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2-butoxy-2-methylbutane, also known as tert-amyl ethyl ether or 2-methoxy-2-methylbutane, is an organic compound with the chemical formula C9H20O. It is a colorless, volatile liquid that is insoluble in water but soluble in most organic solvents. This ether derivative is commonly used as a solvent in various industrial applications, such as in the production of paints, varnishes, and lacquers, as well as in the extraction of essential oils. It is also utilized as a fuel component in racing fuels and as a cleaning agent in the electronics industry. Due to its low boiling point and high vapor pressure, 2-butoxy-2-methylbutane is considered a hazardous substance and requires proper handling and storage to prevent environmental and health risks.

3249-47-6

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3249-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3249-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3249-47:
(6*3)+(5*2)+(4*4)+(3*9)+(2*4)+(1*7)=86
86 % 10 = 6
So 3249-47-6 is a valid CAS Registry Number.

3249-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Butoxy-2-methylbutane

1.2 Other means of identification

Product number -
Other names tert-amyl n-butyl ether

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:3249-47-6 SDS

3249-47-6Relevant academic research and scientific papers

METHOD FOR PRODUCING ASYMMETRIC ALKYL ETHER HAVING TERTIARY ALKYL GROUP

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Paragraph 0030, (2017/01/31)

PROBLEM TO BE SOLVED: To provide a method capable of obtaining an asymmetric alkyl ether having a tertiary alkyl group easily and industrially. SOLUTION: (1) There is provided a method for producing an asymmetric alkyl ether having a tertiary alkyl group by subjecting a tertiary alcohol and a primary alcohol or a secondary alcohol to a dehydration reaction using activated clay as a catalyst. (2) There is provided the method for producing an asymmetric alkyl ether having a tertiary alkyl group according to (1), where the tertiary alcohol is any one selected from the group consisting of tert-butanol, tert-amylalcohol and 1-adamantyl alcohol. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Thermochemistry of branched ethers: Experimental study of chemical equilibrium in the reacting system of tert-amyl alkyl ether synthesis

Verevkin, Sergey P.

, p. 576 - 581 (2007/10/03)

The chemical equilibrium of the reactive systems (alkanol + methylbutenes ? alkyl tert-amyl ether) with the following alkyl substituents: ethyl, propyl, butyl, iso-propyl, sec-butyl, and cyclohexyl, were studied in the liquid phase. Reactions were investigated in the screwed vials in the temperature range (298 to 393) K, and a cation exchanger Amberlist 15 was used as heterogeneous catalyst. Enthalpies of reactions ΔrH m° of teri-amyl alkyl ethers synthesis in the liquid phase were obtained from the temperature dependence of the equilibrium constants and used to derive standard enthalpies of formation, ΔfH m°(1), of tert-amyl alkyl ethers. For the sake of comparison, these enthalpies of formation have been calculated using improved Benson's increments. Calculated values are in close agreement with those from thermochemical measurements.

Thermochemistry of benzyl alcohol: Reaction equilibria involving benzyl alcohol and tert-alkyl ethers

Verevkin, Sergey P.,Vasiltsova, Tatiana V.

, p. 1717 - 1723 (2007/10/03)

Chemical equilibrium of the reactive systems of benzyl alcohol with tert-alkyl ethers was studied in the liquid phase in the temperature range (298 to 373) K and with a cation exchanger Amberlist 15 as a catalyst. Enthalpies of reactions involving benzyl alcohol were obtained from the temperature dependence of the equilibrium constants according to the Second Law and used to derive averaged standard enthalpies of formation of benzyl alcohol ΔfHm(1,298.15K) = -(154-5 ± 1.7) kJ·mol-1 in the liquid state. Vapor pressures and enthalpy of vaporization, ΔlgH m(298.15 K), of benzyl alcohol were determined using transpiration method. The latter value, together with the reliable literature data, provided an averaged result ΔlgHm(298.15 K) = (65.75 ± 0.51) kJ·mol-1. Both averaged results for ΔfHm(1,298.15K)o and ΔfHm(298.15 K) were used to calculate and to recommend the value of enthalpy of formation of benzyl alcohol in the gaseous state ΔfHm(298.15K)o = -(88.8 ± 1.8) kJ·mol-1. Auxiliary data for tert-butyl benzyl ether (energy of combustion, vapor pressures, and enthalpy of vaporization) were measured using calorimetry and transpiration method.

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