Chemical Name: 1,2,3,4-Tetrahydro-5-aminoacridine hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Potent cholinesterase inhibitor, a cognition enhancer in vivo.
Technical Data
M. Wt
234.73
Formula
C13H14N2.HCl
Storage
Desiccate at +4°C
Purity
≥99% (HPLC)
CAS Number
1684-40-8
PubChem ID
15517
InChI Key
ZUFVXZVXEJHHBN-UHFFFAOYSA-N
Smiles
Cl.NC1=C2CCCCC2=NC2=CC=CC=C12
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
23.47
100
water
23.47
100
Preparing Stock Solutions
The following data is based on the product molecular weight 234.73. 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
4.26 mL
21.3 mL
42.6 mL
5 mM
0.85 mL
4.26 mL
8.52 mL
10 mM
0.43 mL
2.13 mL
4.26 mL
50 mM
0.09 mL
0.43 mL
0.85 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
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References
References are publications that support the products' biological activity.
Freeman and Dawson
(1991) Tacrine: a pharmacological review. Prog.Neurobiol. 36 257 PMID: 1714613
Osborne and Christie
(1996) Tetrahydro-9-aminoacridine has mixed actions on muscarinic currents and blocks opioid currents in rat locus ceruleus neurons. J.Pharmacol.Exp.Ther. 276 137 PMID: 8558423
Snapeet al (1999) A comparative study in rats of the in vitro and in vivo pharmacology of the acetylcholinesterase inhibitors tacrine, donepezil and NXX-066. Neuropharmacology 38 181 PMID: 10193909
Summers and Kaufman
(1980) THA- A review of the literature and its use in treatment of five overdose patients. Clin.Toxicol. 16 269 PMID: 6994999