3-(Pyridin-1-ium-1-yl)propane-1-sulfonate

Base Information

• Chemical Name: 3-(Pyridin-1-ium-1-yl)propane-1-sulfonate
• CAS No.: 15471-17-7
• Molecular Formula: C8H11NO3S
• Molecular Weight: 201.246
• Hs Code.: 29333990
• European Community (EC) Number: 239-491-3
• UNII: QN4I6AI9EK
• DSSTox Substance ID: DTXSID3044592
• Wikidata: Q27287352
• Mol file: 15471-17-7.mol

Synonyms:3-(1-pyridinio)-1-propanesulfonate;NDBS cpd

Chemical Property of 3-(Pyridin-1-ium-1-yl)propane-1-sulfonate

Chemical Property:

• Appearance/Colour: white solid
• Vapor Pressure: 0Pa at 25℃
• Melting Point: 275-277 °C
• Flash Point: 160 °C
• PSA: 87.18000
• Density: 1.53[at 20℃]
• LogP: 0.55470
• Storage Temp.: 2-8°C
• Solubility.: Methanol (Slightly), Water (Slightly)
• Water Solubility.: 240.5g/L at 25℃
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 201.04596439
• Heavy Atom Count: 13
• Complexity: 213

Purity/Quality:

98% ^*data from raw suppliers

1-(3-Sulfopropyl)pyridiniumInnerSalt ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-24/25-22

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Nitrogen Compounds -> Pyridines
• Canonical SMILES: C1=CC=[N+](C=C1)CCCS(=O)(=O)[O-]
• Recent ClinicalTrials: 'Prime Boost' Vaccination Strategy Combining Conjugated Anti- Pneumococcal Vaccine (s0) and Polysaccharide Anti- Pneumococcal Vaccine (s4) Compared to Polysaccharide Anti- Pneumococcal Vaccine Alone (s4) In Patients With Common Variable Immunodeficiency
• Uses: Pyridinium propyl sulfobetaine can be used: As a Bronsted acid ionic liquid catalyst in combination with H2SO4 and H3PO4 for the dehydration of glycerol to acrolein via semi-batch reaction technique. As a catalyst in the form of sulfonated heteropoly acid salts for the synthesis of isoamyl isovalerate. In the preparation of molybdenum imido alkylidene NHC catalysts, which are used in biphasic olefin metathesis. To prepare water-stable SO3H-functionalized Br?nsted acidic task-specific ionic liquids (TSILs). In was bright nickel plating, it is a start material to make brightener, A high efficiency brightener and leveler. Because of its high purity, Pyridinium propyl sulfobetaine cannot carry other harmful impurity or salts to baths. 3-(1-Pyridinio)-1-propanesulfonate is a non detergent sulfobetaine used as a mild solubilizing and stabilizing agent for halophilic malate dehydrogenase, halophilic elongation factor Tu (hTu), pig heart malate dehydrogenase, chicken egg w hite lysozyme and E. coli beta-galactosidase. Preserves the antigenic conformation of serine protease gp76. Does not interfere with colorimetric assays using p-nitrophenylphosphate and o-nitrophenyl -b-D-galactopyranoside as substrates. Reduces aggregation and significantly improves protein renaturation. Zwitterionic over a wide pH range. Does not absorb significantly in the near-UV range. Ca n be easily removed by dialysis. Stronger leveling agent in nickel electroplating 3-(1-Pyridinio)-1-propanesulfonate can be used:As a Bronsted acid ionic liquid catalyst in combination with H2SO4 and H3PO4 for the dehydration of glycerol to acrolein via semi-batch reaction technique.As a catalyst in the form of sulfonated heteropoly acid salts for the synthesis of isoamyl isovalerate.In the preparation of molybdenum imido alkylidene NHC catalysts, which are used in biphasic olefin metathesis.To prepare water-stable SO3H-functionalized Br?nsted acidic task-specific ionic liquids (TSILs).
• Description: 3-(1-Pyridinio)-1-propanesulfonate is a white crystalline powder used to prepare electroplating additives.It has good thermal qualitative and chemical stability, and its mechanical strength is also very good. The low polymer molecular weight is prone to disproportionation and cross-linking reactions.

Technology Process of 3-(Pyridin-1-ium-1-yl)propane-1-sulfonate

There total 2 articles about 3-(Pyridin-1-ium-1-yl)propane-1-sulfonate 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: 98.0%

pyridine (110-86-1) + 1,3-propanesultone (1120-71-4) → 1-(3-sulfopropyl)pyridine (15471-17-7)

Guidance literature:

for 1h; Ambient temperature;

Reference yield:

→ 1-(3-sulfopropyl)pyridine (15471-17-7)

Guidance literature:

Pyridin, 1,3-Propansulfon;

upstream raw materials:

pyridine

1,3-propanesultone

Refernces

• 1、 Han, Xiaoxiang,Yan, Wei,Chen, Keke,Hung, Chin-Te,Liu, Li-Li,Wu, Pei-Hao,Huang, Shing-Jong,Liu, Shang-Bin. "Heteropolyacid-based ionic liquids as effective catalysts for the synthesis of benzaldehyde glycol acetal". . p. 149 - 156. Retrieved 2014.
• 2、 Bai, Wei,Gao, Zhanxian,Lu, Xinxin,Wei, Jialun,Yan, Lei,Yu, Limei. "Synthesis of 9,9-bis(4-hydroxyphenyl) fluorene catalyzed by bifunctional ionic liquids". . p. 32559 - 32564. Retrieved 2021/12/07.
• 3、 Yang, Yang,Fu, Renzhong,Liu, Yang,Cai, Jing,Zeng, Xiaojun. "Microwave-promoted one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions". . . Retrieved 2020/06/09.