Description
These mixed disulfides not only form adsorption-resistant SAMs but, at the same time, can be activated in situ or reacted with activated compounds. Monolayers formed with these compounds have exactly 50% surface coverage of reactive groups and avoid phase separation that would otherwise accompany adsorption of -OH and -COOH terminated thiols (Langmuir 2001, 17, 7735-7741). The different lengths of the EG "arm" allow for varying the accessibility of the carboxy group tethered at the end of EG6.Standard Products
| name | catalog no. | m | n | weight | price |
|---|---|---|---|---|---|
| HO-EG-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n1-0.1 | 1 | 100 mg | Log in to see the prices | |
| HO-EG-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n1-0.2 | 1 | 200 mg | ||
| HO-EG-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n1-0.5 | 1 | 500 mg | ||
| HO-EG2-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n2-0.1 | 2 | 100 mg | ||
| HO-EG2-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n2-0.2 | 2 | 200 mg | ||
| HO-EG2-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n2-0.5 | 2 | 500 mg | ||
| HO-EG3-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n3-0.1 | 3 | 100 mg | ||
| HO-EG3-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n3-0.2 | 3 | 200 mg | ||
| HO-EG3-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n3-0.5 | 3 | 500 mg | ||
| HO-EG4-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n4-0.1 | 4 | 100 mg | ||
| HO-EG4-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n4-0.2 | 4 | 200 mg | ||
| HO-EG4-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n4-0.5 | 4 | 500 mg | ||
| HO-EG5-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n5-0.1 | 5 | 100 mg | ||
| HO-EG5-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n5-0.2 | 5 | 200 mg | ||
| HO-EG5-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n5-0.5 | 5 | 500 mg | ||
| HO-EG6-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n6-0.1 | 6 | 100 mg | ||
| HO-EG6-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n6-0.2 | 6 | 200 mg | ||
| HO-EG6-C11-S-S-C11-EG6-OCH2-COOH | DI 006-n6-0.5 | 6 | 500 mg |
Custom synthesis variants
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