274631
1,2,2,6,6-五甲基哌啶
97%
别名:
PMP, 潘必定
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关于此项目
经验公式（希尔记法）:
C10H21N
化学文摘社编号:
分子量:
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
产品名称
1,2,2,6,6-五甲基哌啶, 97%
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
refractive index
n20/D 1.460 (lit.)
bp
187-188 °C (lit.)
density
0.858 g/mL at 25 °C (lit.)
Quality Level
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Application
1,2,2,6,6-五甲基哌啶 (PMP) 作为有机结构导向剂 (OSDA) 用于合成 RTH 型分子筛 。
General description
用 1，2，2，6，6-五甲基哌啶修饰触角中的局灶性 1，8-萘酰亚胺荧光基团，以改善其光稳定性 。
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
存储类别
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
法规信息
危险化学品
此项目有
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)
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
Dean A Myers et al.
Behavioural brain research, 161(1), 39-44 (2005-05-21)
Corticosterone (CORT) micropellets were stereotaxically placed bilaterally at the dorsal margin of the central nucleus of the amygdala (CeA). Both behavioral and physiological responses were recorded (plus maze and colonic discomfort) at 7 days post-implantation. Corticosterone reduced the exploration of
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