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Home > Chemical Reagents > Deuterated Reagents (Find 12 items)

Deuterated Reagents

1,2-Dichlorobenzene-d4

(2199-69-1)
Isotope labelled 1,2-Dichlorobenzene is a side product of the production of chlorobenzene.

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1,2-Benzene-3,4,5,6-d4-dicarboxylic acid, dioctyl ester

(93952-13-7)
A labelled phthalate ester used as plasticizers and additives. Used in toxiciology studies as well as risk assessment studies of food contamination that occurs via migration of phthalates into foodstuffs from food-contact materials (FCM).

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1,3,5-Triazine-2,4,6-triamine-N2,N2,N4,N4,N6,N6-d6

(13550-89-5)
This deuterated Melamine has readily exchangeable deuterium and is not suitable for applications in protic solvents

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Deuterated reagent chemicals are derived from nuclear physics heavy water extraction industry derived products. The introduction of the atomic bomb in the 1940s promoted the rapid development of the seawater and heavy water refining industry, and gradually shifted from military and national defense to high-tech R & D applications. At present, the production process of high-purity deuterated derivatives is mainly controlled by Germany and the United States. "Deuterated Reagents" on ECHEMI mainly supplies raw materials for Deuterated Reagents.

Frequently Asked Questions

What are deuterated reagents and why are they important in scientific research?

Deuterated reagents are chemical compounds in which one or more hydrogen atoms have been replaced with deuterium, a stable isotope of hydrogen. They are essential in fields like NMR spectroscopy, mass spectrometry, and pharmaceutical development because they help track molecular pathways, improve analytical accuracy, and serve as internal standards. Their use enhances the precision and reliability of experimental results.

How do deuterated solvents differ from regular solvents in NMR applications?

Deuterated solvents, such as deuterated chloroform (CDCl₃) or deuterated dimethyl sulfoxide (DMSO-d6), contain deuterium instead of hydrogen, which minimizes interference from solvent proton signals in NMR spectra. This allows clearer observation of the sample’s proton signals, leading to more accurate structural analysis. Choosing high-purity deuterated solvents is critical for reliable NMR data.

Are deuterated reagents used in drug development?

Yes, deuterated reagents play a significant role in drug development. They are used to synthesize deuterated drugs (deuterium-labeled APIs), which can exhibit improved metabolic stability, longer half-lives, and reduced toxicity compared to non-deuterated counterparts. Additionally, deuterated compounds serve as tracers in pharmacokinetic and metabolism studies, aiding in regulatory submissions and clinical trial design.

How should deuterated reagents be stored to maintain their quality?

Deuterated reagents should be stored in tightly sealed containers under inert atmosphere (e.g., argon or nitrogen) to prevent hydrolysis or protium exchange. Most should be kept at low temperatures (2–8°C or –20°C, depending on stability) and protected from light and moisture. Always follow the manufacturer’s storage guidelines and check expiration dates to ensure optimal performance in sensitive analytical or synthetic applications.

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