147753
4-Aminobenzonitrile
98%
Synonym(s):
4-Cyanoaniline
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About This Item
Linear Formula:
H2NC6H4CN
CAS Number:
Molecular Weight:
118.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-850-1
Beilstein/REAXYS Number:
774507
MDL number:
Assay:
98%
Form:
solid
InChI key
YBAZINRZQSAIAY-UHFFFAOYSA-N
InChI
1S/C7H6N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,9H2
SMILES string
Nc1ccc(cc1)C#N
assay
98%
form
solid
mp
83-85 °C (lit.)
Quality Level
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Muta. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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 and characterization of novel azobenzene methacrylate monomers.
Nicolescu FA, et al.
Designed Monomers and Polymers, 12(6), 553-563 (2009)
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)
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
Takashi Nakamura et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 14(4), 741-745 (2012-11-28)
The S1-S0 resonant enhanced multiphoton ionization (REMPI) spectrum as well as the infrared (IR) spectra in the S0 and S1 states of 4-aminobenzonitrile (4ABN) and its van der Waals complex with Ar (4ABN-Ar) were measured by means of IR depletion
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