Description and references
Occurs free in poison sumac (Rhus toxicodendron L., Anacardiaceae), combined in the form of glycosides
of many plants. Preparation: Clark, J. Biol.
Chem. 38, 255 (1919). Structure and configuration:
Fischer, Morrell, Ber. 27, 384 (1894); Fischer, Zach, ibid. 45, 3762 (1912); Hirst, Macbeth, J. Chem. Soc. 1926, 23; Avery, Hirst, ibid. 1929, 2466. Isoln from
walls of gram-negative bacteria: Salton, Biochim. Biophys. Acta 45, 364 (1960); from Afraegle paniculata Engl., Rutaceae: Torto, J. Chem. Soc. 1961, 5234; from
rabbit skin: Malawista, Davidson, Nature 192, 871 (1961); from leaves of Solanum chacoense Bitter, Solanaceae: Kuhn, L"ow, Ber. 94, 1088 (1961).
Derivative
α-Form.
Properties
Always obtained by crystn from H2O
or EtOH. Monohydrate, holohedric rods from water, hemihedric
monoclinic columns from alcohol. Loses water of crystn on heating
and partially changes to the β-modification. Very sweet taste. mp 82-92°: Ghosh, Proc. R. Soc. Edinburgh 36, 216
(1915/16). Sublimes at 105° and 2 mm Hg. d420 1.4708. Shows
mutarotation. [α]D20 -7.7° → +8.9°:
Hudson, Yanovsky, J. Am. Chem. Soc. 39, 1032 (1917).Derivative
β-Form.
Properties
Prepd by heating α-rhamnose monohydrate on a steam
bath; crystallized from anhydr acetone + alcohol. Needles, mp 122-126° (rapid heating). [α]D20 +31.5° (1 min, p = 10). After a short time the rotation
adjusts to the same final value as α-rhamnose. The β-form is hygroscopic
and changes into crystals of the α-modification upon exposure to moist
air.