16-Amino-1-hexadecanethiol, hydrochloride

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16-Amino-1-hexadecanethiol, hydrochloride (10mg) - A458-10

16-Amino-1-hexadecanethiol, hydrochloride (100mg) - A458-12

Item #	Description/Size	Availability	Qty Break	Price	Quantity
A458-10	10 mg	1-2 business days	1	$160.00
A458-12	100 mg	5-10 business days	1	$560.00

*Estimated. Exact shipping date will be notified.
For Research Use Only Products

Application: SAM preparation, amine group coating

Description
Application

Chemical Name: 16-Amino-1-hexadecanethiol, hydrochloride

Appearance: White powder
Purity: ≥95% (HPLC)
MW: 309.98, C₁₆H₃₆ClNS

Storage Condition: ambient temperature
Shipping Condition: ambient temperature

Chemical Structure

Product Description

Aminoalkanethiols are utilized for the modification of a gold surface to introduce amino groups on the surface. Dojindo’s newly developed 16-Amino-1-hexadecanethiol has a 16-carbon chain, which is the longest alkanethiol available in the market. It is expected that 16-Amino-1-hexadecanethiolwill form the most stable SAM on a gold surface among the aminoalkanethiol compounds because of the greater Van-der-Waals force between alkane groups. Five different aminoalkanethiols including Amino-EG6-undecanethiol, hydrochloride are available for gold surface modification. Amino-EG₆-undecanethiol is used for hydrophilic surface preparation. The amino group is usually modified using aminereactivematerials, such as proteins or biomaterials, to functionalize the gold surface. Several researchers have reported SAMs of short alkylchain aminoalkanethiols, and there are an increasing number of reports of long alkyl chain compounds. Takahara and others formed a monolayer of 11-Amino-1-undecanethiol on a gold electrode and studied the effect of the terminal groups on the redox responses of ferrocene derivatives using the voltammetric method. They also reported the relationship between the alkyl chain length of aminoalkanethiols and the redox behavior of 2,3-dichloro-1,4-naphtoquinone attached to the terminal amino group. Tanahashi and coworkers modified a gold surface with SAMs of several kinds of functionalized alkanethiols. They reported the effect of their terminal functional groups on apatite formation in a simulated body fluid using X-ray photoelectron spectroscopic (XPS) measurement and quartz crystal microbalance (QCM) method.

How to prepare the SPR-Chip
Link to Aprication Note

References
1. R. P. Solanki, K. S. Arya, Y. Nishimura, M. Iwamoto, B. D. Malhotra, Langmuir, 2007, 23, 7398-7403.
2. J. M. Brockman, A. G. Fruto and R. M. Corn, J. Am. Chem. Soc., 1999, 121, 8044-8051.