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Key Documents

71220

Sigma-Aldrich

Sodium 2-ethylhexyl sulfate

~50% in H2O

Synonym(s):

2-Ethylhexyl sulfate sodium salt

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About This Item

Empirical Formula (Hill Notation):
C8H17NaO4S
CAS Number:
Molecular Weight:
232.27
Beilstein/REAXYS Number:
5177087
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

description

anionic

Quality Level

form

liquid

mol wt

232.27 g/mol

concentration

4.95% (Na, ICP)
~50% in H2O

technique(s)

protein quantification: suitable

density

1.12 g/mL at 20 °C (lit.)

SMILES string

[Na+].CCCCC(CC)COS([O-])(=O)=O

InChI

1S/C8H18O4S.Na/c1-3-5-6-8(4-2)7-12-13(9,10)11;/h8H,3-7H2,1-2H3,(H,9,10,11);/q;+1/p-1

InChI key

DGSDBJMBHCQYGN-UHFFFAOYSA-M

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Application

Sodium 2-ethylhexyl sulfate is an anionic surfactant that can be used:
  • In suspension polymerization.
  • In the analysis of phenolic compounds through microchip-CE with pulsed amperometric detection.
  • As charge balancing anions in the synthesis of organo-layered double hydroxides (organo-LDHs).

Other Notes

Alkyl sodium sulfate surfactants.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Variation of anions in layered double hydroxides: effects on dispersion and fire properties.
Wang L, et al.
Polymer Degradation and Stability, 94(5), 770-781 (2009)
The effects of alkyl sulfates on the analysis of phenolic compounds by microchip capillary electrophoresis with pulsed amperometric detection.
Ding Y, et al.
Analyst, 132(10), 997-1004 (2007)
Suspension polymerization of thermally expandable core/shell particles.
Jonsson M, et al.
Polymer, 47(10), 3315-3324 (2006)
W M Kluwe
Environmental health perspectives, 65, 271-278 (1986-03-01)
Chronic toxicity and carcinogenicity studies of several phthalic acid esters (PAEs) and compounds containing a 2-ethylhexyl moiety were conducted in Fischer 344 rats and B6C3F1 (hybrid) mice. The compounds studied were phthalic anhydride, di(2-ethylhexyl) phthalate, butyl benzyl phthalate, diallyl phthalate

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