
BHQ-1 NHS | CAS 916753-61-2
| Catalog Number | A20-0007 |
| Category | Black Hole Quencher (BHQ) |
| Molecular Formula | C30H31N7O7 |
| Molecular Weight | 601.62 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| A20-0007 | 25 mg | $998 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BHQ dyes act through a combination of FRET and static quenching to avoid residual background signals or low signal-to-noise ratios common with fluorescent quenchers such as TAMRA. BHQ-1 NHS is a compound that is directly labeled with fluorescently labeled nucleotide.
Chemical Information
Application
QC Data
Chemical Information
| Synonyms | UBQ-1 NHS Ester |
| IUPAC Name | (2,5-dioxopyrrolidin-1-yl) 4-[4-[[2-methoxy-5-methyl-4-[(4-methyl-2-nitrophenyl)diazenyl]phenyl]diazenyl]-N-methylanilino]butanoate |
| SMILES | CC1=CC(=C(C=C1)N=NC2=CC(=C(C=C2C)N=NC3=CC=C(C=C3)N(C)CCCC(=O)ON4C(=O)CCC4=O)OC)[N+](=O)[O-] |
| InChI | InChI=1S/C30H31N7O7/c1-19-7-12-23(26(16-19)37(41)42)32-33-24-18-27(43-4)25(17-20(24)2)34-31-21-8-10-22(11-9-21)35(3)15-5-6-30(40)44-36-28(38)13-14-29(36)39/h7-12,16-18H,5-6,13-15H2,1-4H3 |
| InChIKey | QIDPAHFSJZFKAW-UHFFFAOYSA-N |
| Appearance | Dark Purple Powder |
Application
BHQ-1 NHS is a quencher building block designed for fluorescence signal suppression in conjugation workflows, combining a BHQ-1 quencher core with an NHS ester for efficient coupling to primary amines. This reagent is commonly used by fluorescence assay developers and molecular imaging researchers to create quencher-labeled oligonucleotides, peptides, proteins, and antibody conjugates where background reduction and distance-dependent signal control are required. Its NHS reactivity supports straightforward incorporation into labeling strategies that rely on fluorophore-quencher proximity, including FRET-based and oligonucleotide beacon formats.
1. FRET Quencher Conjugates
BHQ-1 NHS is frequently used to prepare fluorophore-quencher pairs for FRET-based assays, where quenching is engineered by controlling the spatial relationship between donor and acceptor components. Researchers use BHQ-1 NHS to introduce the quencher onto proteins, peptides, or engineered binding constructs that are later paired with a compatible fluorescent donor label. In assay development workflows, quencher conjugation with BHQ-1 NHS helps suppress fluorescence from the donor in the absence of the target-dependent event, supporting cleaner readouts in plate-based fluorescence measurements.
2. Oligonucleotide Beacon Labeling
BHQ-1 NHS is well suited for constructing molecular beacon and related nucleic-acid probe architectures that require quencher placement to minimize fluorescence from a tethered fluorophore. Oligonucleotide labeling teams use the NHS ester functionality to attach BHQ-1 to amine-modified oligos or to quencher-bearing linkers that are incorporated into beacon designs. This approach supports signal control in hybridization and conformational switching assays, where fluorescence recovery occurs when the beacon structure changes donor-quencher proximity.
3. Protein And Antibody Quenching
BHQ-1 NHS is used to generate quencher-labeled proteins and antibody conjugates for fluorescence-based binding studies and reagent development where reduced background is important. In chemical biology and biomolecular assay development, the NHS ester enables coupling to lysine-containing biomolecules, including enzymes used as reporters, affinity reagents used in sandwich formats, and detection antibodies used in fluorescence workflows. By installing BHQ-1 at defined conjugation sites, teams can tailor quenched reporter constructs for proximity-controlled fluorescence readouts.
4. Peptide And Linker Payload Control
BHQ-1 NHS is commonly incorporated into peptide and small-molecule linker systems that are later used to build quenched fluorescence probes and multicomponent labeling reagents. Researchers in biomaterials and molecular imaging workflows use the NHS ester to attach BHQ-1 to amine-bearing peptide handles, spacers, or targeting ligands, enabling controlled quenching when paired with a fluorophore elsewhere in the construct. This strategy is particularly useful when a quencher must be positioned to regulate fluorescence output during assembly of larger probe systems or conjugate libraries.
QC Data
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