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Albiflorin

Albiflorin Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
Email: sales@BioChemBest.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Tel: 13355009207 13355009207
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Company Name: Sichuan Kulinan Technology Co., Ltd  
Tel: 400-1166-196 18981987031
Email: cdhxsj@163.com
Company Name: Shenzhen Sungening Bio-Tech Co., Ltd  
Tel: +86-0755-89668383
Email: sales@sungening.com

Albiflorin manufacturers

  • Albiflorin
  • Albiflorin pictures
  • 2026-09-18
  • CAS:39011-90-0
  • Min. Order: 1g
  • Purity: 98%min
  • Supply Ability: 100G
  • Albiflorin
  • Albiflorin pictures
  • 2026-06-30
  • CAS:39011-90-0
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1000kgs
Albiflorin Basic information
Product Name:Albiflorin
Synonyms:(1R,3R,4R,6S,9S)-9-[(Benzoyloxy)Methyl]-1-(beta-D-glucopyranosyloxy)-4-hydroxy-6-Methyl-7-oxatricyclo[4.3.0.03,9]nonan-8-one;Albiflorin, froM Paeonia lactiflora;ALBIFLORIN;Albiflorin 9-((Benzoyloxy)methyl)-1-(beta-D-glucopyranosyloxy)-4-hydroxy-6-methyl-7-oxatricyclononan-8-one;Albiflorin std;9-((Benzoyloxy)methyl)-1-(beta-D-glucopyranosyloxy)-4-hydroxy-6-methyl-7-oxatricyclononan-8-one;[(benzoyloxy)methyl]-1-(β-D-glucopyranosyloxy)-;4-hydroxy-6-methyl-, (1R, 3R, 4R, 6S)-
CAS:39011-90-0
MF:C23H28O11
MW:480.46
EINECS:
Product Categories:The group of Paeoniflorin;Miscellaneous Natural Products;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract
Mol File:39011-90-0.mol
Albiflorin Structure
Albiflorin Chemical Properties
Melting point 122 °C
Boiling point 722.1±60.0 °C(Predicted)
density 1.58±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 10 mg/ml
pka12.84±0.70(Predicted)
form powder
color White
Major Applicationmetabolomics
vitamins, nutraceuticals, and natural products
InChIKeyJCLNQDVXOFIJKI-ICECTASOSA-N
SMILESC[C@]12C[C@H]3[C@H](O)C[C@@]1(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@]3(COC(=O)c5ccccc5)C(=O)O2
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29389090
Storage Class11 - Combustible Solids
MSDS Information
Albiflorin Usage And Synthesis
Chemical PropertiesDerived from the root of Paeonia albiflora Pall, a plant of the Ranunculaceae family
Usesmetabolomics
vitamins, nutraceuticals, and natural products
DefinitionChEBI: Albiflorin is a monoterpene glycoside with formula C23H28O11, originally isolated from the roots of Paeonia lactiflora. It has a role as a plant metabolite and a neuroprotective agent. It is a benzoate ester, a gamma-lactone, a beta-D-glucoside, a monoterpene glycoside, a secondary alcohol and a bridged compound.
Biological FunctionsAlbiflorin is a natural product isolated from Paeoniae Radix. It enhances mitochondrial function to suppress antimycin A-induced oxidative damage via the preservation of cytochrome c and cardiolipin. Also it may reduce or prevent osteoblast degeneration in osteoporosis.
Biological ActivityAlbiflorin is a natural phenolic compound that has been shown to be an inhibitor of toll-like receptor (TLR) 4.
in vitroAlbiflorin can modulate the TLR-induced inflammatory response by inhibiting the production of proinflammatory cytokines, such as IL-6, IL-8, and TNF-α. This compound also inhibits matrix metalloproteinase activity in tubulointerstitial injury, leading to decreased interstitial inflammation and proteinuria. Albiflorin has been shown to be effective at low doses in experimental models of rheumatoid arthritis. It is believed that this effect may be due to its ability to inhibit TLR4 expression or activation.
Albiflorin Preparation Products And Raw materials
Tag:Albiflorin(39011-90-0) Related Product Information
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