Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

368466

Sigma-Aldrich

4-Aminobenzylamine

99%

Synonym(s):

4-(Aminomethyl)aniline, 4-(Aminomethyl)benzenamine, 4-Aminobenzenemethanamine, 4-Aminomethylphenylamine, Toluene-α,4-diamine, p-(Aminomethyl)aniline, p-Aminobenzylamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
H2NC6H4CH2NH2
CAS Number:
4403-71-8
Molecular Weight:
122.17
MDL number:
MFCD00075513
UNSPSC Code:
12352100
PubChem Substance ID:
24862908
NACRES:
NA.22

Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.61 (lit.)

bp

101 °C/0.05 mmHg (lit.)

mp

37 °C

density

1.078 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCc1ccc(N)cc1

InChI

1S/C7H10N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,5,8-9H2

InChI key

BFWYZZPDZZGSLJ-UHFFFAOYSA-N

Related Categories

General description

4-Aminobenzylamine is an aromatic amine. Diazonium cations of 4-aminobenzylamine were generated in situ with sodium nitrite in aqueous HCl, which were used for the modification of glassy carbon electrode by aryl groups having an aliphatic amine group.

Application

4-Aminobenzylamine may be used:
  • in the electrochemical modification of single-walled carbon nanotubes (SWCNTs), via oxidative coupling
  • in the preparation of a novel acridine-based amino acid
  • in the synthesis of two novel fluorescent Photoinduced Electron Transfer (PET) anion sensors, based on the principle of ′fluorophore-spacer-(anion)receptor′
  • in anodic coupling of SWCNTs
  • in the synthesis of polyacrylamide series containing salicylideneaniline moieties, by a double polymer analogous reaction with reactive precursor polymer poly(pentafluorophenylacrylate) (PPFPA)

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000308970
0000291201
0000250301
0000226479
0000214590

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

Dual responsive chemosensors for anions: the combination of fluorescent PET (Photoinduced Electron Transfer) and colorimetric chemosensors in a single molecule.
Gunnlaugsson T, et al.
Tetrahedron Letters, 44(35), 6575-6578 (2003)
Electrochemical modification of single carbon nanotubes.
Steven Earl Kooi et al.
Angewandte Chemie (International ed. in English), 41(8), 1353-1355 (2002-04-15)
Balasubramanian K, et al.
Advanced Materials, 15(18), 1515-1518 (2003)
C B Carlson et al.
Bioorganic & medicinal chemistry letters, 10(17), 1979-1982 (2000-09-15)
The preparation of a novel acridine-based amino acid is reported. This N-Alloc-protected monomer can be coupled and deprotected under solid-phase peptide synthesis procedures to create acridine peptide conjugates as potential threading intercalators. A peptide containing this novel amino acid undergoes
Temperature-and light-responsive polyacrylamides prepared by a double polymer analogous reaction of activated ester polymers.
Jochum FD and Theato P.
Macromolecules, 42(16), 5941-5945 (2009)
View All Related Papers

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