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    4-Isopropylbenzaldehyde
    4-Isopropylbenzaldehyde
    Information
    CAS No. 122-03-2 Price $30 / 20mg
    Catalog No.CFN70043Purity>=98%
    Molecular Weight148.2Type of CompoundPhenols
    FormulaC10H12OPhysical DescriptionPowder
    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
    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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    4-Isopropylbenzaldehyde

    4-Isopropylbenzaldehyde
    Product Name 4-Isopropylbenzaldehyde
    CAS No.: 122-03-2
    Catalog No.: CFN70043
    Molecular Formula: C10H12O
    Molecular Weight: 148.2 g/mol
    Purity: >=98%
    Type of Compound: Phenols
    Physical Desc.: Powder
    Targets: AChE | BChE
    Source:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $30 / 20mg
    Download: COA    MSDS
    Similar structural: Comparison
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  • Eur J Pharmacol.2018, 832:96-103
  • Nutr Res Pract.2020, 14(3):203-217.
  • Applied Biological Chemistry2022, 65(12)
  • Toxins (Basel).2020, 12(4):210.
  • JEJU National University2022, 10478.
  • Hum Exp Toxicol.2017, 36(11):1169-1176
  • Tropical J. of Pha. Research2017, 16(3):543-552
  • Nutrients.2022, 14(23):4997.
  • Molecules2022, 27(9):2827.
  • Med Sci Monit.2019, 25:9499-9508
  • 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
  • BChE Inhibitor Library
  • Biological Activity
    Description: 4-Isopropylbenzaldehyde shows acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities. 4-Isopropylbenzaldehyde suppressed melanin formation in cultured murine B16-F10 melanoma cells in a dose-dependent decrease up to 0.25 mm without affecting cell growth.
    Targets: AChE | BChE
    In vitro:
    Phytotherapy Research Ptr, 2010, 22(6):809-813.
    Effects of cuminaldehyde on melanoma cells.[Pubmed: 18412105]

    METHODS AND RESULTS:
    Cuminaldehyde (4-Isopropylbenzaldehyde) suppressed melanin formation in cultured murine B16-F10 melanoma cells in a dose-dependent decrease up to 0.25 mm without affecting cell growth. Approximately 30% suppression in melanin production resulted when the cells were cultured with 0.25 mm of cuminaldehyde. This activity was not noticeable with cultured human A375 melanoma cells.
    4-Isopropylbenzaldehyde 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 6.7476 mL 33.7382 mL 67.4764 mL 134.9528 mL 168.691 mL
    5 mM 1.3495 mL 6.7476 mL 13.4953 mL 26.9906 mL 33.7382 mL
    10 mM 0.6748 mL 3.3738 mL 6.7476 mL 13.4953 mL 16.8691 mL
    50 mM 0.135 mL 0.6748 mL 1.3495 mL 2.6991 mL 3.3738 mL
    100 mM 0.0675 mL 0.3374 mL 0.6748 mL 1.3495 mL 1.6869 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:
    Ztschrift Fur Naturforschung C Journal of Bioences, 2008, 63(7-8):547-553.
    Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.[Reference: WebLink]

    METHODS AND RESULTS:
    We have tested acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities of nineteen essential oils obtained from cultivated plants, namely one from Anethum graveolens L. (organic fertilizer), two from Foeniculum vulgare Mill. collected at fully-mature and flowering stages (organic fertilizer), two from Melissa officinalis L. (cultivated using organic and chemical fertilizers), two from Mentha piperita L. and M. spicata L. (organic fertilizer), two from Lavandula officinalis Chaix ex Villars (cultivated using organic and chemical fertilizers), two from Ocimum basilicum L. (green and purple-leaf varieties cultivated using only organic fertilizer), four from Origanum onites L., O. vulgare L., O. munitiflorum Hausskn., and O. majorana L. (cultivated using organic fertilizer), two from Salvia sclarea L. (organic and chemical fertilizers), one from S. officinalis L. (organic fertilizer), and one from Satureja cuneifolia Ten. (organic fertilizer) by a spectrophotometric method of Ellman using ELISA microplate-reader at 1 mg/ml concentration. In addition, a number of single components widely encountered in most of the essential oils [gamma-terpinene, 4-allyl anisole, (-)-carvone, dihydrocarvone, (-)-phencone, cuminyl alcohol, cumol, 4-Isopropylbenzaldehyde, trans-anethole, camphene, iso-borneol, (-)-borneol, L-bornyl acetate, 2-decanol, 2-heptanol, methyl-heptanol, farnesol, nerol, iso-pulegol, 1,8-cineole, citral, citronellal, citronellol, geraniol, linalool, alpha-pinene, beta-pinene, piperitone, iso-menthone, menthofurane, linalyl oxide, linalyl ester, geranyl ester, carvacrol, thymol, menthol, vanilline, and eugenol] was also screened for the same activity in the same manner.
    CONCLUSIONS:
    Almost all of the essential oils showed a very high inhibitory activity (over 80%) against both enzymes, whereas the single components were not as active as the essential oils.
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