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1,4,7,10,13-Pentaoxacyclopentadecane, 2-tetradecyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92588-90-4

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92588-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92588-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,8 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92588-90:
(7*9)+(6*2)+(5*5)+(4*8)+(3*8)+(2*9)+(1*0)=174
174 % 10 = 4
So 92588-90-4 is a valid CAS Registry Number.

92588-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tetradecyl-1,4,7,10,13-pentaoxacyclopentadecane

1.2 Other means of identification

Product number -
Other names 1,4,7,10,13-Pentaoxacyclopentadecane,2-tetradecyl

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:92588-90-4 SDS

92588-90-4Downstream Products

92588-90-4Relevant academic research and scientific papers

Template Synthesis and Ionophorous Properties of Substituted Crown Ethers towards Alkali-metal Ions

Bowsher, Brian R.,Rest, Antony J.,Main, Brian G.

, p. 1421 - 1426 (2007/10/02)

A number of alkyl-substituted crown ethers of the type 2-R-12-crown-4, 2-R-15-crown-5, and 2-R-18-crown-6 (R = Me, Et, octyl, decyl, tetradecyl,icosyl, or Ph) have been prepared in relatively good yields by a novel synthetic route employing the metal-ion template effect.The ionophorous properties of these crown ethers with respect to the transport of lithium, sodium, and potassium picrates across a bulk liquid chloroform membrane were measured and have been compared to those of crown ethers already used as ionophores.Substitution of alkyl and phenyl groups on the crown ethers, making them more lipophilic, does not seem to assist the transport of Na+ and K+ as their picrate salts, but rather appears to make the ionophore more susceptible to remain in the chloroform phase, as the chain length increases, and thereby leads to a reduction in transport.Introduction of alkyl and other groups, however, does seem to assist the transport of Li+ as lithium picrate, although the overall rate of transport is considerably slower for Li+ than the rate for Na+.

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