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Home > Biochemical Engineering > Biosynthetic Natural Products > Kaempferol for Sale > Most Professional Factory Supply High Qulity Kaempferol CAS 520-18-3
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Most Professional Factory Supply High Qulity Kaempferol CAS 520-18-3

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Unit Price: Get Latest Price
CAS No.:

520-18-3

Grade:

Pharmaceutical Grade

Content:

99%

Port:

Durban

Brand:

Custom

Packaging:

As per customer requirement

Price valid (until):

2024-05-21

Company Type:
Distributor
Location:
South Africa
Qualification:
Main Products:

Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

  • Product Description

  • Seller Information

  • Inquiry History

  • Description


      Product Detail  


                                                          1. Introduction to Kaempferol (520-18-3): Kaempferol (520-18-3) is a natural flavonoid compound found in various plant sources, including fruits, vegetables, and medicinal herbs. It is renowned for its diverse pharmacological properties and potential health benefits, contributing to its widespread use in traditional medicine and dietary supplements.

                                                          2. Chemical Structure of Kaempferol (520-18-3): Kaempferol (520-18-3) belongs to the flavonol subclass of flavonoids and is characterized by its distinctive molecular structure, comprising two aromatic rings (A and B) connected by a heterocyclic pyran ring (C) with a hydroxyl group at the 3-position. This unique arrangement confers its biological activity and therapeutic potential.

                                                          3. Natural Sources of Kaempferol: Kaempferol (520-18-3) is widely distributed in nature and can be found in a variety of plant-based foods such as apples, onions, broccoli, tea leaves, and Ginkgo biloba. Its presence in dietary sources underscores its importance as a bioactive compound in human nutrition.

                                                          4. Biological Activities of Kaempferol: Kaempferol (520-18-3) exhibits a broad spectrum of pharmacological activities, including antioxidant, anti-inflammatory, anticancer, cardioprotective, neuroprotective, and antimicrobial effects. These diverse bioactivities contribute to its potential therapeutic applications in various disease conditions.

                                                          5. Antioxidant Properties of Kaempferol: Kaempferol (520-18-3) possesses potent antioxidant properties, scavenging free radicals and reactive oxygen species to protect cells and tissues from oxidative damage. Its ability to modulate oxidative stress pathways contributes to its cytoprotective effects in health and disease.

                                                          6. Anti-Inflammatory Effects of Kaempferol: Kaempferol (520-18-3) exerts anti-inflammatory effects by inhibiting pro-inflammatory mediators and signaling pathways involved in the inflammatory response. Its modulation of inflammatory cytokines and enzymes contributes to its potential therapeutic utility in inflammatory diseases.

                                                          7. Anticancer Potential of Kaempferol: Kaempferol (520-18-3) demonstrates promising anticancer activity by exerting cytotoxic effects on cancer cells, inhibiting tumor growth, and inducing apoptosis (programmed cell death). Its ability to target multiple signaling pathways implicated in cancer progression makes it a subject of intense research in oncology.

                                                          8. Cardioprotective Effects of Kaempferol: Kaempferol (520-18-3) has been shown to exert cardioprotective effects by improving cardiovascular function, reducing oxidative stress, and modulating lipid metabolism. Its vasodilatory and antiplatelet properties contribute to its potential therapeutic value in cardiovascular diseases.

                                                          9. Neuroprotective Properties of Kaempferol: Kaempferol (520-18-3) exhibits neuroprotective effects by attenuating neuroinflammation, oxidative stress, and neuronal apoptosis. Its ability to enhance neurotrophic factors and promote synaptic plasticity may have implications for neurodegenerative disorders such as Alzheimer's disease.

                                                          10. Metabolic Effects of Kaempferol: Kaempferol (520-18-3) has been investigated for its potential metabolic benefits, including anti-obesity and anti-diabetic effects. Its modulation of metabolic pathways involved in glucose and lipid homeostasis holds promise for managing metabolic disorders.

                                                          11. Skin Health and Dermatological Applications: Kaempferol (520-18-3) exhibits beneficial effects on skin health, including antioxidant, anti-inflammatory, and photoprotective properties. Its incorporation into topical formulations may help protect against UV-induced skin damage and mitigate signs of aging.

                                                          12. Bioavailability and Pharmacokinetics: The bioavailability of kaempferol (520-18-3) is influenced by factors such as its absorption, metabolism, and excretion. Strategies to improve its bioavailability, such as formulation optimization and co-administration with enhancers, are being explored to maximize its therapeutic efficacy.

                                                          13. Safety and Toxicity Profile: Kaempferol (520-18-3) is generally regarded as safe when consumed in dietary amounts, with low toxicity reported in preclinical studies. However, high doses may elicit adverse effects, and individuals with certain medical conditions or taking medications should exercise caution.

                                                          14. Regulatory Status and Dietary Supplements: Kaempferol (520-18-3) is commonly included in dietary supplements and herbal products marketed for its potential health benefits. Regulatory agencies oversee the safety and labeling of these products to ensure consumer protection and adherence to quality standards.

                                                          15. Future Directions in Kaempferol Research: Future research on kaempferol (520-18-3) aims to further elucidate its molecular mechanisms of action, explore novel therapeutic applications, and evaluate its efficacy in clinical settings. Collaborative efforts across disciplines will drive innovation and advance our understanding of its health-promoting effects.

