5'-O-(4,4'-Dimethoxytrityl)-2'-deoxythymidine-3'-(methyl-N,N-diisopropyl)phosphoramidite

≥95%

Reagent Code: #221357
fingerprint
CAS Number 84416-85-3

science Other reagents with same CAS 84416-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 721.8 g/mol
Formula C₃₈H₄₈N₃O₉P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the efficient and precise assembly of DNA strands. Its dimethoxytrityl group provides reversible protection for the 5'-hydroxyl, allowing stepwise chain elongation with high coupling efficiency. The 2'-deoxythymidine base ensures correct base pairing in the final sequence, while the phosphoramidite moiety facilitates rapid and selective formation of phosphite linkages on automated synthesizers. Commonly applied in the production of primers, probes, and modified DNA for PCR, sequencing, gene synthesis, and diagnostic assays. Stable under standard synthesis conditions and compatible with high-throughput platforms, making it essential in molecular biology and pharmaceutical development.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿13,060.00
5'-O-(4,4'-Dimethoxytrityl)-2'-deoxythymidine-3'-(methyl-N,N-diisopropyl)phosphoramidite
No image available

Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the efficient and precise assembly of DNA strands. Its dimethoxytrityl group provides reversible protection for the 5'-hydroxyl, allowing stepwise chain elongation with high coupling efficiency. The 2'-deoxythymidine base ensures correct base pairing in the final sequence, while the phosphoramidite moiety facilitates rapid and selective formation of phosphite linkages on automated synthesizers. Commonly applied in the

Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the efficient and precise assembly of DNA strands. Its dimethoxytrityl group provides reversible protection for the 5'-hydroxyl, allowing stepwise chain elongation with high coupling efficiency. The 2'-deoxythymidine base ensures correct base pairing in the final sequence, while the phosphoramidite moiety facilitates rapid and selective formation of phosphite linkages on automated synthesizers. Commonly applied in the production of primers, probes, and modified DNA for PCR, sequencing, gene synthesis, and diagnostic assays. Stable under standard synthesis conditions and compatible with high-throughput platforms, making it essential in molecular biology and pharmaceutical development.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...