THC Science

Robinose
Names
	IUPAC name 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-galactopyranose
	Other names Robinobiose
Identifiers
CAS Number	552-74-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	390161;
PubChem CID	441428;
	InChI InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6-,7+,8-,9+,10+,11+,12+/m0/s1 Key: OVVGHDNPYGTYIT-PEPLWKDOSA-N; InChI=1/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6-,7+,8-,9+,10+,11+,12+/m0/s1 Key: OVVGHDNPYGTYIT-PEPLWKDOBI;
	SMILES O(C[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)[C@@H]2O[C@H]([C@H](O)[C@@H](O)[C@H]2O)C;
Properties
Chemical formula	C12H22O10
Molar mass	326.298 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Robinose is a disaccharide composed of 6″-O-α-rhamnopyranosyl-β-galactopyranoside. The sugar can be found in Acalypha hispida.^[1]

Robinin is a kaempferol-3-O-robinoside-7-O-rhamnoside.

References[edit]

^ Reiersen, Bergitte; Kiremire, Bernard T; Byamukama, Robert; Andersen, Øyvind M (2003). "Anthocyanins acylated with gallic acid from chenille plant, Acalypha hispida". Phytochemistry. 64 (4): 867–71. doi:10.1016/S0031-9422(03)00494-1. PMID 14559283.