Oligonucleotide Synthesis, RNA Raw Materials & Modification

Chemical Phosphorylation Reagent

Oligonucleotide Synthesis, RNA Raw Materials & Modification

Product NoCH65101CAS No108783-02-4Purity98% (HPLC)
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Product summary

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Product family
Oligonucleotide Synthesis, RNA Raw Materials & Modification
MF
C34H45N2O7PS
MW
656.8
Purity
98% (HPLC)

Chemical Phosphorylation Reagent is a non-nucleoside building block for introducing a phosphate group on an oligonucleotide during synthesis: a phosphoramidite carrying a protected phosphate (with a sulfonyl-type, base-labile protecting group and a 5'-O-(4,4'-dimethoxytrityl) handle) plus a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite. Its PubChem-backed identity includes CAS 108783-02-4, molecular formula C34H45N2O7PS, molecular weight 656.8, and PubChem CID 10283145.

It couples at the oligonucleotide terminus like any amidite; after the phosphate protecting group is removed during deprotection, it leaves a phosphate monoester — for example a 5'-phosphate. This provides a terminally phosphorylated oligonucleotide chemically, without an enzymatic phosphorylation step.

Synonyms

CPR; Chemical Phosphorylation Reagent I; 5'-phosphate-ON reagent (sulfonyl-protected phosphate amidite)

Identity and specifications

Catalog No.CH65101
CAS No.108783-02-4
Molecular FormulaC34H45N2O7PS
Molecular Weight656.8
PubChem CID10283145
InChIKeyRJDYWMSSNMDIOO-UHFFFAOYSA-N
Purity98% (HPLC)

Storage conditions

-20 C

Technical attributes

Reagent class
Non-nucleoside phosphorylation phosphoramidite
Installation site
Oligonucleotide terminus
Installed group
Phosphate monoester after deprotection
Structure distinction
Sulfur-containing protected-phosphate structure
Grade
N (Normal)
Packaging
1 mg; 5 mg; 10 mg; 100 mg; 250 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 50 g; 100 g; 500 g; 1 kg; 5 kg; 10 kg; 25 kg; 100 µmol; Custom packaging on request
Water content
<=0.5%
Physical form
colourless to light brown-yellow transparent oily substance
Stability
prepared LK2101 solution: use within 24 h

Application context

  • Chemical Phosphorylation Reagent reference: use this chemical phosphorylation reagent record for oligonucleotide phosphorylation reagent catalog work.
  • Identifier cross-check: compare CAS 108783-02-4, PubChem CID 10283145, formula C34H45N2O7PS, MW 656.8, and the listed InChIKey for catalog identity matching.
  • Inquiry preparation: include catalog number CH65101, the product name, and the identity-matching identifiers when preparing a CHEMOS product inquiry.

Related technical resources

Public references

Frequently Asked Questions

What does a Chemical Phosphorylation Reagent do?

It provides a phosphate group on an oligonucleotide chemically, during solid-phase synthesis, instead of using an enzyme (kinase). It couples like an amidite and, after deprotection, leaves a phosphate monoester — for example a 5'-phosphate.

How does it fit into the synthesis cycle?

It carries a 3'-phosphoramidite and a 5'-DMT handle, so it couples in the normal amidite cycle at the position where the phosphate is wanted. Its phosphate protecting group is removed at final deprotection to reveal the terminal phosphate.

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