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Sodium perborate are chemical compounds with (H2O)x. Commonly encountered salts are the anhydrous form (x = 0) and as a (x = 6). These two species are sometimes called, respectively, "monohydrate" or PBS-1 and "tetrahydrate" or PBS-4, after the historic assumption that would be the anhydrous form). Both the anhydrous and hexahydrate salts are white, odorless, water-soluble solids.

(1994). 9780471936206, John Wiley & Sons.

Peroxyborates are widely used in laundry detergents, as one of the peroxide-based bleaches.

Sodium perborate was first obtained in 1898, independently, by Sebastian Tanatar and by P. Melikoff and L. Pissadewsky; the researchers prepared sodium perborate by treating sodium borate with a solution of hydrogen peroxide and sodium hydroxide, but Tanatar also obtained sodium perborate by electrolysis of a solution of sodium borate.

  • See p. 299.


Structure
Unlike sodium percarbonate, the peroxyborates are not of hydrogen peroxide. Rather, they contain a , which consists of a cyclic core with a pair of bonded to each boron atom. The ring adopts a chair conformation. The hexahydrate has the formula , that is, or .
(2025). 9783527303854

The anhydrous compound is commonly but incorrectly called a "monohydrate" with the historical but misleading formula . Instead, a more descriptive formula is . Likewise, the hexahydrate is usually called "tetrahydrate" and formulated as . Both forms are white, odorless, water-soluble solids. The "monohydrate" and the "tetrahydrate" are the commercially important forms.

A true tetrahydrate , traditionally known as the "trihydrate", is also known but has no industrial significance. There is a for each of the three traditional "hydrates", the three "peroxyborate" versions of each (interpreted as a hydrogen peroxide adduct) and the poorly-defined "anhydrate" , a total of seven.


Chemistry
Sodium perborate (i.e. breaks down in contact with water), producing hydrogen peroxide and :
The resulting then enter in equilibrium with , hydrogen peroxide , the anion , and the tetrahydroxyborate anion :

As the concentration of the solution increases, other peroxoborate species become significant. With excess , the anions , , and eventually appear. At high borate concentrations, the sodium perborate with dimeric anion crystallizes out, due to its relatively low solubility.

The "monohydrate" form dissolves faster than the "tetrahydrate" and has higher heat stability; it is prepared by heating the "tetrahydrate". The commercial "anhydrate", or Oxoborate, is prepared by further heating of "monohydrate" and actually consists of and boron–oxygen radical.


Preparation
Sodium perborate is manufactured by reaction of and NaOH to give sodium metaborate , which is then reacted with hydrogen peroxide to give hydrated sodium perborate:

A may be added to control crystal size.J. Dugua and B.Simon (1978): "Crystallization of sodium perborate from aqueous solutions: I. Nucleation rates in pure solution and in presence of a surfactant". Journal of Crystal Growth, volume 44, issue 3, pages 265-279.J. Dugua and B.Simon (1978): "Crystallization of sodium perborate from aqueous solutions: II. Growth kinetics of different faces in pure solution and in the presence of a surfactant". Journal of Crystal Growth, volume 44, issue 3, pages 280-286.

It may also be produced in the electrolysis of an aqueous solution containing borax, sodium carbonate and sodium bicarbonate (potassium dichromate is added to improve yield along with sodium silicate). A copper pipe is used as a cathode and platinum for the anode, the current being 6 amperes at 7 to 8 volts, and the temperature 10°C.


Uses
Sodium perborate serves as a stable source of in many , laundry detergents, , and laundry . It is a less aggressive bleach than sodium hypochlorite and other chlorine-based bleaches, causing less degradation to and . Sodium perborate releases oxygen rapidly at temperatures greater than 60 °C. Addition of the activator, typically tetraacetylethylenediamine (TAED), makes it active at lower temperatures (40–60 °C).

The compound has properties and can act as a . It is also used as a "disappearing" in some brands of .


Dental use
Sodium perborate monohydrate is quickly hydrolyzed into hydrogen peroxide and on contact with water. A 1979 double-blind suggests that hydrogen peroxide, which is released during the use of this product, may prevent or retard colonization and multiplication of anaerobic bacteria, such as those that inhabit oral wounds.

Sodium perborate is also present in some formulas for non vital root treated teeth. The compound is inserted in the root canal and left in place for an extended period of time to allow it to diffuse into the tooth and bleach stains from the inside out. However, this use has been banned in the .


