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A26209 Sigma-Aldrich

Adenosine 5′-triphosphate disodium salt hydrate

99%

Synonym: 5′-ATP-Na2, ATP disodium salt hydrate

  • CAS Number 34369-07-8

  • Empirical Formula (Hill Notation) C10H14N5Na2O13P3 · xH2O

  • Molecular Weight 551.14 (anhydrous basis)

  •  Beilstein/REAXYS Number 6264880

  •  EC Number 213-579-1

  •  MDL number MFCD00150755

  •  eCl@ss 32160414

  •  PubChem Substance ID 24890675

  •  NACRES NA.22

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Nucleobase, Nucleoside and Nucleotide Derivatives, Nucleoside Chemistry
Quality Level   200
assay   99%
mp   176 °C (dec.) (lit.)
storage temp.   2-8°C
SMILES string   [Na+].[Na+].[H]O[H].Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP(O)(=O)OP([O-])(=O)OP(O)([O-])=O)[C@@H](O)[C@H]3O
InChI   1S/C10H16N5O13P3.2Na.H2O/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20;;;/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20);;;1H2/q;2*+1;/p-2/t4-,6-,7-,10-;;;/m1.../s1
InChI key   NTBQNWBHIXNPRU-MSQVLRTGSA-L

Description

Application

Adenosine 5′-triphosphate disodium salt hydrate has been used as a component of mechanistic target of rapamycin (mTOR) assay start buffer. It has also been used in a feeding behavior study of Rhodnius prolixus as a potent phagostimulant in feeding solutions to enhance the feeding rate.

Packaging

1, 5, 10, 50 g in glass bottle

Other Notes

Contains solvent of crystallization, varying amounts of water

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

MSMLS Online Plate Map

Metabolite descriptors included with the software download upon purchase of the product include: Name, Parent CID, molecular formula, molecular weight, CAS, ChEBI, HMDB ID, PubChem Compound and Subst...
Keywords: Mass spectrometry, Metabolites

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Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
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Peer-Reviewed Papers
15

References

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