Available Variants5 mg
CHA.22700-5mg
Price
€92.00
Available – Dispatch in 14 days
10 mg
CHA.22700-10mg
Price
€158.40
Available – Dispatch in 14 days
50 mg
CHA.22700-50mg
Price
€536.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.22700-5mg | €92.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 mg | CHA.22700-10mg | €158.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
50 mg | CHA.22700-50mg | €536.00 |
≥93%, synthetic (organic), powder
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) | C9H14BrN2O15P3 · xNa+ |
|---|---|
| CAS Number | 161848-60-8 |
| Molecular Weight | 563.04 (free acid basis) |
| UNSPSC Code | 41106305 |
| PubChem Substance ID | 24891977 |
| NACRES | NA.51 |
| Assay | ≥93% |
| Biological source | synthetic (organic) |
| Form | powder |
| Solubility | water: 50 mg/mL, clear, colorless |
| Storage temp. | −20°C |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
5-Bromouridine 5′-triphosphate sodium salt, with a CAS number of 161848-60-8, is a nucleotide analog that has been utilized in various molecular biology applications. This compound is a brominated derivative of uridine triphosphate, where the bromine atom is incorporated at the 5-position of the uracil ring. The sodium salt form of this molecule enhances its solubility in aqueous solutions, making it more suitable for incorporation into nucleic acid synthesis reactions. As a substrate for RNA polymerases, 5-bromouridine 5′-triphosphate sodium salt can be used to synthesize brominated RNA transcripts, which can be employed in a range of downstream applications, including the analysis of RNA structure and function, as well as the study of RNA-protein interactions. Its unique properties make it a valuable tool in molecular biology research.
