DMT-dG(dmf) Phosphoramidite
≥99.0% (reversed phase HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 330628-04-1
Synonym(S): DMT-dG(dmf) Amidite, N-[(dimethylamino)methylene]-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxyguanosine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], N2-Dimethylformamidine-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 6 X 10 G | G115000-6-X-10-G | In Stock | ₹ 1,02,350.38 |
| 100 G | G115000-100-G | In Stock | ₹ 1,49,947.90 |
| 6 X 20 G | G115000-6-X-20-G | In Stock | ₹ 1,91,505.08 |
| 500 G | G115000-500-G | In Stock | ₹ 15,55,530.85 |
| 1 KG | G115000-1-KG | In Stock | ₹ 23,59,373.70 |
G115000 - 6 X 10 G
In Stock
Quantity
1
Base Price: ₹ 1,02,350.38
GST (18%): ₹ 18,423.068
Total Price: ₹ 1,20,773.448
type
for DNA synthesis
Quality Level
200
product line
Proligo Reagents
Assay
≥99% (31P-NMR)≥99.0% (reversed phase HPLC)
form
powder
mol wt
824.90 g/mol
technique(s)
oligo synthesis: suitable
color
white to off-white
λ
conforms (UV/VIS Identity)
nucleoside profile
base: deoxyguanosinebase protecting group: DMF2' protecting group: none5' protecting group: DMTdeprotection: fast
Other Options
Description
- General description: DMT-dG(dmf) Phosphoramidite belongs to fast deprotection phosphoramidites where the deprotection step of automated oligonucleotide synthesis is integral to synthesis time and final product quality. Changing the dG protecting group to the dimethylformamidine (dmf) baseprotecting group enables the rapid synthesis of high-purity, high-yield oligonucleotide, thus increasing the efficiency of high-throughput production.
- Features and Benefits: Key Features of dG(dmf):dG(dmf) is deprotected faster than the conventional dG(ib): the deprotection time in concentrated ammonia is reduced to 2 hours at 55 °C or 1 hour at 65 °CThe dG(dmf)-monomer is especially suitable for G-rich sequences: incomplete deprotection is greatly reduced in comparison with the conventional dG(ib)-monomerdG(dmf)-phosphoramidite is as stable in solution as the standard dA(bz)-, dC(bz)- and dT-phosphoramiditesdG(dmf)-phosphoramidite can directly substitute for dG(ib)-phosphoramiditeNo change is required in the reagents commonly used for DNA synthesis (Except a low concentration iodine oxidizer i.e., 0.02 M in iodine, should be employed)
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable