
Thioflavin T | CAS 2390-54-7
| Catalog Number | A01-0008 |
| Category | Fluorescent Proteins & Nucleotides |
| Molecular Formula | C17H19ClN2S |
| Molecular Weight | 318.86 |
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Product Introduction
Thioflavin T is a benzothiazole fluorescent dye used to detect amyloid fibrils and protein aggregates. It emits bright green fluorescence upon binding.
Chemical Information
Product Specification
Application
Computed Properties
Literatures
Patents
Chemical Information
| Synonyms | Basic Yellow 1;2-(p-(dimethylamino)phenyl)-3,6-dimethylbenzothiazolium chloride; thioflavin S; thioflavine; ThT (dye) |
| Purity | >95.0%(HPLC) |
| IUPAC Name | 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethylaniline;chloride |
| SMILES | CC1=CC2=C(C=C1)[N+](=C(S2)C3=CC=C(C=C3)N(C)C)C.[Cl-] |
| InChI | InChI=1S/C17H19N2S.ClH/c1-12-5-10-15-16(11-12)20-17(19(15)4)13-6-8-14(9-7-13)18(2)3;/h5-11H,1-4H3;1H/q+1;/p-1 |
| InChIKey | JADVWWSKYZXRGX-UHFFFAOYSA-M |
| Solubility | H2O: ≥ 30 mg/mL |
| Appearance | Yellow to ochre-yellow powder |
| Melting Point | 212°C |
| MDL Number | MFCD00011944 |
Product Specification
| Maximum Absorption Wavelength | 412(H2O) nm |
| Storage | Store in a cool and dry place (or refer to the Certificate of Analysis). |
| Signal | Danger |
| GHSHazardStatements | H301 (83.33%): Toxic if swallowed [Danger Acute toxicity, oral] H317 (66.67%): May cause an allergic skin reaction [Warning Sensitization, Skin] H318 (66.67%): Causes serious eye damage [Danger Serious eye damage/eye irritation] H319 (16.67%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H400 (66.67%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard] H410 (66.67%): Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard] H411 (16.67%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] |
| Precautionary Statement Codes | P261, P264, P264+P265, P270, P272, P273, P280, P301+P316, P302+P352, P305+P351+P338, P305+P354+P338, P317, P321, P330, P333+P313, P337+P317, P362+P364, P391, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) |
Application
Thioflavin T is a benzothiazole-based fluorescent dye widely used to monitor amyloid-like beta-sheet formation in vitro. In fluorescence workflows, it is commonly paired with excitation in the visible range and read out as an intensity increase upon binding to amyloid fibrils, enabling kinetic and endpoint measurements of fibrillization processes. Because Thioflavin T is a small, dye-like staining reagent, it is frequently employed in aggregation assays, screening campaigns, and materials/biomolecular studies where fibril formation is the readout.
1. Amyloid Fibrillization Assays
Thioflavin T is routinely used by biochemistry and chemical biology laboratories to quantify amyloid fibril formation from purified proteins, peptides, and synthetic aggregation-prone sequences. Researchers typically follow fibrillization kinetics by tracking fluorescence intensity over time, using Thioflavin T as a binding-dependent reporter for beta-sheet-rich aggregates. This makes the dye a standard tool for comparing aggregation rates across buffer conditions, temperature regimes, ionic strengths, and truncation or mutation variants, and for evaluating how candidate small molecules, polymers, or biomolecules influence fibril growth in controlled in vitro studies.
2. Screening Anti-Aggregation Compounds
Thioflavin T supports fluorescence-based screening workflows in which aggregation modulators are assessed by their impact on fibril-associated signal development. In drug discovery-adjacent research and lead-optimization efforts, Thioflavin T is used to generate concentration-dependent aggregation profiles, including time-resolved readouts that distinguish early-stage effects from later-stage fibril maturation. The dye's straightforward fluorescence measurement format is also leveraged in plate-based assays to compare multiple conditions in parallel, helping teams prioritize compounds or excipients for downstream orthogonal characterization of aggregation state.
3. Endpoint Aggregate Characterization
Thioflavin T is frequently applied for endpoint staining and comparative analysis of amyloid-like aggregates after incubation, where fluorescence intensity serves as a practical proxy for fibril abundance. In many protein chemistry workflows, researchers use Thioflavin T staining alongside complementary characterization such as microscopy, spectroscopy, or biochemical fractionation to corroborate aggregation state and to map how experimental perturbations shift the balance between monomeric, oligomeric, and fibrillar populations. This application is particularly common when investigators need a rapid, dye-based readout to guide sample selection for more detailed structural or morphological analyses.
4. Biomaterials and Surface Studies
Thioflavin T is used in biomaterials research to examine how surfaces, coatings, and material-associated environments influence protein aggregation and fibril deposition. Materials scientists often incorporate the dye into fluorescence readout strategies to compare fibril formation on different substrates, including variations in surface chemistry, charge, hydrophobicity, and functional group density. By providing a convenient measure of amyloid-like aggregate formation in contact or near-surface contexts, Thioflavin T helps teams evaluate material-driven changes in aggregation propensity and fibril growth behavior during material development and interface studies.
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 318.0957475 g/mol |
| Monoisotopic Mass | 318.0957475 g/mol |
| Topological Polar Surface Area | 35.4Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 325 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 27297626 | 2016-11-25 | Hopeahainol A binds reversibly at the acetylcholinesterase (AChE) peripheral site and inhibits enzyme activity with a novel higher order concentration dependence | Chemico-biological interactions |
| 23528352 | 2013-05-05 | Inhibition of human islet amyloid polypeptide or amylin aggregation by two manganese-salen derivatives | European journal of pharmacology |
| 22766284 | 2012-12-01 | Surface chemistry at the nanometer scale influences insulin aggregation | Colloids and surfaces. B, Biointerfaces |
| 22955637 | 2012-11-07 | Unzipping the role of chirality in nanoscale self-assembly of tripeptide hydrogels | Nanoscale |
| 23067245 | 2012-11-05 | Influence of the valine zipper region on the structure and aggregation of the basic leucine zipper (bZIP) domain of activating transcription factor 5 (ATF5) | Molecular pharmaceutics |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-115232195-A | Oligopeptide two-dimensional nanomaterials and their applications | 2022-07-25 |
| CN-115025204-A | A compound of dipeptide compounds that inhibits Aβ42 aggregation and reduces its cytotoxicity | 2022-07-20 |
| CN-115197689-A | A kind of functionalized upconversion nanoparticle of photo-oxidative protein and its preparation method and application | 2022-07-06 |
| CN-115201302-A | Electrochemical sensor, preparation method and application thereof | 2022-07-04 |
| CN-115141265-A | Quaternary allosteric pyruvate isoenzyme M2-type activating peptide and its application in reversing the Warburg effect and tumor chemotherapy | 2022-06-30 |
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