G112080

DMT-dG(tac) Phosphoramidite

configured for PerkinElmer, configured for Polygen

• Synonyme(s) : DMT-dG(tac) amidite
• Formule empirique (notation de Hill): C₅₂H₆₂N₇O₉P
• Numéro CAS: 149989-60-6
• Poids moléculaire : 960.06
• Numéro MDL: MFCD01941141
• Code UNSPSC : 12352200
• ID de substance PubChem : 329799737
• Nomenclature NACRES : NA.51

Propriétés

• Type: for DNA synthesis
• Gamme de produits: Proligo Reagents
• Pureté: ≥98% (³¹P-NMR); ≥98.0% (reversed phase HPLC)
• Forme: powder
• Poids mol.: 960.06 g/mol
• Technique(s): oligo synthesis: suitable
• Couleur: white to light yellow
• Solubilité: acetonitrile: 0.2 M, clear
• λ: conforms (UV/VIS Identity)
• Compatibilité: configured for PerkinElmer; configured for Polygen
• Profil des nucléosides: base: deoxyguanosine; base protecting group: TAC; 2' protecting group: none; 5' protecting group: DMT; deprotection: fast
• Température de stockage: -10 to -25°C
• Chaîne SMILES: COc1ccc(cc1)C(OC[C@H]2O[C@H](C[C@@H]2OP(OCCC#N)N(C(C)C)C(C)C)n3cnc4C(=O)NC(NC(=O)COc5ccc(cc5)C(C)(C)C)=Nc34)(c6ccccc6)c7ccc(OC)cc7
• InChI: 1S/C52H62N7O9P/c1-34(2)59(35(3)4)69(66-29-13-28-53)68-43-30-46(58-33-54-47-48(58)56-50(57-49(47)61)55-45(60)32-64-42-26-16-36(17-27-42)51(5,6)7)67-44(43)31-65-52(37-14-11-10-12-15-37,38-18-22-40(62-8)23-19-38)39-20-24-41(63-9)25-21-39/h10-12,14-27,33-35,43-44,46H,13,29-32H2,1-9H3,(H2,55,56,57,60,61)/t43-,44+,46+,69?/m0/s1
• Clé InChI: MCBSUBQIVLOCIW-YEZUPXOUSA-N

Description

Description générale

Proligo′s DNA phosphoramidites lead to high-yield and high-quality oligonucleotides due to their high coupling efficiency. The deprotection step of automated oligonucleotide synthesis is integral to synthesis time and final product quality. The high coupling efficiency of Proligo′s DNA phosphoramidites leads to high-yield and high-quality oligonucleotides.Substitution of standard protecting groups with the labile TAC (tert.-butylphenoxyacetyl) protecting group results in ultra-fast and easydeprotection under mild conditions, suitable for oligonucleotides with baselabile monomers and reporters as well as in-situ synthesis schemes on glass surfaces.Key Features of TAC Chemistry

• Deprotection of the TAC group is ultra-fast: complete deprotection inconcentrated ammonia occurs within 15 minutes at 55 °C or two hours atroom temperature
• Compatible with the AMA deprotection reagent (a mixture of ≥25%ammonia in water with 40% aqueous methylamine I/I, v/v)
• Highly soluble in acetonitrile. No need to add co-solvents such asdimethylformamide or methylene chloride
• Suitable for the synthesis of oligomers with base-labile units e.g., dyes andmodifiers, because of less exposure to ammonia and the possibility ofroom temperature deprotection
• No change is required in the reagents commonly used for DNA synthesis,except that Proligo′s Fast Deprotection Cap A solution is used instead ofCap A solution
• The application of dA(tac) minimizes depurination and improves thequality of oligonucleotidesDMT-dG(tac) Phosphoramidite configured for Expedite^™ and PolyGen^® Synthesizers.

Informations légales

Expedite is a trademark of Applera Corporation or its subsidiaries in the US and/or certain other countries

PolyGen is a registered trademark of PolyGen GmbH.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable