17297-56-2

Usage

Uses

Used in Environmental Remediation:
Biorobin is used as a bioremediation agent for cleaning up oil spills and contamination. It accelerates the natural process of hydrocarbon degradation in polluted environments, making it an effective solution for environmental cleanup.
Used in Oil Spill Response:
Biorobin is used as a response tool for oil spills, where it helps in the rapid degradation of hydrocarbons, reducing the environmental impact of the spill and facilitating the recovery of affected areas.
Used in Industrial Waste Management:
Biorobin is used as a waste management solution in industries that generate hydrocarbon-contaminated waste. It aids in the breakdown of hydrocarbons, reducing the toxicity of the waste and making it easier to dispose of or recycle.
Used in Soil and Water Treatment:
Biorobin is used as a treatment agent for contaminated soil and water, where it helps in the biodegradation of hydrocarbons, improving the quality of the environment and making it safer for human and ecological health.

Upstream product

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

Downstream Products

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

Relevant academic research and scientific papers

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.