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2433-14-9

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2433-14-9 Usage

General Description

4-Cyclohexylcyclohexanol is a bicyclic compound with a molecular formula of C12H22O. It contains two cyclohexane rings with a cyclohexyl group attached to one of the rings. 4-CYCLOHEXYLCYCLOHEXANOL is a white solid at room temperature and is insoluble in water but soluble in organic solvents. It is commonly used as a fragrance ingredient in various consumer products such as perfumes and cosmetics. It also serves as a chemical intermediate in the synthesis of other organic compounds. In addition, 4-Cyclohexylcyclohexanol has potential applications in pharmaceutical research and drug development due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 2433-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2433-14:
(6*2)+(5*4)+(4*3)+(3*3)+(2*1)+(1*4)=59
59 % 10 = 9
So 2433-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h10-13H,1-9H2

2433-14-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CYCLOHEXYLCYCLOHEXANOL

1.2 Other means of identification

Product number -
Other names 4,4'-bicyclohexanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2433-14-9 SDS

2433-14-9Relevant articles and documents

Extractive hydrogenation: A new and versatile technique broadening gas chromatography applications

Itani, Mohammad,Giese, Roger W.

, p. 1189 - 1197 (1994)

A new technique, "extractive hydrogenation", is combined with gas chromatography (GC) to analyze organic including biological samples. In this method, the sample (or an extract thereof) is subjected to intense hydrogenation under aqueous conditions in the presence of excess (in terms of mass) palladium/carbon catalyst. Products with a saturated hydrocarbon framework result, for example, as alcohols, the larger of which adsorb onto the carbon of the catalyst. These larger products are separately recovered by extracting the washed catalyst with an organic solvent and then detected by GC. Here, the GC was fitted with a flame ionization detector (FID) or an electron impact mass spectrometer (EI-MS). Detection in this way (H2-GC) of the following trace analytes was achieved: (a) 100 μg of an (acetylamino)fluorene-deoxyguanosine DNA adduct spiked into 1 mg of DNA; (b) 1.5 μg of novobiocin, an antibiotic, spiked into 15 mL of milk (followed by extraction prior to H2-GC); and (c) 1 mg of 4-aminobiphenyl, a carcinogen, spiked into 150 mg of hemoglobin (followed by hydrolysis prior to H2-GC). The technique gave somewhat different GC-FID chromatograms for Escherichia coli and Enterococcus bacteria. Unlike pyrolysis (similarly used prior to GC), which tends to convert a biological sample into a char, the hydrogenation technique turns the sample into a clear aqueous solution. Most importantly, the method brings a broad variety of organic-containing samples in a simple way into the scope of GC/EI-MS with its computerized library of spectra.

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