17297-56-2

Basic information

• Product Name: Biorobin
• Synonyms: Biorobin;3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Kaempferol 3-O-robinoside
• CAS NO: 17297-56-2
• Molecular Formula: C₂₇H₃₀O₁₅
• Molecular Weight: 594.5181
• Mol File: 17297-56-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 221-223℃
• Boiling Point: 941.7±65.0 °C(Predicted)
• Appearance: /
• Density: 1.76
• PKA: 6.20±0.40(Predicted)
• CAS DataBase Reference: Biorobin(CAS DataBase Reference)
• NIST Chemistry Reference: Biorobin(17297-56-2)
• EPA Substance Registry System: Biorobin(17297-56-2)

Safety Data

• Hazardous Substances Data: 17297-56-2(Hazardous Substances Data)

Usage

General Description

Biorobin is a bioremediation agent primarily used for cleaning up oil spills and contamination. It is a complex mixture of bacterial strains, enzymes, and nutrients, specifically designed to accelerate the natural process of hydrocarbon degradation in polluted environments. The key bacteria in Biorobin are microorganisms belonging to the Pseudomonas and Bacillus families, which have the ability to degrade a wide variety of hydrocarbons efficiently. These harmless but effective bacteria contribute to the process of bioremediation by consuming the hydrocarbons present in oil, ultimately breaking them down into harmless substances like water and carbon dioxide.

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 
• 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 
• 131559-51-8 kaempferol 3-O-(2^G-xylosylrutinoside)-7-O-glucoside 
• 57526-56-4 kaempherol 3-O-[α-L-rhamnopyranosyl-(1->6)]-β-D-glucopyranosyl-7-O-α-L-rhamnopyranoside 

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 
• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 
• 4205-23-6 D-gulose 
• 634-74-2 D-rhamnose 
• 1318780-82-3 C₃₀H₁₈O₁₃ 
• 61198-83-2 1,2,3,4-tetra-O-benzoyl-6-desoxy-α-L-mannopyranose 
• 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.

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.

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).