721921
Methanol-d4
NMR reference standard, 99.8 atom % D, NMR tube size 3 mm × 8 in.
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About This Item
Formule linéaire :
CD3OD
Poids moléculaire :
36.07
Numéro CE :
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.12
Produits recommandés
Qualité
NMR reference standard
Pureté isotopique
99.8 atom % D
Pureté
99% (CP)
Forme
liquid
Technique(s)
NMR: suitable
Taille du tube de RMN
3 mm × 8 in.
Changement de masse
M+4
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Description générale
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.
The absolute infrared absorption intensities of CD3OD have been reported between 8000 and 350cm-1.
Application
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.
Quantité
3 mm O.D. tube contains 0.235 mL.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
Organes cibles
Eyes,Central nervous system
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
49.5 °F - closed cup
Point d'éclair (°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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