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| (S)-(+)-O-Acetyl-L-mandelic acid Basic information |
| (S)-(+)-O-Acetyl-L-mandelic acid Chemical Properties |
| Melting point | 98-101 °C | | alpha | 153 º (c=2 in acetone) | | Boiling point | 317.8±30.0 °C(Predicted) | | density | 1.259±0.06 g/cm3(Predicted) | | refractive index | 153 ° (C=2, Acetone) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Acetone, Chloroform | | form | Solid | | pka | 2.76±0.10(Predicted) | | color | White | | optical activity | [α]28/D +153°, c = 2 in acetone | | BRN | 2694109 | | InChIKey | YCCSWLJUVZBEAS-VIFPVBQESA-N | | CAS DataBase Reference | 7322-88-5(CAS DataBase Reference) |
| Safety Statements | 22-24/25 | | WGK Germany | 3 | | HS Code | 29181990 |
| (S)-(+)-O-Acetyl-L-mandelic acid Usage And Synthesis |
| Chemical Properties | (S)-(+)-O-Acetyl-L-mandelic acid is white to light yellow crystal powde
| | Uses | (S)-(+)-O-Acetyl-L-mandelic acid is an antibacterial used particularly in the treatment of urinary tract infections.
| | Uses | The (R)- and (S)-isomers are chiral derivatizing agents for NMR determination of enantiomeric purity of α-deuterated carboxylic acids, alcohols, and amines. | | Purification Methods | Recrystallise it from *benzene/hexane or toluene, and it has characteristic NMR and IR spectra. [Pracejus Justus Liebig |
| (S)-(+)-O-Acetyl-L-mandelic acid Preparation Products And Raw materials |
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