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338567

Sigma-Aldrich

Sulfosuccinic acid solution

70 wt. % in H2O

Synonym(s):

2-Sulfobutanedioic acid

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About This Item

Linear Formula:
HOOCCH2CH(SO3H)COOH
CAS Number:
5138-18-1
Molecular Weight:
198.15
Beilstein:
1727687
MDL number:
MFCD00075139
UNSPSC Code:
12162002
PubChem Substance ID:
24860555
NACRES:
NA.23

form

viscous liquid

concentration

70 wt. % in H2O

refractive index

n20/D 1.449

density

1.438 g/mL at 25 °C

SMILES string

OC(=O)CC(C(O)=O)S(O)(=O)=O

InChI

1S/C4H6O7S/c5-3(6)1-2(4(7)8)12(9,10)11/h2H,1H2,(H,5,6)(H,7,8)(H,9,10,11)

InChI key

ULUAUXLGCMPNKK-UHFFFAOYSA-N

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Application

  • Modification of nanocellulose membrane by impregnation method with sulfosuccinic acid for direct methanol fuel cell applications: This study examines the use of sulfosuccinic acid in various concentrations to improve the properties of nanocellulose membranes for fuel cells (Sriruangrungkamol & Chonkaew, 2021).
  • A high-strength polyvinyl alcohol hydrogel membrane crosslinked by sulfosuccinic acid for strontium removal via filtration: Research focusing on using sulfosuccinic acid to enhance polyvinyl alcohol hydrogel membranes for effective strontium filtration (Yoon et al., 2019).
  • Cross-linked poly (vinyl alcohol)/sulfosuccinic acid polymer as an electrolyte/electrode material for H2–O2 proton exchange membrane fuel cells: This paper discusses the application of sulfosuccinic acid in creating cross-linked polyvinyl alcohol for fuel cell membranes (Ebenezer et al., 2016).
  • Preparation of chitosan/polyvinyl alcohol blended films containing sulfosuccinic acid as the crosslinking agent using UV curing process: An investigation into using sulfosuccinic acid to crosslink chitosan/polyvinyl alcohol films for improved mechanical properties (Yun et al., 2017).
  • Investigation on resistive humidity sensing in sulfosuccinic acid doped polyaniline films: This research explores the potential of sulfosuccinic acid doped polyaniline films for humidity sensing applications (Biswas et al., 2021).

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Manmohan Singh et al.
Journal of pharmaceutical sciences, 93(2), 273-282 (2004-01-06)
The adsorption behavior of model proteins onto anionic poly(lactide-co-glycolide) (PLG) microparticles was evaluated. PLG microparticles were prepared by a w/o/w solvent evaporation process in the presence of the anionic surfactant dioctyl sodium sulfosuccinate (DSS). The effect of surfactant concentration and
N I Gerhardt et al.
Biotechnology and bioengineering, 78(1), 60-72 (2002-02-22)
The stability and structure of protein-containing water-in-oil (w/o) microemulsions were investigated by using the large protein immunoglobulin G (IgG, MW 155,000) in a mixture comprised of brine, sulfosuccinic acid bis [2-ethylhexyl]ester (sodium salt), and isooctane. We explored factors affecting the
Maria del Carmen Hernández-Soriano et al.
Journal of environmental monitoring : JEM, 13(10), 2830-2837 (2011-08-24)
Accumulation of metals in soil at elevated concentrations causes risks to the environmental quality and human health for more than one hundred million people globally. The rate of metal release and the alteration of metal distribution in soil phases after
G Oros et al.
General physiology and biophysics, 18(3), 283-292 (2000-03-07)
The strength and selectivity of the phytotoxicity of 11 sulfosuccinic acid ester surfactants were determined on the leaves of Tradescantia bicolor, and the data were evaluated by multivariate mathematical-statistical methods. Spectral mapping technique combined with stepwise regression analysis indicated that
C M Carvalho et al.
Journal of biotechnology, 81(1), 1-13 (2000-08-11)
A transesterification process is analyzed in its multiple kinetic components that include the determination of the kinetic constants for both substrates, butyl acetate (BAc) and hexanol (H), involved in the alcoholysis reaction and for the products formed (hexyl acetate (HAc)
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