Trimethyl(vinyl)ammonium bromide

Product Information

Molecular Formula:
C5H12N.Br
Molecular Weight:
166.06
Description
Trimethyl(vinyl)ammonium bromide is an exceptionally powerful quaternary ammonium compound harnessed in the field of biomedicine and manifesting its commendable potential in inhibiting the augmentation of multifarious microbial organisms. This compound exhibits an immense capability to effectively combat distinctive infections provoked by a diverse array of pathogenic bacteria, viruses, and fungi. Moreover, Trimethyl(vinyl)ammonium bromide impressively assumes the roles of an unparalleled antiseptic, disinfectant, as well as a remarkable preservative within the realms of pharmaceuticals, personal care products, and healthcare environments.
Synonyms
NEURINE BROMIDE; VINYLTRIMETHYLAMMONIUM BROMIDE; TRIMETHYLVINYLAMMONIUM BROMIDE; n,n,n-trimethyl-ethenaminiubromide; n,n,n-trimethylethenaminiumbromide; trimethylvinyl-ammoniubromide; vinyltrimethyl-ammoniubromide; Trimethylvinylaminium·bromide
IUPAC Name
ethenyl(trimethyl)azaniumbromide
Canonical SMILES
C[N+](C)(C)C=C.[Br-]
InChI
InChI=1S/C5H12N.BrH/c1-5-6(2,3)4/h5H,1H2,2-4H31H/q+1/p-1
InChI Key
IDVSELVVGYIOEX-UHFFFAOYSA-M
Melting Point
192-193 °C (decomp)
Purity
>97.0%(T)
Density
g/cm3
Appearance
Solid

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
165.01531 g/mol
Monoisotopic Mass
165.01531 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
49.4
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-111909670-A Ultrahigh-temperature salt-tolerant star polymer fluid loss additive, preparation method thereof and water-based drilling fluid 2020-09-03
CN-111909670-B Ultrahigh-temperature salt-tolerant star polymer fluid loss additive, preparation method thereof and water-based drilling fluid 2020-09-03
CN-108948074-A A method of using poly ion liquid extraction separation purification phosphatidyl choline 2017-05-27
CN-108948074-B Method for extracting, separating and purifying phosphatidylcholine by polyion liquid 2017-05-27
JP-2005249572-A Microchannel chip manufacturing method, microchannel chip, biomolecule separation method using the microchannel chip, and electrophoresis apparatus having the microchannel chip 2004-03-04
JP-4450368-B2 Microchannel chip manufacturing method, microchannel chip, biomolecule separation method using the microchannel chip, and electrophoresis apparatus having the microchannel chip 2004-03-04
US-2010101953-A1 Methods for producing microchannel chips, microchannel chips, methods for separating biomolecules using the microchannel chips, and electrophoretic apparatus having the microchannel chips 2004-03-04
US-8012430-B2 Methods for producing microchannel chips, microchannel chips, methods for separating biomolecules using the microchannel chips, and electrophoretic apparatus having the microchannel chips 2004-03-04
JP-2005062074-A DNA chip and target DNA detection method. 2003-08-19
JP-4161053-B2 DNA chip and target DNA detection method. 2003-08-19
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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