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| (S)-(+)-2-Methylbutyric acid Basic information |
| (S)-(+)-2-Methylbutyric acid Chemical Properties |
| Melting point | -55°C | | Boiling point | 78 °C/15 mmHg (lit.) | | alpha | 19 º (c=neat) | | density | 0.938 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.406(lit.) | | FEMA | 2695 | 2-METHYLBUTYRIC ACID | | Fp | 165 °F | | storage temp. | 2-8°C | | pka | 4.80±0.10(Predicted) | | form | Liquid | | color | Clear colorless | | optical activity | [α]20/D +19°, neat | | BRN | 1720485 | | InChIKey | WLAMNBDJUVNPJU-BYPYZUCNSA-N | | CAS DataBase Reference | 1730-91-2(CAS DataBase Reference) |
| (S)-(+)-2-Methylbutyric acid Usage And Synthesis |
| Chemical Properties | clear colorless liquid | | Uses | (S)-(+)-2-Methylbutyric Acid is a chiral starting reagent used in various synthetic preparations. | | Uses | (S)-(+)-2-Methylbutyric acid may be used in the preparation of the stereoisomers of (R)-lavandulyl (S)-2-methylbutanoate and (R)-maconelliyl (S)-2-methylbutanoate, which are female sex pheromones found in pink hibiscus mealybug. | | Definition | ChEBI: The (S)-enantiomer of 2-methylbutanoic acid. | | Purification Methods | Purify the acid by distilling it in vacuo [Sax & Bergmann J Am Chem Soc 77 1910 1955, Doering & Aschner J Am Chem Soc 75 393 1953 ]. The methyl ester is formed by addition of diazomethane and has b 112-115o/760mm, [] D +21.1o (c 1.7, MeOH). [Beilstein 2 IV 888.] |
| (S)-(+)-2-Methylbutyric acid Preparation Products And Raw materials |
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