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282987

Sigma-Aldrich

Sodium 4-hydroxybenzenesulfonate dihydrate

98%

Synonym(s):

4-Hydroxybenzenesulfonic acid sodium salt, Phenol-4-sulfonic acid sodium salt dihydrate

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About This Item

Linear Formula:
HOC6H4SO3Na·2H2O
CAS Number:
10580-19-5
Molecular Weight:
232.19
Beilstein:
3803250
EC Number:
249-038-1
MDL number:
MFCD00150724
UNSPSC Code:
12352100
PubChem Substance ID:
24857081
NACRES:
NA.22
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Quality Level

100

Assay

98%

functional group

sulfonic acid

SMILES string

[Na+].[H]O[H].[H]O[H].Oc1ccc(cc1)S([O-])(=O)=O

InChI

1S/C6H6O4S.Na.2H2O/c7-5-1-3-6(4-2-5)11(8,9)10;;;/h1-4,7H,(H,8,9,10);;2*1H2/q;+1;;/p-1

InChI key

SXONATFNYJWFNK-UHFFFAOYSA-M

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Application

Sodium 4-hydroxybenzenesulfonate dihydrate has been used in the preparation of:
  • series of layered divalent transition metal benzenesulfonates[1]
  • luminescent ladder-like lanthanide coordination polymers of 4-hydroxybenzenesulfonate[1]
  • new polynorbornene ionomers bearing fluorinated pendant benzenesulfonate groups[2]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD9559V
STBH8759
STBH7730
STBG9382
STBG6725

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Sigma-Aldrich

328596

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Taurine ≥99%

Sigma-Aldrich

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Ying Zhang et al.
Inflammation, 43(2), 417-424 (2020-01-18)
PNU-282987, the α7 acetylcholine receptor(α7nAchR) agonist, has been repeatedly reported to play a key role in anti-inflammatory action of multiple disease. However, little is known about its effect on LPS-induced intestinal epithelial barrier dysfunction. This study investigated the protective effects
Synthesis and structures of layered metal sulfonate salts.
Kosnic EJ, et al.
New. J. Chem., 32(5), 790-793 (2008)
Hitomi Kimura et al.
Scientific reports, 9(1), 5887-5887 (2019-04-12)
Gastrointestinal prokinetic agents function as serotonin-4 receptor (5-HT4R) agonists to activate myenteric plexus neurons to release acetylcholine (ACh), which then induce anti-inflammatory action. Details of this pathway, however, remain unknown. The aim of this study is to clarify the anti-inflammatory
Hongmei Xu et al.
BMC pregnancy and childbirth, 19(1), 188-188 (2019-05-30)
Preeclampsia is associated with chronic inflammation. The cholinergic anti-inflammatory pathway regulates systemic inflammation through activating α7 nicotinic acetylcholine receptors (α7nAChR) expressed in monocytes/macrophages. This study aimed to investigate the role of α7nAChR in peripheral blood monocytes in preeclampsia. Peripheral blood
Megan L Stanchfield et al.
Frontiers in molecular biosciences, 7, 200-200 (2020-09-15)
Previous studies from this lab have determined that dedifferentiation of Müller glia occurs after eye drop application of an α7 nicotinic acetylcholine receptor (nAChR) agonist, PNU-282987, to the adult rodent eye. PNU-282987 acts on α7 nAChRs on retinal pigment epithelial
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