3-Hydroxyphenyltrimethylammonium bromide

Base Information

Chemical Name:3-Hydroxyphenyltrimethylammonium bromide
CAS No.:1620-19-5
Molecular Formula:Br*C₉H₁₄NO
Molecular Weight:232.12
Hs Code.:
UNII:8BBF2W6V08
Wikidata:Q27270137

Synonyms:3-hydroxyphenyltrimethylammonium;3-hydroxyphenyltrimethylammonium bromide;3-hydroxyphenyltrimethylammonium bromide, 14C-labeled;3-hydroxyphenyltrimethylammonium iodide;PTMA

Suppliers and Price of 3-Hydroxyphenyltrimethylammonium bromide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 3-Hydroxyphenyltrimethylammonium bromide

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:231.02588
Heavy Atom Count:12
Complexity:128

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+](C)(C)C1=CC(=CC=C1)O.[Br-]

Technology Process of 3-Hydroxyphenyltrimethylammonium bromide

There total 3 articles about 3-Hydroxyphenyltrimethylammonium bromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 114-80-7
Neostigmine bromide

: 19962-04-0
Dimethylcarbaminsaeure-3-aminophenylester

: 16088-19-0
norneostigmine

: 76418-45-6
Dimethylcarbaminsaeure-3-methylaminophenylester

: 1620-19-5
3-hydroxyphenyltrimethylammonium bromide

: 99-07-0
3-Dimethylaminophenol

Guidance literature:: With water; In various solvent(s); at 70 - 95 ℃; Kinetics; Thermodynamic data; Product distribution; Activation energies in 6 buffer systems with varying pH, influence of buffer concentration, ionic force, oxygen, and pilocarpine hydrochloride on the rates of hydrolysis and demethylation;