76850
1,2,2,6,6-Pentamethylpiperidine
purum, ≥99.0% (GC)
Synonym(s):
PMP, Pempidine
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About This Item
grade
purum
Assay
≥99.0% (GC)
refractive index
n20/D 1.460 (lit.)
n20/D 1.460
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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Other Notes
One of the most strongly basic tertiary amines (sterically hindered and nonquaternizing)
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
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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The Journal of Organic Chemistry, 36, 824-824 (1971)
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
[Tuberculous osteoarthritis revealed by ankle injury].
Presse medicale (Paris, France : 1983), 28(10), 531-532 (1999-04-21)
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
Mediation of passive avoidance learning by nicotinic hippocampo-entorhinal components in young rats.
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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