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Merck
CN

490288

甲胺-15N 盐酸盐

98 atom % 15N

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线性分子式:
CH315NH2·HCl
化学文摘社编号:
分子量:
68.51
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
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产品名称

甲胺-15N 盐酸盐, 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

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.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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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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