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93503-77-6

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93503-77-6 Usage

Chemical Properties

white to light beige crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 93503-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,0 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93503-77:
(7*9)+(6*3)+(5*5)+(4*0)+(3*3)+(2*7)+(1*7)=136
136 % 10 = 6
So 93503-77-6 is a valid CAS Registry Number.

93503-77-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-TERT-AMYLCALIX[8]ARENE

1.2 Other means of identification

Product number -
Other names p-tert-pentylcalix<8>arene

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:93503-77-6 SDS

93503-77-6Downstream Products

93503-77-6Relevant articles and documents

Path to Industrial Production of Calix[8 and 4]arenes

Haase, Cornelius Heinz Werner

, p. 603 - 611 (2020/02/04)

A highly selective and high yield synthesis for the production of calix[8]arenes in concentrated reaction masses is described. Obtained purities are >98% and yields of >80%, with isolation by simple filtration. The developed approach allows for subsequent

Cation Transport from Multiple Alkali Cation Mixtures Using a Liquid Membrane System Containing a Series of Calixarene Carriers

Izatt, Steven R.,Hawkins, Richard T.,Christensen, James J.,Izatt, Reed M.

, p. 63 - 66 (2007/10/02)

Several new p-tert-pentylcalixarenes have been synthesized.These and other calixarenes have been used to study carrier-mediated alkali-metal cation fluxes at 25 deg C in H2O-(organic solvent)-H2O liquid membranes.In addition to single cation systems, all possible equimolar, two-, three-, and four-cation mixtures of NaOH, KOH, RbOH, and CsOH were used in the study.In each case, alkali cation transport was coupled with the reverse flux of protons.Selective transport of Cs(1+) over Rb(1+), K(1+), and Na(1+) was seen in all mixtures studied.The greatest selectivity for Cs(1+) was found for calixarenes, but the largest flux of Cs(1+) as well as the other alkali cations was seen with the calixarenes and calixarenes.The greater flux in these latter cases may be a result of each calixarene binding two cations.In experiments at low -to- ratios, p-tert-butylcalixarene transports Rb(1+) over Cs(1+).As these ratios increase, transport of Cs(1+) becomes favored over that of Rb(1+), indicating that the cation flux depends, in part, on the relative concentrations of the cations in the source phase.

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