5'-O-(4,4'-Dimethoxytrityl)-N4-isobutyryl-5-methyl-2'-deoxycytidine

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Reagent Code: #47925
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CAS Number 176755-84-3

science Other reagents with same CAS 176755-84-3

blur_circular Chemical Specifications

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Weight 613.7 g/mol
Formula C₃₅H₃₉N₃O₇
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in oligonucleotide synthesis, this compound serves as a protected form of 5-methyl-2'-deoxycytidine. The 4,4'-dimethoxytrityl (DMT) group protects the 5'-hydroxyl, while the isobutyryl group safeguards the exocyclic amine, ensuring selective reactions during DNA strand assembly. It is particularly valuable in automated solid-phase synthesis, enabling the production of custom DNA sequences for research, diagnostics, and therapeutic applications. Its stability and ease of deprotection make it a key reagent in molecular biology and genetic engineering workflows.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿4,122.00
inventory 50mg
10-20 days ฿14,400.00

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5'-O-(4,4'-Dimethoxytrityl)-N4-isobutyryl-5-methyl-2'-deoxycytidine
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Used primarily in oligonucleotide synthesis, this compound serves as a protected form of 5-methyl-2'-deoxycytidine. The 4,4'-dimethoxytrityl (DMT) group protects the 5'-hydroxyl, while the isobutyryl group safeguards the exocyclic amine, ensuring selective reactions during DNA strand assembly. It is particularly valuable in automated solid-phase synthesis, enabling the production of custom DNA sequences for research, diagnostics, and therapeutic applications. Its stability and ease of de

Used primarily in oligonucleotide synthesis, this compound serves as a protected form of 5-methyl-2'-deoxycytidine. The 4,4'-dimethoxytrityl (DMT) group protects the 5'-hydroxyl, while the isobutyryl group safeguards the exocyclic amine, ensuring selective reactions during DNA strand assembly. It is particularly valuable in automated solid-phase synthesis, enabling the production of custom DNA sequences for research, diagnostics, and therapeutic applications. Its stability and ease of deprotection make it a key reagent in molecular biology and genetic engineering workflows.

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