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KRYPTOFIX 22 DD is a chemical compound that belongs to the family of crown ethers, known for its high affinity for metal ions and its ability to form stable complexes with them. This makes it a versatile complexing agent and phase transfer catalyst in various chemical reactions, playing a crucial role in extraction, separation processes, organic synthesis, and catalytic reactions.
Usage:
Used in Chemical Synthesis Industry:
KRYPTOFIX 22 DD is used as a complexing agent for the extraction and separation of metal ions, facilitating the transfer of ions between different phases and enhancing the efficiency of chemical reactions.
Used in Organic Synthesis:
KRYPTOFIX 22 DD is used as a phase transfer catalyst to facilitate the transfer of ions between different phases, making it valuable in organic synthesis and catalytic reactions.
Used in Catalytic Reactions:
KRYPTOFIX 22 DD is used as a complexing agent to form stable complexes with metal ions, which is crucial in various catalytic reactions.

79495-97-9

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79495-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79495-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,9 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79495-97:
(7*7)+(6*9)+(5*4)+(4*9)+(3*5)+(2*9)+(1*7)=199
199 % 10 = 9
So 79495-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H66N2O4/c1-3-5-7-9-11-13-15-17-19-33-21-25-35-29-31-37-27-23-34(24-28-38-32-30-36-26-22-33)20-18-16-14-12-10-8-6-4-2/h3-32H2,1-2H3

79495-97-9SDS

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 7,16-didecyl-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

1.2 Other means of identification

Product number -
Other names N,N'-didecyl-4,13-diaza-18-crown-6

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:79495-97-9 SDS

79495-97-9Downstream Products

79495-97-9Relevant academic research and scientific papers

Re-evaluation of the mechanism of cytotoxicity of dialkylated lariat ether compounds

Carrasquel-Ursulaez, Willy,Chanda, Baron,Dehghany, Mahzad,Jones, Corey,Reeves, Ryan D.,Schomaker, Jennifer M.

, p. 40391 - 40394 (2020)

The cytotoxicity of dialkylated lariat ethers has been previously attributed to their ionophoric properties. Herein, we provide evidence that these effects are due to loss of membrane integrity rather than ion transport, a finding with important implications for the future design of synthetic ionophores.

Supramolecular cation transporters alter root morphology in the Arabidopsis thaliana plant

Patel, Mohit B.,Negin, Saeedeh,Stavri, Ariel,Gokel, George W.

, p. 183 - 191 (2017/10/05)

Bibracchial (two-armed) 4,13-diaza-18-crown-6 lariat ether and tris(macrocycle) hydraphile synthetic amphiphiles alter root morphology in Arabidopsis thaliana plants. The effect on root structure and growth depends both on the hydraphile spacer chain length and lariat ether side chain length as well as the concentration of compound in the growth medium. In some cases a correlation to ion transport activity was apparent, but such a correlation is not always manifested. Surprisingly, planar bilayer conductance (BLM) studies showed that lariat ethers and lariat ether amides both exhibited well controlled membrane activity. Pore formation in soybean asolectin membranes occurred readily and the pores were stable and sustained. Low concentrations of active hydraphiles and lariat ethers altered the primary:lateral root density ratio, generally increasing it. The transporter-mediated alterations in lateral root density were suggestive of the activity of plant auxins such as indole-3-acetic acid and 2,4-dichlorophenoxyacetic acid, which are known to depend on cytosolic potassium ion concentrations. The hypothesis that the compounds interfere with the auxin pathway was tested and discounted by using auxin-resistant A. thaliana mutants. Rather than functioning directly as auxin mimics, ionophores affect the ion gradients producing an auxin-like effect on root development.

