site logo
HS-(CH2)m-COO-NHS
HS-(CH2)m-COO-NHS (FT 003)

Description

Harbors molecules onto a SAM-covered surface though an amide bond forming between the NHS ester and the molecule's free amino group. This NHS-ester coupling reaction is extremely easy to carry out, and proceeds in excellent yield. In a typical procedure, a gold slide (~1 cm2) covered with NHS-terminated SAM is immersed for 3 hrs in 0.5 mL of a methylene chloride (chloroform, THF, dry DMF and DMSO, absolute ethanol are also allowed) solution of a molecule bearing free amino group and 1.5 equivalents of NEt3. When the reaction is complete, the substrate should be rinsed with pure solvent and dried under a stream of nitrogen.

Standard Products

name catalog no. m n weight price
HS-C10-COO-NHS FT 003-m10-0.2 10 200 mg Log in to see the prices
HS-C10-COO-NHS FT 003-m10-0.5 10 500 mg
HS-C10-COO-NHS FT 003-m10-1 10 1 g
HS-C11-COO-NHS FT 003-m11-0.1 11 100 mg
HS-C11-COO-NHS FT 003-m11-0.2 11 200 mg
HS-C11-COO-NHS FT 003-m11-0.5 11 500 mg
HS-C11-COO-NHS FT 003-m11-1 11 1 g
HS-C15-COO-NHS FT 003-m15-0.2 15 200 mg
HS-C15-COO-NHS FT 003-m15-0.5 15 500 mg
HS-C15-COO-NHS FT 003-m15-1 15 1 g

Custom synthesis variants

Note, if none of the listed structures fit your specific requirements, please submit your own structure formula within our custom synthesis contact form by clicking button below.

custom product inquire