What is the Monensin?

Monensin is Crystallin solid, while it's Molecular Formula is C36H62O11. Crystallin solid Monensin (2) C36H62O11, a carboxylic acid which is used as its water-soluble sodium salt (Coban, Rumensin). Monensin is also used to treat histomoniasis. The polyether ionophoric antibiotics are capable of complexing and interfacing with specific alkali metal cations to render them lipid-soluble and diffusible across parasite mitochondrial membranes. Related useful polyether antibiotics are narasin and lasalocid (3, Lasalocid A, C34H54O8,).

What is the CAS number for Monensin?

The CAS number of Monensin is 17090-79-8.

What is Monensin (17090-79-8) used for?

Monensin is a polyether antibiotic derived from Streptomyces cinnamonensis, first isolated in 1967. It is a broad-spectrum anticoccidial antibiotic with antifungal and antiviral properties. Monensin forms complexes with monovalent cations, such as Li+, Na+, K+, Rb+, Ag+, and Tl+, and functions as an Na+/H+ antiporter. It is known for its ability to block intracellular protein transport.InChI:InChI=1/C37H64O10.Na/c1-11-35(32-21(4)18-27(43-32)29-20(3)17-22(5)37(41,12-2)46-29)14-13-28(44-35)34(9)15-16-36(47-34)19-26(38)23(6)31(45-36)24(7)30(42-10)25(8)33(39)40;/h20-32,38,41H,11-19H2,1-10H3,(H,39,40);/q;+1/p-1/t20-,21-,22+,23+,24+,25-,26-,27+,28+,29?,30+,31-,32?,34-,35-,36?,37-;/m0./s1

What is the Monensin?

Monensin is Crystallin solid, while it's Molecular Formula is C36H62O11. Crystallin solid Monensin (2) C36H62O11, a carboxylic acid which is used as its water-soluble sodium salt (Coban, Rumensin). Monensin is also used to treat histomoniasis. The polyether ionophoric antibiotics are capable of complexing and interfacing with specific alkali metal cations to render them lipid-soluble and diffusible across parasite mitochondrial membranes. Related useful polyether antibiotics are narasin and lasalocid (3, Lasalocid A, C34H54O8,).

What is the CAS number for Monensin?

The CAS number of Monensin is 17090-79-8.

What is Monensin (17090-79-8) used for?

Monensin is a polyether antibiotic derived from Streptomyces cinnamonensis, first isolated in 1967. It is a broad-spectrum anticoccidial antibiotic with antifungal and antiviral properties. Monensin forms complexes with monovalent cations, such as Li+, Na+, K+, Rb+, Ag+, and Tl+, and functions as an Na+/H+ antiporter. It is known for its ability to block intracellular protein transport.InChI:InChI=1/C37H64O10.Na/c1-11-35(32-21(4)18-27(43-32)29-20(3)17-22(5)37(41,12-2)46-29)14-13-28(44-35)34(9)15-16-36(47-34)19-26(38)23(6)31(45-36)24(7)30(42-10)25(8)33(39)40;/h20-32,38,41H,11-19H2,1-10H3,(H,39,40);/q;+1/p-1/t20-,21-,22+,23+,24+,25-,26-,27+,28+,29?,30+,31-,32?,34-,35-,36?,37-;/m0./s1

Product classification

17090-79-8

Product Name：monensin
Molecular Formula：C₃₆H₆₂O₁₁
Purity：99%
Molecular Weight：670.882

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Product Details;

CasNo： 17090-79-8

Molecular Formula： C₃₆H₆₂O₁₁

Appearance： Crystallin solid

Top quality factory supply 17090-79-8 monensin at low price

Molecular Formula:C36H62O11
Molecular Weight:670.882
Appearance/Colour:Crystallin solid
Vapor Pressure:1.85E-25mmHg at 25°C
Melting Point:103-105 °C
Refractive Index:1.5465 (estimate)
Boiling Point:766.3 °C at 760 mmHg
PKA:6.6 (in 66% DMF)
Flash Point:229.2 °C
PSA：156.20000
Density:1.21 g/cm³
LogP:2.93820

Monensin(Cas 17090-79-8) Usage

Safety Profile	Poison by ingestion and intraperitoneal routes. An eye and skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Brand name	Coban [as sodium salt] (Lilly);Rumensin [as sodium salt] (Lilly).

InChI:InChI=1/C37H64O10.Na/c1-11-35(32-21(4)18-27(43-32)29-20(3)17-22(5)37(41,12-2)46-29)14-13-28(44-35)34(9)15-16-36(47-34)19-26(38)23(6)31(45-36)24(7)30(42-10)25(8)33(39)40;/h20-32,38,41H,11-19H2,1-10H3,(H,39,40);/q;+1/p-1/t20-,21-,22+,23+,24+,25-,26-,27+,28+,29?,30+,31-,32?,34-,35-,36?,37-;/m0./s1

17090-79-8 Relevant articles

Spectroscopic, semi-empirical and antimicrobial studies of a new amide of monensin A with 4-aminobenzo-15-crown-5 and its complexes with Na+ cation at 1:1 and 1:2 ratios

?owicki, Daniel,Huczyński, Adam,Stefańska, Joanna,Brzezinski, Bogumil

, p. 1468 - 1478 (2011)

A new amide of monensin A with 4-aminobe...

Can temperature be used to tune the selectivity of membrane ion-selective electrodes?

Zahran, Elsayed M.,Gavalas, Vasileios,Valiente, Manuel,Bachas, Leonidas G.

, p. 3622 - 3628 (2010)

The selectivity coefficients, KIJpot, of...

1H, 13C NMR, FT-IR, ESI MS and PM5 studies of a new 3,6,9-trioxadecylamide of monensin A and its complexes with Li+, Na+ and K+ cations

?owicki, Daniel,Huczyński, Adam,Brzezinski, Bogumil,Bartl, Franz

experimental part, p. 121 - 131 (2011/04/23)

A new 3,6,9-trioxadecylamide of monensin...

Structural and antimicrobial studies of a new N-phenylamide of monensin A complex with sodium chloride

?owicki, Daniel,Huczyński, Adam,Ratajczak-Sitarz, Ma?gorzata,Katrusiak, Andrzej,Stefańska, Joanna,Brzezinski, Bogumil,Bartl, Franz

experimental part, p. 53 - 59 (2009/09/30)

A complex between a new N-phenylamide of...

17090-79-8 Process route

: 22373-78-0
monensin A sodium salt

: 17090-79-8
monensin

Conditions

Conditions	Yield
With sulfuric acid; In dichloromethane;
With sulfuric acid; In dichloromethane; water; pH=1.5;
With sulfuric acid; In dichloromethane; water; pH=1.5;
With hydrogenchloride; water;
With sulfuric acid; In dichloromethane; water; pH=1.5;

: 17090-79-8
monensin