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268445

Sigma-Aldrich

Isethionic acid ammonium salt

99%

Sinônimo(s):

2-Hydroxyethanesulfonic acid ammonium salt

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About This Item

Fórmula linear:
HOCH2CH2SO3NH4
Número CAS:
Peso molecular:
143.16
Beilstein:
3722656
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

99%

Formulário

solid

pf

138-141 °C (lit.)

grupo funcional

hydroxyl
sulfonic acid

cadeia de caracteres SMILES

N.OCCS(O)(=O)=O

InChI

1S/C2H6O4S.H3N/c3-1-2-7(4,5)6;/h3H,1-2H2,(H,4,5,6);1H3

chave InChI

LLOHIFXFHGMBNO-UHFFFAOYSA-N

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Aplicação

Isethionic acid ammonium salt may be used in chemical synthesis studies.

Pictogramas

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Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Saswata Ghosh et al.
Journal of cosmetic science, 58(3), 229-244 (2007-06-29)
Sodium cocoyl isethionate (SCI) is an important surfactant ingredient in mild, syndet (synthetic detergent) cleansing bars. In vitro and in vivo studies have demonstrated that SCI is mild and less damaging to the skin barrier than soaps and surfactants such
Sonja Weinitschke et al.
Microbiology (Reading, England), 153(Pt 9), 3055-3060 (2007-09-05)
The degradation of taurine, isethionate and sulfoacetate in Cupriavidus necator (Ralstonia eutropha) H16 was shown by enzyme assays to be inducible, and each pathway involved sulfoacetaldehyde, which was subject to phosphatolysis by a common sulfoacetaldehyde acetyltransferase (Xsc, H16_B1870) to yield
Chantal Brüggemann et al.
Microbiology (Reading, England), 150(Pt 4), 805-816 (2004-04-10)
Growth of the alpha-proteobacterium Paracoccus denitrificans NKNIS with taurine or isethionate as sole source of carbon involves sulfoacetaldehyde acetyltransferase (Xsc), which is presumably encoded by an xsc gene in subgroup 3, none of whose gene products has been characterized. The
C Nabel et al.
Pflugers Archiv : European journal of physiology, 438(5), 694-699 (1999-11-11)
The aim of this study was to assess the relevance of chloride channels to the inhibitory effect of angiotensin II (ANGII) on renin secretion. We thus examined the effects of the chloride channels blockers IAA-94 and niflumic acid, the Na-K-Cl
Lei Gong et al.
Toxicological sciences : an official journal of the Society of Toxicology, 122(2), 587-597 (2011-05-13)
Organic anion-transporting polypeptides (Oatp) 1a1 and 1a4 were deleted by homologous recombination, and mice were characterized for Oatp expression in liver and kidney, transport in isolated hepatocytes, in vivo disposition of substrates, and urinary metabolomic profiles. Oatp1a1 and Oatp1a4 proteins

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