277630
Methylamine-13C hydrochloride
99 atom % 13C
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About This Item
Formule linéaire :
13CH3NH2 · HCl
Numéro CAS:
Poids moléculaire :
68.51
Numéro MDL:
Code UNSPSC :
12352116
ID de substance PubChem :
Nomenclature NACRES :
NA.12
Produits recommandés
Pureté isotopique
99 atom % 13C
Niveau de qualité
Forme
solid
Technique(s)
protein expression: suitable
Pf
232-234 °C (lit.)
Changement de masse
M+1
Chaîne SMILES
Cl.[13CH3]N
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i1+1;
Clé InChI
NQMRYBIKMRVZLB-YTBWXGASSA-N
Conditionnement
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.
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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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
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
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
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
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
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