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2-N-PROPYLCYCLOHEXANOL is a cyclohexanol chemical compound, an organic substance with the molecular formula C9H18O and a molecular weight of 142.24 g/mol. It is a colorless liquid with a faint odor, insoluble in water, but soluble in organic solvents. 2-N-PROPYLCYCLOHEXANOL is known for its low toxicity and is not typically associated with significant health or environmental risks, although it should still be handled and disposed of with proper safety measures.

90676-25-8

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90676-25-8 Usage

Uses

Used in Perfumery:
2-N-PROPYLCYCLOHEXANOL is used as a fragrance ingredient for its ability to contribute to the scent profile of various perfumes. Its unique olfactory characteristics make it a valuable component in the creation of complex and appealing fragrances.
Used in Food Industry:
In the food industry, 2-N-PROPYLCYCLOHEXANOL is utilized as a flavoring agent, enhancing the taste of food products by providing a distinct flavor note. Its use in food products is carefully regulated to ensure safety and quality.
Production Methods:
2-N-PROPYLCYCLOHEXANOL can be synthesized through two primary methods: the hydrogenation of 2-N-propylcyclohexanone or the reduction of 2-N-propylcyclohexanone oxime. Both methods are employed to produce 2-N-PROPYLCYCLOHEXANOL for its various applications in the perfumery and food industries.

Check Digit Verification of cas no

The CAS Registry Mumber 90676-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,7 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90676-25:
(7*9)+(6*0)+(5*6)+(4*7)+(3*6)+(2*2)+(1*5)=148
148 % 10 = 8
So 90676-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-2-5-8-6-3-4-7-9(8)10/h8-10H,2-7H2,1H3

90676-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N-PROPYLCYCLOHEXANOL

1.2 Other means of identification

Product number -
Other names cis-2-Propyl-cyclohexanol

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:90676-25-8 SDS

90676-25-8Relevant academic research and scientific papers

Hydrogenation of lignin-derived phenolic compounds over step by step precipitated Ni/SiO2

Shu, Riyang,Zhang, Qi,Xu, Ying,Long, Jinxing,Ma, Longlong,Wang, Tiejun,Chen, Pengru,Wu, Qingyun

, p. 5214 - 5222 (2016/02/05)

The harsh reaction conditions for the valorization of lignin-derived phenolic compounds considerably limit the efficient utilization of the lignin derivatives. Here, we put forward a high efficient and selective hydrogenation process for phenolic compounds at a mild condition over step by step precipitated Ni/SiO2 catalyst. The properties of the Ni/SiO2 catalysts by different preparation methods were detailedly compared using various characterization measurements. Catalytic activity of the catalysts was tested by the hydrogenation of guaiacol, and the results showed that guaiacol could be completely converted into cyclohexanol with 99.9% selectivity at 120 °C, 2 MPa H2 atmosphere for 2 h. Other typical lignin-derived phenolic compounds also had excellent hydrogenation performance and great energy efficiency. Catalyst characterization results demonstrated that the high catalytic activity of the step by step precipitated Ni/SiO2 was mainly ascribed to its polyporous spherical structure, which led to the large specific surface area and high nickel dispersion. The appropriate acidity of the catalyst also promoted the catalytic performance significantly. Furthermore, the catalyst exhibited an excellent recyclability, where no significant loss of the catalytic activity was showed out after 3 runs.

Ruthenium Nanoparticles Stabilized in Cross-Linked Dendrimer Matrices: Hydrogenation of Phenols in Aqueous Media

Maximov, Anton,Zolotukhina, Anna,Murzin, Vadim,Karakhanov, Edward,Rosenberg, Edward

, p. 1197 - 1210 (2015/04/14)

Novel catalysts consisting of ruthenium nanoparticles encapsulated in cross-linked matrices based on the poly(propylene imine) dendrimers of the 1st and 3rd generations have been synthesized with a narrow particle size distribution (3.8 and 1.0 nm, respectively). The resulting materials showed high activity for the hydrogenation of phenols in aqueous media (specific catalytic activity reached turnover frequencies of 2975h-1 with respect to hydrogen uptake). It has been shown that the use of water as a solvent leads to a 1.5 to 50-fold increase in the reaction rate depending upon the nature of the substrate. It has been established that unlike the traditional heterogeneous catalysts based on ruthenium, during the hydrogenation of dihydroxybenzenes, the hydrogenation rate decreases in the order: resorcinol>hydroquinoneacatechol. The maximum specific activity for resorcinol was a turnover frequency of 243150h-1 with respect to hydrogen uptake. The catalyst based on the dendrimer of the 3rd generation containing finer particles has significantly inferior activity to the catalyst based on the dendrimer of the 1st generation by virtue of steric factors, as well as the need for prereduction of the ruthenium oxide contained on the surface. These catalysts showed resistance to metal leaching and may be reused several times without loss of activity.

New active-iron based reducing system for carbonyl compounds and imines. Stereoselective reduction of cyclic ketones

Moglie, Yanina,Alonso, Francisco,Vitale, Cristian,Yus, Miguel,Radivoy, Gabriel

, p. 2812 - 2819 (2007/10/03)

The reaction of different carbonyl compounds and imines with a mixture of iron(II) chloride tetrahydrate, an excess of lithium powder, and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB, 5 mol%) in THF at room temperature, led to the formation of the corresponding alcohols and amines, respectively. The process was also applied to the transformation of α,β-unsaturated carbonyl compounds into the corresponding saturated alcohols. The new reducing system exhibited good to excellent diastereoselectivity toward the reduction of different monocyclic and polycyclic ketones.

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