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| L-(-)-ARABITOL Basic information |
| L-(-)-ARABITOL Chemical Properties |
Melting point | 101-104 °C(lit.) | Boiling point | 194.6°C (rough estimate) | density | 1.1497 (rough estimate) | refractive index | 1.3960 (estimate) | storage temp. | 2-8°C | solubility | H2O: 0.1 g/mL, clear, colorless | pKa | 13.24±0.20(Predicted) | form | Powder | color | White to off-white | Water Solubility | Soluble in water (50 mg/ml). | Sensitive | Hygroscopic | Merck | 14,762 | BRN | 1720521 | Stability: | Hygroscopic | LogP | -2.649 (est) | CAS DataBase Reference | 7643-75-6(CAS DataBase Reference) | EPA Substance Registry System | L-Arabinitol (7643-75-6) |
| L-(-)-ARABITOL Usage And Synthesis |
Chemical Properties | white amorphous powder | Uses | L-Arabitol, a rare sugar alcohol, is being studied as a food additive that reduces fat deposits in the intestines. L-Arabitol is used as an inducer of xylanase expression in Hypocrea jecorina (Trichoderma reesei). L-Arabitol is used to identify, differentiate and characterize L-arabitol dehydrogenase(s). | Definition | ChEBI: The L-enantiomer of arabinitol. | General Description | Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. L-Arabinitol is formed as a by-product of L-arabinose during the xylitol production in corn cob hydrolysates. | Purification Methods | This pentol, which occurs in the urine of pentosuric subjects, is purified by recrystallisation from 90% EtOH or MeOH. It has a higher rotation in the presence of molybdate: [] 20D -130o (c 0.16, acidified molybdate) [Richtmeyer & Hudson J Am Chem Soc 73 2249 1957]. [G.tzi & Reichstein Helv Chim Acta 21 197 1938, Beilstein 1 IV 2832.] |
| L-(-)-ARABITOL Preparation Products And Raw materials |
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