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147753

Sigma-Aldrich

4-Aminobenzonitrile

98%

Synonym(s):

4-Cyanoaniline

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About This Item

Linear Formula:
H2NC6H4CN
CAS Number:
Molecular Weight:
118.14
Beilstein/REAXYS Number:
774507
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

83-85 °C (lit.)

SMILES string

Nc1ccc(cc1)C#N

InChI

1S/C7H6N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,9H2

InChI key

YBAZINRZQSAIAY-UHFFFAOYSA-N

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Application

4-Aminobenzonitrile was used as derivatization reagent in capillary zone electrophoretic analysis of aldoses, ketoses and uronic acid. It was used in the synthesis of methacrylic monomers containing pendant azobenzene structures and polythiophenes containing an azobenzene moiety in the side-chain.

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Muta. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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Piyali Bhanja et al.
ChemSusChem, 10(5), 921-929 (2017-01-07)
The new covalent organic framework material TDFP-1 was prepared through a solvothermal Schiff base condensation reaction of the monomers 1,3,5-tris-(4-aminophenyl)triazine and 2,6-diformyl-4-methylphenol. Owing to its high specific surface area of 651 m
Synthesis of azobenzene-containing polythiophenes and photoinduced anisotropy.
Aubertin F and Zhao Y.
Journal of Polymer Science: Part A, General Papers, 42(14), 3445-3455 (2004)
Synthesis and characterization of novel azobenzene methacrylate monomers.
Nicolescu FA, et al.
Designed Monomers and Polymers, 12(6), 553-563 (2009)
Matthias Schmies et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 14(4), 728-740 (2012-12-05)
IR photodissociation (IRPD) spectra of mass-selected cluster ions of 4-aminobenzonitrile (ABN(+)) with up to four Ar and N2 ligands are recorded over the spectral range of the N-H stretching vibrations (ν(s/a)) of ABN(+) in its (2)B1 ground electronic state. ABN(+)-L(n)
H Schwaiger et al.
Electrophoresis, 15(7), 941-952 (1994-07-01)
Aldoses, ketoses and uronic acids were derivatized successfully within 15 min at a temperature of 90 degrees C by reductive amination with 4-aminobenzonitrile. Subsequently, the derivatives were separated as their borate complexes by capillary zone electrophoresis, using 175 mM borate

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