CHEMICAL AND PHYSICAL PROPERTIES
Color/Form | Yellow, amorphous solid |
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LogP | log Kow = 2.16 |
Stability/Shelf Life | STABLE IN AIR & LIGHT. /HCL/ |
Optical Rotation | Specific optical rotation = +214 deg at 25 °C/D (chloroform) |
Decomposition | When heated to decomposition it emits toxic fumes of /chlorine, oxides of sulfur, and oxides of nitrogen/. |
Ionization Efficiency | Positive |
Dissociation Constants | Characteristic taste; odorless or has faint mercaptan-like odor; freely soluble in water, dimethylformamide, methanol; soluble in alcohol; practically insoluble in acetone; pKa: 7.72 in pure water /Clindamycin hydrochloride/ |
Collision Cross Section | 209.07 Ų [M+Na]+ 202.49 Ų [M+H]+ 204.41 Ų [M-H]- |
Other Experimental Properties | Mol wt: 479.47. White crystals from ethanol-ethyl acetate, mp 141-143 °C. Specific optical rotation = +144 deg at 25 °C/D (water). pKa 7.6. Soluble in water, pyridine, ethanol, DMF /Clindamycin hydrochloride monohydrate/ |
COMPUTED DESCRIPTORS
Molecular Weight | 425.0 g/mol |
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XLogP3 | 2.2 |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 7 |
Exact Mass | 424.1798710 g/mol |
Monoisotopic Mass | 424.1798710 g/mol |
Topological Polar Surface Area | 128 Ų |
Heavy Atom Count | 27 |
Formal Charge | 0 |
Complexity | 502 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 9 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Clindamycin is an antibacterial prescription medicine approved by the U.S. Food and Drug Administration (FDA) for the treatment of certain serious bacterial infections, such as: