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    Natural Products
    Ethyl salicylate
    Ethyl salicylate
    Information
    CAS No. 118-61-6 Price $30 / 20mg
    Catalog No.CFN70034Purity>=98%
    Molecular Weight166.1Type of CompoundPhenols
    FormulaC9H10O3Physical DescriptionOil
    Download COA    MSDSSimilar structuralComparison
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $7.0 / In-stock
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    Ethyl salicylate

    Ethyl salicylate
    Product Name Ethyl salicylate
    CAS No.: 118-61-6
    Catalog No.: CFN70034
    Molecular Formula: C9H10O3
    Molecular Weight: 166.1 g/mol
    Purity: >=98%
    Type of Compound: Phenols
    Physical Desc.: Oil
    Source:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $30 / 20mg
    Download: COA    MSDS
    Similar structural: Comparison
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  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Phenols Compound Library
  • Biological Activity
    Description: Ethyl salicylate has anti-inflammatory and analgesic activities.
    Ethyl salicylate Description
    Source:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: 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

    After receiving: 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.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.0205 mL 30.1023 mL 60.2047 mL 120.4094 mL 150.5117 mL
    5 mM 1.2041 mL 6.0205 mL 12.0409 mL 24.0819 mL 30.1023 mL
    10 mM 0.602 mL 3.0102 mL 6.0205 mL 12.0409 mL 15.0512 mL
    50 mM 0.1204 mL 0.602 mL 1.2041 mL 2.4082 mL 3.0102 mL
    100 mM 0.0602 mL 0.301 mL 0.602 mL 1.2041 mL 1.5051 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Journal of Pharmaceutical and Biomedical Analysis, 2008,48(3):969-973.
    Encapsulation of methyl and ethyl salicylates by β-cyclodextrin: HPLC, UV–vis and molecular modeling studies.[Reference: WebLink]
    The complexation of mEthyl salicylate (MS) and Ethyl salicylate (ES), non-steroidal analgesic, anti-inflammatory and antirrheumatic drugs with β-cyclodextrin (βCD) has been studied from thermodynamic and structural points of view.
    METHODS AND RESULTS:
    The complexation with βCD has been investigated using reversed-phase liquid chromatography. Retention behavior has been analyzed on a reverse-phase column Luna 18(2) 5 μm. The mobile-phase was methanol:water in different ratios (55:45 to 70:30) in which βCD (1–9 mM) was incorporated as a mobile-phase additive. The decrease in retention times with increasing concentrations of βCD enables the determination of the apparent stability constant of the complexes. Values at 30 °C with 55% methanol were KMS:βCD: 15.84 M−1 and KES:βCD: 12.73 M−1 for MS and ES, respectively. The apparent stability constants decrease as the polarity of the solvent decreases. The low solubility of MS and ES in aqueous solution has been improved by complexation with βCD (1–9 mM). The stability constants of the complexes obtained from the phase-solubility diagrams using a UV–vis spectrophotometric method were ḰMS:βCD: 229 M−1 and ḰES:βCD: 166 M−1. In addition, semi-empirical quantum mechanics calculations using AM1 and PM3 methods in vacuum were performed. The energetically favorable inclusion structures were identified and the most favorable orientation for the inclusion process was found to be the head-down orientation for both complexes. Enthalpy for encapsulation processes was found to be favorable (ΔH° < 0), while entropy (ΔS° < 0) and Gibbs free energy were unfavorable (ΔG° > 0).
    CONCLUSIONS:
    By means of HPLC and UV–vis measurements and quantum mechanics calculations, it was found that MS and ES form a 1:1 inclusion complex with βCD. The theoretical results are in agreement with the experimental parameters associated with the encapsulation process.
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