Monensin methyl ester structure
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Common Name | Monensin methyl ester | ||
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CAS Number | 28636-21-7 | Molecular Weight | 684.89700 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C37H64O11 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS06 |
Signal Word | Danger |
Use of Monensin methyl esterMonensin methyl ester, a neutral analog of monensin, is an ion active component for Na+ selective disk electrodes[1]. |
Name | monensin methyl ester |
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Description | Monensin methyl ester, a neutral analog of monensin, is an ion active component for Na+ selective disk electrodes[1]. |
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Related Catalog | |
References |
Molecular Formula | C37H64O11 |
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Molecular Weight | 684.89700 |
Exact Mass | 684.44500 |
PSA | 142.37000 |
LogP | 4.36130 |
Vapour Pressure | 4.17E-26mmHg at 25°C |
Storage condition | 2-8°C |
Symbol |
GHS06 |
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Signal Word | Danger |
Hazard Statements | H301-H310 |
Precautionary Statements | P280-P301 + P310-P302 + P350-P310 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T |
Risk Phrases | 24/25 |
Safety Phrases | 36/37-45 |
RIDADR | UN 2811 6.1 / PGIII |
Monensin A methyl ester complexes with Li+, Na+, and K+ cations studied by ESI-MS, 1H- and 13C-NMR, FTIR, as well as PM5 semiempirical method.
J. Mol. Struct. 788 , 176-183, (2006) Monensin A methyl ester (MON1) was synthesized by a new method and its ability to form complexes with Li+, Na+, and K+ cations was studied by electrospray ionization-mass spectroscopy (ESI-MS), 1H and... |
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[Monensin, an electrically charged carboxyl ionophor, and its neutral methylester as ion active components for Na+ selective disk electrodes].
Biomed. Tech. (Berl.) 32(1-2) , 22-4, (1987)
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Spectroscopic and semiempirical studies of a proton channel formed by the methyl ester of monensin A.
J. Phys. Chem. B 110(31) , 15615-23, (2006) Monensin A is an ionophore able to carry protons and cations through the cell membrane. Its methyl ester (MON1) and its hydrates have been studied in acetonitrile, and its deuterated analogue by Fouri... |