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233560

Sigma-Aldrich

4-Hexadecylaniline

97%

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About This Item

Fórmula linear:
CH3(CH2)15C6H4NH2
Número CAS:
79098-13-8
Peso molecular:
317.55
Número MDL:
MFCD00007920
Código UNSPSC:
12352100
ID de substância PubChem:
24853983
NACRES:
NA.22

Ensaio

97%

p.e.

254-255 °C/15 mmHg (lit.)

pf

53-56 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCCCCCCCCc1ccc(N)cc1

InChI

1S/C22H39N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-17-19-22(23)20-18-21/h17-20H,2-16,23H2,1H3

chave InChI

RBCCQATUVPNPGQ-UHFFFAOYSA-N

Aplicação

4-Hexadecylaniline has been used:
  • in simple solution based method for the gold (Au) metallization of DNA resulting in a Au nanowire network
  • in fabrication of hybrid organized molecular films by Langmuir-Blodgett (LB) technique and their photoluminescent properties has been investigated
  • in seed mediated synthesis of anisotropic rod shaped gold nanoparticles in organic media

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
10720HR
07520KQ
11723LG
09818BI

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S Prathap Chandran et al.
Journal of nanoscience and nanotechnology, 7(8), 2808-2817 (2007-08-10)
A seed mediated approach for the synthesis of anisotropic rod shaped gold nanoparticles in organic media (toluene) is demonstrated. Pre-formed gold nanoparticles stabilized in toluene by 4-hexadecylaniline (HDA) are used as seeds. These when reacted with 1-octadecylamine (ODA) hydrophobised chloroaurate
Marlene Costa et al.
Journal of the science of food and agriculture, 97(2), 564-571 (2016-04-22)
The relationships between the hydrophilic-lipophilic balance (HLB) of antioxidants (AOs) and their distributions and efficiencies in emulsions are not fully understood. Recent reports indicate that, for series of homologous antioxidants of different hydrophobicity, the variation of their efficiency with the
Min Jiang et al.
Journal of colloid and interface science, 316(1), 100-106 (2007-09-04)
Hybrid organized molecular films composed of a polyoxometalate, decatungsteuropate (EuW(10)), and amphiphiles such as hexadecyltrimethylammonium bromide (CTAB), n-octadecylamine (ODA) and 4-hexadecylaniline (HDA) were fabricated by Langmuir-Blodgett (LB) technique and their photoluminescent properties were investigated. The hybrid films, which were formed
Mafalda Meireles et al.
Journal of the science of food and agriculture, 99(8), 3917-3925 (2019-01-31)
Controlling the interfacial concentrations of antioxidants (AOs) in oil-in-water emulsions can be regarded as a unique approach for increasing the efficiency of AOs in inhibiting the oxidation of lipids. Classical methods to determine the AO distribution in binary systems cannot
J Freiría-Gándara et al.
Food & function, 9(8), 4429-4442 (2018-08-03)
The antioxidant (AO) efficiencies and the distributions of gallic acid (GA) and a series of alkyl gallates (propyl, PG, butyl, BG, octyl, OG and lauryl, LG) were determined in intact fish oil-in-water emulsions. The efficiency of the AOs in inhibiting
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