277630
Methylamine-13C hydrochloride
99 atom % 13C
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About This Item
Linear Formula:
13CH3NH2 · HCl
CAS Number:
Molecular Weight:
68.51
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
Isotopic purity:
99 atom % 13C
Mass shift:
M+1
Form:
solid
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i1+1;
SMILES string
Cl.[13CH3]N
InChI key
NQMRYBIKMRVZLB-YTBWXGASSA-N
isotopic purity
99 atom % 13C
form
solid
technique(s)
protein expression: suitable
mp
232-234 °C (lit.)
mass shift
M+1
Quality Level
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
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
Sucismita Chutia et al.
The journal of physical chemistry. B, 116(51), 14788-14804 (2012-11-23)
We study the initial steps of the interaction of water molecules with two unsolvated peptides: Ac-Ala(5)-LysH(+) and Ac-Ala(8)-LysH(+). Each peptide has two primary candidate sites for water adsorption near the C-terminus: a protonated carboxyl group and the protonated ammonium group
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