Basic information Safety Supplier Related

3'-ADENYLIC ACID

Basic information Safety Supplier Related

3'-ADENYLIC ACID Basic information

Product Name:
3'-ADENYLIC ACID
Synonyms:
  • synadenylicacid
  • ADENYLIC ACID, YEAST
  • ADENYLIC ACID
  • ADENYLIC ACID, B
  • ADENOSINE 3'-MONOPHOSPHATE
  • ADENOSINE 3'-PHOSPHATE
  • ADENOSINE 3'-PHOSPHORIC ACID
  • ADENOSINE-3'-MONOPHOSPHORIC ACID
CAS:
84-21-9
MF:
C10H14N5O7P
MW:
347.22
EINECS:
201-521-8
Product Categories:
  • Pharmaceutical Intermediates
  • Nucleotides and Nucleic Acids
  • Nucleic acids
Mol File:
84-21-9.mol
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3'-ADENYLIC ACID Chemical Properties

Melting point:
~210 °C (dec.)
Boiling point:
815.5±75.0 °C(Predicted)
Density 
2.32±0.1 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
Aqueous Base (Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly)
pka
pK1: 3.65(0);pK2: 5.88(-1) (25°C)
form 
Solid
color 
White to Off-White
Water Solubility 
0.5g/L(15 ºC)
Merck 
13,158
BRN 
54478
Stability:
Hygroscopic
EPA Substance Registry System
3'-Adenylic acid (84-21-9)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
RTECS 
AU7480320
10-21

MSDS

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3'-ADENYLIC ACID Usage And Synthesis

Uses

Adenosine 3′-monophosphate (3′-AMP) is a metabolite produced from hydrolysis of 2′,3′-cAMP by a family of metal-dependent phosphodiesterases. 3′-AMP inhibits proliferation of preglomerular vascular smooth muscle cells and glomerular mesangial cells via A2B receptors. 2′,3′-cAMP and 3′-AMP represent a new unexplored pathway for adenosine-based cell regulation.

Definition

ChEBI: 3'-AMP is an adenosine 3'-phosphate with a monophosphate group at the 3'-position. It has a role as a mouse metabolite, a human metabolite and an Escherichia coli metabolite. It is an adenosine 3'-phosphate and a purine ribonucleoside 3'-monophosphate. It is a conjugate acid of a 3'-AMP(2-).

Purification Methods

It crystallises from large volumes of H2O in needles as the monohydrate, but is not very soluble in boiling H2O. Under acidic conditions it forms an equilibrium mixture of 2' and 3' adenylic acids via the 2',3'-cyclic phosphate. When heated with 20% HCl, it gives a quantitative yield of furfural after 3hours, unlike 5'-adenylic acid which only gives traces of furfural. The yellow monoacridine salt has m 175o(dec), and the diacridine salt has m 177o (225o)(dec). [Brown & Todd J Chem Soc 44 1952, Takaku et al. Chem Pharm Bull Jpn 21 1844 1973, NMR: Ts'O et al. Biochemistry 8 997 1969, Beilstein 26 III/IV 3607.]

3'-ADENYLIC ACIDSupplier

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