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86490

Supelco

2,2′:6′,2′′-Terpyridine

for spectrophotometric det. of Ag, Fe, Ru, ≥98.5%

Synonym(s):

α,α′,α″-Tripyridyl, 2,6-Di(2-pyridyl)pyridine

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About This Item

Empirical Formula (Hill Notation):
C15H11N3
CAS Number:
Molecular Weight:
233.27
Beilstein:
11199
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.21

Quality Level

Assay

≥98.5% (GC)
≥98.5%

form

crystals

quality

for spectrophotometric det. of Ag, Fe, Ru

technique(s)

UV/Vis spectroscopy: suitable

mp

89-91 °C (lit.)
90-93 °C

solubility

dioxane: 0.1 g/mL, clear

cation traces

Ag: ≤5 mg/kg
Ba: ≤5 mg/kg
Ca: ≤5 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

c1ccc(nc1)-c2cccc(n2)-c3ccccn3

InChI

1S/C15H11N3/c1-3-10-16-12(6-1)14-8-5-9-15(18-14)13-7-2-4-11-17-13/h1-11H

InChI key

DRGAZIDRYFYHIJ-UHFFFAOYSA-N

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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Reagent for the spectrophotometric det. of Ag and Ru

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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L.C. Kamra et al.
Analytica Chimica Acta, 81, 177-177 (1976)
E. Gagliardi et al.
Mikrochimica Acta, 1175-1175 (1964)
K S Hsu et al.
European journal of pharmacology, 270(1), 89-95 (1994-01-03)
The pharmacological and toxicological activity of 2,2',2''-tripyridine was determined in rat thoracic aorta. 2,2',2''-Tripyridine inhibited norepinephrine (3 microM)-induced phasic and tonic contractions in the thoracic aorta as well as the endothelium-denuded aorta of the rat. The tonic pre-contraction elicited by
S Rahuel-Clermont et al.
Biochemistry, 36(19), 5837-5845 (1997-05-13)
The insulin hexamer is an allosteric protein capable of undergoing transitions between three conformational states: T6, T3R3, and R6. These transitions are mediated by the binding of phenolic compounds to the R-state subunits, which provide positive homotropic effects, and by
S Y Lin-Shiau et al.
British journal of pharmacology, 106(1), 55-60 (1992-05-01)
1. The curare-like action of 2,2',2''-tripyridine (a synthetic by-product of the herbicide, paraquat) was studied in mouse phrenic nerve-diaphragm preparation. The inhibition by 2,2',2''-tripyridine of nerve-evoked twitches was dependent on the concentration, ranging from 1 to 100 microM, which had

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