Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C8H18O4S |
| Molecular Weight | 210.291 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC(CC)COS(O)(=O)=O
InChI
InChIKey=MHGOKSLTIUHUBF-UHFFFAOYSA-N
InChI=1S/C8H18O4S/c1-3-5-6-8(4-2)7-12-13(9,10)11/h8H,3-7H2,1-2H3,(H,9,10,11)
| Molecular Formula | C8H18O4S |
| Molecular Weight | 210.291 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Sodium ethasulfate is a clear, colorless, viscous, and nonflammable liquid that belongs to the sodium sulfate chemical group. Sodium ethasulfate is usually stable; however, it is incompatible with strong oxidizing agents. Due to its unique solubility and penetrating action, it is widely used in various end-user industries such as textile, chemical production, pharmaceuticals, agrochemicals, metal working, and food processing. Sodium ethasulfate is used as wetting agent in the textile industry. The product is used along with calcium hypochlorite as a bleaching agent. The product is used as mercerizing agent for cotton processing in the chemical industry. Sodium ethasulfate is employed as intermediate in anoinic surfactants that are used for dishwashing detergents. It is also used as surfactant in lye washing and peeling process. In the pharmaceutical industry, it is used to enhance the bactericidal properties of generic antiseptics that are more acidic. It is also employed as surfactant in penicillin production for breaking undesired reaction conditions.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Carcinogenic potential of phthalic acid esters and related compounds: structure-activity relationships. | 1986-03 |
|
| Comparative chronic toxicities and carcinogenic potentials of 2-ethylhexyl-containing compounds in rats and mice. | 1985-11 |
|
| Experimental toxicity of sodium 2-ethylhexyl sulfate. | 1970-07 |
|
| Metabolism of 2-ethylhexyl sulfate by the rat and rabbit. | 1966-05 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3709453
Sodium ethasulfate (2-ethylhexyl sulfate) (10,000-40,000 ppm) was administered to groups of rats (10,000-20,000 ppm) and mice (5,000-20,000 ppm) for 2 years.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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