274631
1,2,2,6,6-Pentamethylpiperidine
97%
Synonym(s):
PMP, Pempidine
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About This Item
Empirical Formula (Hill Notation):
C10H21N
CAS Number:
Molecular Weight:
155.28
Beilstein:
103806
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.460 (lit.)
bp
187-188 °C (lit.)
density
0.858 g/mL at 25 °C (lit.)
SMILES string
CN1C(C)(C)CCCC1(C)C
InChI
1S/C10H21N/c1-9(2)7-6-8-10(3,4)11(9)5/h6-8H2,1-5H3
InChI key
XULIXFLCVXWHRF-UHFFFAOYSA-N
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General description
The focal 1,8-naphthalimide fluorophores in the antennae were modified with 1,2,2,6,6-pentamethylpiperidine to improve their photostability.
Application
1,2,2,6,6-Pentamethylpiperidine (PMP) was used as an organic structure directing agent (OSDA) in the synthesis of the RTH-type zeolites.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
131.0 °F - closed cup
Flash Point(C)
55 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Nikolai I Georgiev et al.
Journal of fluorescence, 21(1), 51-63 (2010-07-20)
This paper reports on the divergent synthesis, photophysical properties and photodegradation of novel PAMAM dendrons, core and peripherally functionalized with 1,8-naphthalimide fluorophores. The novel compounds were configured as light-harvesting antennae where the system surface is labeled with blue emitting 4-allyloxy-1,8-naphthalimide
Ming Liu et al.
Physical chemistry chemical physics : PCCP, 16(9), 4155-4164 (2014-01-24)
In addition to the original preparation route of the RTH-type zeolites using 1,2,2,6,6-pentamethylpiperidine (PMP) as an organic structure directing agent (OSDA), we have found that simpler organic amines such as N-methylpiperidine and pyridine can be used as alternative OSDAs in
[Tuberculous osteoarthritis revealed by ankle injury].
O Louletzian et al.
Presse medicale (Paris, France : 1983), 28(10), 531-532 (1999-04-21)
C Maccarrone et al.
Life sciences, 42(25), 2633-2638 (1988-01-01)
Decentralization of the superior cervical ganglion (S.C.G.) of the rat elevated the neuropeptide-Y immunoreactivity (NPY-ir) content of the ganglion on day 1 (+43%) but not on day 3 post-surgery. The content of NPY-ir in the iris was increased by decentralization
G I Wilkie et al.
Neurochemical research, 21(9), 1141-1148 (1996-09-01)
The modulation of [3H]ACh release by nicotinic compounds was studied in superfused rat hippocampal synaptosomes loaded with [3H]choline, (-)-Nicotine (0.1-10 microM) evoked a dose-dependent increase in [3H]ACh release; higher concentrations were less effective. Nicotine-evoked release was Ca(2+)-dependent, and blocked by
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