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Methanol-d4 -Lösung

NMR reference standard, 99.8 atom % D, NMR tube size 3 mm × 8 in.

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About This Item

Lineare Formel:
CD3OD
Molekulargewicht:
36.07
EG-Nummer:
212-378-6
UNSPSC-Code:
41116107
NACRES:
NA.12

Qualität

NMR reference standard

Isotopenreinheit

99.8 atom % D

Assay

99% (CP)

Form

liquid

Methode(n)

NMR: suitable

NMR-Röhrchengröße

3 mm × 8 in.

Massenverschiebung

M+4

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Allgemeine Beschreibung

Methanol-d4 (CD3OD) is a deuterated NMR solvent used for NMR-based research and analyses. It has the highest isotopic enrichment and will not interfere with the desired level of detection.
The absolute infrared absorption intensities of CD3OD have been reported between 8000 and 350cm-1.

Anwendung

Methanol-d4 may be used as a removable internal standard to limit contamination during the quantification of lipophilic shellfish toxins using quantitative nuclear magnetic resonance technique (qNMR). The purity and ability of the lipophilic shellfish toxins to serve as authentic reference standards is also determined. It may also be used as a solvent in investigating the utility of matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry to monitor peptide and protein conformational changes of bradykinin, α-melanocyte stimulating hormone, and melittin.

Menge

3 mm O.D. tube contains 0.235 mL.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Zielorgane

Eyes,Central nervous system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

49.5 °F - closed cup

Flammpunkt (°C)

9.7 °C - closed cup

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Infrared intensities of liquids. XVII. Infrared refractive indices from 8000 to 350 cm-1, absolute integrated absorption intensities, transition moments, and dipole moment derivatives of methan-d3-ol and methanol-d4 at 25?C.
Bertie JE and Zhang SL.
J. Chem. Phys. , 101(10), 8364-8379 (1994)
Alexis Lavaud et al.
Phytochemistry, 109, 103-110 (2014-12-04)
Ten tocotrienol derivatives, i.e., amplexichromanols (1-10), were isolated from stem bark of Garcinia amplexicaulis Vieill. ex Pierre collected in Caledonia. The structures of the compounds 1-5 were determined to be chromanol derivatives substituted by a polyprenyl chain oxidized in terminal
Cheng-Kun Lin et al.
Organic & biomolecular chemistry, 13(7), 2100-2107 (2014-12-20)
A straightforward synthesis of novel, 2-heterocyclyl polyhydroxylated pyrrolidines is described. Stereocontrolled additions of nucleophiles to cyclic nitrones generated the corresponding 2,3-trans adducts, allowing the synthesis of the corresponding pyrrolidines via key intermediates bearing an alkyne and a nitrile oxide. Three
Jon Kapla et al.
Physical chemistry chemical physics : PCCP, 17(34), 22438-22447 (2015-08-08)
The disaccharide trehalose (TRH) strongly affects the physical properties of lipid bilayers. We investigate interactions between lipid membranes formed by 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and TRH using NMR spectroscopy and molecular dynamics (MD) computer simulations. We compare dipolar couplings derived from DMPC/TRH
Athina Dimopoulou et al.
Nucleosides, nucleotides & nucleic acids, 34(4), 289-308 (2015-03-17)
We report the synthesis of novel thiopurine pyranonucleosides. Direct coupling of silylated 6-mercaptopurine and 6-thioguanine with the appropriate pyranoses 1a-e via Vorbrüggen nucleosidation, gave the N-9 linked mercaptopurine 2a-e and thioguanine 4a-e nucleosides, while their N-7 substituted congeners 10a-e and
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