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

75006-56-3

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75006-56-3 Usage

Chemical compound

A chemical compound with a cycloalkane structure.

Building block

Used in the design and synthesis of novel surfactants and polymers.

Molecular structure

Unique molecular structure with a long hydrophobic alkyl chain, cyclic ether, and amine groups.

Micelle formation

Suitable for forming micelles in aqueous solutions.

Detergent properties

Acts as a detergent due to its hydrophobic alkyl chain.

Flexibility and versatility

Cyclic ether and amine groups provide flexibility and versatility.

Industrial applications

Used in various industrial applications such as adhesives, coatings, and personal care products.

Pharmaceutical industry

Used in drug delivery and as a stabilizer in vaccines.

Check Digit Verification of cas no

The CAS Registry Mumber 75006-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75006-56:
(7*7)+(6*5)+(5*0)+(4*0)+(3*6)+(2*5)+(1*6)=113
113 % 10 = 3
So 75006-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H45NO4/c1-2-3-4-5-6-7-8-9-10-11-12-23-13-15-24-17-19-26-21-22-27-20-18-25-16-14-23/h2-22H2,1H3

75006-56-3SDS

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 13-dodecyl-1,4,7,10-tetraoxa-13-azacyclopentadecane

1.2 Other means of identification

Product number -
Other names 1,4,7,10-Tetraoxa-13-azacyclopentadecane,13-dodecyl

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:75006-56-3 SDS

75006-56-3Relevant academic research and scientific papers

Lipophilic Bis(monoaza crown ether) Derivatives: Synthesis and Cation-Complexing Properties

Sakamoto, Hidefumi,Kimura, Keiichi,Koseki, Yasuaki,Matsuo, Mitsunori,Shono, Toshiyuki

, p. 4974 - 4979 (2007/10/02)

Eleven lipophilic bis(monoaza crown ether) derivatives were synthesized, in which two monoaza crown ethers with 9-, 12-, 15-, or 18-membered rings are linked through the nitrogen atoms by an alkane-, diether-, or diester-type bridge chain bearing a dodecyl group.Sodium and potassium binding with the bis(monoaza crown ether) was determined potentiometrically and compared with those for previous bis(crown ethers) 5 (n = 1 - 3) and corresponding monocyclic analogues 4 and 6 (n = 1 - 3).Marked bis(crown ether) effect was observed only for the alkane-type bis(monoaza-12-crown-4) and bis(monoaza-15-crown-5) derivatives 1 (n = 1,2) on complexing Na+ and K+, respectively.It was suggested that in some of the other bis(monoaza crown ethers) lariat-ether effect works instead.Bis(monoaza-9-crown-3) derivatives 1 and 2 (n = 0) possess very poor cation-complexing ability.Acidity constant values gave some hints about the bis(crown ether) effect.

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