
QSY9 NHS Ester | CAS 304014-17-3
| Catalog Number | A20-0050 |
| Category | QSY |
| Molecular Formula | C43H38N4O13S3 |
| Molecular Weight | 914.98 |
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Product Introduction
QSY9 NHS Ester has a wide and intense quenching range from 500-600 nm. The NHS ester group can be applied to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.
Chemical Information
Application
Chemical Information
| Synonyms | QSY-9-succinimidyl ester; SY-9 NHS ester |
| IUPAC Name | 4-[[9-[2-[4-(2,5-dioxopyrrolidin-1-yl)oxycarbonylpiperidin-1-yl]sulfonylphenyl]-6-[methyl-(4-sulfophenyl)azaniumylidene]xanthen-3-yl]-methylamino]benzenesulfonate |
| SMILES | CN(C1=CC=C(C=C1)S(=O)(=O)[O-])C2=CC3=C(C=C2)C(=C4C=CC(=[N+](C)C5=CC=C(C=C5)S(=O)(=O)O)C=C4O3)C6=CC=CC=C6S(=O)(=O)N7CCC(CC7)C(=O)ON8C(=O)CCC8=O |
| InChI | InChI=1S/C43H38N4O13S3/c1-44(28-7-13-32(14-8-28)62(53,54)55)30-11-17-34-37(25-30)59-38-26-31(45(2)29-9-15-33(16-10-29)63(56,57)58)12-18-35(38)42(34)36-5-3-4-6-39(36)61(51,52)46-23-21-27(22-24-46)43(50)60-47-40(48)19-20-41(47)49/h3-18,25-27H,19-24H2,1-2H3,(H-,53,54,55,56,57,58) |
| InChIKey | UFGPPUDYRGLQJT-UHFFFAOYSA-N |
| Appearance | Purple Solid |
Application
QSY9 NHS Ester is an NHS-ester activated form of the QSY9 quencher, designed for efficient covalent attachment to primary amines on proteins, peptides, and other amine-containing biomolecules. As a fluorescence-quenching reagent, it is used to suppress donor emission in labeled constructs and to tune background in fluorescence-based assay and imaging workflows, including oligonucleotide and protein conjugates. Its quencher functionality is commonly leveraged when robust, stable signal control is required after conjugation.
1. Protein Conjugation Quenching
QSY9 NHS Ester is frequently used by protein engineering and chemical biology groups to generate quencher-labeled proteins for fluorescence assay development. After coupling to lysine-rich targets or amine-functionalized protein domains, the resulting quencher conjugates help reduce unwanted donor fluorescence in FRET pairs, quenched reporters, and multi-label biomolecular constructs. Researchers use these conjugates in assay optimization workflows where controlling residual fluorescence from labeled components is essential for reliable readout.
2. FRET Pair Signal Suppression
QSY9 NHS Ester is widely applied in FRET-based assay design where a quencher must be positioned on a donor-containing system to manage fluorescence output. Conjugation to amine-bearing biomolecules enables construction of donor-quencher architectures used in fluorescence monitoring formats, including proximity-dependent reporter systems and distance-controlled labeling strategies. This quencher format is particularly useful when a stable covalent handle is needed to ensure consistent quenching behavior across prepared conjugate lots.
3. Oligonucleotide Reporter Construction
QSY9 NHS Ester is commonly incorporated into fluorescence reporter designs that require quenched oligonucleotide constructs, especially when a covalent quencher attachment to amine-modified nucleic acids is desired. By coupling to amino-functionalized linkers or modified nucleotides, teams building molecular beacons or quenched hybridization reporters can suppress fluorescence from an attached dye until a target-dependent event changes the reporter geometry or separation. This approach is also used in nucleic-acid assay reagent development where background suppression is a key practical requirement.
4. Biomaterial Surface Functionalization
QSY9 NHS Ester is used in biomaterials and surface chemistry workflows to install quencher functionality onto amine-presenting polymers, coatings, and biointerfaces. Covalent immobilization supports fluorescence signal control in labeled surface assays, where quencher-modified materials can reduce stray emission from nearby fluorophores and improve the interpretability of microscopy or plate-based fluorescence measurements. This makes QSY9 NHS Ester relevant for researchers developing functionalized matrices, sensor surfaces, and immobilized reporter platforms that rely on controlled fluorescence output.
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