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    Natural Products
    1-(4-Hydroxyphenyl)propan-1-one
    Information
    CAS No. 70-70-2 Price $30 / 20mg
    Catalog No.CFN97700Purity>=98%
    Molecular Weight150.17Type of CompoundPhenylpropanoids
    FormulaC9H10O2Physical DescriptionPowder
    Download     COA    MSDS    SDFSimilar structuralComparison (Web)  (SDF)
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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
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    1-(4-Hydroxyphenyl)propan-1-one

    1-(4-Hydroxyphenyl)propan-1-one
    Product Name 1-(4-Hydroxyphenyl)propan-1-one
    CAS No.: 70-70-2
    Catalog No.: CFN97700
    Molecular Formula: C9H10O2
    Molecular Weight: 150.17 g/mol
    Purity: >=98%
    Type of Compound: Phenylpropanoids
    Physical Desc.: Powder
    Targets: Estrogen receptor
    Source: The herbs of Cedrus deodara
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $30 / 20mg
    Inquire / Order: manager@chemfaces.com
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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
  • Phenylpropanoids Compound Library
  • Estrogen receptor Inhibitor Library
  • Biological Activity
    Description: Paroxypropione(1-(4-Hydroxyphenyl)propan-1-one) is a manufactured, nonsteroidal estrogen which has been used medically as an antigonadotropin.
    Targets: Estrogen receptor
    1-(4-Hydroxyphenyl)propan-1-one Description
    Source: The herbs of Cedrus deodara
    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 6.6591 mL 33.2956 mL 66.5912 mL 133.1824 mL 166.478 mL
    5 mM 1.3318 mL 6.6591 mL 13.3182 mL 26.6365 mL 33.2956 mL
    10 mM 0.6659 mL 3.3296 mL 6.6591 mL 13.3182 mL 16.6478 mL
    50 mM 0.1332 mL 0.6659 mL 1.3318 mL 2.6636 mL 3.3296 mL
    100 mM 0.0666 mL 0.333 mL 0.6659 mL 1.3318 mL 1.6648 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:
    Modern Chinese Medicine, 2008,10(11):13-5.
    Studies on the Chemical Constituents of Alpinia Calanga Willd.[Reference: WebLink]
    To study the chemical constituents of Alpinia galanga Willd.
    METHODS AND RESULTS:
    The chem- ical constituents were isolated by various column chromatographic methods,and the structures were elucidated on the basis of UV,IR,MS,~1H-NMR,~(13)C-NMR spectral analysis. Eleven compounds were isolated and their structures were elucidated as 4-[(E)-3-hydroxyprop-1-enyl]phenyl acetate(1),trans-p-hydroxylcinnamaldehyde acetate(2),5-hydroxy-7-(4″-hydroxy-3″-methoxyphenyl)-1-phenyl-3-heptanone(3),7-(4″-hydroxy-3″-me- thoxyphenyl)-1-phenylhep-4-en-3-one(4),[1′S]-1′-acetoxyeugenol acetate(5),trans-p-hydroxylcinnamalde- hyde(6),p-hydroxybenzaldehyde(7),1-(4-Hydroxyphenyl)propan-1-one(8),galangin(9),trans-p-coumaryl diacetate(10),β-sitosterol(11).
    CONCLUSIONS:
    Compound 1 was obtained from nature for the first time,com- pound 2 was obtained from this genus for the first time,and compounds 3 and 4 were obtained from this plant for the first time.
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