179341-69-6

Basic information

• Product Name: 4-N-DODECYLOXYBENZAMIDE
• Synonyms: 4-N-DODECYLOXYBENZAMIDE;4-DODECYLOXYBENZAMIDE
• CAS NO: 179341-69-6
• Molecular Formula: C₁₉H₃₁NO₂
• Molecular Weight: 305.45
• Product Categories: Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates
• Mol File: 179341-69-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 441.6 °C at 760 mmHg
• Flash Point: 140.1 °C
• Appearance: /
• Density: 0.973 g/cm³
• Vapor Pressure: 5.38E-08mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: 4-N-DODECYLOXYBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-N-DODECYLOXYBENZAMIDE(179341-69-6)
• EPA Substance Registry System: 4-N-DODECYLOXYBENZAMIDE(179341-69-6)

Safety Data

• Hazardous Substances Data: 179341-69-6(Hazardous Substances Data)

Usage

General Description

4-N-dodecyloxybenzamide is a chemical compound with the molecular formula C20H29NO2. It is a long-chain alkyl benzamide, with a dodecyl (C12) group attached to the benzene ring. 4-N-DODECYLOXYBENZAMIDE is used as a surfactant, emulsifier, and dispersing agent in various industrial and cosmetic applications. It is also used as a corrosion inhibitor and lubricant additive. 4-N-dodecyloxybenzamide has surfactant properties due to the presence of the dodecyl chain, making it an effective dispersing agent in applications such as polymer production, paints, adhesives, and personal care products. Due to its emulsifying properties, it is also used in the formulation of creams and lotions. Additionally, it is used as a lubricant additive to improve the performance and stability of industrial oils.

InChI:InChI=1/C19H31NO2/c1-2-3-4-5-6-7-8-9-10-11-16-22-18-14-12-17(13-15-18)19(20)21/h12-15H,2-11,16H2,1H3,(H2,20,21)

Upstream product

• 619-57-8 p-hydroxybenzamide 
• 143-15-7 1-dodecylbromide 
• 24083-19-0 4-n-dodecyloxybenzaldehyde 
• 29147-92-0 4-(dodecyloxy)benzonitrile 
• 4292-19-7 1-Iodododecane 
• 767-00-0 4-cyanophenol 

Downstream Products

• 65039-19-2 4-(dodecyloxy)aniline 

Relevant articles and documents

Photoresponsive behavior of hydrophilic/hydrophobic-based novel azobenzene mesogens: Synthesis, characterization and their application in optical storage devices

Three series of alkoxy chain-bearing azobenzene-derived quaternary ammonium iodides with an alkoxy chain at one end, namely N,N-diethanol-6-(4-((4′-alkyloxyphenyl)diazenyl)phenoxy)hexan-1-ammonium iodides, N-ethyl-N-ethanol-6-(4-((4′-alkyloxyphenyl)diazenyl)phenoxy)hexan-1-ammonium iodides and N,N-diethyl-6-(4-((4′-alkyloxyphenyl)diazenyl)phenoxy)hexan-1-ammonium iodides were synthesized and characterized. Their mesomorphic and photoswitching properties were examined via polarising optical microscopy (POM), differential scanning calorimetry (DSC) and UV-vis spectrophotometry. The liquid crystalline tilted schlieren texture of smectic C, non-tilted natural focal conic texture of smectic A and smectic B phases were observed in the N,N-diethanol- and N-ethyl-N-ethanol-bearing ammonium group substituted at the terminal via the alkoxy chain of the azo moiety. In these azo moieties, the equilibrium time for trans-cis isomerization was about 1 min and cis-trans isomerization occurred at around 590 min, which had the highest alkoxy chain and no hydroxyl group on their head group. The absence of a hydroxyl group on the terminal head group resulted in slow thermal back relaxation, whereas the hydroxyl group-bearing head group showed fast thermal back relaxation. These results suggest that the influence of the substituent on the cationic ammonium head group and alkoxy chain length on the photoisomerization of the azo compounds is vital for optical storage devices. Furthermore, the device fabricated using these materials demonstrated that they are excellent candidates for optical image storage applications.

Utilization of evaporation during the crystallization process: Self-templation of organic parallelogrammatic pipes

Analogues of 4-dodecyloxy-2-trifluoromethylbenzamide (12FH2) consisting of a hydrophobic alkyl chain, a trifluoromethylated aromatic ring, and a self-complementary hydrogenbonding amido group were synthesized, and the structural effect of each component o

Naphthyridine-based helical foldamers and macrocycles: Synthesis, cation binding, and supramolecular assemblies

(Figure Presented) Unraveling the factors that control the conformation of molecular chains is of great interest both for understanding the shape of biological molecular strands and for designing artificial ones that adopt desired forms. Thus, a variety of artificial folding codons have been identified that enforce the formation, among others, of helices, strands, and loops, the major emphasis being on the shape of the foldamer. We report herein the synthesis and study of a family of foldamers and macrocycles based on the 1,8-naphthyridine and pyrimidine units, whose internal cavity is large enough to accommodate ionic substrates, and focus on the impact of guest binding within a cylindrical environment. Interestingly, the binding event within these large oligomers is translated to the outside of the receptors and affects the interaction of the overall complexes with the outside world. For instance, alkali cations bind to the one-turn helices and macrocycles to promote fibril formation and aggregation. Also, polyammonium substrates are able to tune the length of the overall helix assemblies and the rigidity of long oligomers. The reported data on one-turn, two-turn helices and macrocycles not only allows one to devise a model for the ion-controlled supramolecular assembly of such systems but also provides evidence that such controlled scaffolds bear promise in the design of complex systems.