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CL11430

Sigma-Aldrich

DMT-locMeC(bz) Phosphoramidite

configured for ABI

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Empirical Formula (Hill Notation):
C48H54N5O9P
CAS Number:
Molecular Weight:
875.94

biological source

non-animal source (BSE/TSE no Risk)

Quality Level

product line

Proligo Reagents

Assay

≥98.0% (31P-NMR)
≥98.0% (reversed phase HPLC)

form

powder

impurities

≤3 wt. % Residual Solvent Content
<0.4% Water Content (Karl Fischer)
<0.5% Single unspecified Impurity (reversed phase HPLC)

color

white to off-white

solubility

acetonitrile: 0.2 M, clear, colorless

absorption

<0.1 in acetonitrile at 0.2 M

suitability

conforms to structure for H-NMR
conforms to structure for LC-MS

compatibility

configured for ABI

storage temp.

−20°C

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This Item
CL11480AL11430C111000
Sigma-Aldrich

CL11430

DMT-locMeC(bz) Phosphoramidite

Sigma-Aldrich

CL11480

DMT-locMeC(bz) Phosphoramidite

Sigma-Aldrich

AL11430

DMT-locA(bz) Phosphoramidite

DMT-dC(bz) Phosphoramidite

C111000

DMT-dC(bz) Phosphoramidite

Quality Level

300

Quality Level

300

Quality Level

300

Quality Level

200

form

powder

form

powder

form

powder

form

powder or granules

assay

≥98.0% (31P-NMR), ≥98.0% (reversed phase HPLC)

assay

≥98.0% (31P-NMR), ≥98.0% (reversed phase HPLC)

assay

≥98.0% (31P-NMR), ≥98.0% (reversed phase HPLC)

assay

≥99% (31P-NMR), ≥99.0% (reversed phase HPLC)

solubility

acetonitrile: 0.2 M, clear, colorless

solubility

acetonitrile: 0.2 M, clear, colorless

solubility

soluble, clear, colorless

solubility

-

color

white to off-white

color

white to off-white

color

white to off-white

color

white to off-white

General description

DMT-locMeC(bz) Phosphoramidite belongs to the group of LNA phosphoramidite. It is known as DMT-5-Me-locCytidine(N4-Benzoyl)- ß-Cyanoethylphosphoramidite. The synthesis cycle for Locked Nucleic Acid (LNA) oligonucleotides consists of the same series of reactions as the cycle that is employed for DNA monomers. However, the rate of coupling for LNA monomers is slower compared to that of DNA monomers (a coupling time of 8 minutes is recommended for LNA monomers compared to 90 seconds for DNA monomers). With the exception of the LNA monomers, LNA synthesis is accomplished with the same reagents as DNA synthesis.

Features and Benefits

Key Features of LNA Phosphoramidites:

  • LNA oligonucleotides are prepared by phosphoramidite chemistry
  • Standard DNA synthesizer platforms can be employed. No change is required in the reagents commonly used for DNA synthesis.
  • To further enhance the hybridization characteristics of LNA, 5-methyl-cytidine is employed instead of cytidine.
  • LNA monomers are as soluble in acetonitrile as their DNA counterparts (except for the 5-methyl-cytidine derivative, which requires the application of 10-20%, dichloromethane as a co-solvent)
  • Mixmer oligonucleotides containing LNA, DNA and/or RNA monomers can be assembled easily
  • LNA oligonucleotides with predefined melting temperatures (Tm) can be designed and prepared.

Other Notes

LNA phosphoramidites from Merck are diluted with dryacetonitrile, except for locMeC(bz)-phosphoramidite.This phosphoramidite requires the application of a cosolventto prevent crystallization from the solution onthe synthesizer. Dichloromethane or tetrahydrofuran(THF) can be applied as co-solvents with acetonitrile tocompletely dissolve locMeC(bz)-phosphoramidite.

Legal Information

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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