U211130
别名:
DMT-2′O-甲基-rU酰胺
1 of 10
Sigma-Aldrich
U211150
DMT-2′O-Methyl-rU Phosphoramidite
A211100
DMT-2′O-Methyl-rA(bz) 磷酰胺
G211230
DMT-2′Fluoro-dG(ib) Phosphoramidite
C213130
DMT-2′O-Methyl-rC(ac) Phosphoramidite
U211200
DMT-2′Fluoro-dU Phosphoramidite
C213140
T111050
DMT-dT亚磷酰胺
A211150
A211050
DMT-2′O-TBDMS-rA (bz) 亚磷酰胺
U211140
non-animal source (no BSE/TSE risk)
Proligo Reagents
≥99% (31P-NMR)≥99.0% (reversed phase HPLC)
powder
oligo synthesis: suitable
≤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
white to off-white
conforms (UV/VIS Identity)
conforms to structure for H-NMRconforms to structure for LC-MS
configured for ABI
base: uridinebase protecting group: none2' protecting group: methyl5' protecting group: DMTdeprotection: fast/standard
2-8°C
CO[C@@H]1[C@H](OP(OCCC#N)N(C(C)C)C(C)C)[C@@H](COC(c2ccccc2)(c3ccc(OC)cc3)c4ccc(OC)cc4)O[C@H]1N5C=CC(=O)NC5=O
1S/C40H49N4O9P/c1-27(2)44(28(3)4)54(51-25-11-23-41)53-36-34(52-38(37(36)49-7)43-24-22-35(45)42-39(43)46)26-50-40(29-12-9-8-10-13-29,30-14-18-32(47-5)19-15-30)31-16-20-33(48-6)21-17-31/h8-10,12-22,24,27-28,34,36-38H,11,25-26H2,1-7H3,(H,42,45,46)/t34-,36-,37-,38-,54?/m1/s1
UVUOJOLPNDCIHL-XKZJCBTISA-N
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11 - Combustible Solids
WGK 3
Not applicable
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