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

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

Uses

Used in Dye Production:
2,6-Bis(dodecyloxy)benzaldehyde is used as a precursor in the synthesis of dyes, contributing to the creation of various colorants for different applications.
Used in Perfumery:
2,6-Bis(dodecyloxy)benzaldehyde is used as a fragrance ingredient in perfumes, taking advantage of its strong odorous properties to enhance the scent of various products.
Used in Aromatic Compounds Synthesis:
2,6-Bis(dodecyloxy)benzaldehyde is used as a building block in the production of other aromatic compounds, which are essential in the flavor and fragrance industry.
Used in Liquid Crystal Synthesis:
2,6-Bis(dodecyloxy)benzaldehyde is used as a starting material in the synthesis of liquid crystals, which have potential applications in display technologies and other specialized fields.
Used in Surfactant Production:
2,6-Bis(dodecyloxy)benzaldehyde is used as a component in the manufacturing of surfactants, which are utilized in various industrial processes to reduce surface tension between liquids and solids.
Used in Scent Manufacturing:
2,6-Bis(dodecyloxy)benzaldehyde is used as a key ingredient in the production of scented products, leveraging its strong aromatic properties to create appealing fragrances for consumer goods.

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.

Zinc porphyrins with a pyridine-ring-anchoring group for dye-sensitized solar cells

Anchoring groups are extremely important in controlling the performance of dye-sensitized solar cells (DSCs). The design and characterization of sensitizers with new anchoring groups, in particular non-carboxylic acid groups, has become a recent focus of DSC research. Herein, new donor-p-acceptor zinc-porphyrin dyes with a pyridine ring as an anchoring group have been designed and synthesized for applications in DSCs. Photophysical and electrochemical investigations demonstrated that the pyridine ring worked effectively as an anchoring group for the porphyrin sensitizers. DSCs that were based on these new porphyrins showed an overall powerconversion efficiency of about 4.0% under full sunlight (AM 1.5G, 100 mWcm-2).

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.

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 cm2 than Dye I with a 2-(phenylethynyl)thiophene (PCE = 3.5%) anchored through a cyanoacrylic group.

Dye sensitized solar cells: TiO2 sensitization with a bodipy-porphyrin antenna system

A zinc porphyrin derivative (2) and zinc porphyrin-bodipy dyad (3) have been prepared and applied to dye-sensitized solar cells (DSSCs). On the basis of absorption and fluorescence excitation spectra, dyad 3 efficiently transfers energy from the bodipy to zinc porphyrin constituent. The 3-sensitized solar cell demonstrates higher solar spectral coverage, based on incident photon to current efficiency (IPCE) spectra, and an improved power conversion efficiency (η = 1.55%) compared to that of the 2-sensitized cell (η = 0.84%). The better performance of the 3-sensitized cell is attributed largely to the gain in spectral absorbance provided by the bodipy constituent of 3. Also evident, however, are secondary effects reflecting (a) fill-factor improvement and (b) a slight gain in porphyrin red-edge absorbance due to bodipy-conjugate formation.