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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
Structure of 2-ETHYLHEXYL HYDROGEN SULFATE

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)

HIDE SMILES / InChI

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

Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
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

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
by admin
on Mon Mar 31 21:36:26 GMT 2025
Edited
by admin
on Mon Mar 31 21:36:26 GMT 2025
Record UNII
8NX2133F3J
Record Status Validated (UNII)
Record Version
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Name Type Language
2-ETHYLHEXYL HYDROGEN SULFATE
Systematic Name English
ETASULFATE
WHO-DD  
Preferred Name English
2-ETHYLHEXYL SULFATE
Systematic Name English
2-ETHYLHEXYL BISULFATE
Systematic Name English
SURFARON A 6008
Brand Name English
ETHASULFATE
Common Name English
EMPICOL 0585A
Brand Name English
SULFURIC ACID, MONO(2-ETHYLHEXYL) ESTER
Systematic Name English
Etasulfate [WHO-DD]
Common Name English
Code System Code Type Description
CHEBI
87808
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
CAS
72214-01-8
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
PUBCHEM
31364
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID7047988
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
FDA UNII
8NX2133F3J
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
CHEBI
88117
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
SMS_ID
300000056085
Created by admin on Mon Mar 31 21:36:26 GMT 2025 , Edited by admin on Mon Mar 31 21:36:26 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY