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:
Product Name
Methylamine-13C hydrochloride, 99 atom % 13C
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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T A Kuznetsova et al.
Prikladnaia biokhimiia i mikrobiologiia, 48(6), 606-611 (2013-01-22)
Methanol dehydrogenase (MDG) of the facultative methylotrophic phytosymbiont Methylobacterium nodulans has been purified for the first time to an electrophoretically homogeneous state and characterized. The native protein with a molecular mass of 70 kDa consists of large (60 kDa) and
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
Chaehyuk Ko et al.
The journal of physical chemistry. B, 117(1), 316-325 (2012-12-15)
Proton-coupled electron transfer can occur through concerted (electron-proton transfer, EPT) or sequential mechanisms, but this distinction becomes less well-defined for photoinduced reactions. These issues have been examined with transient absorption experiments on a hydrogen-bonded complex consisting of p-nitrophenylphenol and t-butylamine.
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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