Skip to Content
Merck
CN

Key Documents

View All Documentation

325430

Triphenylmethylamine

99%

Synonym(s):

Tritylamine

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

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
Assay:
99%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

assay

99%

form

solid

bp

223 °C/14 mmHg (lit.)

mp

102-104 °C (lit.)

functional group

amine, phenyl

SMILES string

NC(c1ccccc1)(c2ccccc2)c3ccccc3

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

InChI key

BZVJOYBTLHNRDW-UHFFFAOYSA-N

General description

Reaction of triphenylmethylamine with borontrifluoride was studied.

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.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCH6086
MKBZ7831V
MKBH2603V
MKBH3275V
MKBD8899V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
View All Related Papers

Global Trade Item Number

SKUGTIN
325430-5G04061826713037