Ordering
Available Variants12 x 1 g
CHA.92262-12x1g
Price
€264.80
Available – Dispatch in 14 days
12 x 2 g
CHA.92262-12x2g
Price
€540.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
12 x 1 g | CHA.92262-12x1g | €264.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
12 x 2 g | CHA.92262-12x2g | €540.80 |
configured for PerkinElmer, configured for Polygen
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) | C46H52N5O8P |
|---|---|
| CAS Number | 102212-98-6 |
| Molecular Weight | 833.91 |
| NACRES | NA.51 |
| PubChem Substance ID | 329774852 |
| UNSPSC Code | 41116107 |
| MDL number | MFCD00036315 |
| Assay | ≥99% (31P-NMR), ≥99.0% (reversed phase HPLC) |
| Biological source | non-animal source (no BSE/TSE risk) |
| Form | powder or granules |
| Storage temp. | 2-8°C |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 1 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
DMT-dC(bz) Phosphoramidite, with a CAS number of 102212-98-6, is a crucial reagent in the synthesis of oligonucleotides. This compound is a protected deoxycytidine phosphoramidite, where the 5-hydroxyl group is protected by a dimethoxytrityl (DMT) group and the N4 position of the cytosine base is protected by a benzoyl group. The phosphoramidite moiety allows for efficient coupling to other nucleoside phosphoramidites during solid-phase oligonucleotide synthesis. The DMT group can be easily removed after synthesis, while the benzoyl group remains to protect the base during subsequent steps. This reagent is widely used in the production of therapeutic and diagnostic oligonucleotides, and its high purity and reactivity make it an essential tool in molecular biology research and applications. Its chemical properties and reactivity are well-characterized, ensuring reliable and efficient oligonucleotide synthesis.
