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233552

Sigma-Aldrich

4-Tetradecylaniline

97%

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About This Item

Fórmula lineal:
CH3(CH2)13C6H4NH2
Número de CAS:
91323-12-5
Peso molecular:
289.50
MDL number:
MFCD00009804
UNSPSC Code:
12352100
PubChem Substance ID:
24853982
NACRES:
NA.22

assay

97%

form

solid

mp

46-49 °C (lit.)

SMILES string

CCCCCCCCCCCCCCc1ccc(N)cc1

InChI

1S/C20H35N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-19-15-17-20(21)18-16-19/h15-18H,2-14,21H2,1H3

InChI key

WKYFQPQIOXXPGE-UHFFFAOYSA-N

Categorías relacionadas

Application

4-Tetradecylaniline has been used:
  • as standard during the quantitative determination of trans content of fats and oils and margarine by FTIR spectroscopy
  • to investigate the quenching of the triplet state of n-alkyl 3-nitrophenyl ethers in aqueous micellar sodium dodecyl sulfate (SDS) solutions by laser flash photolysis
  • in amidation and esterification of oxidised single-walled carbon nanotubes (SWCNTs)

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKBL2503V
MKBH6668V
37298PJ
13514TE
14822EO

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Prabhpreet Singh et al.
Chemical Society reviews, 38(8), 2214-2230 (2009-07-23)
Since carbon nanotubes (CNTs) display unique structures and remarkable physical properties, a variety of applications have emerged in both materials and life sciences. In terms of applications, the functionalisation of nanotubes is extremely important, as it increases their solubility and
Trans fatty acid determination in fats and margarine by fourier transform infrared spectroscopy using a disposable infrared card.
Ma K, et al.
Journal of the American Oil Chemists' Society, 76(12), 1399-1404 (1999)
Photoreactions of n-alkyl-3-nitrophenyl ethers with aromatic amines in SDS micelles: A laser flash photolysis study.
Rigoli IC, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 222(1), 34-39 (2011)
Kristiana T Santoso et al.
Bioorganic & medicinal chemistry, 27(16), 3532-3545 (2019-07-03)
A library of thirty-two quinolinequinones (QQs) with various amine substituents at the 6- and 7-positions were synthesised efficiently and in good yields for evaluation as potential anti-tuberculosis agents. Mycobacterium tuberculosis growth inhibition assays demonstrated that QQs bearing moderate length alkyl

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