Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C13H14N2 · HCl · xH2O
CAS Number:
Molecular Weight:
234.72 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥99%
Form:
solid
Quality Level
assay
≥99%
form
solid
mp
284-286 °C (lit.)
SMILES string
O.Cl.Nc1c2CCCCc2nc3ccccc13
InChI
1S/C13H14N2.ClH.H2O/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13;;/h1,3,5,7H,2,4,6,8H2,(H2,14,15);1H;1H2
InChI key
PXGRMZYJAOQPNZ-UHFFFAOYSA-N
Application
9-Amino-1,2,3,4-tetrahydroacridine hydrochloride hydrate is a well-known cholinesterase inhibitor commonly used in pharmacological studies.
Still not finding the right product?
Explore all of our products under 9-Amino-1,2,3,4-tetrahydroacridine hydrochloride hydrate
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Acetylcholinesterase capillary enzyme reactor for screening and characterization of selective inhibitors.
da Silva JI, et al.
Journal of Pharmaceutical and Biomedical Analysis, 73, 44-52 (2013)
Comparison of inhibitory activities of donepezil and other cholinesterase inhibitors on acetylcholinesterase and butyrylcholinesterase in vitro.
Ogura H, et al.
Methods and Findings in Experimental and Clinical Pharmacology, 22(8), 609-614 (2000)
The ameliorating effects of stigmasterol on scopolamine-induced memory impairments in mice.
Park SJ, et al.
European Journal of Pharmacology, 676(1-3), 64-70 (2012)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A79922-5G | 04061833390924 |
| A79922-1G | 04061833390917 |

