76850
1,2,2,6,6-Pentamethylpiperidine
purum, ≥99.0% (GC)
Synonym(s):
PMP, Pempidine
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About This Item
Empirical Formula (Hill Notation):
C10H21N
CAS Number:
Molecular Weight:
155.28
EC Number:
201-211-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
103806
MDL number:
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
grade
purum
assay
≥99.0% (GC)
bp
187-188 °C (lit.)
density
0.858 g/mL at 25 °C (lit.)
Other Notes
One of the most strongly basic tertiary amines (sterically hindered and nonquaternizing)
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
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
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H.Z. Sommer et al.
The Journal of Organic Chemistry, 36, 824-824 (1971)
[Tuberculous osteoarthritis revealed by ankle injury].
O Louletzian et al.
Presse medicale (Paris, France : 1983), 28(10), 531-532 (1999-04-21)
M L Kemel et al.
Neuroscience, 50(3), 597-610 (1992-10-01)
Previously, using a new in vitro microsuperfusion procedure, we have demonstrated marked differences in the cholinergic presynaptic regulation of the release of [3H]dopamine continuously synthesized from [3H]tyrosine in two close striosomal- and matrix-enriched areas of the cat caudate nucleus. A
L Tremblay et al.
Proceedings of the National Academy of Sciences of the United States of America, 89(23), 11214-11218 (1992-12-01)
Using a sensitive in vitro microperfusion method, the effects of selective and potent agonists of NK1, NK2, and NK3 tachykinin receptors ([Pro9]SP, ([Lys5,MeLeu9,Nle10]NKA-(4-10), and [Pro7]NKB, respectively) on the presynaptic control of dopamine release were investigated in striosomal-enriched (area rich in
T J Martin et al.
The Journal of pharmacology and experimental therapeutics, 254(1), 45-51 (1990-07-01)
The nature of mecamylamine's and pempidine's antagonism of nicotine in the central nervous system has not been defined clearly. Although these compounds are thought to be noncompetitive antagonists in the brain due to the fact that they do not compete
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