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Tritylamine, 98%, Thermo Scientific Chemicals
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Catalog number A13864.06
also known as A13864-06
Price (USD)/ Each
91.90
-
Quantity:
5 g
Price (USD)/ Each
91.90
Tritylamine, 98%, Thermo Scientific Chemicals
Catalog numberA13864.06
Price (USD)/ Each
91.90
-
Chemical Identifiers
CAS5824-40-8
IUPAC Nametriphenylmethanamine
Molecular FormulaC19H17N
InChI KeyBZVJOYBTLHNRDW-UHFFFAOYSA-N
SMILESNC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Melting Point (clear melt)100.0-106.0?C
Appearance (Color)White to cream
Assay (Non-aqueous acid-base Titration)≥97.5 to ≤102.5%
Triphenylmethylamine was used to prepare diamondoid porous organic salt.1 It was also used in preparation of N-tritylated β-amino alcohols, useful building blocks in organic synthesis. It is used in the preparation of trityl- cysteine analogs as inhibitors of human mitotic kinesin.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Triphenylmethylamine was used to prepare diamondoid porous organic salt.1 It was also used in preparation of N-tritylated β-amino alcohols, useful building blocks in organic synthesis. It is used in the preparation of trityl- cysteine analogs as inhibitors of human mitotic kinesin.
Solubility
Soluble in chloroform, methanol. Insoluble in water.
Notes
Air sensitive. Store in a cool, dry, well-ventilated area. Store away from oxidizing agent.
Triphenylmethylamine was used to prepare diamondoid porous organic salt.1 It was also used in preparation of N-tritylated β-amino alcohols, useful building blocks in organic synthesis. It is used in the preparation of trityl- cysteine analogs as inhibitors of human mitotic kinesin.
Solubility
Soluble in chloroform, methanol. Insoluble in water.
Notes
Air sensitive. Store in a cool, dry, well-ventilated area. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Atsushi Yamamoto; Tetsuya Hasegawa; Tomoya Hamada; Tomofumi Hirukawa; Ichiro Hisaki; Mikiji Miyata; Norimitsu Tohnai. Role-allocated combination of two types of hydrogen bonds towards constructing a breathing diamondoid porous organic salt. Chemistry: A European Journal. 2013, 19 (9), 3006-3016.
- Sushil K. Sharma; Michael F. Songster; Tracey L. Colpitts; Peter Hegyes; George Barany; Francis J. Castellino. Reductive amination with tritylamine as an ammonia equivalent: efficient preparation of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)valeric acid (PAL) handle for peptide synthesis. J. Org. Chem., 1993, 58 (18), 4993-4996.
- Protected form of ammonia: the trityl group is removable by strong acid. For use in the synthesis of 1-aminoalkanephosphonic esters or acids, see: Synthesis, 370 (1988):