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Propargyl-3-sulfopropyl ether sodium salt

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Propargyl-3-sulfopropyl ether sodium salt Basic information

Product Name:
Propargyl-3-sulfopropyl ether sodium salt
Synonyms:
  • popsliquid
  • SODIUM 3-(PROP-2-YNYLOXY)PROPANE-1-SULFONATE
  • Sodium 3-(prop-2-yn-1-yloxy)propane-1-sulfonate
  • sodium 3-(1-sulfohex-5-yn-3-yloxy)-5-hexyne-1-sulfonate
  • sodium,3-(1-sulfohex-5-yn-3-yloxy)hex-5-yne-1-sulfonate
  • POPS
  • PROPARGYL (3-SULFOPROPYL) ETHER, SODIUM SALT
  • 3-(2-Propynyloxy)-1-propanesulfonic acid, sodium salt
CAS:
30290-53-0
MF:
C6H11NaO4S
MW:
202.2
EINECS:
608-454-7
Mol File:
30290-53-0.mol
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Propargyl-3-sulfopropyl ether sodium salt Chemical Properties

Density 
1.21 at 20℃
vapor pressure 
0-2992.94Pa at 25℃
form 
Liquid
InChI
InChI=1S/C6H10O4S.Na.H/c1-2-4-10-5-3-6-11(7,8)9;;/h1H,3-6H2,(H,7,8,9);;
InChIKey
QZGFGSLFVLDKEY-UHFFFAOYSA-N
SMILES
C(S(O)(=O)=O)CCOCC#C.[NaH]
LogP
-4.1
Surface tension
72.53-72.79mN/m at 1g/L and 19.9℃
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Propargyl-3-sulfopropyl ether sodium salt Usage And Synthesis

Description

Propargyl-3-sulfopropyl ether sodium salt is a sulfonate used as a co-brightener with glycerol in the electroplating industry. It is also used as an alkaline industrial chemical that can be used to remove tellurium from glass and ceramics. Propargyl-3-sulfopropyl ether sodium salt is prepared by reacting propargyl alcohol with sodium sulfite and ethylene diamine. This reaction produces propargyl sulfonic acid, which reacts with ethylene oxide to form the desired product.

Uses

Propargyl-3-sulfopropyl ether sodium salt is a sulfonate used as a co-brightener with glycerol in the electroplating industry. It is also used as an alkaline industrial chemical for removing tellurium from glass and ceramics.

Synthesis

Propargyl-3-sulfopropyl ether sodium salt is prepared by the reaction of 1,3-propanesultone and propargyl alcohol. The specific synthesis steps are as follows:
To a chilled (5 °C) slurry of NaH (60% in mineral oil, 1.60 g, 40.9 mmol, 1.0 equiv.) in dry DMF (30 mL) was added dropwise a solution of propargyl alcohol (2.4 mL, 40.9 mmol, 1.0 equiv.) in dry DMF (30 mL) over a ten minute period. I ,3-Propanesultone (5.0 g, 40.9 minol, 1.0 equiv.) was dissolved in dry DMF (30mL), and the resulting solution added dropwise over a five minute period to the chilled sodium propargylate solution. After stirring for ten minutes in the ice bath, the flask was transferred to an oil bath and heated at 60°C for three hours. Most of the DMF was then removed by rotavap, and the remaining oil was triturated with 200 mL diethyl ether to yield a white solid, which was collected by vacuum filtration. The product was driedunder vacuum to provide Propargyl-3-sulfopropyl ether sodium salt as a white powder (7.4 g, 90%).

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