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24634-61-5

  • Product NamePotassium sorbate
  • Molecular FormulaC6H7KO2
  • Molecular Weight150.219
  • Purity99%
  • Appearancewhite crystals or powder
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  • CasNo: 24634-61-5
  • Molecular Formula: C6H7KO2
  • Appearance: white crystals or powder
  • Purity: 99%

Cost-effective and customizable Potassium sorbate 24634-61-5 for sale

  • Molecular Formula:C6H7KO2
  • Molecular Weight:150.219
  • Appearance/Colour:white crystals or powder 
  • Vapor Pressure:<1 Pa (20 °C) 
  • Melting Point:270 °C 
  • Boiling Point:233 °C at 760 mmHg 
  • PKA:4.69[at 20 ℃] 
  • Flash Point:139.9 °C 
  • PSA:40.13000 
  • Density:1,361 g/cm3 
  • LogP:-0.13140 

Potassium sorbate(Cas 24634-61-5) Usage

Overview

Potassium sorbate is petitioned for use in organic livestock production as mold inhibitor[1-3]. Sorbic acid was first discovered in the Mountain Ash Tree (Sorbus aucuparia or Sorbus americana). Today most potassium sorbate is made synthetically. Potassium sorbate is a naturally occurring unsaturated fatty acid and is completely safe with regard to health and has the lowest allergenic potential of all food preservatives. Potassium sorbate was also petitioned for use in liquid livestock medications primarily aloe vera juice as a substitute for antibiotics and other various hormones[1-4]. The use of chemical food preservatives, except for salts, sugars, spices, vinegar, etc., was not very widespread until the last 200 years. Progress in the development of food preservatives has not been steady. With a view to developing more effective, simpler, and less expensive means of food preservation, many chemicals having strong antimicrobial properties were initially utilized for food preservation but were subsequently abandoned when their undesirable physiological and biochemical properties were discovered. For example, boric acid, salicyclic acid, creosote, and formaldehyde, which were utilized as preservatives in foods during the 19th century, are no longer used. On the other hand, sorbic acid (SA), benzoic acid, p-hydroxy benzoic acid esters, and sulfur dioxide have proved very useful in various food preservation applications and their use has been officially permitted in almost all countries of the world [1,4]. Figure 1 the chemical structure of potassium sorbate

Application

When dissolved in water, potassium sorbate ionizes to form sorbic acid which is effective against yeasts, molds, and select bacteria, and is widely used at 250 ppm to 1000 ppm levels in cheeses, dips, yogurt, sour cream, bread, cakes, pies and fillings, baking mixes, doughs, icings, fudges, toppings, beverages, margarine, salads, fermented and acidified vegetables, olives, fruit products, dressings, smoked and salted fish, confections and mayonnaise. Therefore, it is generally used as a powerful food preservative.

Antimicrobial effect

Antimicrobial properties of sorbic acid were discovered independently in 1939 and 1940 by Muller and Gooding in Germany and the USA, respectively[2, 10]. After this discovery, sorbic acid and its salts were tested and used in a variety of consumer products for inhibition of yeast and molds and certain bacteria. But its use as a food preservative had to wait until 1950 when commercial production commenced. Initially sorbates were known to be effective inhibitors of yeast and molds, and less so of bacteria. In 1974 Tompkin et al.[8] reported that addition of 0.1 % potassium sorbate to uncured sausages delayed the growth of Salmonella spp. and Staphylococcus aureus as well as growth and toxin production by Clostridium botulinum. Following these findings, extensive studies were undertaken on the potential use of sorbic acid or its salts as antibotulinal agents and preservatives in various types of meats and meat products. These compounds were tested in combination with low levels of sodium nitrite for the preservation of cured meats and the reduction of potentially carcinogenic nitrosamine in products such as bacon[9, 10]. Most recently sorbic acid has played a very important role in the development of intermediate-moisture foods. The water activity of these foods is low enough to control the growth of bacteria but not growth of yeast and molds; therefore, sorbic acid is used as a very effective antimycotic agent in these products[11]. Sorbic acid and its salts are also being used as one of the various "hurdles" employed to control microbial growth in intermediate moisture foods[12]. Unfortunately, grain and feed provides an ideal environment for molds to proliferate. Raw materials or feeds in bulk storage are rich sources of energy, proteins and moisture and, thus, are highly conducive to mold growth[13]. Potassium sorbate is the potassium salt of sorbic acid, and is much more soluble in water than the acid. Potassium sorbate will produce sorbic acid once it is dissolved in water and is the most widely used food preservative in the world. It is effective up to pH 6.5 but effectiveness increases as the pH decreases. Potassium sorbate has about 74% of the antimicrobial activity of the sorbic acid, thus requiring higher concentrations to obtain the same results that pure sorbic acid provides. Potassium sorbate is effective against yeasts, molds, and select bacteria, and is widely used at 0.025 to 0.10 % levels in cheeses, dips, yogurt, sour cream, bread, cakes, pies and fillings, baking mixes, doughs, icings, fudges, toppings, beverages, margarine, salads, fermented and acidified vegetables, olives, fruit products, dressings, smoked and salted fish, confections and mayonnaise. Maximum level allowable by law is 0.1%. It is important to know that the addition of sodium benzoate and/or potassium sorbate to a food product will raise the pH by approximately 0.1 to 0.5 pH units depending on the amount, pH, and type of product. Additional adjustment of the pH might be needed to keep the pH at a safe level[14].

