Oligonucleotide Synthesis, RNA Raw Materials & Modification

3'-O-allyl-2'-dCTP

Oligonucleotide Synthesis, RNA Raw Materials & Modification

Product NoCH66023CAS No917766-45-1Purity>=98%
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Product summary

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Product family
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Purity
>=98%

3'-O-allyl-2'-dCTP is a 3'-O-allyl modified dCTP reversible terminator. The 3'-hydroxyl is capped with a reversible blocking group so that polymerase extension stops after a single incorporation cycle. Key identifiers are CHEMOS CH66023, CAS 917766-45-1, molecular formula C12H20N3O13P3, and molecular weight 507.22.

3'-O-modified nucleotides are used in cyclic reversible-terminator sequencing-by-synthesis workflows: DNA polymerase incorporates the nucleotide, extension pauses after one base, and cap removal regenerates the 3'-OH so synthesis can continue.

Synonyms

3'-O-allyl-dCTP; 3'-O-(prop-2-en-1-yl)-2'-deoxycytidine-5'-triphosphate

Identity and specifications

Catalog No.CH66023
Product Name3'-O-allyl-2'-dCTP
CAS No.917766-45-1
Molecular FormulaC12H20N3O13P3
Molecular Weight507.22
Product Type3'-O-allyl reversible-terminator dCTP
Base AddedCytosine
Purity>=98%

Technical attributes

Nucleotide class
Reversible-terminator dNTP
Parent nucleotide
dCTP
3'-O blocking group
Allyl
Deblocking outcome
Regenerates the 3'-OH
Packaging
Custom packaging on request

Application context

  • Reversible terminator nucleotide: used as the cytosine member of a 3'-O-blocked dNTP set.
  • Sequencing-by-synthesis context: incorporation pauses extension for one cycle before cap removal allows synthesis to continue.
  • Modified nucleotide cataloging: relevant to oligonucleotide synthesis, sequencing reagent, and modified dNTP product organization.

Related technical resources

Public references

Frequently Asked Questions

What is 3'-O-allyl-2'-dCTP?

3'-O-allyl-2'-dCTP is a 3'-O-allyl modified dCTP used as a reversible-terminator nucleotide in sequencing-by-synthesis research workflows.

How does a reversible terminator work?

DNA polymerase incorporates the nucleotide, the 3'-O blocking group pauses further extension, and removal of the cap regenerates the 3'-OH so synthesis can continue.

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