6130-58-1

Basic information

• Product Name: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside
• CAS NO: 6130-58-1
• Molecular Weight: 594.526
• Mol File: 6130-58-1.mol

Chemical Properties

• CAS DataBase Reference: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(6130-58-1)
• EPA Substance Registry System: kaempferol 3-O-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside(6130-58-1)

Safety Data

• Hazardous Substances Data: 6130-58-1(Hazardous Substances Data)

Upstream product

• 131573-90-5 kaempferol 3-O-(2^G-xylosylrutinoside) 
• 34336-18-0 7-O-β-D-glucopyranosyloxy-4',5-dihydroxy-3-[O-α-L-rhamnopyranosyl-(1->6)-3-O-β-D-glucopyranosyloxy]flavone 
• 57526-56-4 kaempherol 3-O-[α-L-rhamnopyranosyl-(1->6)]-β-D-glucopyranosyl-7-O-α-L-rhamnopyranoside 
• 131559-51-8 kaempferol 3-O-(2^G-xylosylrutinoside)-7-O-glucoside 
• 135095-52-2 3-O-[(2-O-β-D-galactopyranosyl-6-O-α-L-rhamnopyranosyl)-β-D-glucopyranosyl]-kaempferol 
• 131573-90-5 kaempferol 3-O-β-D-<2^G-O-β-D-xylopyranosyl-6^G-O-α-L-rhamnopyranosyl>glucopyranoside 
• 131559-50-7 kaempferol 3-O-(2^G-glucosylrutinoside)-7-O-glucoside 

Downstream Products

• 33978-17-5 pelargonidin 3-O-β-rutinoside 
• 2280-44-6 D-Glucose 
• 520-18-3 kaempferol 
• 73-34-7 D-rhamnose 
• 552-74-9 6-O-α-L-rhamnopyranosyl-β-D-glucopyranose 
• 61198-83-2 1,2,3,4-tetra-O-benzoyl-6-desoxy-α-L-mannopyranose 
• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 
• 1318780-82-3 C₃₀H₁₈O₁₃ 
• 4205-23-6 D-gulose 
• 634-74-2 D-rhamnose 
• 58947-55-0 biorobin nonaacetate 
• 26184-96-3 rutinose 

Relevant articles and documents

Kaempferol and its glycosides from Equisetum silvaticum L. from the khanty-mansi autonomous area

Three flavonoids were isolated from the aerial part of the wood horsetail (Equisetum silvaticum L.); two of them were found for the first time. The compounds were identified as kaempferol, kaempferol 3-O-β-D-galactopyranosyl-7-O-α-L-rhamnopyranoside and kaempferol 3-O-rutinosyl-7-O-L-rhamnopyranoside on the basis of the chemical transformations and IR, UV, 1H-NMR and mass spectra.

Method For Preparing Kaempferol-3-0-Rutinoside and Composition of Skin External Application Comprising Thereof

Disclosed is a method for the preparation of kaempferol-3-O-rutinoside and a composition of a skin external application comprising kaempferol-3-O-rutinoside as an active ingredient. The method for isolating kaempferol-3-O-rutinoside through hydrolysis uses an enzyme or microbe that removes the sugar selectively from kaempferol-3-O-rutinoside glycosides in a plant extract. Disclosed also is a composition of a skin external application comprising kaempferol-3-O-rutinoside that prevents skin wrinkle.

Two flavonol glycosides from seeds of Camellia sinensis.

Two novel flavonol triglycosides, camelliaside A and B, have been isolated from seeds of Camellia sinensis. The structures were determined to be kaempferol 3-O-[2-O-beta-D- galactopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside and kaempferol 3-O-[2-O-beta- D-xylopyranosyl-6-O-alpha-L-rhamnopyranosyl]-beta-D-glucopyranoside on the basis of spectroscopic, chemical and enzymatic studies. These types of interglycosidic linkages, Gal(1----2)[Rha(1----6)]Glc and Xyl(1----2)[Rha(1----6)]Glc, have not been reported previously in flavone and flavonol glycosides.

KAEMPFEROL GLYCOSIDES FROM HOSTA VENTRICOSA

Leaves of Hosta ventricosa yielded eight kaempferol glycosides, of which six: the 3-(2G-glucosylrutinoside)-7-glucoside, 3-sophoroside-7-glucoside, 3-rutinoside-7-glucoside, 3-(2G-glucosylrutinoside), 3-sophoroside, 3-rutinoside were fully characterized and two: 3-xylosylrutinoside-7-glucoside and 3-xylosylrutinoside were tentatively identified.Investigations included 1H-1H-COSY and 1H-1H 2D J NMR analysis.

Constituents of Cupuliferae, II. - A New Acylated Flavonoid Glycoside from Castanea sativa Mill.

From leaves of Castanea sativa Mill. in addition to tiliroside , 3>, a new acylated flavonoid glycoside has been isolated and identified as kaempferol 3-O-Glc-(p-coumaroyl)-α-L-rhamnopyranosyl-(1->6)-β-D-glucopyranoside> (1).

The final structure of robinin and biorobin and their total synthesis

Robinin has been proved by total synthesis and by methylation analysis using GC-MS to be kaempferol-3- O-(6-O-α-l-rhamnopyranosyl -β-d-galactopyranoside)-7-O-α-l-rhamnopyranoside and not, as claimed by Maksjutina et al., a mixture of 4 glycosides containing the 7-O-rhamnosyl moiety in the α- and β-furanoside as well as in the α- and β-pyranoside forms. The assumption that the 3-O-rhamnosido -galactose moiety contained furanoid rings was also disproved.