490288
Methylamine-15N hydrochloride
98 atom % 15N
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Fórmula lineal:
CH315NH2·HCl
Número CAS:
Peso molecular:
68.51
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
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Permítanos ayudarleNombre del producto
Methylamine-15N hydrochloride, 98 atom % 15N
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i2+1;
SMILES string
Cl.C[15NH2]
InChI key
NQMRYBIKMRVZLB-CGOMOMTCSA-N
isotopic purity
98 atom % 15N
form
solid
mp
232-234 °C (lit.)
mass shift
M+1
Quality Level
Categorías relacionadas
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
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N Cecilia Martinez-Gomez et al.
Journal of bacteriology, 195(10), 2359-2367 (2013-03-19)
The methylotroph Methylobacterium extorquens AM1 oxidizes methanol and methylamine to formaldehyde and subsequently to formate, an intermediate that serves as the branch point between assimilation (formation of biomass) and dissimilation (oxidation to CO₂). The oxidation of formaldehyde to formate is
Yongqian Zhang et al.
Analytica chimica acta, 752, 106-111 (2012-10-30)
Both endogenous and exogenous methylamine have been found to be involved in many human disorders. The quantitative assessment of methylamine has drawn considerable interest in recent years. Although there have been many papers about the determination of methylamine, only a
Frank Weinhold
Journal of computational chemistry, 33(30), 2440-2449 (2012-07-28)
We have developed a "Natural Bond Critical Point" (NBCP) module for the natural bond orbital (NBO) program that allows mutual analysis of NBO-based versus Bader-type quantum theory of atoms in molecules (QTAIM) topological descriptors of chemical bonding interactions. Conventional QTAIM
Sheeza Khan et al.
Protein and peptide letters, 20(1), 61-70 (2012-06-08)
Kidney cells of animals including human and marine invertebrates contain high amount of the protein denaturant, urea. Methylamine osmolytes are generally believed to offset the harmful effects of urea on proteins in vitro and in vivo. In this study we
Nicolas Fleury-Brégeot et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(31), 9564-9570 (2012-07-07)
Ammoniomethyl trifluoroborates are very powerful reagents that can be used to access biologically relevant aryl- and heteroaryl-methylamine motifs via Suzuki-Miyaura cross-couplings. Until now, this method was limited to the production of tertiary and primary amines. The synthesis of a large
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