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A111000

DMT-dA(bz) Phosphoramidite

Synonym(s):

DMT-dA(bz) Amidite, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxyadenosine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], N6-Benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyadenosine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]

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Size/SKUAvailabilityPrice
6 x 5 g

Available to ship TODAYfromHamburg

€300.00
6 x 10 g

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€1,030.00
100 g

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€1,580.00
6 x 20 g
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€1,980.00
500 g
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€6,850.00
20 x 40 g
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€13,700.00
1 kg
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€14,120.00

About This Item

Empirical Formula (Hill Notation):
C47H52N7O7P
CAS Number:
Molecular Weight:
857.93
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
Assay:
≥99% (31P-NMR), ≥99.0% (reversed phase HPLC)
Biological source:
non-animal source (no BSE/TSE risk)
Form:
powder or granules
Storage temp.:
2-8°C

€300.00


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biological source

non-animal source (no BSE/TSE risk)

Quality Segment

type

for DNA synthesis

product line

Proligo Reagents

assay

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

form

powder or granules

technique(s)

oligo synthesis: suitable

impurities

≤0.3 wt. % water content (Karl Fischer)

color

white to off-white

λ

conforms (UV/VIS Identity)

nucleoside profile

base: deoxyadenosine
base protecting group: benzoyl
2' protecting group: none
5' protecting group: DMT
deprotection: standard

storage temp.

2-8°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)n3cnc4c(NC(=O)c5ccccc5)ncnc34)(c6ccccc6)c7ccc(OC)cc7

InChI

1S/C47H52N7O7P/c1-32(2)54(33(3)4)62(59-27-13-26-48)61-40-28-42(53-31-51-43-44(49-30-50-45(43)53)52-46(55)34-14-9-7-10-15-34)60-41(40)29-58-47(35-16-11-8-12-17-35,36-18-22-38(56-5)23-19-36)37-20-24-39(57-6)25-21-37/h7-12,14-25,30-33,40-42H,13,27-29H2,1-6H3,(H,49,50,52,55)/t40-,41+,42+,62?/m0/s1

InChI key

GGDNKEQZFSTIMJ-AKWFTNRHSA-N

General description

DMT-dA(bz) Phosphoramidite belongs to the group of DNA Phosphoramidites.

Its key features include:

  • Exocyclic amine functions are protected by a benzoyl group (dA(bz) anddC(bz)) or isobutyryl group (dG(ib))
  • Recommended cleavage and deprotection conditions are 8 hours at 55 °Cor 24 hours at room temperature using concentrated ammonia solution,for standard base-protected oligonucleotides
  • The high coupling efficiency of Proligo′s DNA phosphoramidites leads tohigh-yield and high-quality oligonucleotides

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This Item
A111040A111030A11100P
description

-

description

configured for MerMade

description

configured for ABI

description

-

biological source

non-animal source (no BSE/TSE risk)

biological source

non-animal source (no BSE/TSE risk)

biological source

non-animal source (no BSE/TSE risk)

biological source

non-animal source (no BSE/TSE risk)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

300

form

powder or granules

form

powder or granules

form

powder or granules

form

powder or granules

assay

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

assay

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

assay

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

assay

≥99.5% (reversed phase HPLC), >99.5% (31P-NMR)

color

white to off-white

color

white to off-white

color

white to off-white

color

white to off-white

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C


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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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