• Product NameMonensin sodium
  • CasNo. 22373-78-0
  • MFC36H61NaO11
  • MW692.864
  • Purity
  • Appearancelight cream amorphous powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 22373-78-0

MF: C36H61NaO11

Appearance: light cream amorphous powder

Manufacturer Supply Best Quality Monensin sodium 22373-78-0 with Efficient Transportation

  • Molecular Formula:C36H61NaO11
  • Molecular Weight:692.864
  • Appearance/Colour:light cream amorphous powder 
  • Vapor Pressure:4.13E-27mmHg at 25°C 
  • Melting Point:267-269 °C 
  • Boiling Point:766.3 °C at 760 mmHg 
  • Flash Point:229.2 °C 
  • PSA:165.43000 
  • LogP:2.87390 

Monensin sodium salt(Cas 22373-78-0) Usage

Biochem/physiol Actions

Na+ ionophore; blocks glycoprotein secretion; may induce catecholamine secretion from chromaffin cells. Useful in potentiometric and spectroscopic studies of alkali metal ion complexes.

Purification Methods

Crystallise it from EtOH/H2O [Cox et al. J Am Chem Soc 107 4297 1985].

General Description

Monensin is a polyether ionophoric antibiotic, which is produced by Streptomyces cinnamonensis. It is used to treat bacterial, fungal and parasitic infections. Monensin prevents the growth of colon cancer cells. It facilitates the transport of sodium and potassium ions between intracellular and extracellular spaces. Monensin prevents coccidiosis?in poultry production.

InChI:InChI=1/C36H62O11.Na/c1-10-34(31-20(3)16-26(43-31)28-19(2)15-21(4)36(41,18-37)46-28)12-11-27(44-34)33(8)13-14-35(47-33)17-25(38)22(5)30(45-35)23(6)29(42-9)24(7)32(39)40;/h19-31,37-38,41H,10-18H2,1-9H3,(H,39,40);/q;+1/p-1/t19-,20+,21+,22+,23+,24+,25-,26-,27+,28-,29-,30-,31-,33+,34-,35+,36-;/m0./s1

22373-78-0 Relevant articles

Thermodynamics of Reaction in Heterogeneous Systems (Water-Organic Phases) between the Ionophore Monensin and Alkali-Metal Cations

Hebrant, Marc,Pointud, Yvon,Juillard, Jean

, p. 3653 - 3662 (1991)

Gibbs functions, enthalpies, entropies, ...

Rates and Equilibria of Alkali Metal and Silver Ion Complex Formation with Monensin in Ethanol

Cox, B. G.,Truong, Ng van,Rzeszotarska, J.,Schneider, H.

, p. 5965 - 5969 (1984)

Measurements are reported on the stabili...

Synthesis of monensin. Reconstruction from degradation products

Cai,Still

, p. 4641 - 4643 (2007/10/02)

-

BIOSYNTHESIS OF THE POLYETHER ANTIBIOTIC MONENSIN-A. RESULTS FROM THE INCORPORATIONS OF LABELLED ACETATE AND PROPIONATE AS A PROBE OF THE CARBON CHAIN ASSEMBLY PROCESSES

Sood, Gulshan R.,Ashworth, Doreen M.,Ajaz, Abid A.,Robinson, John A.

, p. 3183 - 3194 (2007/10/02)

The incorporation of sodium - and (S)--p...

BUTYRATE METABOLISM IN STREPTOMYCETES. CHARACTERIZATION OF AN INTRAMOLECULAR VICINAL INTERCHANGE REARRANGEMENT LINKING ISOBUTYRATE AND BUTYRATE IN STREPTOMYCES CINNAMONENSIS

Reynolds, Kevin A.,O'Hagan, David,Gani, David,Robinson, John A.

, p. 3195 - 3208 (2007/10/02)

The incorporations of varicus carbon-13 ...

22373-78-0 Process route

C<sub>36</sub>H<sub>61</sub>O<sub>11</sub><sup>(1-)</sup>
76948-58-8

C36H61O11(1-)

monensin A sodium salt
22373-78-0

monensin A sodium salt

Conditions
Conditions Yield
With sodium cation; at 25 ℃; Thermodynamic data; ΔH-, Γ-, TΔS-;
 
monensin<sup>(1-)</sup> ion

monensin(1-) ion

monensin sodium salt
22373-78-0

monensin sodium salt

Conditions
Conditions Yield
With sodium cation; In ethanol; at 25 ℃; Rate constant;
 

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