2-[(2-Amino-2-oxoethyl)ammonio]ethanesulfonate

Base Information

• Chemical Name: 2-[(2-Amino-2-oxoethyl)ammonio]ethanesulfonate
• CAS No.: 7365-82-4
• Molecular Formula: C4H10N2O4S
• Molecular Weight: 182.2
• Hs Code.: 29241900
• Mol file: 7365-82-4.mol

Synonyms:2-[(2-amino-2-oxoethyl)ammonio]ethanesulfonate;CHEBI:39062;N-(2-acetamido)-2-aminoethanesulfonate

Chemical Property of 2-[(2-Amino-2-oxoethyl)ammonio]ethanesulfonate

Chemical Property:

• Appearance/Colour: White crystals
• Vapor Pressure: 0Pa at 25℃
• Melting Point: 270-295 °C
• Refractive Index: 1.536
• Boiling Point: 404.49℃
• PKA: 6.8(at 25℃)
• PSA: 117.87000
• Density: 1.484 g/cm³
• LogP: 0.12110
• Storage Temp.: Store at RT.
• Solubility.: H2O: 0.1 M at 20 °C, clear, colorless
• Water Solubility.: soluble
• XLogP3: -4.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 182.03612798
• Heavy Atom Count: 11
• Complexity: 203

Purity/Quality:

99%, ^*data from raw suppliers

ACES ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CS(=O)(=O)[O-])[NH2+]CC(=O)N
• Uses: N-(Carbamoylmethyl)taurine can be used to study biological buffers and zwitterionic compounds. ACES has been used in a study to determine the levels of ibuprofen and flurbiprofen in pharmaceuticals by capillary zone electrophoresis. Buffer for biological systems. ACES is used as a Good's buffer is an ideal separator in the resolution of protein systems, a zwitterionic compound used in biochemical and biological research.

Technology Process of 2-[(2-Amino-2-oxoethyl)ammonio]ethanesulfonate

There total 4 articles about 2-[(2-Amino-2-oxoethyl)ammonio]ethanesulfonate 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: 82.0%

C4H9NO5S → N-(2-acetamido)-2-aminoethanesulfonic acid (7365-82-4)

Guidance literature:

With ammonia; In tetrahydrofuran; at 60 ℃; for 8h; under 7500.75 Torr;

Reference yield: 82.0%

C5H11NO5S → N-(2-acetamido)-2-aminoethanesulfonic acid (7365-82-4)

Guidance literature:

With ammonia; In tetrahydrofuran; at 60 ℃; for 8h; under 3750.38 Torr;

Reference yield: 80.0%

N-(ethyl acetate)-2-aminoethanesulfonic acid → N-(2-acetamido)-2-aminoethanesulfonic acid (7365-82-4)

Guidance literature:

With ammonia; In acetonitrile; at 60 ℃; for 8h; under 3750.38 Torr;

Refernces

• 1、 -. "Stabilizing labeled antibody using amino acids". . . Retrieved 2011/11/07.
• 2、 -. "Isolation of nucleic acids". . . Retrieved 2008/06/13.