• Product NameHydroxylamine-O-sulfonic acid
  • CasNo. 2950-43-8
  • MFH3NO4S
  • MW113.094
  • Purity
  • Appearancewhite to slightly beige crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 2950-43-8

MF: H3NO4S

Appearance: white to slightly beige crystalline powder

Trustworthy Factory Supply High Purity 99% 2950-43-8 with Lowest Price

  • Molecular Formula:H3NO4S
  • Molecular Weight:113.094
  • Appearance/Colour:white to slightly beige crystalline powder 
  • Vapor Pressure:0-53.329Pa at 25-39℃ 
  • Melting Point:210 °C (dec.)(lit.) 
  • Refractive Index:1.534 
  • Boiling Point:39 °C(Press: 0.4 Torr) 
  • PKA:-6.47±0.18(Predicted) 
  • PSA:98.00000 
  • Density:1.98 g/cm3 
  • LogP:0.46060 

Hydroxylamine-O-sulfonic acid(Cas 2950-43-8) Usage

Purification Methods

Stir the solid vigorously with anhydrous Et2O and filter it off using large volumes of dry Et2O. Drain dry at the pump for 5minutes and then for 12-14hours in a vacuum. Store it in a vacuum desiccator over conc H2SO4. Determine the purity by oxidation of iodide to I2. It must be stored in a dry atmosphere at 0-4o. It decomposes slowly in H2O at 25o and more rapidly above this temperature. [Matsuguma & Andrieth Inorg Synth V 122 1957.]

General Description

Hydroxylamine-O-sulfonic acid is a versatile synthetic reagent. It is widely employed as a nucleophile and as an electrophile in various organic syntheses. It can be synthesized by reacting hydroxylamine sulfate with 30% fuming H2SO4.

InChI:InChI=1/H3NO4S/c1-5-6(2,3)4/h1H2,(H,2,3,4)

2950-43-8 Relevant articles

Synthesis of novel 7-azaindole derivatives containing pyridin-3-ylmethyl dithiocarbamate moiety as potent PKM2 activators and PKM2 nucleus translocation inhibitors

Liu, Bin,Yuan, Xia,Xu, Bo,Zhang, Han,Li, Ridong,Wang, Xin,Ge, Zemei,Li, Runtao

, p. 1 - 15 (2019/03/17)

Multiple lines of evidence have indicate...

Multigram Synthesis of Functionalized Spirocyclic Diazirines

Martyloga, Oleksandr V.,Myronenko, Artamon,Tkachenko, Anton M.,Matvienko, Vitalii O.,Kuchkovska, Yuliya O.,Grygorenko, Oleksandr O.

, p. 3744 - 3750 (2019/06/28)

An approach to the synthesis of spirocyc...

Method for the production of O-substituted hydroxylamines

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, (2008/06/13)

A new method for the production of O-sub...

Antimicrobial 1,3-disubstituted/imidazolium salts

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, (2008/06/13)

The imidazolium compounds of the formula...

2950-43-8 Process route

nitromethane
75-52-5

nitromethane

sulfur trioxide
7446-11-9

sulfur trioxide

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

aminosulfonic acid
5329-14-6

aminosulfonic acid

hydroxylamine-O-sulfonic acid
2950-43-8

hydroxylamine-O-sulfonic acid

Conditions
Conditions Yield
above 0°C;
 
4-phenyl-3-butyne-2-one
1817-57-8

4-phenyl-3-butyne-2-one

pyridazin-1-ium-1-amine iodide

pyridazin-1-ium-1-amine iodide

1,2-diazine
289-80-5

1,2-diazine

hydroxylamine-O-sulfonic acid
2950-43-8

hydroxylamine-O-sulfonic acid

Conditions
Conditions Yield
With potassium hydrogencarbonate; potassium hydroxide; In water;
44%

2950-43-8 Upstream products

  • 75-52-5
    75-52-5

    nitromethane

  • 7446-11-9
    7446-11-9

    sulfur trioxide

  • 7803-49-8
    7803-49-8

    hydroxylamine

  • 7664-93-9
    7664-93-9

    sulfuric acid

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    133541-45-4

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