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About This Item
Empirical Formula (Hill Notation):
C17H26N3O2S · ClO4
CAS Number:
Molecular Weight:
435.92
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI key
JALGRPFYCOBGHM-UHFFFAOYSA-M
SMILES string
[O-]Cl(=O)(=O)=O.CN(C)c1cccc2c(cccc12)S(=O)(=O)NCC[N+](C)(C)C
InChI
1S/C17H26N3O2S.ClHO4/c1-19(2)16-10-6-9-15-14(16)8-7-11-17(15)23(21,22)18-12-13-20(3,4)5;2-1(3,4)5/h6-11,18H,12-13H2,1-5H3;(H,2,3,4,5)/q+1;/p-1
form
solid
reaction suitability
reagent type: oxidant
storage temp.
−20°C
Application
- Used as a guest for multivalent macrocyclic hosts in histone surface recognition
- Dye for fluorescence spectroscopy
Fluorescent probe for receptor proteolipid from electric organ of Electrophorus electricus
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Hugo R Arias et al.
Biochemistry, 45(7), 2014-2026 (2006-02-16)
We investigated the molecular mechanisms and the binding site location for the fluorophor crystal violet (CrV), a noncompetitive antagonist of the nicotinic acetylcholine receptor (AChR). To this end, radiolabeled competition binding, fluorescence spectroscopy, Schild-type analysis, patch-clamp recordings, and molecular dynamics
A Szatanik-Kloc et al.
Plant physiology and biochemistry : PPB, 120, 194-201 (2017-10-22)
It is widely believed that pectin are responsible for the vast majority of cation binding positions in the root cell walls. To estimate the role of particular kinds of pectin, we studied the cell wall material isolated from the roots
Agonists of Torpedo nicotinic receptors: essential role of a positive charge.
A Y Jeng et al.
Annals of the New York Academy of Sciences, 358, 370-373 (1980-01-01)
R Narayanan et al.
International journal of peptide and protein research, 17(2), 170-180 (1981-02-01)
The interaction of the cholinergic fluorescent probes, 1-(5-dimethyl-aminoaphthalene-1-sulfonamido) ethane-2-trimethylammonium perchlorate, 1-(5-dimethylaminoaphthalene-1-sulfonamido) pentane-5-trimethylammonium tartarate and 1-(5-dimethylaminonaphthalene-1-sulfonamido) decane-10- trimethylammonium tartarate with horse serum cholinesterase has been examined by fluorescence and n.m.r. methods. Fluorescence titrations show binding of the decane derivative to two
The use of a cholinergic fluorescent probe for the study of the receptor proteolipid.
G Weber et al.
Molecular pharmacology, 7(5), 530-537 (1971-09-01)
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