- TRIPHENYLMETHYLAMINE
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- $9.00
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2026-05-28
- CAS:5824-40-8
- Min. Order: 1KG
- Purity: 99.8%
- Supply Ability: 100tons
- TRIPHENYLMETHYLAMINE
-
- $25.00
-
2026-03-20
- CAS:5824-40-8
- Min. Order: 100KG
- Purity: 99.5%
- Supply Ability: 100 mt
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| | Triphenylmethylamine Basic information |
| | Triphenylmethylamine Chemical Properties |
| Melting point | 102-104 °C (lit.) | | Boiling point | 223 °C/14 mmHg (lit.) | | density | 0.9242 (rough estimate) | | refractive index | 1.7500 (estimate) | | Fp | 223°C/14mm | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | pka | 7.77±0.10(Predicted) | | color | Off-White | | Water Solubility | Insoluble | | Sensitive | Air Sensitive | | BRN | 2113674 | | InChI | 1S/C19H17N/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H,20H2 | | InChIKey | BZVJOYBTLHNRDW-UHFFFAOYSA-N | | SMILES | NC(c1ccccc1)(c2ccccc2)c3ccccc3 | | CAS DataBase Reference | 5824-40-8(CAS DataBase Reference) | | NIST Chemistry Reference | Tritylamine(5824-40-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | F | 10-23 | | HS Code | 29214990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | Triphenylmethylamine Usage And Synthesis |
| Chemical Properties | Triphenylamine is a white to light yellow powder that exhibits a certain degree of basicity and readily forms corresponding hydrochlorides when treated with hydrochloric acid. Its structure contains three benzene rings, and it is commonly used as a starting material for synthesizing organic optoelectronic molecules in fundamental chemical research. | | Uses | Triphenylmethylamine is a trityl derivative that is structurally related to Clotrimazole (C587400). Triphenylmethylamine is used in the preparation of trityl-cysteine analogs as inhibitors of human mi
totic kinesin. Triphenylmethylamine is also used as a fireproofing agent. | | Uses | Triphenylmethylamine was used to prepare diamondoid porous organic salt. It was also used in preparation of N-tritylated β-aminoalcohols, useful building blocks in organic synthesis. | | General Description | Reaction of triphenylmethylamine with borontrifluoride was studied. | | References | [1] M. SOROKA W. G. Tritylamine (triphenylmethylamine) in organic synthesis; II. The reaction of tritylamine with oxiranes – synthesis of N-trityl-β-aminoalcohols[J]. Arkivoc, 2003, 24 1. DOI:10.3998/ARK.5550190.0004.C05.
[2] NORIMITSU TOHNAI DR. Well-Designed Supramolecular Clusters Comprising Triphenylmethylamine and Various Sulfonic Acids†[J]. Angewandte Chemie International Edition, 2007, 46 13: 2220-2223. DOI:10.1002/anie.200603841. |
| | Triphenylmethylamine Preparation Products And Raw materials |
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