Abstract
The crystalline xylitol prepared by Wolfrom and Kohn [3] in 1942 was a hygroscopic and metastable product with a melting point of 61–61.5 °C. The product was formed during prolonged standing of xylitol syrup in an ice box. From this form of xylitol Carson et al. [4] separated approximately 1 year later a stable anhydrous xylitol which was more suitable for chemical and biological studies than the earlier product. The product of Carson et al. [4] was finally recrystallized from ether (methanol and ethanol were also suitable) as colorless crystals with a melting point of 93–94.5 °C. The low-melting monoclinic form usually changes in a few days into the high-melting rhombic form on exposure to the air at room temperature. The crystallization of the low-melting metastable form is easily achieved from alcoholic solution when lath-shaped crystals with oblique ends result. An aqueous viscous syrup also yields complete large crystals on standing several weeks at room temperature.
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© 1978 Springer Basel AG
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Mäkinen, K.K. (1978). Xylitol as a chemical compound. In: Biochemical Principles of the Use of Xylitol in Medicine and Nutrition with Special Consideration of Dental Aspects. Experientia Supplementum, vol 30. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-5757-4_2
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DOI: https://doi.org/10.1007/978-3-0348-5757-4_2
Publisher Name: Birkhäuser, Basel
Print ISBN: 978-3-0348-5758-1
Online ISBN: 978-3-0348-5757-4
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