54890-03-8

Basic information

• Product Name: Cyclohexanedodecol
• Synonyms: Cyclohexanedodecol
• CAS NO: 54890-03-8
• Molecular Formula: C₆H₁₂O₁₂
• Molecular Weight: 276.1523
• Mol File: 54890-03-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 137.4°Cat760mmHg
• Flash Point: 32°C
• Appearance: /
• Density: 4.535g/cm³
• Vapor Pressure: 2.98mmHg at 25°C
• Refractive Index: 3.229
• PKA: 9.06±0.70(Predicted)
• CAS DataBase Reference: Cyclohexanedodecol(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanedodecol(54890-03-8)
• EPA Substance Registry System: Cyclohexanedodecol(54890-03-8)

Safety Data

• Hazardous Substances Data: 54890-03-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H12O12/c7-1(8)2(9,10)4(13,14)6(17,18)5(15,16)3(1,11)12/h7-18H

Upstream product

• 319-89-1 tetrahydroxy-1,4-quinone 
• 7697-37-2 nitric acid 
• 7782-50-5 chlorine 
• 608-80-0 benzenehexol 
• 118-76-3 rhodizonic acid 
• 925665-97-0 hexa-O-nitro-myo-inositol 
• 527-31-1 hexaketocyclohexane 

Downstream Products

• 608-80-0 benzenehexol 
• 118-76-3 rhodizonic acid 
• 124-38-9 carbon dioxide 

Relevant articles and documents

Highly conductive PEDOT:PSS films prepared through a treatment with geminal diols or amphiphilic fluoro compounds

Poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films with high conductivity can have important application as the transparent electrode of optoelectronic devices. In this paper, we report the significant conductivity enhancement of PEDOT:PSS through a treatment with germinal diols which have two hydroxyl groups connected to one carbon atom or amphiphilic fluoro compounds which have hydrophobic fluorocarbon groups and hydrophilic hydroxyl or carboxylic groups. Several compounds, including hexafluoroacetone, cyclohexanehexone, formaldehyde, acetaldehyde, and perfluorobenzophenone, which could convert into geminal diols, were used to treat PEDOT:PSS films. The conductivity enhancements are generally consistent with the equilibrium constants for the conversion of these compounds into geminal diols. PEDOT:PSS films were also treated with several amphiphilic fluoro compounds. The conductivity was significantly enhanced when PEDOT:PSS films were treated with hexafluoroisopropanol, trifluoroacetic acid and heptafluorobutyric acid, while it hardly changed when they were treated with 2,2,2-trifluoroethanol. Conductivities of more than 1000 S cm-1 were observed on the treated PEDOT:PSS films. The mechanism for the conductivity enhancement of PEDOT:PSS through the treatment with geminal diols or amphiphilic fluoro compounds is attributed to the phase segregation of PSSH from PEDOT:PSS and conformational change of the PEDOT chains as the results of the compounds-induced reduction in the Coulombic attraction between the positively charged PEDOT and negatively charged PSS chains.