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Molecular Probes™ 5-(Aminomethyl)Fluorescein, Hydrochloride
Description
The primary aliphatic amine of 5-(aminomethyl)fluorescein can be reversibly coupled to aldehydes and ketones to form a Schiff base - which can be reduced to a stable amine derivative by sodium borohydride (NaBH4) or sodium cyanoborohydride (NaCNH3) to form new probes. Carboxylic acids of proteins and other water-soluble biopolymers can be coupled to this molecule in aqueous solution using water-soluble carbodiimides such as EDAC (E2247).
Specifications
Specifications
| CAS | 138588-53-1 |
| Color | Orange-Yellow |
| Packaging | 1 Each |
| Molecular Formula | C21H15NO5 |
| Quantity | 10 mg |
| Synonym | 5-aminomethyl fluorescein, 5-aminomethyl fluorescein hydrochloride, 5-amfl, 6-aminomethyl-3',6'-dihydroxyspiro 2-benzofuran-3,9'-xanthene-1-one, 5'-aminomethyl-3,6-dihydroxyspiro 9h-xanthene-9,1' 3'h-isobenzofuran-3'-one, 5-aminomethyl-3',6'-dihydroxy-3h-spiro isobenzofuran-1,9'-xanthen-3-one |
| InChI Key | FKQRDXNGJULUOJ-UHFFFAOYSA-N |
| Molecular Weight (g/mol) | 361.35 |
| PubChem CID | 132166 |
For Research Use Only. Not for use in diagnostic procedures.
Product Title
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