G211040

DMT-2′O-TBDMS-rG(ib)-phosphoramidit

configured for MerMade

• Synonym(e): N-(2-methyl-1-oxopropyl)-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-[(1,1-dimethylethyl)dimethylsilyl]-guanosin, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidit]
• Empirische Formel (Hill-System): C₅₀H₆₈N₇O₉PSi
• CAS-Nummer: 147201-04-5
• Molekulargewicht: 970.18
• MDL-Nummer: MFCD00080299
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 329799856
• NACRES: NA.51

Eigenschaften

• Biologische Quelle: non-animal source (no BSE/TSE risk)
• Qualitätsniveau: 300
• Produktlinie: Proligo Reagents
• Assay: ≥99% (³¹P-NMR); ≥99.0% (reversed phase HPLC)
• Form: powder
• Methode(n): oligo synthesis: suitable
• Verunreinigungen: ≤0.3% water content (Karl Fischer); ≤0.5% P(III) Impurities 100-169ppm (³¹P-NMR); ≤0.5% single Impurity (reversed phase HPLC); ≤3% residual Solvent content
• Farbe: white to off-white
• λ: conforms (UV/VIS Identity)
• Eignung: conforms to structure for H-NMR; conforms to structure for LC-MS
• Kompatibilität: configured for MerMade
• Nukleosidprofil: base: guanosine; base protecting group: isobutyryl; 2' protecting group: TBDMS; 5' protecting group: DMT; deprotection: standard
• Lagertemp.: −20°C
• SMILES String: COc1ccc(cc1)C(OC[C@H]2O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2OP(OCCC#N)N(C(C)C)C(C)C)n3cnc4C(=O)NC(NC(=O)C(C)C)=Nc34)(c5ccccc5)c6ccc(OC)cc6
• InChI: 1S/C50H68N7O9PSi/c1-32(2)45(58)54-48-53-44-41(46(59)55-48)52-31-56(44)47-43(66-68(12,13)49(7,8)9)42(65-67(63-29-17-28-51)57(33(3)4)34(5)6)40(64-47)30-62-50(35-18-15-14-16-19-35,36-20-24-38(60-10)25-21-36)37-22-26-39(61-11)27-23-37/h14-16,18-27,31-34,40,42-43,47H,17,29-30H2,1-13H3,(H2,53,54,55,58,59)/t40-,42-,43-,47-,67?/m1/s1
• InChIKey: PGJKESPHANLWME-FTZVBZPOSA-N

Beschreibung

Allgemeine Beschreibung

RNA phosphoramidites, along with RNA CPG, and analogous to DNA synthesis support the synthesis of sequence-specific RNA oligonucleotides for RNA interference (RNAi) and can be used in target validation and other drug development techniques.Modern phosphoramidite-mediated synthesis has enabled routine high-yielding preparations of RNA oligonucleotides. High-quality RNA phosphoramidites are key to low failure rates, the high biological activity of synthesis products, and cost-effectiveness.Key Features

• Industry-standard 2′O-TBDMS protective group
• Consistent lot-to-lot purity and performance
• Compatible with deprotection methods based on methylamine or AMA
• Standard RNA phosphoramidites provide excellent coupling results whenused with ETT or BTT as an activator; best results are obtained withActivator 42®
• Capping with standard acetic anhydride capping reagent rather than withFast Deprotection Cap A
• Manufactured under a certified ISO 9001 quality systemDMT-2′O-TBDMS-rG(ib)

Phosphoramidite is configured for MerMade Synthesizers.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 2
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable