1,3-PROPANEDISULFONIC ACID DISODIUM SALT
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
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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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1,3-PROPANEDISULFONIC ACID DISODIUM SALT(36589-58-9)Related Product Information
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- 1,3-PROPANEDISULFONIC ACID DISODIUM SALT, 99% (DRY WT.),1,3-PROPANEDISULFONIC ACID DISODIUM SALT