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    4-(Dimethylamino)cinnamaldehyde
    Information
    CAS No. 6203-18-5 Price $70 / 100mg
    Catalog No.CFN98120Purity>=98%
    Molecular Weight175.23Type of CompoundAlkaloids
    FormulaC11H13NOPhysical DescriptionYellow powder
    Download Manual    COA    MSDS    SDFSimilar structuralComparison (Web)
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    4-(Dimethylamino)cinnamaldehyde Description
    Source: The barks of Cinnamomum cassia Presl.
    Biological Activity or Inhibitors: 1. The 4-(dimethylamino)cinnamaldehyde (DMAC) assay is currently used to quantify proanthocyanidin (PAC) content in cranberry products.
    2. 4-Dimethylaminocinnamaldehyde is a photometric reagent for primary aromatic amines.
    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.
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 5.7068 mL 28.5339 mL 57.0679 mL 114.1357 mL 142.6696 mL
    5 mM 1.1414 mL 5.7068 mL 11.4136 mL 22.8271 mL 28.5339 mL
    10 mM 0.5707 mL 2.8534 mL 5.7068 mL 11.4136 mL 14.267 mL
    50 mM 0.1141 mL 0.5707 mL 1.1414 mL 2.2827 mL 2.8534 mL
    100 mM 0.0571 mL 0.2853 mL 0.5707 mL 1.1414 mL 1.4267 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.
    4-(Dimethylamino)cinnamaldehyde References Information
    Citation [1]

    J Agric Food Chem. 2012 May 9;60(18):4578-85.

    Comparison of isolated cranberry (Vaccinium macrocarpon Ait.) proanthocyanidins to catechin and procyanidins A2 and B2 for use as standards in the 4-(dimethylamino)cinnamaldehyde assay.[Pubmed: 22533362]
    The 4-(Dimethylamino)cinnamaldehyde (DMAC) assay is currently used to quantify proanthocyanidin (PAC) content in cranberry products. However, this method suffers from issues of accuracy and precision in the analysis and comparison of PAC levels across a broad range of cranberry products. Current use of procyanidin A2 as a standard leads to an underestimation of PACs content in certain cranberry products, especially those containing higher molecular weight PACs. To begin to address the issue of accuracy, a method for the production of a cranberry PAC standard, derived from an extraction of cranberry (c-PAC) press cake, was developed and evaluated. Use of the c-PAC standard to quantify PAC content in cranberry samples resulted in values that were 2.2 times higher than those determined by procyanidin A2. Increased accuracy is critical for estimating PAC content in relationship to research on authenticity, efficacy, and bioactivity, especially in designing clinical trials for determination of putative health benefits.
    Citation [2]

    J. Anal. Chem., 2004, 59(4):335-44.

    4-Dimethylaminocinnamaldehyde As a Photometric Reagent for Primary Aromatic Amines[Reference: WebLink]
    The interaction of primary aromatic amines (PAAs) with 4-(Dimethylamino)cinnamaldehyde (DMACA) is studied in various media by UV, IR, and 1 H NMR spectroscopy. The optimum conditions for these reactions have been found, and the reasons for better analytical effects in the condensation reaction of PAAs with this reagent have been revealed. The physicochemical properties of the analytical form are studied using the aniline–DMACA model system as an example. A correlation has been found between the pH opt of the reactions under study and the p K a values of arylamines.