TBdms-peg5-1-o-(b-cyanoethyl-n,n-diisopropyl)phosphoramidite

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Reagent Code: #244924
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CAS Number 1807521-08-9

science Other reagents with same CAS 1807521-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 508.71 g/mol
Formula C₂₃H₄₉N₂O₆PSi
badge Registry Numbers
MDL Number MFCD28142479
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase oligonucleotide synthesis, particularly in the preparation of DNA probes and primers. Its primary role is to introduce a polyethylene glycol (PEG) spacer with a terminal protected hydroxyl group, enabling conjugation with other molecules such as fluorophores, biotin, or peptides. The TBdms (tert-butyldimethylsilyl) group protects the hydroxyl during synthesis, while the phosphoramidite moiety allows for efficient coupling to the growing DNA chain. The β-cyanoethyl group stabilizes the phosphate intermediate and prevents side reactions. After synthesis, the protecting groups are removed under standard deprotection conditions, freeing the hydroxyl for downstream conjugation. This reagent is especially valuable in diagnostic assays, labeled probes, and functionalized nucleic acids for research and therapeutic applications.

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inventory 250mg
10-20 days ฿31,490.00

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TBdms-peg5-1-o-(b-cyanoethyl-n,n-diisopropyl)phosphoramidite
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Used in solid-phase oligonucleotide synthesis, particularly in the preparation of DNA probes and primers. Its primary role is to introduce a polyethylene glycol (PEG) spacer with a terminal protected hydroxyl group, enabling conjugation with other molecules such as fluorophores, biotin, or peptides. The TBdms (tert-butyldimethylsilyl) group protects the hydroxyl during synthesis, while the phosphoramidite moiety allows for efficient coupling to the growing DNA chain. The β-cyanoethyl group stabilizes the

Used in solid-phase oligonucleotide synthesis, particularly in the preparation of DNA probes and primers. Its primary role is to introduce a polyethylene glycol (PEG) spacer with a terminal protected hydroxyl group, enabling conjugation with other molecules such as fluorophores, biotin, or peptides. The TBdms (tert-butyldimethylsilyl) group protects the hydroxyl during synthesis, while the phosphoramidite moiety allows for efficient coupling to the growing DNA chain. The β-cyanoethyl group stabilizes the phosphate intermediate and prevents side reactions. After synthesis, the protecting groups are removed under standard deprotection conditions, freeing the hydroxyl for downstream conjugation. This reagent is especially valuable in diagnostic assays, labeled probes, and functionalized nucleic acids for research and therapeutic applications.

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