• 1. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Evolved polymerases facilitate selection of fully 2′-OMe-modified aptamers?
  Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
• 3. Fate of Sb(v) and Sb(iii) species along a gradient of pH and oxygen concentration in the Carnoulès mine waters (Southern France)
  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Secondary amines

N-(2-Chloroethyl)-1,2-Ethanediamine Dihydrochloride: A Comprehensive Overview

N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride, also known by its CAS number 5590-29-4, is a chemical compound with significant applications in various industries. This compound is a derivative of ethylenediamine, a widely used amine in chemical synthesis. The molecule consists of a two-carbon chain with two amine groups and a chloroethyl substituent, making it a versatile compound with unique chemical properties.

N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride is often utilized as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its structure allows for easy modification and functionalization, which is critical in the development of advanced materials and compounds. Recent studies have highlighted its role in the synthesis of metal-organic frameworks (MOFs) and coordination polymers, where its ability to act as a ligand has been exploited to create porous materials with high surface areas.

The compound's chemical stability and reactivity make it an ideal candidate for various industrial applications. For instance, in the pharmaceutical industry, N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride is employed as an intermediate in the production of antibiotics and antiviral agents. Its ability to form stable complexes with metal ions has also led to its use in catalytic processes and as a chelating agent in water treatment systems.

Recent research has focused on optimizing the synthesis of N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride to enhance yield and reduce environmental impact. Novel methods involving green chemistry principles have been developed, such as using microwave-assisted synthesis or enzymatic catalysis. These advancements not only improve the efficiency of production but also align with global efforts to promote sustainable chemical manufacturing.

In terms of safety and handling, N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride should be treated with care due to its potential to cause skin and eye irritation. Proper personal protective equipment (PPE) should be worn during handling, and storage should be in accordance with standard chemical storage practices to prevent contamination or degradation.

Overall, N-(2-Chloroethyl)-1,2-ethanediamine dihydrochloride remains a vital compound in modern chemistry, with ongoing research exploring its potential in emerging fields such as nanotechnology and biotechnology. Its versatility and reactivity ensure that it will continue to play a pivotal role in the development of innovative chemical products and processes.

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• 334-22-5(bis(2-chloroethyl)amine)
• 50871-01-7((2-chloroethyl)(ethyl)amine)
• 102092-04-6(Bis(2-chloroethyl)-d8-amine HCl)
• 53502-60-6(Piperazine,1-(2-chloroethyl)-, hydrochloride (1:2))
• 101418-39-7(1,2-Ethanediamine,N1,N2-bis(2-chloroethyl)-N1,N2-dimethyl-)
• 100517-14-4(1,2-Ethanediamine,N1,N1-bis(2-chloroethyl)-)
• 63980-44-9(Piperazine,1,4-bis(2-chloroethyl)-, hydrochloride (1:1))
• 821-48-7(Bis(2-chloroethyl)amine hydrochloride)
• 352431-06-2(Bis(2-chloroethyl)-1,1,2,2-d4-amine Hydrochloride)