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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:
79-55-0
Molecular Weight:
155.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856594
EC Number:
201-211-2
Beilstein/REAXYS Number:
103806
MDL number:
MFCD00006493
Assay:
97%
Form:
liquid
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Quality Level

200

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

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.

pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN7123
BCCL1685
BCCG2968
BCBV4885
BCBQ4177V

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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
P M Plotsky et al.
Life sciences, 41(10), 1311-1317 (1987-09-07)
Secretion of corticotropin releasing factor (CRF) from the hypothalamic paraventricular nuclei into the hypophysial-portal circulation is modulated by a variety of neuronal afferents. Effects of intracerebroventricular acetylcholine (ACH), gamma-aminobutyric acid (GABA) and epinephrine (EPI) on immunoreactive (ir) CRF concentration in
D Blozovski
Developmental psychobiology, 18(4), 355-366 (1985-07-01)
Young rats, 11, 16, and 20 days of age, received bilateral injections of three antinicotinic agents into the posteroventral hippocampo-subiculo-entorhinal area, and were trained to learn a cool-draft-stimulus, passive-avoidance task shortly after (17 min). Gallamine triethiodide had no action at
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Global Trade Item Number

SKUGTIN
274631-5G04061837775710