14535-90-1

Basic information

• Product Name: adenosine 5'-pentaphosphate
• Synonyms: adenosine 5'-pentaphosphate;adenosine 5'-(hexahydrogen pentaphosphate)
• CAS NO: 14535-90-1
• Molecular Formula: C10H18N5O19P5
• Molecular Weight: 667.14
• Mol File: 14535-90-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 1086.3°Cat760mmHg
• Flash Point: 610.7°C
• Appearance: /
• Density: 2.83g/cm³
• PKA: 0.57±0.50(Predicted)
• CAS DataBase Reference: adenosine 5'-pentaphosphate(CAS DataBase Reference)
• NIST Chemistry Reference: adenosine 5'-pentaphosphate(14535-90-1)
• EPA Substance Registry System: adenosine 5'-pentaphosphate(14535-90-1)

Safety Data

• Hazardous Substances Data: 14535-90-1(Hazardous Substances Data)

Usage

Definition

ChEBI: A nucleoside pentaphosphate that is adenosine in which a hexahydrogen pentaphosphate is attached at the 5' position.

Upstream product

• 61-19-8 5'-adenosine monophosphate 
• 56-65-5 ATP 

Relevant articles and documents

Facile and Selective Synthesis of Diadenosine Polyphosphates through Catalysis by Leucyl t-RNA Synthetase Coupled with ATP Regeneration

Leucyl t-RNA synthetase from a thermophilic bacterium, Bacillus stearothermophillus, effectively catalyzed the synthesis of p1,p4-di(adenosine 5'-)tetraphosphate (Ap4A), p1,p5-di(adenosine 5'-)pentaphosphate (Ap5A) and adenosine 5'-tetraphosphate (p4A).In particular, when the reaction was coupled with an ATP recycling system involving thermostable acetate kinase and adenylate kinase, Ap4A and Ap5A were produced selectively in high yields.This reaction is selective, gives high yields and does not require protection of the functional groups of nucleotides, and also it can be carried out in an aqueous solution.This method is superior to the conventional organic synthesis and provides a practical means of the synthesizing diadenosine polyphosphates (ApnA), biologically important compounds.