129236-97-1 Usage
Description
1,4-Bis(decyloxy)benzene 98, also known as 1,4-di(decyloxy)benzene, is a chemical compound characterized by a benzene ring with two decyloxy groups attached at the 1 and 4 positions. 1 4-BIS(DECYLOXY)BENZENE 98 is notable for its high purity level of 98% and is recognized for its surfactant, dispersant, and intermediate properties in the production of various substances. Its ability to enhance the solubility and stability of other compounds, along with its surfactant and dispersant properties, makes it a valuable ingredient in the formulation of detergents, emulsifiers, and other industrial products. Furthermore, it finds applications in organic synthesis and materials science due to its unique chemical characteristics.
Uses
Used in Detergent Industry:
1,4-Bis(decyloxy)benzene 98 is used as a surfactant and dispersant for improving the solubility and stability of detergent formulations. Its properties contribute to the effectiveness of cleaning agents by reducing the surface tension of water, allowing it to mix with oil and dirt, thus facilitating their removal from various surfaces.
Used in Emulsifier Industry:
In the emulsifier industry, 1,4-bis(decyloxy)benzene 98 is utilized as a key component in the production of emulsifiers. It aids in the formation of stable emulsions by reducing the interfacial tension between two immiscible liquids, such as oil and water, enabling them to mix and remain stable for extended periods.
Used in Organic Synthesis:
1,4-Bis(decyloxy)benzene 98 serves as an intermediate in organic synthesis, where it is used to produce a variety of other chemical compounds. Its unique structure allows for further chemical reactions, leading to the creation of new substances with different properties and applications.
Used in Materials Science:
Within the field of materials science, 1,4-bis(decyloxy)benzene 98 is employed in the development and enhancement of various materials. Its chemical properties make it a useful additive in the formulation of materials with specific characteristics, such as improved solubility, stability, or other desired attributes.
Check Digit Verification of cas no
The CAS Registry Mumber 129236-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,3 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129236-97:
(8*1)+(7*2)+(6*9)+(5*2)+(4*3)+(3*6)+(2*9)+(1*7)=141
141 % 10 = 1
So 129236-97-1 is a valid CAS Registry Number.
129236-97-1Relevant articles and documents
Benzothiadiazole, hexylthiophen and alkoxy benzene based solution processable copolymer: Effect of the electron withdrawing substituents (fluorine atoms) on electrochemical, optical and electrochromic properties
Xu, Zhen,Du, Hongmei,Yin, Mengjie,Wang, Bozhen,Zhao, Jinsheng,Xie, Yu
, p. 1 - 9 (2018)
4,7-Bis(4-hexyl-5-(trimethylstannane) -2-thienyl) ?2,1,3-benzothiadiazole (HTBT) coupled with 2,5-bis (decyloxy)-1,4-dibromobenzene to afford the donor-π-bridge-donor-acceptor conjugated poly (4,7-bis (4-hexyl-2-thienyl) ?2,1,3-benzothiadiazole-co-p-didec
Synthesis and Properties of Triphenodioxazine-Based Conjugated Polymers for Polymer Solar Cells
Gong, Xiaohui,Han, Pei,Wen, Hui,Sun, Ying,Zhang, Xueqin,Yang, Hong,Lin, Baoping
, p. 3689 - 3698 (2017/07/22)
As a fused-ring conjugated unit, triphenodioxazine, has been applied in two series of thiophene-free conjugated polymers for polymer solar cells. The polymers were synthesized through a multi-step synthetic route, and the substituents had a great effect on the reactivity of the reactants. Relationships among the polymer structures as well as thermal, optical, and electrochemical properties were investigated in detail by experimental data analysis and theoretical simulation. The polymers possess highly planar backbones, broad Vis/NIR absorption bands, suitable frontier molecular orbital energies, and low band gaps ranging from 1.3 to 1.8 eV. The power conversion efficiencies of their photovoltaic devices are about 1 %. Introducing longer alkyl side chains into a polymer can bring about a better film-forming ability and improve the photovoltaic performance.
Aryl trihydroxyborate salts: Thermally unstable species with unusual gelation abilities
Moy, Cheryl L.,Kaliappan, Raja,McNeil, Anne J.
experimental part, p. 8501 - 8507 (2011/12/04)
A series of aryl trihydroxyborate salts were synthesized and found to form gels in benzene. The compounds were thermally unstable and readily underwent protodeboronation in solution and the solid state. Gelation could be induced without decomposition via sonication. Subsequent characterization studies revealed an unusual dependence of gel properties on alkyl chain length.
