Neurine

Base Information

• Chemical Name: Neurine
• CAS No.: 463-88-7
• Molecular Formula: C5H12 N . H O
• Molecular Weight: 103.164
• Hs Code.: 2923900090
• European Community (EC) Number: 207-344-2
• NSC Number: 56349
• UNII: G6RL36OO0J
• DSSTox Substance ID: DTXSID70196803
• Wikipedia: Neurine
• Wikidata: Q408180
• Metabolomics Workbench ID: 44788
• Mol file: 463-88-7.mol

Synonyms:NEURINE;trimethylvinylammonium hydroxide;Vitaloid;Neurin;463-88-7;Neirin;Neirine;N,N,N-Trimethylethenaminium hydroxide;Vinyltrimethylammonium hydroxide;Trimethyl vinyl ammonium hydroxide;ethenyl(trimethyl)azanium;hydroxide;Ethenaminium, N,N,N-trimethyl-, hydroxide;Trimethyl(vinyl)ammonium hydroxide;EINECS 207-344-2;NSC 56349;UNII-G6RL36OO0J;G6RL36OO0J;Ammonium, trimethylvinyl-, hydroxide;NSC-56349;NEURINE [MI];C5H12N.HO;SCHEMBL239297;ethenyltrimethylazanium oxidanide;DTXSID70196803;C5-H12-N.H-O;CHEBI:165174;NSC56349;TRIMETHYLVINYLAMMONIUMHYDROXIDE;AKOS006229479;WLN: 1U1K1&1&1 &Q;Ethenaminium,N,N-trimethyl-, hydroxide;LS-19174;FT-0694054;Q408180

Chemical Property of Neurine

Chemical Property:

• Melting Point: <25 °C
• Refractive Index: 1.4147 (estimate)
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 23.06000
• Density: g/cm³
• LogP: 0.65930
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 103.099714038
• Heavy Atom Count: 7
• Complexity: 49.4

Purity/Quality:

99%, ^*data from raw suppliers

TRIMETHYLVINYLAMMONIUM HYDROXIDE 98.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Highly toxic.
• Hazard Codes: Highly toxic.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+](C)(C)C=C.[OH-]
• Uses: Biochemical research.

Technology Process of Neurine

There total 8 articles about Neurine 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:

→ choline (62-49-7) + Neurin (463-88-7)

Guidance literature:

With silver nitrate;

Reference yield:

bromocholine (10250-82-5) → Neurin (463-88-7)

Guidance literature:

With silver orthophosphate; ethanol; unter Ausschluss von Licht;

Reference yield:

(2-bromoethyl)trimethylammonium bromide (2758-06-7) → Neurin (463-88-7)

Guidance literature:

With silver(l) oxide;

upstream raw materials:

bromocholine

(2-bromoethyl)trimethylammonium bromide

ethylene dibromide

trimethylamine

Downstream raw materials:

trimethylamine

N,N-dimethylvinylamine

acetaldehyde

formic acid