Jump to content

Laminaribiose

From Wikipedia, the free encyclopedia

This is the current revision of this page, as edited by LegionMammal978 (talk | contribs) at 14:27, 3 May 2023 (fix mistake, add semisystematic name). The present address (URL) is a permanent link to this version.

(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
Laminaribiose
Names
IUPAC name
3-β-D-Glucopyranosyl-(1→3)-D-glucose
Systematic IUPAC name
(2R,3S,4R,5R)-2,4,5,6-Tetrahydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanal
Other names
3-β-D-Glucosyl-D-glucose
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C12H22O11/c13-1-3-5(15)7(17)8(18)12(22-3)23-10-6(16)4(2-14)21-11(20)9(10)19/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8-,9-,10+,11?,12+/m1/s1 ☒N
    Key: QIGJYVCQYDKYDW-LCOYTZNXSA-N ☒N
  • O([C@H]1[C@H](O)[C@H](OC(O)[C@@H]1O)CO)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O
Properties
C12H22O11
Molar mass 342.30 g/mol
Density 1.768 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Laminaribiose C12H22O11 is a disaccharide which is used notably in the agricultural field and as an antiseptic. It is in general obtained by hydrolysis or by acetolysis of natural polysaccharides of plant origin.[1] It is also a product of the caramelization of glucose. [2]

References

[edit]
  1. ^ US 6632940 
  2. ^ Sugisawa, Hirqshi; Edo, Hiroshi (1966). "The Thermal Degradation of Sugars I. Thermal Polymerization of Glucose". Journal of Food Science. 31 (4): 561. doi:10.1111/j.1365-2621.1966.tb01905.x.