Monensin

Monensin Basic information
Product Name:Monensin
Synonyms:2-(5-ethyltetrahydro-5-(tetrahydro-3-6-dioxaspiro(4.5)decane-7-butyricacid;a3823a;elancoban;gamma,2,8-tetramethyl--furyl)-2-furyl)-9-hydroxy-beta-methoxy-alph;monelan;Monensine sodium;4-[2-[2-Ethyl-5-(6-hydroxy-6-hydroxymethyl-3,5-dimethyltetrahydropyran-2-yl)-3-methyloctahydro-[2,2]bifuranyl-5-yl]-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]-3-methoxy-2-methylpentanoic acid;Monensin A
CAS:17090-79-8
MF:C36H62O11
MW:670.87
EINECS:241-154-0
Product Categories:Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;API's
Mol File:17090-79-8.mol
Monensin Structure
Monensin Chemical Properties
Melting point 103-105°C
alpha D +47.7°
Boiling point 608.24°C (rough estimate)
density 1.0773 (rough estimate)
refractive index 1.5465 (estimate)
storage temp. 2-8°C
pka6.6 (in 66% DMF)
CAS DataBase Reference17090-79-8(CAS DataBase Reference)
EPA Substance Registry SystemMonensin (17090-79-8)
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 36/37/39-45
WGK Germany 3
RTECS JH2830000
Hazardous Substances Data17090-79-8(Hazardous Substances Data)
ToxicityLD50 of monensin complex in mice, chicks (mg/kg): 43.8 ± 5.2, 284 ± 47 orally (Haney, Hoehn)
Monensin Usage And Synthesis
Chemical PropertiesCrystallin Solid
UsesMonensin A is a polyether antibiotic first isolated from Streptomyces cinnamonensis in 1967. Monensin A is a broad-spectrum anticoccicidial antibiotic, also exhibiting antifungal and antiviral activity. Monensin A forms complexes with monovalent cations such as Li+, Na+, K+, Rb+, Ag+ and Tl+ and is thus able to transport these cations across lipid membranes of cells, playing an important role as an Na+/H+ antiporter. It blocks intracellular protein transport and is used in animals to prevent coccidiosis, promote growth and prevent bloat. Derivatives of monensin, monensin methyl ester and particularly monensin decyl ester, are used in ion selective electrodes.
UsesMonensin (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,).
UsesPoliether antibiotic. Coccidiostat
DefinitionChEBI: Monensin A is a spiroketal, monensin A is the major component of monensin, a mixture of antibiotic substances produced by Streptomyces cinnamonensis. An antiprotozoal, it is used as the sodium salt as a feed additive for the prevention of coccidiosis in poultry and as a growth promoter in cattle. It has a role as a coccidiostat, an antifungal agent and an ionophore. It is a monocarboxylic acid, a cyclic hemiketal, a spiroketal and a polyether antibiotic.
Brand nameCoban [as sodium salt] (Lilly);Rumensin [as sodium salt] (Lilly).
Safety ProfilePoison by ingestion and intraperitoneal routes. An eye and skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Monensin Preparation Products And Raw materials
Raw materialsMonensin sodium salt
Methylparaben Ivermectin Nystatin Methyl Abamectin Bensulfuron methyl Monensin 26-[N-(2-phenylethyl)carbamate] Parathion-methyl MONENSIN, [3H(G)] Kresoxim-methyl Thiophanate-methyl MONENSIN DECYL ESTER MONENSIN SODIUM SALT HYDRATE,monensin,monosodiumsal Methyl salicylate Methyl bromide CHLOROPHOSPHONAZO III METSULFURON METHYL Monensin

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