Skip to Content
Merck
All Photos(1)

Key Documents

372072

Sigma-Aldrich

Sodium deuteroxide solution

40 wt. % in D2O, 99.5 atom % D

Synonym(s):

Sodium deuteroxide solution, Sodium hydroxide-d

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
NaOD / D2O
CAS Number:
Molecular Weight:
41.00
MDL number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.12

isotopic purity

99.5 atom % D

form

liquid

concentration

40 wt. % in D2O

technique(s)

NMR: suitable

refractive index

n20/D 1.418

mass shift

M+1

SMILES string

[Na+].[O-][2H]

InChI

1S/Na.H2O/h;1H2/q+1;/p-1/i/hD

InChI key

HEMHJVSKTPXQMS-DYCDLGHISA-M

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Sodium deuteroxide solution is an isotopic analog of sodium hydroxide. It is used as a deuterium source to produce other deuterated compounds.

Application

Sodium deuteroxide solution is used:
  • As a deuterated solvent to measure the extent of hydrolysis of CEE (creatine ethyl ester) by NMR spectroscopy.
  • To prepare deuterated THPM (tetrahydropyrimidine).
  • To study the preparation, stability and biodegradability of surface-active amide.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Juan Carro et al.
Biochemistry, 57(11), 1790-1797 (2018-02-28)
The mechanism of dioxygen reduction by the flavoenzyme aryl-alcohol oxidase was investigated with kinetic isotope, viscosity, and pL (pH/pD) effects in rapid kinetics experiments by stopped-flow spectrophotometry of the oxidative half-reaction of the enzyme. Double mixing of the enzyme in
Mary Jo Weiss-Errico et al.
The journal of physical chemistry. B, 121(35), 8359-8366 (2017-08-12)
Legacy perfluoroalkyl substances (PFASs) are known environmental pollutants with serious adverse health effects. Perfluoroethercarboxylic acids (PFECAs), emerging PFASs now being substituted for legacy PFASs, have recently been detected in the environment. Cyclodextrins (CDs) have been proposed as agents for the
Ricardo Dias et al.
International journal of biological macromolecules, 112, 1029-1037 (2018-02-16)
Celiac Disease (CD) is now recognized as a worldwide epidemic. Although a gluten free diet usually induces clinical improvements within days or weeks, adhering to this routine is still troublesome. Therefore, new solutions are needed for quality-of-life improvement of CD
Adam R Offenbacher et al.
The journal of physical chemistry. B, 124(2), 345-354 (2020-01-07)
Proton-coupled electron transfer (PCET) is fundamental to many important biological reactions, including solar energy conversion and DNA synthesis. For example, class Ia ribonucleotide reductases (RNRs) contain a tyrosyl radical-diiron cofactor with one aspartate ligand, D84. The tyrosyl radical, Y122•, in
Jolanda E Reusser et al.
Environmental science. Processes & impacts, 22(4), 1084-1094 (2020-03-20)
Inositol phosphates, particularly myo-inositol hexakisphosphate (myo-IP6), are an important pool of soil organic phosphorus (P) in terrestrial ecosystems. To measure concentrations of myo-IP6 in alkaline soil extracts, solution 31P nuclear magnetic resonance (NMR) spectroscopy is commonly used. However, overlap of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service