Organic synthesis
Sodium perborate is also used as an reagent in organic synthesis. For example, it converts into and . Another use of sodium perborate in organic synthesis is as a convenient alternative to , for example in the 2 step conversion of an to a (the first step is a Miyaura borylation). Spirocycloheptanes as inhibitors of rock


Safety
In the , sodium perborate, like most perborates, was classified as "carcinogenic, mutagenic, or toxic for reproduction" (CMR), category 1B of Regulation (EC) 790/2009, as a result of being included in Part 3 of Annex VI of the regulation 1272/2008 on Classification, Labelling and Packaging (CLP) of substances and mixtures. As a result, their use has been automatically banned in cosmetic products in the EU, in any concentration, starting 1 December 2010. That extends to the use of perborates for tooth whitening.Nature Inc. (2015): "Chemical used in beauty salon teeth whitening banned by EU". BDJ Team, volume 2, article 15075, 26 June 2015.


Brands

Bocasan
Bocasan was an oral wound cleanser manufactured in the by Knox Laboratories Ltd of London from 1960–1975, before being rebranded as an product Medicines: The Comprehensive Guide edited by Dr. Ian Morton, Judith M. Hall. Royal Society of Medicine. Bloomsbury Publishing, London, 2002. Pg 118

Production of Bocasan appears to have ceased by 2003. A similar product, was available for a period before also ceasing production in 2010. As of 2013, a pharmacy offers the same formulation under the name Bikosan

It was used to aid treatment, in adults or children over 5 years old, of conditions such as , denture irritation, orthodontic irritation, or after dental procedures.

Bocasan was packaged in a 1.7 gram envelope, and contained 69.72% sodium perborate monohydrate and 29.68% sodium hydrogen tartrate anhydrous. To use, the contents were dissolved in 30 cubic centimetres of warm water. Half the amount was swilled around the mouth for two minutes and discarded, and the procedure repeated with the remainder. Treatment was recommended three times a day after meals.

A 1979 double-blind crossover study suggests that hydrogen peroxide, which is released during the use of this product, may prevent or retard colonization and multiplication of anaerobic bacteria, such as those that inhabit oral wounds. A small (n=12) 1998 RCT shows that Bocasan combined with mouthwash is better than chlorhexidine alone in preventing plaque. A further study (n=28) shows that Bocasan reduces the staining associated with chlorhexidine.


Drug facts
  • Active ingredient: Sodium perborate monohydrate
  • Inactive ingredients: Sodium hydrogen tartrate
  • Purpose: Oral cleanser
  • Normal use: Use up to three times daily, after meals or as directed by a dentist


Amosan
Amosan is an oral . It contains 68.635% sodium perborate monohydrate by weight. Sold as a powder customarily packaged in 1.7g envelopes, it reconstitution with warm water, after which it is used as a mouth rinse. It is used to aid in the prevention of, as well as speed the recovery from , denture irritation, orthodontic irritation, and oral injuries or after dental procedures.


History
Amosan was originally made by ; a mention of the powder appeared in the February 6, 1970 . Federal register Between 2005 and 2010, Amosan was manufactured in and sold under the Oral-B brand, belonging to Procter & Gamble after its 2005 acquisition of Gillette. In December 2010, its use was banned in the EU, as the product is based on borate, which the union considers "carcinogenic, mutagenic, or toxic for reproduction".Nature Inc. (2015): "Chemical used in beauty salon teeth whitening banned by EU". BDJ Team, volume 2, article 15075, 26 June 2015.

Vintage Brands Limited began manufacturing and selling Amosan Oral Antiseptic Rinse in 2014 because many consumers were disappointed that it was no longer available. Amosan Oral Products Facebook Product review pages on Amazon and public comment forums elsewhere indicate a high level of frustration with the discontinuation by users who could find no effective alternative treatment.

In April 2012, it was reported that Shoppers Drug Mart in Canada had produced a comparable product under their house brand: 'Life Brand Oral Wound Cleanser'. Also, Jean Coutu and Rexall has their own house brand versions.


Drug facts
  • Active ingredient: Sodium perborate monohydrate 1.2 g
  • Inactive ingredients: L-, , flavors
  • Purpose: Oral wound cleanser
  • Normal use: Use up to 4 times daily, after meals and before bedtime or as directed by a dentist or physician


See also


External links

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