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10100-95-5

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10100-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10100-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,0 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10100-95:
(7*1)+(6*0)+(5*1)+(4*0)+(3*0)+(2*9)+(1*5)=35
35 % 10 = 5
So 10100-95-5 is a valid CAS Registry Number.

10100-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-methylpropan-2-yl)oxy]pentane

1.2 Other means of identification

Product number -
Other names Amyl-t-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:10100-95-5 SDS

10100-95-5Relevant articles and documents

IODINE MEDIATED SYNTHESIS OF ALKYL TERTIO-ALKYL ETHERS

Jenner G.

, p. 2445 - 2448 (1988)

Mixed alkyl t-alkyl ethers have been prepared by the selective coupling of the alcohol precursors.Dehydration was promoted by iodine under hydrogen pressure at 100 deg C.

Kinetics of the reactions of tert-butanol with C2-C5 alcohols on sulfo cation exchangers

Golovanov,Pisareva,Levshenkov

, p. 179 - 183 (2013)

The kinetics of etherification of tert-butanol with aliphatic alcohols on gel KU-2×8 and macroporous KU-23 sulfo cation exchangers was studied. The first order of reaction with respect to tert-butanol and the -SO3H groups of a catalyst was established. The activation energy of the process observed on KU-2×8 was 60-95 kJ/mol. It was shown that the etherification of tert-butanol on KU-2×8 occurred in a surface layer. The reactivity of primary alcohols introduced into the reaction with tert-butanol increased with their molecular weights (C2-C5). The rate of reaction with secondary alcohols was lower than that with primary alcohols.

Investigation of the equilibria of the reaction: CH3(CH2)4OH + (CH3)2C:CH2 = CH3(CH2)4OC(CH3)3

Rozhnov, A. M.,Barkov, V. I.,Sharonov, K. G.,Tsvetkov, V. S.

, p. 327 - 333 (1990)

Equilibria have been studied of the reaction of synthesis of amyl t-butyl ether (ATBE) from n-pentan-1-ol and 2-methylpropene in the liquid (313 to 413 K) and gas (399 to 447 K) phases.It has been found that in the liquid phase (ATBE + n-pentan-1-ol + 2-methylpropane) is non-ideal.Its mole-fraction equilibrium product Kx depends on the composition of the reaction mixture at constant temperature.With n(C5H11OH)/n 2 in the starting mixture, Kx is approximately constant.It has been shown that the values of Kx found for n(C5H11OH)/n =4 can be used for the establishment of the enthalpy of reaction without corrections for non-ideality of the mixture.An ebulliometric method was used to find the vapour pressure of ATBE. ΔrHm0 = -(67.09 +/- 4.94) kJ*mol-1 and ΔrSm0 = -(173.1 +/- 11.6) J*K-1*mol-1 were found for the reaction: CH3(CH2)4OH + (CH3)2C:CH2 = CH3(CH2)4OC(CH3)3 in the gas phase for T = 423 K.The following values of thermodynamic quantities of ATBE have been found both from chemical equilibria and (p,T) results: ΔfHm0(298.15 K,g) = -(380.6 +/- 6.8) kJ*mol-1; ΔvapHm(298.15 K) = (46.89 +/- 0.99) kJ*mol-1, and ΔvapHm = (39.1 +/- 3.1) kJ*mol-1 at the normal boiling temperature, 419.156 K.

A convenient synthesis of tert-butyl ethers under microwave condition

Mahammed,Keshava Murthy,Mohana Raju

, p. 575 - 578 (2008/09/20)

Synthesis of tert-butyl ethers from various alcohols and substituted phenols can be achieved using tert-butyl bromide in the presence of basic lead carbonate as a catalyst under microwave irradiation in absence of solvent. The catalyst is easily recovered via filtration and reused up to three times without appreciable loss of activity.

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