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Merck

8.14925

Kryptofix® 222

special quality for synthesis

greener alternative

Greener Alternative

Synonym(s):

Kryptofix® 222, 4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

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About This Item

Empirical Formula (Hill Notation):
C18H36N2O6
CAS Number:
Molecular Weight:
376.49
UNSPSC Code:
12352005
EC Index Number:
245-962-4
NACRES:
NA.22
MDL number:
Form:
powder
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Quality Segment

form

powder

potency

300-2000 mg/kg LD50, oral (Rat)

reaction suitability

core: cryptand, reaction type: phase-transfer

sustainability

Sustainability features

mp

70-73 °C

greener alternative category

storage temp.

2-8°C

SMILES string

N21CCOCCOCCN(CCOCCOCC2)CCOCCOCC1

InChI

1S/C18H36N2O6/c1-7-21-13-14-24-10-4-20-5-11-25-17-15-22-8-2-19(1)3-9-23-16-18-26-12-6-20/h1-18H2

InChI key

AUFVJZSDSXXFOI-UHFFFAOYSA-N

General description

We are committed to providing greener alternatives that adhere to the 12 Principles of Green Chemistry. This catalyst enables efficient catalytic transformations aligned with green chemistry principles, promoting atom economy and waste reduction. Click here for more information.

Application

  • Improved, one-pot synthesis of 6-[(18) F]fluorodopamine and quality control testing for use in patients with neuroblastoma.: This study presents an improved method for synthesizing 6-[(18) F]fluorodopamine using Kryptofix 222. The one-pot synthesis process enhances efficiency and quality control, making it suitable for clinical applications in neuroblastoma patients (Vāvere et al., 2018).
  • Efficient radiosynthesis and non-clinical safety tests of the TSPO radioprobe [(18)F]FEDAC: Prerequisites for clinical application.: Kryptofix 222 is utilized in the radiosynthesis of [(18)F]FEDAC, a radioprobe for TSPO imaging. The study highlights the efficiency and safety of the synthesis process, facilitated by Kryptofix 222, and its potential for clinical application (Kawamura et al., 2016).
  • Fully automated one-pot radiosynthesis of O-(2-[18F]fluoroethyl)-L-tyrosine on the TracerLab FX(FN) module.: This research demonstrates the automated synthesis of O-(2-[18F]fluoroethyl)-L-tyrosine, employing Kryptofix 222 as a phase transfer catalyst. The automated process significantly improves the synthesis efficiency (Bourdier et al., 2011).
  • Electrochemical concentration of no-carrier-added [(18)F]fluoride from [(18)O]water in a disposable microfluidic cell for radiosynthesis of (18)F-labeled radiopharmaceuticals.: Kryptofix 222 plays a crucial role in the electrochemical concentration of [(18)F]fluoride, facilitating the radiosynthesis of various (18)F-labeled radiopharmaceuticals in a microfluidic cell, enhancing the overall efficiency and yield (Saiki et al., 2010).

Analysis Note

Assay (perchloric acid titration): ≥ 99
Purity (GC): ≥ 99
Identity (IR-spectrum): passes test
Melting point: 69 - 72
Biggest singly impurity (GC): ≤ 0.1 %
Acetone (HS-GC): ≤ 5000 ppm
Acetonitrile (HS-GC): ≤ 410 ppm
Dichloromethane (HS-GC): ≤ 600 ppm
n-Hexane (HS-GC): ≤ 290 ppm
Methanol (HS-GC): ≤ 3000 ppm
petroleum ether (HS-GC): ≤ 290 ppm
Pyridine (HS-GC): ≤ 200 ppm
Sulfated ash: ≤ 0.1 %
Water (according to Karl Fischer): ≤ 0.5
E.coli: passes test
Salmonella species: passes test
Staphylococcus aureus: passes test
Pseudomonas aeruginosa: passes test
Colony count (aerobic bacteria): ≤ 5000 CFU/g
Colony count (Yeasts and moulds): ≤ 500 CFU/g
Endotoxins: ≤ 50 I.U./g

Legal Information

Kryptofix is a registered trademark of Merck KGaA, Darmstadt, Germany


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Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

WGK

WGK 3

Hazard Codes



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