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    3-(Hydroxymethyl)cyclopentanol
    Information
    CAS No. 1007125-14-5 Price
    Catalog No.CFN99022Purity>=98%
    Molecular Weight116.2 Type of CompoundMiscellaneous
    FormulaC6H12O2Physical DescriptionOil
    Download Manual    COA    MSDS    SDFSimilar structuralComparison (Web)
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    3-(Hydroxymethyl)cyclopentanol Description
    Source: The fruits of Illicium verum
    Biological Activity or Inhibitors: Reference standards.
    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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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.
    doi:10.1016/j.phymed.2017.12.030

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 8.6059 mL 43.0293 mL 86.0585 mL 172.117 mL 215.1463 mL
    5 mM 1.7212 mL 8.6059 mL 17.2117 mL 34.4234 mL 43.0293 mL
    10 mM 0.8606 mL 4.3029 mL 8.6059 mL 17.2117 mL 21.5146 mL
    50 mM 0.1721 mL 0.8606 mL 1.7212 mL 3.4423 mL 4.3029 mL
    100 mM 0.0861 mL 0.4303 mL 0.8606 mL 1.7212 mL 2.1515 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.
    3-(Hydroxymethyl)cyclopentanol References Information
    Citation [1]

    Org Lett. 2008 Nov 6;10(21):4735-8.

    Synthesis of D- and L-carbocyclic nucleosides via rhodium-catalyzed asymmetric hydroacylation as the key step.[Pubmed: 18816138]
    D- and L-carbocyclic nucleosides were obtained by a new procedure involving an enantioselective rhodium/duphos-catalyzed hydroacylation reaction as the key step. The 3-(Hydroxymethyl)cyclopentanol intermediate was obtained by stereoselective reduction of ketone and by dynamic kinetic resolution (DKR).