61168-09-0

Basic information

• Product Name: 4-(DIMETHYLAMINO) CYCLOHEXANOL
• Synonyms: 4-(DIMETHYLAMINO) CYCLOHEXANOL;4-(dimethylamino)cyclohexan-1-ol
• CAS NO: 61168-09-0
• Molecular Formula: C₈H₁₇NO
• Molecular Weight: 143.22668
• Mol File: 61168-09-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 216.4 °C at 760 mmHg
• Flash Point: 86.1 °C
• Appearance: /
• Density: 0.97 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(DIMETHYLAMINO) CYCLOHEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(DIMETHYLAMINO) CYCLOHEXANOL(61168-09-0)
• EPA Substance Registry System: 4-(DIMETHYLAMINO) CYCLOHEXANOL(61168-09-0)

Safety Data

• Hazardous Substances Data: 61168-09-0(Hazardous Substances Data)

Usage

General Description

4-(Dimethylamino) cyclohexanol, also known as DMAC, is a chemical compound with the molecular formula C10H21NO. It is a cyclic amine and alcohol derivative with a dimethylamino group attached to the cyclohexane ring. DMAC is commonly used as a solvent in various industrial applications, including the production of polyurethanes, adhesives, and coatings. It is also used as a reagent in organic synthesis and as a precursor for the synthesis of pharmaceuticals and agrochemicals. DMAC exhibits both acidic and basic properties and is known for its ability to dissolve a wide range of organic compounds. It is considered a hazardous material and should be handled with care due to its potential health and environmental hazards.

Upstream product

• 619-60-3 4-(N,N-dimethylamino)phenol 
• 7732-18-5 water 
• 50-00-0 formaldehyd 
• 6850-65-3 p-hydroxycyclohexylamine 
• 23363-88-4 trans-N-acetyl-4-hydroxycyclohexylamine 

Downstream Products

• 1396316-15-6 N,N,N-trimethyl-4-(thiophen-3-ylmethylene)cyclohexanaminium bromide 
• 40594-34-1 4-(dimethylamino)cyclohexanone 

Relevant articles and documents

A novel polythiophene derivative as a sensitive colorimetric and fluorescent sensor for anionic surfactants in water

A novel cationic polythiophene derivative, poly[N,N,N-trimethyl-4- (thiophen-3-ylmethylene)cyclohexanaminium chloride] (PTCA-Cl), has been prepared successfully and applied as a colorimetric and fluorometric probe for the detection of anionic surfactants. In particular, a new method for the polymerization of cationic polythiophene derivatives is found, which has not been reported previously. The colorimetric and fluorescent response of PTCA-Cl to anionic surfactants have been investigated by absorption and emission spectroscopy. The sensing interaction can be apparently observed by the naked eye, which presents a great advantage for its practical applications. Moreover, the sensor (PTCA-Cl) shows high selectivity towards anionic surfactants in the presence of other negatively charged analytes, as well as high sensitivity with a detection limit at 10-9 M by using fluorimetry, which is the lowest ever achieved among all synthetic anionic surfactants sensors available. Therefore, the water soluble polythiophene derivative can be applied as a colorimetric and fluorescent probe for the detection of anionic surfactants with high selectivity and sensitivity.