C113050

DMT-dC(ac)-phosphoramidit

configured for ABI

• Synonym(e): DMT-dC(ac)-amidit, N-acetyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxycytidin, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidit], N4-Acetyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidin-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidit]
• Empirische Formel (Hill-System): C₄₁H₅₀N₅O₈P
• CAS-Nummer: 154110-40-4
• Molekulargewicht: 771.84
• NACRES: NA.51
• PubChem Substance ID: 329774865
• UNSPSC Code: 12352200
• MDL number: MFCD09842112
• Assay: ≥98% (³¹P-NMR), ≥99.0% (reversed phase HPLC)
• Biological source: non-animal source (no BSE/TSE risk)
• Form: powder
• Storage temp.: -10 to -25°C

Eigenschaften

• biological source: non-animal source (no BSE/TSE risk)
• Quality Segment: 200
• type: for DNA synthesis
• product line: Proligo Reagents
• assay: ≥98% (³¹P-NMR), ≥99.0% (reversed phase HPLC)
• form: powder
• packaging: pkg of 1 × 10 g C113050-10G
• technique(s): oligo synthesis: suitable
• color: white to off-white
• λ: conforms (UV/VIS Identity)
• compatibility: configured for ABI
• nucleoside profile: base: deoxycytidine; base protecting group: acetyl; 2' protecting group: DMT; 5' protecting group: DMT; deprotection: fast/standard
• storage temp.: -10 to -25°C
• SMILES string: COc1ccc(cc1)C(OC[C@H]2O[C@H](C[C@@H]2OP(OCCC#N)N(C(C)C)C(C)C)N3C=CC(NC(C)=O)=NC3=O)(c4ccccc4)c5ccc(OC)cc5
• InChI: 1S/C41H50N5O8P/c1-28(2)46(29(3)4)55(52-25-11-23-42)54-36-26-39(45-24-22-38(43-30(5)47)44-40(45)48)53-37(36)27-51-41(31-12-9-8-10-13-31,32-14-18-34(49-6)19-15-32)33-16-20-35(50-7)21-17-33/h8-10,12-22,24,28-29,36-37,39H,11,25-27H2,1-7H3,(H,43,44,47,48)/t36-,37+,39+,55?/m0/s1
• InChI key: MECWEBCHRKVTNV-RLWDVSNXSA-N

Beschreibung

General description

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. DMT-dC(ac) Phosphoramidite is an acetyl-protected DNA phosphoramidite used in fast deprotection chemistry for the rapid and high-yield synthesis of high-purity oligonucleotides. Key Features of dC(ac): •

• Ultrafast deprotection: 10 minutes at 65°C with AMA reagent
• Key component in oligonucleotide synthesis
• Industry standard for fast deprotection chemistry
• Operating for AMA deprotection methods without changes
• Consistent lot-to-lot high purity and performance
• Manufactured under a certified ISO 9001 quality system

The product belongs to ÄKTA® Synthesizers.

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable