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About This Item
Empirical Formula (Hill Notation):
C13H18N5O13P3 · xNa+
Molecular Weight:
545.23 (free acid basis)
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
assay
≥95% (HPLC)
Quality Segment
form
solid
reaction suitability
reaction type: click chemistry
solubility
10 mM Tris-HCl, pH 7.5: soluble
shipped in
wet ice
storage temp.
−20°C
SMILES string
O[C@@H]([C@H]1O)[C@@H](COP(O)(OP(O)(OP(O)(O)=O)=O)=O)O[C@@H]1N2C=NC3=C2N=CN=C3NCC#C
InChI
1S/C13H18N5O13P3/c1-2-3-14-11-8-12(16-5-15-11)18(6-17-8)13-10(20)9(19)7(29-13)4-28-33(24,25)31-34(26,27)30-32(21,22)23/h1,5-7,9-10,13,19-20H,3-4H2,(H,24,25)(H,26,27)(H,14,15,16)(H2,21,22,23)/t7-,9-,10-,13?/m1/s1
InChI key
MUOIWXPACQCYQC-RJNFYWFKSA-N
Application
N6-Propargyl-ATP is suitable for in vitro AMPylation of proteins as well as in vitro polyadenylation of RNA. The resulting alkyne-functionalized protein or RNA can be processed using Cu(I)-catalyzed click chemistry to attach azide-labeled molecules. This gives options such as introduction of a biotin group for purification tasks, introduction of a fluorescent group for detection, or crosslinking to other azide-functionalized biomolecules.
Storage Class
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
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