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Chemical Structure
Chemical Structure
Chemical Structure

Fulvic acid [479-66-3]

Research Use Only
AG-CN2-0135
AdipoGen Life Sciences
CAS Number479-66-3
Product group Chemicals
Estimated Purity>95%
Molecular Weight308.2
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Fulvic acid
  • Delivery Days Customer
    10
  • CAS Number
    479-66-3
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Warning
  • Molecular Formula
    C14H12O8
  • Molecular Weight
    308.2
  • Scientific Description
    Chemical. CAS: 479-66-3. Formula: C14H12O8. MW: 308.2. Isolated from Penicillium sp. strain FKP-0046. Free radical scavenger and antioxidant. Potential compound to neutralize radioactive and toxic wastes and heal soils. Chelates and binds scores of minerals into a bioavailable form used by cells. Shown to incorporate into bone and cartilage of rats. Antibacterial. Antifungal. beta-Hexosaminidase release inhibitor. Anti-inflammatory. Tau fibrils aggregation inhibitor (Alzheimers Disease). Antiseptic. Interrupts the dimer formation of Abeta(17-42) peptides. - Free radical scavenger and antioxidant [1]. Potential compound to neutralize radioactive and toxic wastes and heal soils. Chelates and binds scores of minerals into a bioavailable form used by cells [1]. Shown to incorporate into bone and cartilage of rats [2]. Antibacterial [3]. Antifungal [3]. beta-Hexosaminidase release inhibitor [4]. Anti-inflammatory [5]. Tau fibrils aggregation inhibitor (Alzheimers Disease) [6]. Antiseptic [7]. Interrupts the dimer formation of Abeta(17-42) peptides [8].
  • SMILES
    CC1(O)CC2=C(CO1)C(=O)C1=C(C(O)=O)C(O)=C(O)C=C1O2
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • Studies in the biochemistry of micro-organisms: Fulvic acid, a new crystalline yellow pigment, a metabolic product of P. griseo-fulvum Dierckx, P. flexuosum Dale and P. Brefeldianum Dodge: A.E. Oxford, et al.; Biochem. J. 29, 1102 (1935)
  • The evidence for the incorporation of fulvic acid into the bone and cartilage of rats: C. Wang, et al. Sci. Total Environ. 19, 197 (1996)
  • An in vitro investigation of the antimicrobial activity of oxifulvic acid: C.E. J. van Rensburg, et al.; J. Antimicrob. Chemother. 46, 853 (2000)
  • Properties of fulvic acid extracted from excess sludge and its inhibiting effect on beta-hexosaminidase release: H. Motojima, et al.; Biosci. Biotechnol. Biochem. 73, 2210 (2009)
  • Carbohydrate-derived fulvic acid (CHD-FA) inhibits carrageenan-induced inflammation and enhances wound healing: efficacy and toxicity study in rats: R. Sabi, et al.; Drug Dev. Res. 73, 18 (2011)
  • Fulvic acid inhibits aggregation and promotes disassembly of tau fibrils associated with Alzheimer's disease: A. Cornejo, et al.; J. Alzheim. Dis. 27, 143 (2011)
  • Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms: L. Sherry, et al.; Front. Microbiol. 3, 116 (2012)
  • The effect of fulvic acid on pre- and postaggregation state of Abeta(17-42): Molecular dynamics simulation studies: S. Verma, et al.; Biochim. Biophys. Acta 1834, 24 (2013)