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1-Methyl-1-propylcyclohexane is an organic compound with the molecular formula C??H??. It is a cyclic alkane, specifically a cyclohexane derivative, with a methyl group (CH?) and a propyl group (C?H?) attached to the same carbon atom in the ring. 1-Methyl-1-propylcyclohexane. is a colorless liquid with a low melting point and boiling point, and it is insoluble in water but soluble in organic solvents. It is used as a solvent and as a precursor in the synthesis of other organic compounds. Due to its non-polar nature, 1-methyl-1-propylcyclohexane is also used in chromatography as a stationary phase in gas chromatography.

4258-93-9

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4258-93-9 Usage

Chemical structure

A six-membered cyclohexane ring with a methyl and propyl group attached at different carbon atoms.

Physical state

Colorless liquid.

Odor

Faint, sweet.

Solubility

Insoluble in water, soluble in organic solvents.

Usage

Primarily used as a solvent in various industrial applications, such as manufacturing of adhesives, paints, and coatings.

Potential uses

May have applications in pharmaceutical and fragrance industries.

Toxicity

Low toxicity.

Environmental impact

Low environmental impact, making it a relatively safe and environmentally friendly option for solvent applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4258-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4258-93:
(6*4)+(5*2)+(4*5)+(3*8)+(2*9)+(1*3)=99
99 % 10 = 9
So 4258-93-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H20/c1-3-7-10(2)8-5-4-6-9-10/h3-9H2,1-2H3

4258-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-propylcyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexane, 1-methyl-1-propyl-

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:4258-93-9 SDS

4258-93-9Relevant academic research and scientific papers

High-performance ring-opening catalysts based on iridium-containing zeolite Beta in the hydroconversion of decalin

Santi, Dominic,Holl, Tobias,Calemma, Vincenzo,Weitkamp, Jens

, p. 46 - 57 (2013/06/04)

Decalin was converted in a flow-type reactor under a hydrogen pressure of 5.2 MPa on Ir/H,A-Beta zeolite catalysts, where A stands for an alkali metal cation. In one series of catalysts, the Ir content was 3 wt.%, and the nature of A was varied from lithi

IONIC ALKYLATION OF TERTIARY ALKYL HALIDES WITH TETRAALKYLSILANES

Bolestova, G. I.,Parnes, Z. N.

, p. 32 - 36 (2007/10/02)

In the reaction of tertiary alkyl halides with tetraethyl-, tetrapropyl-, tetrabutyl-, and tetraamylsilane in the presence of AlX3 the halogen atom is substituted by the alkyl group with the formation of the corresponding saturated hydrocarbons containing a quaternary carbon atom.As a result of the hydride mobility of the β-hydrogen atom in the tetraalkylsilane ionic hydrogenolysis of the substrate occurs in addition to alkylation, and the degree of hydrogenolysis depends on the alkyl substituent in the silane.

IONIC HYDROMETHYLATION OF OLEFINS BY THE (CH3)4Si-HCl-AlCl3 SYSTEM

Bolestova, G. I.,Parnes, Z. N.,Kursanov, D. N.

, p. 2175 - 2179 (2007/10/02)

The ionic hydromethylation of olefins with the (CH3)4Si-HCl-AlCl3 system was realized for the first time.A method was developed on the basis of this system for the production of high yields of difficultly obtainable saturated hydrocarbons with a quaternary carbon atom (including bicyclic compounds with an angular methyl group) from acyclic, monocyclic, and bicyclic olefins.

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