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About This Item
Linear Formula:
CH3(CH2)5C6H4NH2
CAS Number:
Molecular Weight:
177.29
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
grade
technical grade
Assay
90%
form
liquid
refractive index
n20/D 1.525 (lit.)
bp
279-285 °C (lit.)
density
0.919 g/mL at 25 °C (lit.)
SMILES string
CCCCCCc1ccc(N)cc1
InChI
1S/C12H19N/c1-2-3-4-5-6-11-7-9-12(13)10-8-11/h7-10H,2-6,13H2,1H3
InChI key
OVEMTTZEBOCJDV-UHFFFAOYSA-N
General description
4-Hexylaniline reacts with isatin (1H-indole-2,3-dione) to form Schiff base ligand (HL). Mesomorphic properties of imine compounds derived from 4-hexylaniline has been investigated using polarised light optical microscopy and differential scanning calorimetry.
Application
4-Hexylaniline has been used in the preparation of stable ruthenium nanoparticles.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 1
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Liquid crystals based on semiperfluorinated imines and salicylaldimato metal complexes. A comparative study of alkyl, alkoxy and polyether substituents.
Bilgin-Eran B, et al.
Journal of Materials Chemistry, 17(22), 2319-2328 (2007)
Solid-state electronic conductivity of ruthenium nanoparticles passivated by metal-carbon covalent bonds.
Ghosh D and Chen S.
Chemical Physics Letters, 465(1), 115-119 (2008)
Novel Isatin-Schiff Base Cu (H) and Ni (H) Complexes. X-ray Crystal Structure of Bis [3-(4-hexylphenylimino)-1H-indol-2 (3H)-one]-dichlorocopper (H) Complex.
Ercag A, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 17(2) (2006)
Kyle A Brown et al.
Nature methods, 16(5), 417-420 (2019-04-17)
We report the identification of a photocleavable anionic surfactant, 4-hexylphenylazosulfonate (Azo), which can be rapidly degraded by ultraviolet irradiation, for top-down proteomics. Azo can effectively solubilize proteins with performance comparable to that of sodium dodecyl sulfate (SDS) and is compatible
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