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39905-46-9

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39905-46-9 Usage

General Description

p-Tetradecyloxyaniline is a chemical compound that belongs to the group of aromatic amines. It is an aniline derivative with a tetradecyloxy group attached to the para position of the aromatic ring. p-Tetradecyloxyaniline is commonly used in the production of organic pigments and dyes, as well as in the synthesis of pharmaceuticals and agrochemicals. p-Tetradecyloxyaniline is also known for its use as an intermediate in the production of various industrial chemicals and is considered to have low to moderate toxicity. However, caution should be taken when handling this chemical, as exposure to high concentrations may cause irritation to the skin and eyes. Additionally, it is important to follow proper safety procedures and protocols when working with p-Tetradecyloxyaniline.

Check Digit Verification of cas no

The CAS Registry Mumber 39905-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,0 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39905-46:
(7*3)+(6*9)+(5*9)+(4*0)+(3*5)+(2*4)+(1*6)=149
149 % 10 = 9
So 39905-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H35NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-18-22-20-16-14-19(21)15-17-20/h14-17H,2-13,18,21H2,1H3

39905-46-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tetradecoxyaniline

1.2 Other means of identification

Product number -
Other names 4-(tetradecyloxy)anilin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39905-46-9 SDS

39905-46-9Relevant articles and documents

Thermotropic Liquid-Crystalline and Light-Emitting Properties of Bis(4-aalkoxyphenyl) Viologen Bis(triflimide) Salts

Agra-Kooijman, De?a M.,Al-Karawi, Muhammed Kareem M.,Bhowmik, Pradip K.,Chang, Anthony,Chen, Si L.,Cortez, Raymond G.,Dizon, Erenz J.,Fisch, Michael R.,Gutierrez, Bryan,Han, Haesook,Ho, Andy,Killarney, Shane T.,Kim, Jongin,Kumar, Satyendra,Mandal, Hari D.,Mendez, Klarissa,Principe, Ronald Carlo G.,Sharpnack, Lewis

, (2020/05/29)

A series of bis(4-alkoxyphenyl) viologen bis(triflimide) salts with alkoxy chains of different lengths were synthesized by the metathesis reaction of respective bis(4-alkoxyphenyl) viologen dichloride salts, which were in turn prepared from the reaction of Zincke salt with the corresponding 4-n-alkoxyanilines, with lithium triflimide in methanol. Their chemical structures were characterized by 1H and 13C nuclear magnetic resonance spectra and elemental analysis. Their thermotropic liquid-crystalline (LC) properties were examined by differential scanning calorimetry, polarizing optical microscopy, and variable temperature X-ray diffraction. Salts with short length alkoxy chains had crystal-to-liquid transitions. Salts of intermediate length alkoxy chains showed both crystal-to-smectic A (SmA) transitions, Tms, and SmA-to-isotropic transitions, Tis. Those with longer length of alkoxy chains had relatively low Tms at which they formed the SmA phases that persisted up to the decomposition at high temperatures. As expected, all of them had excellent thermal stabilities in the temperature range of 330-370 ?C. Their light-emitting properties in methanol were also included.

Structurally simple trimesic amides as highly selective anion channels

Yuan, Lin,Shen, Jie,Ye, Ruijuan,Chen, Feng,Zeng, Huaqiang

, p. 4797 - 4800 (2019/05/02)

Trimesic amide molecules, which contain simple alkyl chains in their periphery, exhibit interesting anion-transport functions. The most active and highly selective channel TA12 efficiently transports ClO4? anions across membranes, with other anions conducted in the order of I? > NO3? > Br? > Cl?.

Luminescent mesogenic borondifluoride complexes with the Schiff bases containing salicylideneamines and β-enaminoketones core systems

Lei, Zih-Yang,Lee, Gene-Hsiang,Lai, Chung K.

, p. 44 - 56 (2018/04/02)

Three new families of borondifluoride complexes 1a–c derived from salicylideneamines 2a and β-enaminoketonates 2b–c were reported, and their mesomorphic and optical properties were also investigated. One single crystal and molecular structure of nonmesogenic BF2 complex 1c (n = 10) was resolved and the geometry of the central boron atom was tetrahedron. A larger dihedral angle of 81.3° between the two phenyl rings observed in crystal lattice was attributed to the lack of liquid crystallinity. Boron complexes 1a formed monotropic SmA phases, while boron complexes 1b exhibited enantiotropic SmC mesophases. The optical property of the boron complexes was dependent on their molecular structures, and they emitted a blue–to–green emission at λmax = 476–541 nm in the solution and 488–550 nm in the solid state. This is the first group of mesogenic BF2 complexes with the Schiff bases derived from respective salicylideneamines and β-enaminoketones.

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