490288
Methylamine-15N hydrochloride
98 atom % 15N
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Cambia visualizzazione
1 G
CHF 676.00
About This Item
Formula condensata:
CH315NH2·HCl
Numero CAS:
Peso molecolare:
68.51
Numero MDL:
Codice UNSPSC:
12352116
ID PubChem:
NACRES:
NA.12
Prodotti consigliati
Purezza isotopica
98 atom % 15N
Livello qualitativo
Stato
solid
Punto di fusione
232-234 °C (lit.)
Spostamento di massa
M+1
Stringa SMILE
Cl.C[15NH2]
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i2+1;
NQMRYBIKMRVZLB-CGOMOMTCSA-N
Categorie correlate
Confezionamento
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.
Avvertenze
Warning
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 4 Oral
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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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