Other grades of this product :
| ETHYL MANDELATE Basic information |
| Product Name: | ETHYL MANDELATE | | Synonyms: | DL-ETHYL MANDELATE;DL-MANDELIC ACID ETHYL ESTER;ETHYL DL-MANDELATE;ETHYL ALPHA-HYDROXYPHENYLACETATE;ETHYL PHENYLGLYCOLATE;ETHYL MANDELATE;DL-MANDELIC ACID ETHYL ESTER 93+%;ethyl à-hydroxyphenylacetate | | CAS: | 4358-88-7 | | MF: | C10H12O3 | | MW: | 180.2 | | EINECS: | 610-127-9 | | Product Categories: | | Mol File: | 4358-88-7.mol |
| ETHYL MANDELATE Chemical Properties |
| Melting point | 35.5°C | | alpha | [α]D20 -0.1～+0.2° (neat) | | Boiling point | 253-255 °C(lit.) | | density | 1.115 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.512(lit.) | | Fp | >230 °F | | storage temp. | Refrigerator | | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) | | form | Oil | | color | Colourless | | CAS DataBase Reference | 4358-88-7(CAS DataBase Reference) |
| Safety Statements | 24/25 | | WGK Germany | 2 | | RTECS | OO7397000 | | HS Code | 29172090 |
| ETHYL MANDELATE Usage And Synthesis |
| Chemical Properties | Appearance :white solid or liquid | | Uses | Ethyl Mandelate is used as a reagent in the synthesis of several organic compounds including that of volatile methylsiloxanes which have the potential to be a more environmentally sustainable alternative as solvents in chemical synthesis to non-polar organic solvents. It was found to act as a substrate for (S)-mandelate dehydrogenase which is a flavin mononucleotide dependent enzyme that oxidises (S)-mandelate to benzoylformate. | | Synthesis Reference(s) | Journal of the American Chemical Society, 107, p. 3981, 1985 DOI: 10.1021/ja00299a038The Journal of Organic Chemistry, 49, p. 3241, 1984 DOI: 10.1021/jo00191a048 |
| ETHYL MANDELATE Preparation Products And Raw materials |
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