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Thermo Scientific Chemicals
Sodium perborate tetrahydrate, 97%
CAS: 10486-00-7 | NaBO3·4H2O
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Catalog number A10189.36
also known as A10189-36
Price (JPY)
-
Quantity:
500 g
Specifications
CAS10486-00-7
Chemical Name or MaterialSodium perborate tetrahydrate
DOT InformationTransport Hazard Class: 5.1; Packing Group: III; Proper Shipping Name: OXIDIZING SOLID, N.O.S.
Density1.73
EINECS Number239-172-9
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This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Suitable for battery materials development.
Applications
Sodium perborate tetrahydrate is considered as a source of active hydrogen used in detergents, cleaning products, laundry detergents and bleaches. It finds application as a tooth bleaching agent utilized for tooth. It has antiseptic properties and acts as disinfectant as well as preservative in eye drops. Further, it is mixed with suitable activator, tetraacetylethylenediamine in order to release oxygen at lower temperatures.
Solubility
Soluble in water.
Notes
Moisture sensitive.Incompatible with metals, metallic salts, acids, bases and reducing agents.
Sodium perborate tetrahydrate is considered as a source of active hydrogen used in detergents, cleaning products, laundry detergents and bleaches. It finds application as a tooth bleaching agent utilized for tooth. It has antiseptic properties and acts as disinfectant as well as preservative in eye drops. Further, it is mixed with suitable activator, tetraacetylethylenediamine in order to release oxygen at lower temperatures.
Solubility
Soluble in water.
Notes
Moisture sensitive.Incompatible with metals, metallic salts, acids, bases and reducing agents.
RUO – Research Use Only
General References:
- Useful, inexpensive oxidant. Reviews: Chemtech, 566 (1991); Tetrahedron, 51, 6145 (1995); Synthesis, 1325 (1995); J. Chem. Soc., Perkin 1, 471 (2000). Examples: Oxidation of secondary alcohols to ketones, and ɑ-hydroxy acids to keto acids: Synthesis, 765 (1989). Mild epoxidation of ɑß-unsaturated ketones: Synth. Commun., 19, 3579 (1989); Tetrahedron Lett., 36, 663 (1995). Partial hydrolysis of nitriles to amides: Tetrahedron, 45, 3299 (1989); Synth. Commun., 20, 563 (1990). Oxidation (in AcOH) of sulfides to sulfoxides or sulfones, arylamines to nitro compounds, and Baeyer-Villiger oxidation of ketones to esters: Tetrahedron, 43, 1753 (1987). Oxidation (in AcOH) of aromatic aldehydes to acids: Tetrahedron, 45, 3299 (1989); or oximes to nitro compounds: Synlett, 337 (1992). Oxidative conversion of organoboranes to alcohols: Org. Synth. Coll., 9, 522 (1998).
- In combination with triflic acid for hydroxylation of aromatics: Synlett, 39 (1991).
- In combination with acetic anhydride, cyclic acetals are cleaved to their respective esters: Synlett., 329 (1995).
- For phase-transfer oxidation of alcohols to ketones, catalyzed by Chromium(VI) oxide, 12522, see: Synth. Commun., 21, 575 (1991).
- For a brief feature on uses in synthesis, see: Synlett, 2513 (2006).
- Qin, S.; Yin, B.; Zhang, Y.; Zhang, Y. Leaching kinetics of szaibelyite ore in NaOH solution. Hydrometallurgy 2015, 157, 333-339.
- Hematian, S.; Hormozi, F. Drying kinetics of coated sodium percarbonate particles in a conical fluidized bed dryer. Powder Technol. 2015, 269, 30-37.