724771-79-3

Upstream product

• 724771-76-0 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(8-acetoxy-octyloxy)-tetrahydro-pyran-4-yl ester 
• 724771-77-1 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(8-iodo-octyloxy)-tetrahydro-pyran-4-yl ester 
• 29836-26-8 n-octyl β-D-glucopyranoside 
• 188778-83-8 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(8-hydroxy-octyloxy)-tetrahydro-pyran-4-yl ester 
• 111-87-5 octanol 
• 38954-67-5 octyl (2,3,4,6-tetra-O-acetyl)-β-D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 108-24-7 acetic anhydride 
• 724771-78-2 (2R,3R,4S,5S,6R)-2-Octyloxy-6-trityloxymethyl-tetrahydro-pyran-3,4,5-triol 

Downstream Products

• 38954-67-5 octyl (2,3,4,6-tetra-O-acetyl)-β-D-glucopyranoside 
• 168288-10-6 octyl α-L-arabinopyranosyl(1-6)-β-D-glucopyranoside hexaacetate 

Relevant academic research and scientific papers

Synthesis of sugar-based chelating surfactants for metal removal from wastewater

Four chelating surfactants were synthesized in a few steps from octyl d-glucosides. Their main interfacial properties were determined, and their flotation properties were evaluated on a laboratory scale using Fe(III) as a model contaminant metal. The performance on metal extraction was mainly dependent on the complexing functional group, but the surfactant efficiency was also important.

Chemoenzymatic synthesis of rhodiooctanoside isolated from Chinese medicines, rhodiolae radix

Direct β-glucosidation between 1,8-octanediol 5 and D-glucose 6 using the immobilized β-glucosidase (EC 3.2.1.21) from almonds with the synthetic prepolymer ENTP-4000 gave mono-β-glucoside 3 in 58% yield, which was converted into n-octyl β-D-glucopyranoside 2 by means of a chemoenzymatic method. The coupling of n-octyl β-D-glucopyranoside congener 15 and 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl bromide 17, followed by deprotection afforded the synthetic rhodiooctanoside 1, which was identical with natural 1 with respect to the spectral data and specific rotation.