Oligonucleotide Conjugation & Delivery Ligands

2'-O-C16-G (iBu) Phosphoramidite

Oligonucleotide Conjugation & Delivery Ligands

Product NoCH65109CAS No2382942-32-5Purity99.98%
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Product summary

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Product family
Oligonucleotide Conjugation & Delivery Ligands
MF
C60H86N7O9P
MW
1080.3
Purity
99.98%

2'-O-C16-G (iBu) Phosphoramidite is a lipophilic 2'-modified RNA building block: 5'-O-(4,4'-dimethoxytrityl)-N2-isobutyrylguanosine with a 2'-O-hexadecyl (C16) group and a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite. Its PubChem-backed identity includes CAS 2382942-32-5, molecular formula C60H86N7O9P, molecular weight 1080.3, and PubChem CID 167312664.

The 2'-O-C16 chain is a permanent 2'-O-modification — a long, fatty-acid-type lipophilic substituent rather than a protecting group. The cited 2'-modification literature discusses 2'-position sugar modifications in relation to nuclease/metabolic stability, and cited lipophilic-oligonucleotide literature discusses fatty-acid-type moieties in relation to lipid-particle and plasma-protein affinity. The monomer couples through a standard 3'-phosphoramidite (3'→5' linkages), the 5'-DMT is removed each cycle, and N2-isobutyryl protection is removed during final deprotection.

Synonyms

5'-O-DMT-N2-iBu-2'-O-hexadecylguanosine 3'-CE phosphoramidite; 2'-O-C16 (palmityl-type) guanosine amidite

Identity and specifications

Catalog No.CH65109
CAS No.2382942-32-5
Molecular FormulaC60H86N7O9P
Molecular Weight1080.3
PubChem CID167312664
InChIKeyUOYPBRBOXKOJLE-ZGTMVWBUSA-N
Purity99.98%

Storage conditions

-20 C

Technical attributes

Modifier type
Lipophilic nucleoside phosphoramidite
Nucleoside scaffold
Guanosine
2'-O substituent
Hexadecyl (C16)
Base protection
N2-Isobutyryl
Packaging
5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g; 2 g; 5 g; 10 g; 50 g; 100 g; 500 g; 1 kg; 5 kg; Custom packaging on request
Water content
<=0.5%
Physical form
white to off-white powder
Stability
1 year under stated storage

Application context

  • Lipophilic 2'-O-C16 modification: provides a long hexadecyl (C16) chain at the 2'-position — a permanent, fatty-acid-type lipophilic substituent.
  • Cited 2'-modification context: the cited literature discusses 2'-position sugar modifications in relation to nuclease/metabolic stability.
  • Cited lipophilic-moiety context: the cited literature discusses fatty-acid-type moieties in relation to lipid-particle and plasma-protein affinity.
  • 3'→5' coupling monomer: couples through a 3'-phosphoramidite; 5'-DMT is removed each cycle; N2-isobutyryl protection is removed during final deprotection.

Related technical resources

Public references

Frequently Asked Questions

What is the 2'-O-C16 modification?

It is a 2'-O-hexadecyl group — a long, fatty-acid-type lipophilic chain permanently attached at the 2'-position. It is not a protecting group; it stays on the finished oligonucleotide.

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