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Merck
CN

C113030

DMT-dC(ac) Phosphoramidite

configured for ABI

Synonym(s):

DMT-dC(ac) Amidite, N-acetyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxycytidine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], N4-Acetyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]

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About This Item

Empirical Formula (Hill Notation):
C41H50N5O8P
CAS Number:
Molecular Weight:
771.84
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (31P-NMR), ≥99.0% (reversed phase HPLC)
Biological source:
non-animal source (no BSE/TSE risk)
Form:
powder
Solubility:
water: insoluble
Storage temp.:
-10 to -25°C
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biological source

non-animal source (no BSE/TSE risk)

Quality Segment

type

for DNA synthesis

product line

Proligo Reagents

assay

≥98% (31P-NMR), ≥99.0% (reversed phase HPLC)

form

powder

technique(s)

oligo synthesis: suitable

color

white to off-white

solubility

water: insoluble

λ

conforms (UV/VIS Identity)

compatibility

configured for ABI

nucleoside profile

base: deoxycytidine
base protecting group: acetyl
2' protecting group: none
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

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 ABI Synthesizers.

Legal Information

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


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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