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26576-85-2

26576-85-2 Structure

26576-85-2 Structure
IdentificationBack Directory
[Name]

N-BUTYL-3-METHYLPYRIDINIUM BROMIDE
[CAS]

26576-85-2
[Synonyms]

[BMPy]Br
[C4MPy]Br
N-butyl-3-metylpyridinium bromide
N-BUTYL-3-METHYLPYRIDINIUM BROMIDE
1-Butyl-3-methylpyridinium Bromide
1-n-butyl-3-methylpyridinium bromide
1-Butyl-3-methylpyridiniumBromide>
1-Butyl-3-methylpyridin-1-ium bromide
PyridiniuM,1-butyl-3-Methyl-, broMide (1:1)
1-BUTYL-3-METHYLPYRIDINIUM BROMIDE,98.0+%(LC)(T)
N-BUTYL-3-METHYLPYRIDINIUM BROMIDE ISO 9001:2015 REACH
[EINECS(EC#)]

678-235-9
[Molecular Formula]

C10H16BrN
[MDL Number]

MFCD01632121
[MOL File]

26576-85-2.mol
[Molecular Weight]

230.14
Chemical PropertiesBack Directory
[Melting point ]

70-80°
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder to crystal
[color ]

White to Light yellow to Light orange
[CAS DataBase Reference]

26576-85-2
Questions And AnswerBack Directory
[Uses]

1-Butyl-3-methylpyridinium bromide is a 1-alkyl-3-alkyl-pyridinium halide compound. 1-alkyl-3-alkyl-pyridinium halides can be used as bromine-complexing agents in aqueous zinc bromide solutions used in zinc/bromine rechargeable batteries (i.e., both membrane-equipped and membraneless zinc/bromine flow batteries). It has been found that complexes formed by using 1-alkyl-3-methylpyridinium bromide or mixtures thereof do not solidify at temperatures as low as 0°C or even -5°C, thereby maintaining the fluidity of electrolyte solutions with different compositions corresponding to different states of charge of the battery over a wide operating temperature range.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[TSCA ]

TSCA listed
[HS Code ]

2933.39.9200
[REACH Registrations]

Active
Spectrum DetailBack Directory
[Spectrum Detail]

N-BUTYL-3-METHYLPYRIDINIUM BROMIDE(26576-85-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Equip the double-sided reactor with a magnetic stirrer, condenser, thermowell and dropping funnel. The reactor was purged with nitrogen during the entire step. 3-Methylpyridine (465 g) was charged to the reactor and the reactor was heated to 79°C. Then, n
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