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Key Documents

100358

Sigma-Aldrich

3-Aminoquinuclidine dihydrochloride

98%

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About This Item

Empirical Formula (Hill Notation):
C7H14N2 · 2HCl
CAS Number:
Molecular Weight:
199.12
Beilstein/REAXYS Number:
3681298
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

321-323 °C (dec.) (lit.)

SMILES string

Cl.Cl.NC1CN2CCC1CC2

InChI

1S/C7H14N2.2ClH/c8-7-5-9-3-1-6(7)2-4-9;;/h6-7H,1-5,8H2;2*1H

InChI key

STZHBULOYDCZET-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Enantiomeric purity determination of 3-aminoquinuclidine by diastereomeric derivatization and high-performance liquid chromatographic separation.
I Demian et al.
Journal of chromatography, 466, 415-420 (1989-04-19)
Christopher J Magnus et al.
Science (New York, N.Y.), 333(6047), 1292-1296 (2011-09-03)
Ionic flux mediates essential physiological and behavioral functions in defined cell populations. Cell type-specific activators of diverse ionic conductances are needed for probing these effects. We combined chemistry and protein engineering to enable the systematic creation of a toolbox of
Sofia M Morozova et al.
Membranes, 10(9) (2020-09-24)
The growing concern for climate change and global warming has given rise to investigations in various research fields, including one particular area dedicated to the creation of solid sorbents for efficient CO2 capture. In this work, a new family of

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