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Merck

C112000

Sigma-Aldrich

DMT-dC(tac) Phosphoramidite

别名:

DMT-dC(tac)酰胺

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About This Item

经验公式(希尔记法):
C51H62N5O9P
分子量:
920.04
分類程式碼代碼:
12352202
NACRES:
NA.51

種類

for DNA synthesis

產品線

Proligo Reagents

化驗

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

形狀

powder

技術

oligo synthesis: suitable

&lambda ;

conforms (UV/VIS Identity)

核苷譜

base: deoxycytidine
base protecting group: TAC
2' protecting group: none
5' protecting group: DMT
deprotection: fast

儲存溫度

-10 to -25°C

SMILES 字串

CC(C)N(C(C)C)P(OCCC#N)O[C@H]1C[C@@H](O[C@@H]1COC(c2ccccc2)(c3ccccc3)c4ccccc4)N5C=CC(NC(=O)COc6ccc(cc6)C(C)(C)C)=NC5=O

InChI

1S/C49H58N5O7P/c1-35(2)54(36(3)4)62(59-31-17-29-50)61-42-32-46(53-30-28-44(52-47(53)56)51-45(55)34-57-41-26-24-37(25-27-41)48(5,6)7)60-43(42)33-58-49(38-18-11-8-12-19-38,39-20-13-9-14-21-39)40-22-15-10-16-23-40/h8-16,18-28,30,35-36,42-43,46H,17,31-34H2,1-7H3,(H,51,52,55,56)/t42-,43+,46+,62?/m0/s1

InChI 密鑰

NHKNJNORWFDRBB-ROEGVEHFSA-N

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一般說明

DMT-dC(tac) Phosphoramidite is a TAC Protected Phosphoramidite. Substitution of standard protecting groups with the labile TAC (tert.-butylphenoxyacetyl) protecting group results in ultra-fast and easy deprotection under mild conditions, suitable for oligonucleotides with base labile monomers and reporters as well as in-situ synthesis schemes on glass surfaces.

其他說明

  • The deprotection of oligonucleotide synthesis products with the AMAreagent is ultra-fast: complete deprotection requires 10 minutes at 65 °C
  • Side reactions at C-monomers through transamination are eliminated
  • Not compatible with some base-labile modified nucleosides
  • dC(tac)-phosphoramidite can directly substitute for dC(bz)-phosphoramidite
  • No change is required in the reagents commonly used for DNA synthesis.Acetonitrile is used to dissolve phosphoramidite. The standard aceticanhydride capping reagent can be employed.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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