147753
4-Aminobenzonitrile
98%
Synonym(s):
4-Cyanoaniline
Sign In to View Organizational & Contract Pricing.
Select a Size
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:
Product Name
4-Aminobenzonitrile, 98%
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
Looking for similar products? Visit Product Comparison Guide
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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
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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service