1-Ethylpyridinium Chloride

Base Information

• Chemical Name: 1-Ethylpyridinium Chloride
• CAS No.: 2294-38-4
• Molecular Formula: C7H10ClN
• Molecular Weight: 143.616
• Hs Code.: 29332990
• European Community (EC) Number: 680-003-7
• UNII: 38BQL5563G
• DSSTox Substance ID: DTXSID30883823
• Wikidata: Q27256774
• Mol file: 2294-38-4.mol

Synonyms:1-Ethylpyridinium Chloride;2294-38-4;Ethylpyridinium chloride;1-ethylpyridin-1-ium chloride;n-ethylpyridinium chloride;1-ethylpyridin-1-ium;chloride;Pyridinium, 1-ethyl-, chloride;Pyridinium, 1-ethyl-, chloride (1:1);UNII-38BQL5563G;38BQL5563G;pyridine ethochloride;1-ethylpyridin-1-ium,chloride;1-Ethyl Pyridinium Chloride;1-ethylpyridin-1-iumchloride;SCHEMBL365128;DTXSID30883823;MFCD03093293;AKOS015833116;CS-W016405;AS-62685;E0544;FT-0634184;D83482;A816437;J-014910;Q27256774

Chemical Property of 1-Ethylpyridinium Chloride

Chemical Property:

• Appearance/Colour: beige crystals and agglomerates
• Melting Point: 100 °C
• PSA: 3.88000
• LogP: -2.00200
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility.: Soluble in water
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 143.0501770
• Heavy Atom Count: 9
• Complexity: 55.4

Purity/Quality:

98%, ^*data from raw suppliers

1-Ethylpyridin-1-iumChloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+]1=CC=CC=C1.[Cl-]
• Uses: 1-Ethylpyridin-1-ium Chloride can be used as a lubricating oil.

Technology Process of 1-Ethylpyridinium Chloride

There total 6 articles about 1-Ethylpyridinium Chloride 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: 83.4%

→ 1-Ethylpyridinium chloride (2294-38-4)

Guidance literature:

Reference yield:

benzoic acid ethyl ester (93-89-0,99341-95-4) + pyridine hydrochloride (628-13-7) → chloroethane (75-00-3) + 1-Ethylpyridinium chloride (2294-38-4) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

DOI:10.1007/BF00913843

Reference yield:

pyridine (110-86-1) + ethyl bromide (74-96-4) → 1-Ethylpyridinium chloride (2294-38-4)

Guidance literature:

pyridine; bromure d'ethyle; at 120 ℃; for 36h; Inert atmosphere;

With Amberlite IRA-400 Cl^- exchange resin; In water monomer;

DOI:10.1016/j.molliq.2022.118673

upstream raw materials:

benzoic acid ethyl ester

pyridine hydrochloride

pyridine

diethyl ether

Downstream raw materials:

1-ethyl-1,2,5,6-tetrahydropyridine

Refernces

• 1、 Ananikov, Valentine P.,Egorova, Ksenia S.,Gordeev, Evgeniy G.,Posvyatenko, Alexandra V.,Seitkalieva, Marina M.,Strukova, Elena N.,Vavina, Anna V.. "Merging structural frameworks of imidazolium, pyridinium, and cholinium ionic liquids with cinnamic acid to tune solution state behavior and properties". . . Retrieved 2022/03/14.
• 2、 -. "Alkylation process". . . Retrieved 2008/06/13.