M9046
1-Methylpiperidine solution
15% in methanol: water
Synonym(s):
N-Methylpiperidine
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About This Item
Empirical Formula (Hill Notation):
C6H13N
CAS Number:
Molecular Weight:
99.17
PubChem Substance ID:
UNSPSC Code:
12352204
Beilstein/REAXYS Number:
1560282
MDL number:
SMILES string
CN1CCCCC1
InChI
1S/C6H13N/c1-7-5-3-2-4-6-7/h2-6H2,1H3
InChI key
PAMIQIKDUOTOBW-UHFFFAOYSA-N
concentration
15% in methanol: water
storage temp.
2-8°C
Packaging
20% price reduction on quantities of 4 or more
Disclaimer
Shake well prior to use.
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Nithyanandhan Jayaraj et al.
Langmuir : the ACS journal of surfaces and colloids, 25(24), 13820-13832 (2010-06-22)
Supramolecular complexation behavior of cucurbiturils with paramagnetic nitroxide spin probes was examined by (1)H NMR, X-ray diffraction studies of crystals, computation, and EPR. Both cucurbit[7]uril (CB7) and cucurbit[8]uril (CB8) form a 1:1 complex with 4-(N,N,N-trimethylammonium)-2,2,6,6-tetramethylpiperidinyl-N-oxy bromide (CAT1). The structure of
A Kolocouris et al.
The Journal of organic chemistry, 66(15), 4989-4997 (2001-07-21)
When a 1-adamantyl or a 2-adamantyl substituent is introduced at the 2-position in N-methylpiperidine, four different chair conformations are possible. Experimental observation using dynamic NMR spectroscopy and molecular mechanics calculations agree that the chair conformation with an equatorial adamantyl group
[The mechanism of reverse inhibition of cholinesterases by thionphosphonates].
N N Kovalev et al.
Izvestiia Akademii nauk SSSR. Seriia biologicheskaia, (6)(6), 926-929 (1988-11-01)
Francisc Potmischil et al.
Magnetic resonance in chemistry : MRC, 45(3), 231-235 (2007-01-16)
The (15)N chemical shifts of 13 N-methylpiperidine-derived mono-, bi- and tricycloaliphatic tertiary amines, their methiodides and their N-epimeric pairs of N-oxides were measured, and the contributions of specific structural parameters to the chemical shifts were determined by multilinear regression analysis.
N D Henderson et al.
Anti-cancer drug design, 11(6), 421-438 (1996-09-01)
Bioreducible anti-tumour agents are prodrugs which are intended to be inactive in normal cells, but are able to undergo metabolic reduction in cancer cells to produce toxic species that can damage biomolecules. A series of N-oxides of heterocyclic aliphatic amines
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