141676-54-2

Usage

Uses

Used in Dye and Pigment Production:
p-Undecyloxyaniline is used as a key intermediate in the synthesis of dyes and pigments, contributing to the coloration and stability of these products.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, p-Undecyloxyaniline serves as an intermediate in the organic synthesis of various medicinal compounds, playing a crucial role in drug development and production.
Used in Polymer and Coating Industries:
p-Undecyloxyaniline is utilized in the manufacturing of polymers and coatings, enhancing their properties and performance in various applications.
Used as a Corrosion Inhibitor:
In industrial settings, p-Undecyloxyaniline functions as a corrosion inhibitor, protecting materials from degradation and extending their lifespan.
Used as an Antistatic Agent:
p-Undecyloxyaniline is also employed as an antistatic agent, helping to reduce the buildup of static electricity in various industrial applications, thereby improving safety and product quality.

InChI:InChI=1/C17H29NO/c1-2-3-4-5-6-7-8-9-10-15-19-17-13-11-16(18)12-14-17/h11-14H,2-10,15,18H2,1H3

Upstream product

• 87960-81-4 NB-11 
• 100-02-7 4-nitro-phenol 
• 103-90-2 4-acetaminophenol 
• 693-67-4 bromoundecane 

Downstream Products

• 124368-95-2 4-(heptyloxy)-N-(C₆H₄OC₁₁H₂₃)benzaldimine-2-ol 
• 87739-51-3 6,6-Dimethyl-1-(4-undecyloxy-phenyl)-1,6-dihydro-[1,3,5]triazine-2,4-diamine; hydrochloride 
• 1256341-27-1 C₂₅H₃₃NO₄ 

Relevant academic research and scientific papers

Mesogenicity of organophosphazenes: The effect of phosphazene rings and side groups on the phase transition

Cyclotriphosphazene and cyclotetraphosphazene derivatives with mesogenic 4-N-(4-alkoxyphenyl)iminomethyl)phenoxy and 4-(4′-alkoxy) biphenoxy moieties were synthesized. Schiff base moiety has higher mesomorphic stability than that in biphenyl moiety both in cyclotriphosphazene and cyclotetraphosphazene. Cyclotriphosphazenes possess higher thermal stability in the mesomorphic phase than the cyclotetraphosphazenes, suggesting the difference in the molecular structure.

Heterolithic azobenzene-containing supermolecular tripedal liquid crystals self-organizing into highly segregated bilayered smectic phases

Synthesis, self-organization, and optical properties of supermolecular tripedal liquid crystals incorporating various prototypical mesogenic units such as alkoxy-azobenzene (AZB), alkoxy-biphenylene (BPH) or alkoxy-cyanobiphenyl (OCB) derivatives are repo

Electro-optical switching studies on 1,3-phenylene based banana shaped liquid crystals

This work deals with the study of the thermotropic liquid crystalline properties of new asymmetric bent core liquid crystals. The thermotropic properties was analyzed by polarized optical microscopy, differential scanning calorimetric analysis and variable temperature X-ray diffraction measurements. Effect of equal terminal chain with asymmetric bent core system on mesomorphic behavior was examined. The shorter methyl chain compound 10a of exhibits B 1 mesophase and higher homologs (10b and 10c) shows antiferroelectric B2 mesophases, which was studied by electro-optical measurements.

Synthesis and biological evaluation of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as PTP1B inhibitors

Based on the fact that petroselinic acid showed good inhibitory activity (IC50=6.99μmol/L) against protein tyrosine phophatase 1B(PTP1B) in vitro, a series of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives were designed and synthesized. The results indicated that most of the derivatives showed more potent activities against PTP1B. Especially, compound 13 had obvious activity with an IC50 of 106nmol/L in vitro.

Synthesis of symmetric liquid crystal dimers based on azo and imine groups and investigation of phase behaviour by varying alkoxy terminal chain length

With the objective to study the effect of alkoxy terminal chain length on mesomorphic properties of liquid crystals, we have synthesized two (Azo and Imine) different series of dimesogens by varying terminal alkoxy chain length (n = 6-12) with a short spacer unit in between two mesogens. Transition temperatures and phase characterization were studied by DSC, POM and XRD analysis. It was found that all the dimers show mesomorphic properties and the change in terminal alkoxy chain length has pronounced effect on the smectic phase window. In the DSC cooling scan, the smectic phase window of azo compounds increased from 6.4°C (2A6) to 16.0°C(2A12), whereas in Schiff base compounds, it increased from 9.2°C (2S6) to 31.0°C(2S12). Further, the 2A11 dimer was found to undergo photo induced configurational changes.

Synthesis and liquid crystalline properties of novel triazene-1-oxide derivatives

A new group of compounds, C6H5-N(O)=N-NH-C6H4-C(O)-O-C6H4-CH=N-C6H4-OR, (1), [R=n-alkyl group; 1a (R=C7H15 ) to 1h (R=C14H29)], has been designed and synthesized to develop triazene-1-oxide based liquid crystals. All the compounds have been characterized on the basis of their spectral data. Their thermal behavior has been examined and found to exhibit thermotropic liquid crystalline behavior over a wide range of temperature. All members of this family uniformly show nematic phase behavior on melting up to the clearing point during heating as well as on phase entering up to the solidification during cooling. An odd-even effect on transition temperatures has been observed during heating as well as cooling.