5-Carboxy-1-pentanethiol

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5-Carboxy-1-pentanethiol (10mg) - C387-10

5-Carboxy-1-pentanethiol (100mg) - C387-12

Item #	Description/Size	Availability	Qty Break	Price	Quantity
C387-10	10 mg	5-10 business days	1	$125.00
C387-12	100 mg	5-10 business days	1	$330.00

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

Application: SAM preparation, carboxylate coating

Description
Application

Chemical Name: 5-Carboxy-1-pentanethiol
CAS: 17689-17-7

Appearance: Colorless or slightly yellow liquid
Purity: ≥97.0% (HPLC)
MW: 148.22, C₆H₁₂O₂S

Storage Condition: 0-5ºC, protect from metal
Shipping Condition: ambient temperature

Structural Formula

Product Description

Carboxyalkanethiols are utilized for the modification of a gold surface to introduce carboxylic groups on it. The carboxylic group is often converted to activated N-hydroxysuccinimide ester, which reacts with an amine group of biomaterials. Dojindo’s newly developed 15-Carboxy-1-pentadecanethiol has a 15-carbon chain, which is the longest alkanethiol available in the market among carboxyalkanethiols. Five different carboxyalkanethiols including Carboxy-EG₆-undecanethiol are available for gold surface modification. Malone and others fabricated a highly sensitive SPR sensor using 15-Carboxy-1-pentadecanethiol. Glenn and coworkers used carboxyalkanethiol and poly-L-lysine to create an immobilized cytochrome b5 multilayer electrode. Mizutani and others fabricated immobilized glucose oxidase multilayer electrodes in a similar manner. Both groups reported electron transfer from biomaterials to a gold surface. These kinds of multilayer film electrodes are well suited for studies of diffusion electron transfer. Frisbie and others developed a new method, chemical force microscopy, for obtaining the adhesive interactions and the friction image of patterned sample surfaces. They used atomic force microscopy (AFM) to measure the interactions and spatial mapping of chemically distinct functional groups. Frisbie and others formed carboxyalkanethiol monolayers on the gold surfaces of AFM cantilever tips. They used AFM to measure the adhesive and friction forces between molecularly modified probe tips and organic monolayers terminating in a lithographically defined pattern of distinct functional groups.

References

1. J. D. H. Glenn and E. F. Bowden, Diffusionless Electrochemistry of Cytochrome b5 Adsorbed on a Multilayer Film Electrode, Chem. Lett., 1996, 399.
2. F. Mizutani, Y. Sato, S. Yabuki and Y. Hirata, Enzyme Ultra-thin Layer Electrode Prepared by the Co-adsorption of Poly-L-lysine and Glucose Oxidase onto a Mercaptopropionic Acid-Modified Gold Surface, Chem. Lett., 1996, 251.
3. C. D. Frisbie, F. Rozsnyai, A. Noy, M. S. Wrighton and C. M. Lieber, Functional Group Imaging by Chemical Force Microscopy, Science, 1994, 265, 2071.