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About This Item
Linear Formula:
HOCH2CH2SO3NH4
CAS Number:
Molecular Weight:
143.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
260-656-0
Beilstein/REAXYS Number:
3722656
MDL number:
Assay:
99%
Form:
solid
InChI key
LLOHIFXFHGMBNO-UHFFFAOYSA-N
InChI
1S/C2H6O4S.H3N/c3-1-2-7(4,5)6;/h3H,1-2H2,(H,4,5,6);1H3
SMILES string
N.OCCS(O)(=O)=O
assay
99%
form
solid
mp
138-141 °C (lit.)
functional group
hydroxyl, sulfonic acid
Application
Isethionic acid ammonium salt may be used in chemical synthesis studies.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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
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
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
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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