274631
1,2,2,6,6-Pentamethylpiperidine
97%
Synonym(s):
PMP, Pempidine
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C10H21N
CAS Number:
Molecular Weight:
155.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-211-2
Beilstein/REAXYS Number:
103806
MDL number:
Assay:
97%
Form:
liquid
InChI key
XULIXFLCVXWHRF-UHFFFAOYSA-N
InChI
1S/C10H21N/c1-9(2)7-6-8-10(3,4)11(9)5/h6-8H2,1-5H3
SMILES string
CN1C(C)(C)CCCC1(C)C
assay
97%
form
liquid
Quality Level
refractive index
n20/D 1.460 (lit.)
bp
187-188 °C (lit.)
density
0.858 g/mL at 25 °C (lit.)
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F - closed cup
flash_point_c
55 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
V E Gmiro et al.
Eksperimental'naia i klinicheskaia farmakologiia, 63(2), 16-20 (2000-06-02)
Pyrilene acts as a central H-cholinoblocker upon intramuscular injection at a dose of 0.02-0.08 mg/kg, and as an NMDA-blocker, when the dose is increased to 0.2-0.8 mg/kg. Similarly, amantadine exhibits the properties of H-cholinoblocker and NMDA-blocker in the dose intervals
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
M L Kemel et al.
Proceedings of the National Academy of Sciences of the United States of America, 86(22), 9006-9010 (1989-11-01)
By use of a sensitive in vitro microsuperfusion method, the cholinergic prsynaptic control of dopamine release was investigated in a prominent striosome (areas poor in acetylcholinesterase activity) located within the core of cat caudate nucleus and also in adjacent matrix
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service