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1,3-PROPANEDISULFONIC ACID DISODIUM SALT

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1,3-PROPANEDISULFONIC ACID DISODIUM SALT Basic information

Product Name:
1,3-PROPANEDISULFONIC ACID DISODIUM SALT
Synonyms:
  • 1,3-Propanedisulfonic acid disodium salt, 99%(dry wt.), water <5%
  • 1,3-Propanedisulfonic acid, disodium salt,99%
  • Eprodisate disodium
  • NC 503
  • 1,3-Propanedisulfonic disodium
  • Eprodisate Sodium
  • 1,3-PROPANEDISULFONIC ACID DISODIUM SALT
  • DISODIUM PROPANE-1,3-DISULFONATE
CAS:
36589-58-9
MF:
C3H6Na2O6S2
MW:
248.19
Product Categories:
  • Organic Building Blocks
  • Sulfonic/Sulfinic Acid Salts
  • Sulfur Compounds
Mol File:
36589-58-9.mol
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1,3-PROPANEDISULFONIC ACID DISODIUM SALT Chemical Properties

Melting point:
>300°C
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Almost white
Water Solubility 
Partially soluble in cold water, hot water.
Sensitive 
Hygroscopic
BRN 
3767479
CAS DataBase Reference
36589-58-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29041000

MSDS

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1,3-PROPANEDISULFONIC ACID DISODIUM SALT Usage And Synthesis

Chemical Properties

White coarse powder

Uses

keratolytic

Uses

It is used as a reactant involved in synthesis of cadmium(II) bipyridine complex metal-organic frameworks with alkanedisulfonates, alkylenedisulfonate inorganic-organic hybrid materials and glycosaminoglycan mimetic involved in pharmacological studies for the treatment of amyloid A amyloidosis.

Uses

Reactant involved in synthesis of:

  • Cadmium(II) bipyridine complex metal-organic frameworks with alkanedisulfonates
  • Alkylenedisulfonate inorganic-organic hybrid materials

Glycosaminoglycan mimetic involved in pharmacological studies for the treatment of amyloid A amyloidosis

Synthesis

90566-47-5

36589-58-9

Step 3: To a methanolic (15 mL) suspension of the disulfone compound (0.62 g, 2.23 mmol) obtained in Step 2, a methanolic solution of 0.5 M sodium methanol (8.9 mL, 4.58 mmol) was slowly added. The reaction mixture was stirred at room temperature for 24 hours. After completion of the reaction, the homogeneous reaction solution was concentrated under reduced pressure to give a solid. The solid was suspended in ethanol (20 mL) and stirred at room temperature for 1 hour. Subsequently, the solid was separated by filtration and the filter cake was washed sequentially with ethanol (2 x 10 mL) and ether (2 x 10 mL). The resulting solid was dissolved in water (2 mL) and purified by passing through a C8 reversed-phase silica gel pad, using water as eluent. The eluate containing sodium 1,3-propanedisulfonate (P1, disodium salt) was collected and lyophilized to give sodium 1,3-propanedisulfonate (0.41 g, 85% yield) in white solid form. The structure of the product was confirmed by 1H NMR (D2O, 500 MHz): δ 1.84 (quintuple peak, J = 8.0 Hz, 2H), 2.44 (triple peak, J = 8.0 Hz, 4H).

References

[1] Patent: WO2011/17800, 2011, A1. Location in patent: Page/Page column 100

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