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2,5-Dibromopyridine

CAS No.
624-28-2
Chemical Name:
2,5-Dibromopyridine
Synonyms
Dibromopyridine;NSC 76597;5-DibroMop;2,5-DBr-Py;5-DibroMopyridine;2,5-Dibrompyridin;2,5-dibromopyridin;2,5 dibromopyrdine;3,6-DibroMopyridine;2,5-DIBROMOPYRIDINE
CBNumber:
CB7283491
Molecular Formula:
C5H3Br2N
Molecular Weight:
236.89
MDL Number:
MFCD00006221
MOL File:
624-28-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-23 17:18:35

2,5-Dibromopyridine Properties

Melting point 92-95 °C (lit.)
Boiling point 235 °C / 772mmHg
Density 2.0383 (rough estimate)
refractive index 1.5800 (estimate)
Flash point 62℃
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
pka -1.57±0.10(Predicted)
form Crystalline Powder
color Almost white or light beige to brown
Water Solubility insoluble
BRN 109099
InChI InChI=1S/C5H3Br2N/c6-4-1-2-5(7)8-3-4/h1-3H
InChIKey ZHXUWDPHUQHFOV-UHFFFAOYSA-N
SMILES C1(Br)=NC=C(Br)C=C1
CAS DataBase Reference 624-28-2(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H335-H302+H312+H332-H315-H319
Precautionary statements  P280a-P304+P340-P305+P351+P338-P405-P501a-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P501
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-20/21/22
Safety Statements  26-37/39-36/37/39-36
RIDADR  UN2811
WGK Germany  3
HazardClass  IRRITANT
HS Code  29333999
Storage Class 11 - Combustible Solids
REACH Registrations Inactive
NFPA 704
0
2 0

2,5-Dibromopyridine price More Price(90)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D43107 2,5-Dibromopyridine 98% 624-28-2 10g $106 2026-04-30 Buy
TCI Chemical D1217 2,5-Dibromopyridine >99.0%(GC) 624-28-2 5g $25 2026-04-30 Buy
TCI Chemical D1217 2,5-Dibromopyridine >99.0%(GC) 624-28-2 25g $68 2026-04-30 Buy
Usbiological D3483 2,5-Dibromopyridine 20g $312 2026-06-03 Buy
TRC TRC-D425472-10G 2,5-Dibromopyridine 624-28-2 10g $72 2026-06-03 Buy
Product number Packaging Price Buy
D43107 10g $106 Buy
D1217 5g $25 Buy
D1217 25g $68 Buy
D3483 20g $312 Buy
TRC-D425472-10G 10g $72 Buy

2,5-Dibromopyridine Chemical Properties, Uses, Production

Description

Pyridine and its derivatives are distributed widely by nature. Many plant constituents are as contain pyridine ring compounds in the structure of alkaloids, etc.; they are the bases producing many vital compounds and are indispensable raw materials during medicine, agricultural chemicals, dyestuff, tension-active agents, rubber ingredients, fodder additives, foodstuff additives, tackiness agents, etc. are produced.2,5-dibromo pyridine is an important intermediate of organic synthesis and is mainly used in medicine intermediate, organic synthesis, and organic solvent, can also be applicable to aspects such as DYE PRODUCTION, pesticide production and spices. Selective monolithiation of 2,5-dibromopyridine at either the 2-position or the 5-position is reported. Solvent and concentration strongly influence the selectivity. Coordinating solvents and higher concentration favour the 5-position, while non-coordinating solvents and lower concentration favour the 2-position[1].

Chemical Properties

2,5-Dibromopyridine is an off-white crystalline solid. It is insoluble in water but soluble in strong polar organic solvents. It exhibits strong alkalinity.

Uses

2,5-Dibromopyridine (cas# 624-28-2) is a compound useful in organic synthesis.

Preparation

To synthesize 2,5-dibromopyridine, follow these steps:
Add 2-amino-5-bromopyridine (13.0 kg) into a water-cooled solution at 10 °C.
Slowly add 47% aqueous hydrogen bromide (37 L) to the mixture.
Introduce liquid bromine (11 L) into the mixture.
Maintain the reaction temperature below 10 °C.
Prepare a solution of NaNO2 (16.1 kg) and H2O (19 L) and add it dropwise to the mixture while keeping the temperature between 0-5 °C.
Stir the reaction mixture for 30 minutes.
Treat the mixture with a solution of NaOH (28.0 kg) in water (30 L) at a controlled rate below 20-25 °C.
Extract the reaction mixture with diethyl ether (3 × 40 L).
Dry the organic layer with anhydrous Na2SO4.
Remove the desiccant by filtration.
Evaporate the resulting filtrate under reduced pressure to dryness.
Suspend the residue in heptane (10 L).
Collect the target product molecule, 2,5-dibromopyridine, by filtration.
Synthesis method of 2,5-dibromopyridine

Application

2,5-Dibromopyridine is the important intermediate of organic synthesis, is mainly used in medicine intermediate, organic synthesis, organic solvent, also can be applicable to the aspects such as DYE PRODUCTION, pesticide producing and spices.

References

[1] Xin Wang. “Selective monolithiation of 2,5-dibromopyridine with butyllithium.” Tetrahedron Letters 41 1 (2000): 4335–4338.

13466-38-1
624-28-2
Synthesis of 2,5-Dibromopyridine from 2-Hydroxy-5-bromopyridine
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2,5-DIBROMOPYRIDINE PYRIDINE, 2,5-DIBROMO- 2,5-Dibromopyridine, 97+% 2,5-dibromopyridin 2,5-DIBROMOPYRIDINE 2,5-DIBROMOPYRIDINE 2,5-Dibromo pyridine ,98% 2,5-DibroMopyridine, 97% 10GR 3,6-DibroMopyridine NSC 76597 5-DibroMopyridine 2, 5-2 broMide pyridine 2,5 Di bromo pyridne 2,5-Dibromopyridine > Perampanel Impurity 9 2,5-Dibromopyridine ISO 9001:2015 REACH 2,5-Dibrompyridin 2,5 dibromopyrdine Hot Sale?2, 5-Dibromopyridine CAS?624-28-2?with Best Price Pyronoprene Impurity 17 Nicotinic Acid Impurity 13 Dibromopyridine 5-DibroMop 2,5-DBr-Py Pyridine-2,5-dibromide 624-28-2 324-28-2 1450-73-9 Building Blocks Pyridines Halogenated Heterocycles Heterocyclic Building Blocks Bromopyridines Halopyridines alkyl bromide Building Blocks C5 Chemical Synthesis Halogenated Heterocycles Heterocyclic Building Blocks Brominated heterocyclic series Aromatics Bases & Related Reagents Nucleotides Aromatics Compounds Bromopyridines Halopyridines Pyridine series C5Heterocyclic Building Blocks Halogenated Heterocycles Heterocyclic Building Blocks Nitrogen cyclic compounds blocks Bromides Pyridines pyridine derivative Pyridines, Pyrimidines, Purines and Pteredines Halides Pyridine