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Merck
CN

325430

Triphenylmethylamine

99%

Synonym(s):

Tritylamine

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About This Item

Linear Formula:
(C6H5)3CNH2
CAS Number:
5824-40-8
Molecular Weight:
259.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24859510
MDL number:
MFCD00008047
Beilstein/REAXYS Number:
2113674

Key Documents

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Product Name

Triphenylmethylamine, 99%

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

SMILES string

NC(c1ccccc1)(c2ccccc2)c3ccccc3

InChI key

BZVJOYBTLHNRDW-UHFFFAOYSA-N

assay

99%

form

solid

bp

223 °C/14 mmHg (lit.)

mp

102-104 °C (lit.)

functional group

amine
phenyl

Quality Level

100

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Application

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH6086
MKBZ7831V
MKBH2603V
MKBH3275V
MKBD8899V

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Atsushi Yamamoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 3006-3016 (2013-01-12)
A diamondoid porous organic salt (d-POS) composed of 8-hydroxyquinoline-5-sulfonic acid (HQS) and triphenylmethylamine (TPMA) shows reversible structure contraction and expansion ("breathing") in response to guest desorption and adsorption. This flexible structure is designed hierarchically by utilizing two different types of
Reaction of triphenylmethylamines with boron trihalides.
Ronan RJ, et al.
Journal of the American Chemical Society, 93(25), 6811-6814 (1971)
Tritylamine (triphenylmethylamine) in organic synthesis; II. The reaction of tritylamine with oxiranes-synthesis of N-trityl-? aminoalcohols.
Soroka M and Goldeman W.
ARKIVOC (Gainesville, FL, United States), 12, 31-37 (2003)
Grant A McNaughton-Smith et al.
Journal of medicinal chemistry, 51(4), 976-982 (2008-02-01)
Sickle cell disease (SCD) is a hereditary condition characterized by deformation of red blood cells (RBCs). This phenomenon is due to the presence of abnormal hemoglobin that polymerizes upon deoxygenation. This effect is exacerbated when dehydrated RBCs experience a loss
Silke B Bodendiek et al.
Frontiers in pharmacology, 3, 106-106 (2012-06-12)
The paucity of specific pharmacological agents has been a major impediment for delineating the roles of gap junction (GJ) channels formed by connexin proteins in physiology and pathophysiology. Here, we used the selective optimization of side activities (SOSA) approach, which
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