233714
Sodium bisulfate monohydrate
ReagentPlus®, 99%
Synonyme(s) :
Sodium hydrogen sulfate monohydrate
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A propos de cet article
Formule linéaire :
NaHSO4 · H2O
Numéro CAS:
Poids moléculaire :
138.08
NACRES:
NA.55
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-665-7
MDL number:
Assay:
99%
Form:
moist crystals
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Laissez-nous vous aiderInChI key
JXHZRQHZVYDRGX-UHFFFAOYSA-M
InChI
1S/Na.H2O4S.H2O/c;1-5(2,3)4;/h;(H2,1,2,3,4);1H2/q+1;;/p-1
SMILES string
[Na+].[H]O[H].OS([O-])(=O)=O
product line
ReagentPlus®
assay
99%
form
moist crystals
Quality Level
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Catégories apparentées
General description
Sodium bisulfate monohydrate can be used as a reagent for the oxidation of benzylic alcohols to aldehydes and ketones, diarylcarbazides to diaryl carbazones, 1,2-dihydroquinolines to quinoline derivatives, and 1,4-dihydropyridines to pyridine derivatives. It can also be used as a catalyst in the esterification of carboxylic acids and alcohols to synthesize esters. Additionally, it is an effective oxygen scavenger to inhibit corrosion.
Application
- Preservative and Sanitizer in Food Microbiology: Sodium bisulfate monohydrate is effectively used as a preservative in apple juice and as an alternative sanitizer for washing cherry tomatoes. Its antimicrobial properties help control pathogens like Listeria monocytogenes and Escherichia coli, ensuring food safety. This application is crucial for chemists working in food microbiology and safety, highlighting the compound′s role in maintaining the quality and safety of food products (Chen et al., International Journal of Food Microbiology, 2022).
- One-Step Hydrolysis for Xylooligosaccharides Production: Sodium bisulfate monohydrate is employed in a one-step hydrolysis process for the efficient production of xylooligosaccharides from poplar. This method enhances the yield and purity of xylooligosaccharides, which are valuable in various industrial applications, including food additives and pharmaceuticals. This research underscores its importance in bioprocessing and green chemistry initiatives (Liao et al., SSRN Electronic Journal, 2022).
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
The product is not intended for use as a biocide under global biocide regulations, including but not limited to the US EPA′s Federal Insecticide Fungicide and Rodenticide Act, the European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR), and others.
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Danger
hcodes
Hazard Classifications
Eye Dam. 1
Classe de stockage
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Oxidation of 1, 2-dihydroquinolines under mild and heterogeneous conditions
Damavandi J, et al.
Synthetic Communications, 31, 3183-3187 (2001)
Selective and efficient oxidation of diaryl carbazide to diaryl carbazone with NaNO2/NaHSO4? H2O/SiO2
Li X, et al.
J. Chem. Res. (M), 2002, 234-235 (2002)
The role of protein extracts in the induction of disease in Acanthaster planci
Rivera-Posada J, et al.
Journal of Experimental Marine Biology and Ecology, 429, 1-6 (2012)
Oxidation of 1, 4-dihydropyridines under mild and heterogeneous conditions
Zolfigol M, et al.
Synthetic Communications, 30, 2945-2950 (2000)
NaBrO3/NaHSO4.H2O as a versatile reagent system for the oxidation of benzylic alcohols and aldehydes
Shirini F, et al.
Synthetic Communications, 36, 2833-2840 (2006)
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