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| | L-LEUCIC ACID Basic information |
| | L-LEUCIC ACID Chemical Properties |
| Melting point | 78-80 °C(lit.) | | Boiling point | 277.83°C (rough estimate) | | density | 1.0160 (rough estimate) | | refractive index | -26 ° (C=2, 1 %NaOH) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Aqueous Base (Slightly), DMSO (Sparingly), Water (Slightly) | | form | Solid | | pka | 3.86±0.21(Predicted) | | color | White to Off-White | | optical activity | [α]22/D 26.3°, c = 1 in 1 M NaOH | | Water Solubility | almost transparency | | LogP | 0.710 | | CAS DataBase Reference | 13748-90-8(CAS DataBase Reference) | | EPA Substance Registry System | Pentanoic acid, 2-hydroxy-4-methyl-, (2S)- (13748-90-8) |
| Safety Statements | 24/25 | | WGK Germany | 3 | | HS Code | 29181990 |
| | L-LEUCIC ACID Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powde | | Uses | L-Leucic Acid is a reagent in the synthesis of cryptophycins based macrocyclic depsipeptides which are used as tubulin inhibitors. | | Definition | ChEBI: The (S)-enantiomer of 2-hydroxy-4-methylpentanoic acid. Derived from the metabolism of the branched-chain amino acids, it belongs to the 2-hydroxycarboxylic acid group of amino acid metabolites. |
| | L-LEUCIC ACID Preparation Products And Raw materials |
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