Chemical Name: 2,2,6,6-Tetramethylpiperidin-4-yl heptanoate
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Potent non-competitive antagonist of neuronal nicotinic ACh receptors (nAChRs). Produces long-lasting inhibition of neuronal nAChRs formed by the combination of the most abundant α and β subunits (i.e. α3, α4 and β2, β4 respectively). Displays little inhibition of muscle-type (α1β1γδ) or α7 receptors.
Licensing Information
Sold under license from the University of Florida Research Foundation Inc.
Compound Libraries
TMPH hydrochloride is also offered as part of the
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Technical Data
M. Wt
305.88
Formula
C16H31NO2.HCl
Storage
Desiccate at RT
Purity
≥98% (HPLC)
CAS Number
849461-91-2
PubChem ID
16079014
InChI Key
XIDDVJIJIFWGIX-UHFFFAOYSA-N
Smiles
CC1(C)NC(C)(C)CC(OC(CCCCCC)=O)C1.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
30.59
100
water
30.59
100
Preparing Stock Solutions
The following data is based on the product molecular weight 305.88. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.27 mL
16.35 mL
32.69 mL
5 mM
0.65 mL
3.27 mL
6.54 mL
10 mM
0.33 mL
1.63 mL
3.27 mL
50 mM
0.07 mL
0.33 mL
0.65 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Papkeet al (2005) The effects of subunit composition on the inhibition of nicotinic receptors by the amphipathic blocker 2,2,6,6-tetramethylpiperidin-4-yl heptanoate. Mol.Pharmacol. 67 1977 PMID: 15761116