Tetramethylrhodamine isothiocyanate Isomer R
SIAL/T3163 - powder
Synonym: 6-TRITC; Tetramethylrhodamine-
CAS Number: 80724-20-5
Empirical Formula (Hill Notation): C25H21N3O3S
Molecular Weight: 443.52
MDL Number: MFCD00063517
Linear Formula: C25H21N3O3S
Product Type: Chemical
| application(s) | diagnostic assay manufacturing hematology histology |
| composition | Dye content, ≥80% |
| description | labeling efficiency with bovine albumin >= 50% |
| form | powder |
| InChI | 1S/C25H21N3O3S/c1-27(2)16 |
| InChI key | OBYNJKLOYWCXEP-UHFFFAOYSA |
| Quality Level | 200 ![]() |
| SMILES string | CN(C)c1ccc2c(OC3=CC(C=CC |
| solubility | 1 M NH4OH: 10 mg/mL (Faint Red to Very Dark Red to Very Dark Purple solution) |
| storage temp. | 2-8°C |
| Application: | • TRITC is used to label a wide variety of biomolecules, including immunoglobulins, lectins, nucleic acids, polynucleotides, and polysaccharides for affinity, immuno-, and in situ hybridization, fluorescent probes, and flow cytometry. • Lectins are TRITC-Iabeled reagents for the affinity staining of sections and cell monolayers to distinguish the sialomucins of salivary glands. • TRITC-antibodies are used to identify pathogenic amoebae. • TRITC-oligonucleotides are used in the in-situ hybridization staining of soil microorganisms. • TRITC-Iabeled reagents have also been used as fluorescent probes of live cells. • Flow cytometry of TRlTC-Iabeled slime mold cells has been used to study their aggregation behavior. |
| General description: | Tetramethylrhodamine isothiocyanate Isomer R (TRITC) is the R isomer of tetramethylrhodamine isothiocyanate and is also known as 6-tetramethylrhodamine isothiocyanate. It is a strongly fluorescent compound soluble in ethanol, methanol, dimethylformamide, dimethylsulfoxide, and water. TRITC is a moderately-sized aminoxanthene dye carrying carboxylic acid and isothiocyanate substituents on the non-planar pendant phenyl ring. It forms a lipophilic cation in acidic pH and a hydrophilic zwitterion around neutral pH. The isothiocyanate group reacts with nucleophilic substituents (e.g., amino, hydroxyl, thiol) of biomolecules, providing the means of attaching a fluorescent label. TRITC also reacts with water and hydroxide ions and is unstable in aqueous solutions. TRITC is commercially available as a zwitterion or as a chloride. |
| Packaging: | 5, 10 mg in glass bottle |
| Hazard statements | H412 |
| Precautionary statements | P273 |
| Risk Statements | 52/53 |
| Safety Statements | 61 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 2 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | 2-8°C |
| UNSPSC | 12171500 |

