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Sigma-Aldrich

Pyridine hydrobromide

98%

Synonym(s):

Pyridinium bromide

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About This Item

Empirical Formula (Hill Notation):
C5H5N · HBr
CAS Number:
18820-82-1
Molecular Weight:
160.01
Beilstein:
3615336
EC Number:
242-600-7
MDL number:
MFCD00012801
UNSPSC Code:
12352100
PubChem Substance ID:
24858596
NACRES:
NA.22

Assay

98%

form

solid

mp

200 °C (dec.) (lit.)

SMILES string

Br[H].c1ccncc1

InChI

1S/C5H5N.BrH/c1-2-4-6-5-3-1;/h1-5H;1H

InChI key

BBFCIBZLAVOLCF-UHFFFAOYSA-N

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Application

Pyridine hydrobromide may be used in chemical synthesis studies.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Sabyasachi Ta et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 196-200 (2016-09-24)
Combination of pyridine, antipyrine and indole in a single molecule (L2) allows selective recognition of Fe3+ colorimetrically in CH3CN. The structure of L2 is confirmed from single crystal X-ray diffraction analysis. The probe displays two different visible bands at 541nm
Wen Zhou et al.
Inorganic chemistry, 52(5), 2271-2273 (2013-02-20)
The reaction of 2,2'-bipyridine (bpy) with monomeric chromium(II) precursors was used to prepare the S = 1 complexes Cr(tBu-acac)2(bpy) (1) and (η(5)-Cp)(η(1)-Cp)Cr(bpy) (3), as well as the S = 2 compound Cr[N(SiMe3)2]2(bpy) (4). The crystallographically determined bond lengths indicate that
Bidyut Akhuli et al.
Dalton transactions (Cambridge, England : 2003), 42(16), 5818-5825 (2013-03-05)
A pentafluorophenyl (–C6F5) substituted 3-pyridyl urea, L(1), is explored extensively to demonstrate SO4(2-) binding exclusively via second sphere coordination in the cavity of a 1D polymeric self-assembly of L(1), selectively assisted by Cu2+. A single crystal X-ray diffraction study depicts
Takayoshi Arai et al.
Chemical communications (Cambridge, England), 49(71), 7776-7778 (2013-08-01)
A series of bis(oxazolidine)pyridine ligands (the PyBodines) were newly designed and synthesized for the development of a highly efficient, tailor-made catalyst for the [3+2] cycloaddition of azomethine imines with propiolates. The PyBodine(l-Ala)-Cu(OAc)2 catalyst was selected on the basis of solid-phase
Harry Adams et al.
Journal of the American Chemical Society, 135(5), 1853-1863 (2013-01-31)
The association constants for a family of 96 closely related zinc porphyrin-pyridine ligand complexes have been measured in two different solvents, toluene and 1,1,2,2-tetrachloroethane (TCE). The zinc porphyrin receptors are equipped with phenol side arms, which can form intramolecular H-bonds
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