    Items Specifications
    Chemical Structure Kaempferol is a flavonoid compound, characterized by a flavonol structure with a phenyl group and several hydroxyl groups.
    Molecular Formula C₁₅H₁₀O₆
    IUPAC Name 3,4',5,7-Tetrahydroxyflavone
    Synonyms 3,5,7,4'-Tetrahydroxyflavone; 3,4',5,7-Tetrahydroxy-2-phenyl-4H-1-benzopyran-4-one
    Chemical Class Flavonol
    Solubility Sparingly soluble in water, soluble in organic solvents like ethanol and acetone.
    Source Found in various plant sources, including tea leaves, cruciferous vegetables, and some fruits.
    Biological Role Exhibits antioxidant, anti-inflammatory, and anticancer properties, among other pharmacological activities.
    Health Benefits Studied for potential benefits in cardiovascular health, cancer prevention, and neuroprotection.
    Metabolism Metabolized in the liver and excreted mainly through urine and feces.
    Dietary Sources Commonly found in foods such as tea, broccoli, grapes, tomatoes, and apples.
    Pharmacological Use Investigated for its potential therapeutic effects in various diseases, including diabetes and neurodegenerative disorders.
    Bioavailability Limited by factors such as low water solubility and first-pass metabolism.
    Structural Isomers Exists as a single compound without structural isomers.
    Research Areas Active area of research in pharmacology, nutraceuticals, and drug discovery for its diverse biological activities.
    Industrial Uses Utilized in the food and beverage industry as a natural colorant and flavoring agent, and in cosmetics for its antioxidant properties.


      Product Detail  


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    Basic Info
    Product Name:

    Kaempferol

    Other Name:

    4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-(4-hydroxyphenyl)-;Flavone,3,4′,5,7-tetrahydroxy-;3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;C.I. 75640;Indigo Yellow;Kaempferol;Kempferol;Rhamnolutin;Robigenin;Swartziol;3,5,7,4′-Tetrahydroxyflavone;Trifolitin;5,7,4′-Trihydroxyflavonol;Kaempherol;Kaemferol;3,4′,5,7-Tetrahydroxyflavone;Nimbecetin;Populnetin;Rhamnolutein;Pelargidenolon;Kampcetin;Pelargidenon;NSC 407289;NSC 656277;3′-Deoxyquercetin;CSU-2056;CSU 2056;3,5,7-Trihydroxy-2-(4-hydroxyphenyl)chromen-4-one;ST 030560;14461-95-1

    CAS No.:

    520-18-3

    Molecular Formula:

    C15H10O6

    InChIKeys:

    InChIKey=IYRMWMYZSQPJKC-UHFFFAOYSA-N

    Molecular Weight:

    286.23600

    Exact Mass:

    286.24

    EC Number:

    208-287-6

    UNII:

    731P2LE49E

    NSC Number:

    656277|407289

    DSSTox ID:

    DTXSID7020768

    Color/Form:

    Yellow needles from alcohol and water

    HScode:

    2914501900

    Characteristics
    PSA:

    111.13000

    XLogP3:

    2.28240

    Appearance:

    Solid

    Density:

    1.688 g/cm3

    Melting Point:

    277 °C

    Boiling Point:

    582.1ºC at 760 mmHg

    Flash Point:

    226.1ºC

    Refractive Index:

    1.767

    Water Solubility:

    ethanol: 20 mg/mL;In water, 440 mg/L at 25 deg C (est)

    Storage Conditions:

    -20ºC

    Vapor Pressure:

    1.1X10-13mm Hg at 25 deg C (est)

    Henrys Law Constant:

    Henry's Law constant = 6.3X10-17 atm cu m/mole at 25 °C (est)

    Collision Cross Section:

    162.9 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|160.32 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|165.99 Ų [M+H]+ [CCS Type: DT, Method: stepped-field]|187.2 Ų [M+Na]+ [CCS Type: DT, Method: stepped-field]|165.92 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|159.2 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]|165.4 Ų [M-H]-

    Experimental Properties:

    Hydroxyl radical reaction rate constant = 2.4X10-10 cu cm/molecule-sec at 25 °C (est)

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 3, Oral

    Germ cell mutagenicity, Category 2

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Danger

    Hazard statement(s)

    H301 Toxic if swallowed

    H341 Suspected of causing genetic defects

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P270 Do not eat, drink or smoke when using this product.

    P203 Obtain, read and follow all safety instructions before use.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    Response

    P301+P316 IF SWALLOWED: Get emergency medical help immediately.

    P321 Specific treatment (see ... on this label).

    P330 Rinse mouth.

    P318 IF exposed or concerned, get medical advice.

    Storage

    P405 Store locked up.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Distributor

    Main Products:

    Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

    Location:

    13 PROTEA PARK MILKWOOD STREET RANGEVIEW GAUTENG 1739

    Payment Terms:

    TT against copy of documents,TT against B/L draft before shipment

    Average lead Time:

    60

    Total Annual Revenue:

    $1 million-$2.5 million

    Total Employees:

    11-50

    Year of Establishment:

    2012

  • Inquiry History
    3 Inquiries
    Country Product Purchase Quantity Date Posted
    China

    Kaempferol

    25 KG Mar 13, 2026
    India

    Kaempferol

    1 KG Dec 11, 2024
    Nigeria

    kaempferol

    6 KG Jan 24, 2024
    Post an enquiry for this product
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