
Chemical Phosphorylation Reagent II | CAS 171285-25-9
| Catalog Number | A19-0083 |
| Category | DNA Stains |
| Molecular Formula | C39H51N2O9P |
| Molecular Weight | 722.80 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| A19-0083 | 1 g | $299 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
N,N-diisopropylphosphoramidite, a catalytic compound, is an essential building block for oligonucleotide synthesis used in various therapeutic domains such as antisense therapy, siRNA, and gene editing. This efficient and highly pure chemical ensures the production of top-quality therapeutic oligonucleotides.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | O-DMT-2,2-di(ethoxycarbonyl)propan-1,3-diol; CPⅡ; CPRII; 2-[(4,4'-Dimethoxytrityloxy)methyl]-2-[[(diisopropylamino)(2-cyanoethoxy)phosphinooxy]methyl]malonic acid diethyl ester; 3-(4,4'-dimethoxytrityloxy)-2,2-dicarboxyethyl]propyl(2-cyanoethyl)(N, N-diisopropyl)phosphoramidite; (2-Cyanoethyl) (2,2-bis(ethoxycarbonyl)-3-(4,4'-dimethoxytrityloxy)propyl-1) N,N-diisopropylphosphoramidite |
| Purity | ≥95% |
| IUPAC Name | diethyl 2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-2-[[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxymethyl]propanedioate |
| SMILES | CCOC(=O)C(COC(C1=CC=CC=C1)(C2=CC=C(C=C2)OC)C3=CC=C(C=C3)OC)(COP(N(C(C)C)C(C)C)OCCC#N)C(=O)OCC |
| InChI | InChI=1S/C39H51N2O9P/c1-9-46-36(42)38(37(43)47-10-2,28-50-51(49-26-14-25-40)41(29(3)4)30(5)6)27-48-39(31-15-12-11-13-16-31,32-17-21-34(44-7)22-18-32)33-19-23-35(45-8)24-20-33/h11-13,15-24,29-30H,9-10,14,26-28H2,1-8H3 |
| InChIKey | IEKIULVSVQLVMS-UHFFFAOYSA-N |
| Appearance | Colorless semisolid |
| Boiling Point | 740.0±60.0°C at 760 mmHg |
Product Specification
| Storage | Store at -20 °C |
Application
Chemical Phosphorylation Reagent II is a phosphorylation-focused chemical reagent designed to install phosphate groups onto biomolecule scaffolds used in chemical biology and materials research. In fluorescence- and click-compatible workflows, phosphorylated intermediates are frequently leveraged as handles for downstream conjugation, affinity enrichment, or construction of functional probes and biomaterials. Researchers use this reagent when they need controlled introduction of phosphate functionality to enable subsequent labeling strategies, surface immobilization chemistries, or nucleic-acid/protein modification pipelines.
1. Phosphorylated Biomolecule Labeling
Chemical Phosphorylation Reagent II is used by chemical biology groups to generate phosphorylated protein, peptide, or nucleic-acid derivatives that serve as substrates or binding motifs in downstream assays. In practice, the reagent supports preparation of phosphate-bearing conjugates for studies where phosphorylation state is a key experimental variable, including workflows that compare labeled versus non-phosphorylated controls. Teams developing affinity reagents and biochemical tools often rely on this phosphorylation step to create consistent functional groups for subsequent coupling to reporters, linkers, or detection tags.
2. Surface Immobilization And Coatings
Chemical Phosphorylation Reagent II is commonly applied in biomaterials and surface chemistry to introduce phosphate functionality onto polymer surfaces, hydrogel matrices, or coating layers prior to further functionalization. Materials scientists incorporate phosphorylated surfaces to enable controlled attachment of biomolecules, to tune interactions with phosphate-recognizing components, or to prepare substrates for immobilized assay formats. This use case is especially relevant for building research-grade platforms such as microarray surfaces, capture surfaces for biomolecule enrichment, and reusable assay supports where phosphate presentation improves workflow consistency.
3. Phosphate-Mediated Conjugate Construction
Chemical Phosphorylation Reagent II is utilized to prepare phosphate-bearing intermediates that can be carried forward into multistep conjugation schemes, including fluorescent labeling and probe assembly strategies. In molecular imaging reagent development, phosphorylation can provide a defined chemical handle that improves the modularity of conjugate construction, allowing researchers to attach fluorophores, affinity tags, or other reporter groups in a later stage. This approach is frequently adopted in probe optimization studies where modular linker placement and functional-group density are tuned to support robust assay handling and reproducible reagent performance.
4. Nucleic Acid Modification Workflows
Chemical Phosphorylation Reagent II is used in nucleic acid analysis and oligonucleotide workflow development to generate phosphorylated oligonucleotide species required for downstream enzymatic processing or ligation-based assembly strategies. Research groups preparing labeled oligonucleotide probes, sequencing-adjacent constructs, or hybridization reagents often require phosphate installation as a prerequisite step to enable subsequent steps in probe construction. By standardizing phosphorylation of oligonucleotide backbones or termini, the reagent helps streamline preparation of research-grade nucleic acid tools used in fluorescence readouts and hybridization assays.
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