70568-60-4

Basic information

• Product Name: 4-BUTYLCYCLOHEXANOL
• Synonyms: 4-BUTYLCYCLOHEXANOL;4-N-BUTYLCYCLOHEXANOL;4-n-Butylcyclohexanol (cis- and trans- mixture);4-N-BUTYLCYCLOHEXANOL (CIS+TRANS);4-N-BUTYLCYCLOHEXANOL (CIS- AND TRANS- MIXTURE) 98+%;4-Butylcyclohexanol (cis- and trans- mixture);4-Butylcyclohexanol (cis- and trans- mixture)
• CAS NO: 70568-60-4
• Molecular Formula: C₁₀H₂₀O
• Molecular Weight: 156.27
• Mol File: 70568-60-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 83 °C
• Boiling Point: 122 °C / 15mmHg
• Flash Point: 87.9 °C
• Appearance: /
• Density: 0.91
• Vapor Pressure: 0.0276mmHg at 25°C
• Refractive Index: 1.4630-1.4670
• PKA: 15.32±0.40(Predicted)
• CAS DataBase Reference: 4-BUTYLCYCLOHEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BUTYLCYCLOHEXANOL(70568-60-4)
• EPA Substance Registry System: 4-BUTYLCYCLOHEXANOL(70568-60-4)

Safety Data

• Hazardous Substances Data: 70568-60-4(Hazardous Substances Data)

Usage

General Description

4-Butylcyclohexanol is a chemical compound with the molecular formula C10H20O. It is a colorless liquid with a floral odor and is used as a fragrance ingredient in various personal care and cosmetic products. 4-Butylcyclohexanol is also utilized in the production of flavors and fragrances, as well as in the synthesis of other organic compounds. It is synthesized through the reduction of 4-butylcyclohexanone and is known to have low acute toxicity. However, prolonged or repeated exposure to 4-butylcyclohexanol may cause irritation to the skin, eyes, and respiratory system. This chemical is also known to biodegrade easily and poses minimal risk to the environment.

InChI:InChI=1/C10H20O/c1-2-3-4-9-5-7-10(11)8-6-9/h9-11H,2-8H2,1H3

Upstream product

• 1009-11-6 1-(4-hydroxyphenyl)-butan-1-one 
• 61203-82-5 4-butylcyclohexanone 
• 4731-84-4 1,1-bis(4-hydroxyphenyl)-n-butane 
• 108-95-2 phenol 

Downstream Products

• 106148-88-3 p-(1-butylcyclohexyl)benzoic acid 
• 67861-29-4 4-(4-butyl-cyclohex-1-enyl)-morpholine 
• 1383149-15-2 C₂₃H₃₈O₂ 
• 1226494-73-0 (R)-4-(6-(4-butylcyclohexyl)oxynaphthalen-2-yl)-4-methyloxazolidin-2-one 
• 132310-87-3 2-(4-Butyl-cyclohexyl)-propane-1,3-diol 
• 132310-87-3 2-(trans-4-butylcyclohexyl)-1,3-propanediol 
• 67590-13-0 trans-4-n-Butyl-cyclohexanol 
• 61203-82-5 4-butylcyclohexanone 
• 106148-84-9 p-(1-butylcyclohexyl)toluene 
• 179245-36-4 1-Bromo-4-butyl-cyclohexane 
• 81978-13-4 7-Butyl-9,10-dihydro-phenanthrene-2-carboxylic acid 4-butyl-cyclohexyl ester 
• 133883-36-0 4-(5-Hexyl-pyrimidin-2-yl)-benzoic acid 4-butyl-cyclohexyl ester 

Relevant articles and documents

Aliphatic Liquid Crystals, 2. Some Nematic Derivatives of all-trans-Perhydrophenanthrene

A stereoselective synthesis of the all-trans-7-alkylperhydro-2-phenanthrenols 15a-f in 11 steps and 28 liquid crystalline esters 16 of 15a-f are described, additionally some further derivatives of 7-alkylperhydro-2-phenanthrenol.An X-ray structure analysis of ester 16ec is reported.

ENZYMATIC "IN VITRO" REDUCTIONS OF KETONES. PART 12. REDUCTION OF 1-ALKYL-4-PIPERIDONES IN AN ETHANOL-NAD+-HLAD-SYSTEM.

The steady state initial rate equation for a ketone-ethanol-NAD+-HLAD recycling system is checked for 1-n-butyl-4-piperidone.All reaction parameters are discussed in order to optimize the reduction of this substrate.For a series of 1-alkyl-4-piperidones the thermodynamic activation parameters for the reduction in this system are determined and discussed.