U211250

DMT-2′Fluoro-dU Phosphoramidite

configured for (ÄKTA^® and OligoPilot^®)

• Synonyme(s) : DMT-2′-Fluoro-dU amidite
• Formule empirique (notation de Hill): C₃₉H₄₆FN₄O₈P
• Numéro CAS: 146954-75-8
• Poids moléculaire : 748.78
• Numéro MDL: MFCD11113919
• Code UNSPSC : 12352200
• ID de substance PubChem : 329827617
• Nomenclature NACRES : NA.21

Propriétés

• Source biologique: non-animal source (no BSE/TSE risk)
• Niveau de qualité: 300
• Gamme de produits: Proligo Reagents
• Pureté: ≥99% (³¹P-NMR); ≥99.0% (reversed phase HPLC)
• Forme: powder
• Technique(s): oligo synthesis: suitable
• Impuretés: ≤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
• Couleur: white to off-white
• λ: conforms (UV/VIS Identity)
• Adéquation: conforms to structure for H-NMR; conforms to structure for LC-MS
• Compatibilité: configured for (ÄKTA^® and OligoPilot^®)
• Profil des nucléosides: base: deoxyuridine; base protecting group: none; 2' protecting group: fluoro; 5' protecting group: DMT; deprotection: fast/standard
• Température de stockage: −20°C
• Chaîne SMILES: COc1ccc(cc1)C(OC[C@H]2O[C@H]([C@H](F)[C@@H]2OP(OCCC#N)N(C(C)C)C(C)C)N3C=CC(=O)NC3=O)(c4ccccc4)c5ccc(OC)cc5
• InChI: 1S/C39H46FN4O8P/c1-26(2)44(27(3)4)53(50-24-10-22-41)52-36-33(51-37(35(36)40)43-23-21-34(45)42-38(43)46)25-49-39(28-11-8-7-9-12-28,29-13-17-31(47-5)18-14-29)30-15-19-32(48-6)20-16-30/h7-9,11-21,23,26-27,33,35-37H,10,24-25H2,1-6H3,(H,42,45,46)/t33-,35-,36-,37-,53?/m1/s1
• Clé InChI: HQHQPAYRJJMYQX-DJTPZYMWSA-N

Description

Description générale

DMT-2′Fluoro-dU Phosphoramidite is a 2′Fluoro phosphoramidite used to synthesize oligonucleotides that are more thermally stable and provide increased nuclease resistance.Its key features are-

• Can be employed together with DNA or RNA phosphoramidites
• Recommended deprotection conditions are 8 hours at 55 °C using concentrated ammonia solution, or with AMA for 10 minutes at 65 °C
• Synthesis of 2′Fluoro oligonucleotides is similar to standard DNA synthesis but requires an elongated coupling time (recommended is 3 minutes compared to 90 seconds for DNA monomers)
• Consistent lot-to-lot high purity and performance
• Manufactured under a certified ISO 9001 quality system

Application

DMT-2′Fluoro-dU Phosphoramidite is suitable for use in the synthesis of 2′-fluoro modified oligonucleotide sequences by employing automated solid-phase chemistry.

Informations légales

OligoPilot is a registered trademark of Cytiva

ÄKTA is a registered trademark of Cytiva

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