Barbaloin-related compound A

Barbaloin-related compound A
Product Name Barbaloin-related compound A
CAS No.: 473225-21-7
Catalog No.: CFN95453
Molecular Formula: C42H42O18
Molecular Weight: 834.8 g/mol
Purity: >=98%
Type of Compound: Anthraquinones
Physical Desc.: Powder
Source: The herbs of Aloe vera L.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $318/5mg
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Food Chem.2022, 378:131975.
  • Front Pharmacol.2019, 10:1355
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  • Curr Pharm Des.2024, 30(1):71-80.
  • J Microbiol Biotechnol.2022, 32(2):141-148.
  • EXCLI J.2023, 22:482-498.
  • Plant Cell Physiol.2023, 64(7):716-728.
  • Phytomedicine.2024, 129:155645.
  • Eur J Pharmacol.2020, 889:173589.
  • Journal of Applied Pharmaceutical Science2022, 0(00), pp:001-007
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    Shokuhin Eiseigaku Zasshi . 2002 Jun;43(3):115-121.
    [Structural analyses of barbaloin-related compounds in aloe drinks][Pubmed: 12238147]
    Four kinds of barbaloin (BA)-related compounds (A, B, C, D) in aloe drinks were isolated by using preparative HPLC. LC/MS analyses of these compounds showed the identical quasimolecular ion peak at m/z 833 [M-H]-. The chemical structures were mainly determined by NMR, including 1H-1H two-dimensional correlation spectroscopy (COSY), nuclear Overhauser and exchange spectroscopy (NOESY), heteronuclear multiple quantum coherence (HMQC), and heteronuclear multiple-bond connectivity (HMBC) experiments. They were identified as BA-related compounds A (10R, 10"S), B (10S, 10"S), C (10S, 10"R), and D (10R, 10"R) coupled through a C-10 to C-7' linkage, and newly found in nature. These results suggested that BA is converted to dimers during storage of aloe drinks.
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