543047
Deuterium chloride solution
35 wt. % in D2O, ≥99 atom % D
Synonym(s):
Hydrochloric acid-d solution
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About This Item
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isotopic purity
≥99 atom % D
Quality Level
concentration
35 wt. % in D2O
technique(s)
NMR: suitable
mass shift
M+1
SMILES string
Cl[2H]
InChI
1S/ClH/h1H/i/hD
InChI key
VEXZGXHMUGYJMC-DYCDLGHISA-N
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General description
Lithium deuteride is isotopically labeled analogue of Lithium hydride.
Application
Deuterium chloride solution has been used to study:
- The kinetics of chitosan reacetylation using acetic anhydride and acetic acid.
- Regioselective terminal group activation of chitosan by thioacetylation.
- The complex formation between cyclodextrin and captopril in aqueous solution using NMR spectroscopy.
Lithium deuteride can act as semiconductor at 30GPa and room temperature. It is used as the polarized deuteron target material for the measurement of proton and neutron structure
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Inclusion complex formation of captopril with $\alpha$-and $\beta$-cyclodextrins in aqueous solution: NMR spectroscopic and molecular dynamic studies.
Journal of Pharmaceutical Sciences, 91(11), 2390-2398 (2002)
Kinetics and efficiency of chitosan reacetylation.
Carbohydrate Polymers, 87(2), 1192-1198 (2012)
Nature communications, 11(1), 6140-6140 (2020-12-03)
Hydrogen-Deuterium eXchange coupled to Mass Spectrometry (HDX-MS) is now common practice in structural biology. However, it is most of the time applied to rather small oligomeric complexes. Here, we report on the use of HDX-MS to investigate conformational differences between
Regioselective chitosan end-group activation: the triskelion approach
Royal Society of Chemistry Advances, 7(30), 18628-18638 (2017)
PloS one, 15(10), e0239982-e0239982 (2020-10-02)
Magnetic resonance spectroscopy (MRS) allows the analysis of biochemical processes non-invasively and in vivo. Still, its application in clinical diagnostics is rare. Routine MRS is limited to spatial, chemical and temporal resolutions of cubic centimetres, mM and minutes. In fact
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