233714
Sodium bisulfate monohydrate
ReagentPlus®, 99%
Sinónimos:
Sodium hydrogen sulfate monohydrate
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Acerca de este artículo
Fórmula lineal:
NaHSO4 · H2O
Número CAS:
Peso molecular:
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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Permítanos ayudarleInChI 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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Categorías relacionadas
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Synthesis of 2, 4-D butylate with Sodium Bisulfate Catalyst [J].
Wang Y and Zhang W.
Chemical World, 3, 15-15 (2009)
Catalytic esterifications of carboxylic acids and alcohols by sodium bisulfate monohydrate [J].
Yiqun L.
Modern Chemical Industry, 4 (1999)
Christian A Lenz et al.
Frontiers in microbiology, 6, 652-652 (2015-07-21)
Cold-tolerant, neurotoxigenic, endospore forming Clostridium (C.) botulinum type E belongs to the non-proteolytic physiological C. botulinum group II, is primarily associated with aquatic environments, and presents a safety risk for seafood. High pressure thermal (HPT) processing exploiting the synergistic effect
Oxidation of 1, 2-dihydroquinolines under mild and heterogeneous conditions
Damavandi J, et al.
Synthetic Communications, 31, 3183-3187 (2001)
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)
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