1198467-57-0

Basic information

• Product Name: 2,6-bis(dodecyloxy)benzaldehyde
• Synonyms: 2,6-bis(dodecyloxy)benzaldehyde;2,6-di(dodecyloxy)benzaldehyde
• CAS NO: 1198467-57-0
• Molecular Formula: C₃₁H₅₄O₃
• Molecular Weight: 474.75866
• EINECS: -0
• Mol File: 1198467-57-0.mol
• Article Data: 6

Chemical Properties

• Appearance: Pale yellow/Solid
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2,6-bis(dodecyloxy)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-bis(dodecyloxy)benzaldehyde(1198467-57-0)
• EPA Substance Registry System: 2,6-bis(dodecyloxy)benzaldehyde(1198467-57-0)

Safety Data

• Hazardous Substances Data: 1198467-57-0(Hazardous Substances Data)

Usage

General Description

2,6-Bis(dodecyloxy)benzaldehyde is a chemical compound that consists of a benzene ring with two dodecyloxy (C12H25O) groups attached to the 2 and 6 positions and an aldehyde functional group (CHO) attached to the 1 position. It is commonly used in the production of various products such as dyes, perfumes, and other aromatic compounds. This chemical is a pale yellow solid at room temperature, and it is insoluble in water but soluble in organic solvents. It is also known for its strong odorous properties and is often used in the manufacturing of scented products. Additionally, it has been studied for its potential application in the synthesis of liquid crystals and as a surfactant in various industrial processes.

Upstream product

• 41662-92-4 1,3-bis(dodecyloxy)benzene 
• 68-12-2 N,N-dimethyl-formamide 
• 4292-19-7 1-Iodododecane 
• 143-15-7 1-dodecylbromide 
• 108-46-3 recorcinol 

Downstream Products

• 1198467-58-1 meso-(2,6-di(dodecyloxy)phenyl)dipyrromethane 

Relevant articles and documents

Zinc and linkage effects of novel porphyrin-containing polyimides on resistor memory behaviors

A new class of porphyrin-containing polyimides, ZnPor-s-DSDA, ZnPor-t-DSDA, Por-s-DSDA and Por-t-DSDA, were synthesized from porphyrin-containing diamines and 3,3′,4,4′-diphenylsulfone tetracarboxylic dianhydride for resistor-type memory applications. The effect of the linkage and zinc metal was investigated by electrochemistry, molecular simulations, and memory behaviors. The memory devices with different retention times derived from polymers ZnPor-s-DSDA (WORM, >3 h) and ZnPor-t-DSDA (DRAM, 30 s) demonstrated the importance of the linkage effect, and the insulation property of polyimides Por-s-DSDA and Por-t-DSDA also implies a crucial memory behavior by metal chelation.

Fluorous hydrophobic fluorescent (E)-Stilbene derivatives for application on security paper

(E)-Stilbene hydrophobic fluorophores possessing long perfluorinated or hydrocarbonated chains have been prepared through a stereoselective Wittig-Schlosser reaction. When covalently grafted upon paper, they give rise to a fluorescent-labeled paper upon i

Novel π-extended porphyrin derivatives for use in dye-sensitized solar cells

Two novel donor-π-acceptor (D-π-A type) porphyrin dyes were successfully synthesized and use in a dye-sensitized solar cell (DSSC). The molecular structures of both porphyrins are composed of the same dialkyl-substituted diphenylamino unit acting as the donor part, and two bisalkoxyphenyl substituents at the 5,15-meso positions. The acceptor part is composed of different ethyne-linked π-extended bridges, and a cyanoacrylic acid (Dye I) or carboxyphenyl (Dye II) moiety acting as anchoring groups. In order to investigate the effects of including the π-extended bridge between the porphyrin and acceptor unit, two different π-extended bridges such as 2,2′-bithiophene and 2-(phenylethynyl)-thiophene, were employed. In particular, Dye II contains two triple bonds between donor substituted porphyrin and carboxylic acid group. These modifications could potentially reduce dye aggregation on the TiO2 surface. The charge recombination resistance and diffusion length for the cells with Dye II were relatively higher for all the measured ranges of bias potentials, implying that electron recombination loss from injected electrons was highly suppressed when Dye II molecules were adsorbed on the TiO2 surface. Eventually, Dye II containing a 2,2′-bithiophene π-spacer and anchored trough a carboxyphenyl group exhibited a superior power conversion efficiency of 6.7% under AM 1.5 illumination (100 mW.cm-2) in a photoactive area of 0.46 cm 2 than Dye I with a 2-(phenylethynyl)thiophene (PCE = 3.5%) anchored through a cyanoacrylic group.