Amino-EG6-undecanethiol, hydrochloride

Amino-EG6-undecanethiol, hydrochloride

Catalog Number:
CFA1108338DOJ
Mfr. No.:
A483-10
Price:
$790
  • Size:
    10 mg
    Quantity:
    Add to Cart:
      • Overview
        • Polyethyleneglycols (PEGs) are widely used for material modifications to improve hydrophilicity of the surface. PEG-coated materials are usually more stable under physiological conditions. Since Amino-EG6-undecanethiol has 6 ethylene glycol units, 11 carbon atoms, and an SH group at the end, it can be used to prepare a highly oriented and hydrophilic SAM on a gold surface. This is suitable for biomaterial labeling on the surface due to the improved hydrophilicity. The hydrophilic surface can prevent proteins or other biomaterials from non-specific binding. Therefore, the SAM prepared by this reagent will provide a better surface to develop biomaterial sensors or DNA/ protein microarrays. To prepare an Amino-EG6-SAM on a gold surface, hydroxy-EGn-undecanethiols (n=3, 6) are used to dilute the number of amino groups according to the density of the molecules being introduced onto the surface.

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      • Properties
        • Categories
          PEG alkanethiol
          CAS Number
          496839-01-1 (free base)
          Molecular Formula
          C23H60ClNO6S
          Molecular Weight
          504.16
          Appearance
          white or pale yellow powder
          Purity
          ≥90.0% (HPLC, derivatization)
          Storage
          -20°C, protect from light and metal
          Shipping
          ambient temperature

          * For research use only

      • Applications
        • Application Description
          Example of Solvents
          10 mmol/L (Water, Methyl alcohol, Chloroform, Ethyl alcohol, Tetrahydrofuran)
          How to Prepare SAM
          1. Soak a gold-coated glass plate in Piranha solutiona) for 10-15 minutes. Wash the plate with purified water.a)
          2. Dissolve aminoalkanethiol compound in ethanol to prepare several mM to several ten mM solutions.
          3. Soak the plate in the aminoalkanethiol solution for a certain time period.b)
          4. Wash the SAM-coated plate with ethanol and then water.
          5. Dry the plate under nitrogen atmosphere, if necessary.
          a)Piranha solution: sulfuric acid and 30% hydrogen peroxide, 3:1. Piranha solution is a strong oxidizing agent. Extreme care is necessary when using it.
          Do not apply Piranha solution to resin-coated plates; it may erode the resin.
          b)To prepare a SAM-coated plate with the best performance, aminoalkanethiol concentration and soaking time should be individually determined.
          Application of SAM-Preparation of DNA Array
          1. Use SF10 glass slides (Schott Glass Technologies) coated with 5 nm chromium and 45 nm gold thin film.
          2. Soak the glass slide in a 1 mM 1-octadecanethiol (ODT)/ethanol solution overnight to prepare ODT SAM-coated slide.
          3. Draw 500 μm x 500 μm patterns on the ODT SAM-coated slide by UV irradiation with an Hg-Xe arc lamp.a)
          4. Soak the slide in a 1 mM 11-amino-1-undecanethiol (AUT)/ethanol solution for 2 hours to form AUT SAM on the 500 μm x 500 μm photopatterned area.
          5. Drop 2 mM SPDP solutionb) onto the slide and leave the slide at room temperature.
          6. Wash the slide and dry under nitrogen atmosphere.
          7. Apply 1 mM thiol-DNA solutionc) to each 500 μm x 500 μm pattern and incubate at room temperature overnight.
          8. Incubate the slide with a sample solution for 10 minutes and wash with phosphate buffer, followed by SPR imaging.
          a)Irradiation time: 1-1.5 hours
          b)SPDP: N-succinimidyl 3-(2-pyridyldithio)propionate. Dissolve SPDP in DMSO to prepare 50 mM solution. Dilute it 25 times with 100 mM triethanolamine buffer, pH 7.0.
          c)Dissolve thiol-DNA with 100 mM triethanolamine buffer, pH 8.0.


          When it is difficult to take out all the powder from the container, please add the solvent into a container and dissolve it before its use.
      • Reference
        • 1) C. Pale-Grosdemange, E. S. Simon, K. L. Prime and G. M. Whitesides, Anal. Chem., 1999, 71, 777.

          2) M. Kyo, K.Usui-Aoki, H. Koga, Anal. Chem, 2005, 77, 7115.

          3) G. B. Sigal, M. Mrksich and G. M. Whitesides, J. Am. Chem. Soc., 1998, 120, 3464.

          4) Y. Li, H. J. Lee and R. M. Corn, Nucleic Acids Research, 2006, 34, 6416.

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