147753
4-Aminobenzonitrile
98%
Synonym(s):
4-Cyanoaniline
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About This Item
Linear Formula:
H2NC6H4CN
CAS Number:
Molecular Weight:
118.14
Beilstein:
774507
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Muta. 2
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, 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
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
Ranjit Kulkarni et al.
Nature communications, 10(1), 3228-3228 (2019-07-22)
Fully-aromatic, two-dimensional covalent organic frameworks (2D COFs) are hailed as candidates for electronic and optical devices, yet to-date few applications emerged that make genuine use of their rational, predictive design principles and permanent pore structure. Here, we present a 2D
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)
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