U211150

DMT-2′O-Methyl-rU Phosphoramidite

configured for ÄKTA® and OligoPilot®

Manufacturer: Sigma Aldrich

CAS Number: 110764-79-9

Synonym(S): 5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-methyl-uridine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], DMT-2′O-Methyl-rU amidite

Select a Size

Pack Size SKU Availability Price
2 G U211150-2-G In Stock ₹ 19,203.55
5 G U211150-5-G In Stock ₹ 48,853.23
10 G U211150-10-G In Stock ₹ 97,630.68

U211150 - 2 G

₹ 19,203.55

In Stock

Quantity

1

Base Price: ₹ 19,203.55

GST (18%): ₹ 3,456.639

Total Price: ₹ 22,660.189

biological source

non-animal source (no BSE/TSE risk)

Quality Level

300

product line

Proligo Reagents

Assay

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

form

powder

technique(s)

oligo synthesis: suitable

impurities

≤0.1% single unspecified Impurity (reversed phase HPLC)≤0.3% mU2 (reversed phase HPLC, Hydrolysate)≤0.3% mU3 (reversed phase HPLC, DMT-rme)≤0.3% water content (Karl Fischer)≤0.5% P(III) Impurities 100-169ppm (31P-NMR)≤1.0% mU1 (reversed phase HPLC, DMT-rUme-DMT)≤3% residual Solvent content

color

white to off-white

λ

conforms (UV/VIS Identity)

suitability

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

Other Options

Image Product Name Manufacturer Price Range
50-244-0934
eMolecules​ Ambeed / (2R3R4R5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(24-dioxo-34-dihydropyrimidin-1(2H)-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite / 1g / 552739332 / A513418 / / 110764-79-9 / MFCD00792626 / 760.825 / C40H49N4O9P
eMolecules​ ₹ 4,255.75
50-235-5046
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 5GR
STA PHARMACEUTICAL US LLC ₹ 11,319.59
50-235-6277
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 1GR in 60 mL K&A (20-400)
STA PHARMACEUTICAL US LLC ₹ 4,962.48
50-235-4816
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 5GR in 250 mL MerMade (28-400)
STA PHARMACEUTICAL US LLC ₹ 11,319.59
50-235-5170
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 1GR
STA PHARMACEUTICAL US LLC ₹ 4,962.48
50-175-8987
Sigma Aldrich Fine Chemicals Biosciences DMT-2'O-Methyl-rU Phosphoramidite configured for PerkinElmer, configured for Polygen | 110764-79-9 | MFCD00792626 | 0.5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 10,103.78
50-175-8984
Sigma Aldrich Fine Chemicals Biosciences DMT-2'O-Methyl-rU Phosphoramidite configured for MerMade | 110764-79-9 | MFCD00792626 | 1G
Sigma Aldrich Fine Chemicals Biosciences ₹ 11,005.58
50-175-8986
Sigma Aldrich Fine Chemicals Biosciences DMT-2'O-Methyl-rU Phosphoramidite configured for ÄKTA(R) and OligoPilot(R) | 110764-79-9 | MFCD00792626 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 43,738.27
50-235-4817
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 1GR in 30 mL K&A (20-400)
STA PHARMACEUTICAL US LLC ₹ 4,962.48
50-235-5047
STA PHARMACEUTICAL US LLC WuXi TIDES 2‘-OMe U amidite | 110764-79-9, 5GR in 100 mL AKTA (Septum)
STA PHARMACEUTICAL US LLC ₹ 11,319.59

Description

  • General description: DMT-2′O-Methyl-rU Phosphoramidite belongs to the class of 2′O-Methyl RNA Phosphoramidites.
  • Application: 2′O-Methyl RNA nucleoside including DMT-2′O-Methyl-rU Phosphoramidite can be advantageously incorporated in nucleic acid probes with RNA or DNA for in-vivo or in-vitro applications to convey nuclease resistance.
  • Features and Benefits: Its key features include: High yield of crude oligonucleotides Compatible with DNA synthesis Can be employed together with DNA or RNA phosphoramidites in the same synthesis to produce mixmer oligonucleotides Recommended deprotection conditions are 8 hours at 55 °C using concentrated ammonia solution, or with AMA (concentrated ammonia/ 40% aqueous methylamine I/I, v/v) for 10 minutes at 65 °C Purification and other downstream processing of fully modified 2′OMethyl RNA oligonucleotides are simpler than in the case of RNA, as no special precautions are required to provide protection against nucleolytic degradation Synthesis of 2′O-Methyl RNA oligonucleotides is similar to standard DNA synthesis but requires an elongated coupling time (recommended is 6 minutes compared to 90 seconds for DNA monomers) 2′O-Methyl RNA phosphoramidites are also available with fast deprotection chemistry
  • Other Notes: The unique combination of properties of 2′O-Methyl RNA had found widespread use in the fields of: Diagnostic probes Aptamer and ribozyme development Mixed 2′O-Methyl-RNA/DNA antisense molecules
  • Legal Information: OligoPilot is a registered trademark of Cytiva

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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product line:
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form:
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technique(s):
oligo synthesis: suitable

impurities:
≤0.1% single unspecified Impurity (reversed phase HPLC)≤0.3% mU2 (reversed phase HPLC, Hydrolysate)≤0.3% mU3 (reversed phase HPLC, DMT-rme)≤0.3% water content (Karl Fischer)≤0.5% P(III) Impurities 100-169ppm (31P-NMR)≤1.0% mU1 (reversed phase HPLC, DMT-rUme-DMT)≤3% residual Solvent content

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

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

form:
powder

technique(s):
oligo synthesis: suitable

impurities:
≤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

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Proligo Reagents

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

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technique(s):
oligo synthesis: suitable

impurities:
≤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

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white to off-white

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conforms (UV/VIS Identity)

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

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Proligo Reagents

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≥98% (31P-NMR)≥98.0% (reversed phase HPLC)

form:
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oligo synthesis: suitable

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≤0.3 wt. % water content (Karl Fischer)≤0.5% 3′-TC isomer (reversed phase HPLC)≤0.5% P(III) Impurities 145-155ppm (31P-NMR)

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white to light yellow

λ:
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