53490
1-甲基哌啶 溶液
BioReagent, suitable for protein sequencing, ~40% in 1-butanol
别名:
N-甲基哌啶
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关于此项目
经验公式（希尔记法）:
C6H13N
化学文摘社编号:
分子量:
99.17
PubChem Substance ID:
UNSPSC Code:
12352200
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
product line
BioReagent
concentration
~40% in 1-butanol
refractive index
n20/D 1.406
suitability
suitable for protein sequencing
storage temp.
−20°C
Packaging
专用包装，可直接用于常用测序仪。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system, Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
82.4 °F - closed cup
flash_point_c
28 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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
[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.
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
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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