1753-68-0 Usage
Uses
Used in Medical Imaging:
2,5-bis(1-piperidylmethyl)benzene-1,4-diol is used as a contrast agent in medical imaging for enhancing the visibility of certain tissues and organs in radiographic examinations. Its chelating properties allow for improved diagnostic accuracy in various imaging modalities.
Used in Heavy Metal Poisoning Treatment:
In the medical field, 2,5-bis(1-piperidylmethyl)benzene-1,4-diol is used as a treatment for heavy metal poisoning. It is administered orally or intravenously to bind with toxic metal ions, facilitating their safe removal from the body and mitigating the harmful effects of heavy metal exposure.
Used in Industrial Applications:
2,5-bis(1-piperidylmethyl)benzene-1,4-diol is used as a metal ion sequestrant in industrial processes. It helps in managing and controlling the presence of metal ions, which is crucial for various manufacturing and production activities.
Used in Water Treatment:
In the water treatment industry, 2,5-bis(1-piperidylmethyl)benzene-1,4-diol is employed for its ability to chelate and remove heavy metal ions from water sources. This contributes to the purification of water and ensures the safety of water supplies for various uses.
It is important to handle 2,5-bis(1-piperidylmethyl)benzene-1,4-diol with care due to its potential toxicity if ingested or absorbed through the skin, emphasizing the need for proper safety measures during its use in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1753-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1753-68:
(6*1)+(5*7)+(4*5)+(3*3)+(2*6)+(1*8)=90
90 % 10 = 0
So 1753-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H28N2O2/c21-17-12-16(14-20-9-5-2-6-10-20)18(22)11-15(17)13-19-7-3-1-4-8-19/h11-12,21-22H,1-10,13-14H2
1753-68-0Relevant academic research and scientific papers
Investigation of Alkyl Amine Substituted Quinone Derivatives for the Redox Flow Battery Applications in Acidic Medium
Aidhen, Indrapal Singh,Khan, Harun,Murugan, Raja,Ramanujam, Kothandaraman,Sivanadanam, Jagadeeswari
, (2022/03/07)
2,5-bis((dimethylamino)methyl)benzene-1,4-diol (H2QDMA), a redox-active molecule and its derivatives are synthesised by a onestep chemical method using Mannich reaction has been explored as catholyte with vanadium (V2+/V3+) anolyte for aqueous redox flow battery applications. The solubility of H2QDMA was 0.75 M in 3 M H2SO4. H2QDMA showed one sharp redox peak at the formal potential 0.6 V vs Ag/AgCl, and it was stable for 100 continuous CV cycles without any appreciable change in colour. The battery delivered a discharge capacity of 2 Ah L?1, which faded with cycles. We have carried out a post cycle analysis of catholyte and anolyte to understand the origin of the capacity fading. Towards this, the oxidized form of H2QDMA, i.e., QDMA, was synthesized. The stability of QDMA in acidic solution was low, and the colour of the solution changed to intense brown with time. The UV Visible spectrum and CV curves of the QDMA reflects the same behaviour as observed with the catholyte solution obtained post galvanostatic charge-discharge analysis. This study concluded that the QDMA undergoes faster chemical transformation, presumably through the Michael addition reaction process, compared to its participation in the desired electrochemical process.
