DMT-dC(bz) Phosphoramidite
configured for MerMade
Manufacturer: Sigma Aldrich
CAS Number: 102212-98-6
Synonym(S): Cytidine, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxy-, 3′-[2-cyanoethyl bis(1-methylethyl)phosphoramidite], DMT-dC(bz) amidite, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxycytidine, 3′-[2-cyanoethyl N,N-?bis(1-methylethyl)phosphoramidite], N4-Benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 6 X 9.24 G | C111040-6-X-9.24-G | In Stock | ₹ 78,308.05 |
C111040 - 6 X 9.24 G
In Stock
Quantity
1
Base Price: ₹ 78,308.05
GST (18%): ₹ 14,095.449
Total Price: ₹ 92,403.499
biological source
non-animal source (no BSE/TSE risk)
Quality Level
200
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)
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Thermo Scientific Beta Cyanoethyl Phosphoramidite, dC(Bz), 102212-98-6, MFCD00036315, 2 g | -- | ₹ 2,943.26 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES DNA C(Bz) amidite | 102212-98-6, 1GR in 60 mL K&A (20-400) | -- | ₹ 3,251.28 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES DNA C(Bz) amidite | 102212-98-6, 1GR in 30 mL MerMade (28-400) | -- | ₹ 3,251.28 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES DNA C(Bz) amidite | 102212-98-6, 5GR in 100 mL AKTA (Septum) | -- | ₹ 5,818.08 | |
| | Bz Dc Beta-Cyanoethyl Phosphoramidite | -- | ₹ 69,550.63 | |
| | DMT-dC(bz) Phosphoramidite | -- | ₹ 1,17,148.15 - ₹ 20,04,432.78 | |
| | DMT-dC(bz) Phosphoramidite | -- | ₹ 1,540.08 - ₹ 71,784.84 | |
| | 102212-98-6 | Dmt-dc(bz) phosphoramidite | -- | ₹ 598.92 - ₹ 71,784.84 |
Related Products
Description
- 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. Exocyclic amine functions are protected by a benzoyl group (dA(bz) and dC(bz)) or isobutyryl group (dG(ib))Key features of DNA phosphoramidites :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 oligonucleotidesThe product belongs to MerMade synthesizers.
- Packaging: C111040-1G packaged in a 1 oz bottle with a 28-400 capC111040-10G packaged in a 8 oz bottle with a 28-400 capC111040-6x5G packaged in a 8 oz bottle with a 28-400 capC111040-6x10G packaged in a 8 oz bottle with a 28-400 capC111040-20x10G packaged in a 1 L bottle with GL 45
SAFETY INFORMATION
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable