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Methylamin-13C -hydrochlorid
99 atom % 13C
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250 MG
€ 326,00
1 G
€ 821,00
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Größe auswählen
Ansicht ändern
250 MG
€ 326,00
1 G
€ 821,00
About This Item
Lineare Formel:
13CH3NH2 · HCl
CAS-Nummer:
Molekulargewicht:
68.51
MDL-Nummer:
UNSPSC-Code:
12352116
PubChem Substanz-ID:
NACRES:
NA.12
Empfohlene Produkte
Isotopenreinheit
99 atom % 13C
Qualitätsniveau
Form
solid
Methode(n)
protein expression: suitable
mp (Schmelzpunkt)
232-234 °C (lit.)
Massenverschiebung
M+1
SMILES String
Cl.[13CH3]N
InChI
1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i1+1;
InChIKey
NQMRYBIKMRVZLB-YTBWXGASSA-N
Verwandte Kategorien
Verpackung
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.
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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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
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
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
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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