307475
Pyridine hydrobromide
98%
Synonym(s):
Pyridinium bromide
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About This Item
Empirical Formula (Hill Notation):
C5H5N · HBr
CAS Number:
Molecular Weight:
160.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-600-7
Beilstein/REAXYS Number:
3615336
MDL number:
Product Name
Pyridine hydrobromide, 98%
InChI key
BBFCIBZLAVOLCF-UHFFFAOYSA-N
InChI
1S/C5H5N.BrH/c1-2-4-6-5-3-1;/h1-5H;1H
SMILES string
Br[H].c1ccncc1
assay
98%
form
solid
mp
200 °C (dec.) (lit.)
Quality Level
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Related Categories
Application
Pyridine hydrobromide may be used in chemical synthesis studies.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - 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
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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
Ye Wei et al.
Journal of the American Chemical Society, 135(10), 3756-3759 (2013-02-27)
We describe here a [3+3]-type condensation reaction of O-acetyl ketoximes and α,β-unsaturated aldehydes that is synergistically catalyzed by a copper(I) salt and a secondary ammonium salt (or amine). This redox-neutral reaction allows modular synthesis of a variety of substituted pyridines
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