COMPOSITIONS AND METHODS FOR SYNTHETIC AMPHIPHILE-INDUCED CHANGES IN PLANT ROOT MORPHOLOGY

-

Paragraph 0105, (2016/04/04)

The disclosure provides a method for increasing the lateral root development of a plant by exposing said plant to a composition containing a synthetic amphiphile. By increasing the number of lateral roots, the surface area of the root structure is increased, making the plants better able to survive such stresses as drought or low nutrients

Macrocyclic ligands with partially fluorinated sidearms: Synthesis and metal ion complexation

Elshani, Sadik,Kobzar, Evgeny,Bartsch, Richard A.

, p. 3291 - 3301 (2007/10/03)

Derivatives of aza-12-crown-4, aza-15-crown-5, aza-18-crown-6, 1,10- diaza-18-crown-6 and 1,4,8,12-tetraazacyclopentadecane with partially fluorinated substituents attached to nitrogen are prepared. Their efficiencies and selectivities in alkali metal and

Syntheses and Binding Properties of Bibracchial Lariat Ethers (BIBLEs): Survey of Synthetic Methods and Cation Selectivities

Gatto, Vincent J.,Arnold, Kristin A.,Viscariello, Anthony M.,Miller, Steven R.,Morgan, Charles R.,Gokel, George W.

, p. 5373 - 5384 (2007/10/02)

A new, two-step method for the synthesis of 4,10-diaza-15-crown-5 and 4,13-diaza-18-crown-6 and their N,N'-disubstituted derivatives from bis(secondary amines) and 1,2-bis(2-iodoethoxy)ethane is described.Essentially, the method utilizes the incipient sidearms as nitrogen-protecting groups prior to cyclization.The yields for cyclization are high, ranging from 32percent to 77percent.The N,N'-disubstituted derivatives of 4,10-diaza-15-crown-5 produced by alkylation or acylation (A), acylation followed by reduction (AR), cyclization (C), hydrogenolysis (H), or single-step cyclization (O) have the following sidearms: H (H, 91percent), MeOCH2CH2 (C, 38percent), EtOCOCH2 (A, 62percent), PhCH2 (C,72percent), 2-MeOPh (C, 52percent), 2-furanylmethyl (C, 67percent), and 2-nitrobenzyl (A, 50percent).N,N'-Dibenzyl-4,10-diaza-18-crown-6 was obtained by cyclization in 63percent yield.The N,N'-disubstituted derivatives of 4,13-diaza-18-crown-6 produced with the new method have the following sidearms: H (H, 92percent), CO-Et (A, 100percent), n-propyl (AR, 78percent), n-butyl (C, 77percent), n-hexyl (C, 32percent; A, 50percent; O, 7percent), n-octyl (AR, 45percent), CO-n-heptyl (A, 71percent), n-nonyl (O, 11percent;A, 45percent;AR, 39percent), CO-n-undecyl (A, 87percent), n-tetradecyl (AR, 26percent), CO-n-tridecyl (A, 78percent), n-hexadecyl (A, 25percent), n-octadecyl (AR, 60percent), CO-n-heptadecyl (A, 100percent), allyl (O, 26percent), propargyl (O, 22percent), HOCH2CH2 (O, 28percent), MeOCH2CH2 (C, 43percent; AR, 76percent), HOCOCH2 (hydrolysis, 81percent), EtOCOCH2 (A, 92percent), PhCH2 (O, 29percent;C, 66percent), 2-furanylmethyl (O, 27percent, C, 62percent), 2-hydroxybenzyl (A, 85percent), 2-methoxybenzyl (O, 30percent), 2-cyanobenzyl (A, 95percent), 2-nitrobenzyl (A, 90percent), 3-nitrobenzyl (A, 95percent), and 4-nitrobenzyl (A, 70percent).The new cyclization method is compared with other, previously published cyclization reactions with respect to overall yield and ease of purification.When this new cyclization cannot be used, diaza crown ethers can be prepared by alkylation of 4,10-diaza-15-crown-5 or 4,13-diaza-18-crown-6.The homogeneous equilibrium cation binding constants (log Ks) have been determined in anhydrous methanol solution for many of the compounds described herein with Na+, K+, and Ca+.The cation selectivities are rationalized in terms of polar, structural, and lipophilicity effects.

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