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

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

Uses

Used in Personal Care and Cosmetic Products:
4-Butylcyclohexanol is used as a fragrance ingredient in various personal care and cosmetic products for its floral scent, enhancing the sensory experience of these products.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, 4-Butylcyclohexanol is utilized as a key component in creating distinct and appealing scents for a wide range of applications, from perfumes to household products.
Used in Organic Compound Synthesis:
4-Butylcyclohexanol is also used as a building block in the synthesis of other organic compounds, contributing to the development of new chemical entities for various industrial applications.
Used in Environmentally Friendly Practices:
Due to its biodegradable nature, 4-Butylcyclohexanol is favored in industries that prioritize eco-friendly practices, ensuring minimal environmental impact from its use and disposal.

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

Upstream product

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

Downstream Products

• 61203-82-5 4-butylcyclohexanone 
• 106148-84-9 p-(1-butylcyclohexyl)toluene 
• 67590-13-0 trans-4-n-Butyl-cyclohexanol 
• 67861-29-4 4-(4-butyl-cyclohex-1-enyl)-morpholine 
• 132310-87-3 2-(trans-4-butylcyclohexyl)-1,3-propanediol 
• 132310-87-3 2-(4-Butyl-cyclohexyl)-propane-1,3-diol 
• 1383149-15-2 C₂₃H₃₈O₂ 
• 1226494-73-0 (R)-4-(6-(4-butylcyclohexyl)oxynaphthalen-2-yl)-4-methyloxazolidin-2-one 
• 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 
• 106148-88-3 p-(1-butylcyclohexyl)benzoic acid 

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.

Liquid crystal substituted trans-4-n-alkylcyclohexanes and subst.-3-subst.-benzoyloxy-[trans-4-n-alkylcyclohexane]s

The invention relates to liquid crystal nematic substances for electro-optical devices for the modulation of light, for the reproduction of numerals, signs and images as well as an orienting medium for spectroscopy and gas chromatography.It was found that compounds containing two or three rings, connected by carboxyl groups are new liquid crystal nematic substances of the general formula STR1 where R 1 =C n H 2n+1, CN; R 2 =C m H 2m+1, CN;R 3 =H, CH 3, C 2 H 5 Cl, Br; x=0 or 1; m,n=numbers from 1 to 10 are suitable for electro-optical arrangements for the modulation of transmitted or reflected light as well as for the reproduction of numeral signals and images, and further, as an orienting medium for spectroscopy and gas chromotography.Other liquid crystal substances or non-liquid crystalline substances, particularly dyes, may be added to the substances according to the invention.