Immunomodulatory effect

While one recent study reported that potassium sorbate can contribute to the activation of inflammatory pathways[15], other studies indicate that sorbate is primarily anti-inflammatory in vivo and acts to downregulate many immune signaling pathways responsible for inflammation, glial cell activation, switching of T-helper cells, modulation of regulatory T cells, cell-to-cell contact, and migration[16]. These latter, anti-inflammatory effects of sorbate would appear to resemble those of sodium salicylate, the active metabolite of the well-known nonsteroidal anti-inflammatory drug aspirin (acetylsalicylic acid). In mouse microglia, sorbate inhibits NF-kappaB activation, modulates the mevalonate pathway, and suppresses the activation of p21ras[17]. Recently, sorbate administration was shown to induce the expression of TGF-beta in splenocytes and also to upregulate regulatory T cells during experimental autoimmune encephalomyelitis, a mouse model of multiple sclerosis (MS)[18]. Interleukin 4 (IL-4) is known to improve the clinical manifestations in this animal model of MS, and the administration of sorbate to human subjects has been shown to induce IL-4 production in their peripheral blood mononuclear cells. Sorbate might therefore deserve consideration as a useful candidate for conjunctive therapy in treating MS, the most common human demyelinating disease of the central nervous system.

Health concern

Until recently, the extensive use of sorbate salts for large-scale food and drink preservation was regarded as completely safe. Claims to this effect are often still issued by the organizations that represent the soft drink industry. Such statements reflect the long history of apparently safe use of these preservatives and a safety testing that has largely focused on the maximum levels of these compounds that could be tolerated without adverse effects in the diet of laboratory animals[19]. The maximum levels of benzoate and sorbate permitted in food and drinks are based on these studies. Ever since these original safety tests, there have been dramatic advances in the technologies available to investigate damage to cells and tissues, providing opportunities for much deeper investigation of the effects of these additives and the consequences of their long-term, large-scale dietary consumption. Indeed, we are now aware of mechanisms of damage to biological systems that were completely unknown at the time of much of the original safety testing of these preservatives. There are more and more concerns regarding the safety use of sorbate. Sorbic acid and potassium sorbates have a very low mammalian toxicity. There is a general consensus that they are intrinsically devoid of carcinogenic activity, but have the potential to undergo a conversion to potential mutagens. In tests on Syrian hamster embryo fibroblasts, Chinese hamster ovary cells, or bone marrow cells, no genotoxic or cell-transforming activity was detected with freshly prepared sodium sorbate solution. However, products of sodium sorbate with genotoxic and cell-transforming properties were formed under conditions of heating and storage. Sorbate can undergo oxidation to 4,5-oxohexanoate[20] and oxidized potassium sorbate can react with ascorbic acid in the presence of ferrous iron[21]. Much attention has been focused on the reactions between sorbate and nitrite at pH2-4.2, conditions that mimic the gastric environment. Among the products of such reactions are the mutagenic agents 1,4dinitro-2-methylpyrrole and ethylnitrolic acid[22]. There is one report of hepatoma arising from the feeding of mice on a diet of very high (15% w/v) sorbic acid, this being correlated with a depletion of the levels of reduced glutathione (GSH) in the mouse liver. Causation of this hepatoma was attributed to the oxidative stress caused by the depleted GSH pool, together with the gradual production of various mutagens in the intestine, mutagens that following their absorption were transferred to the liver where they were, in turn, metabolically activated to carcinogenic compounds[23]. There are also concerns regarding the effect of sorbate on the mitochondrial function. The study of artificial phospholipid bilayer membranes has revealed that sorbate cause significant increases in membrane conductance and proton permeability, mainly by acting as lipid soluble anions at neutral pH and as proton carriers when the pH approximates to the pK of the acid[24]. The action of sorbate on membranes is thought to be exerted mainly through a disruptive effect on membrane structure[25]. This weak acid has a pronounced effect on mitochondrial function, generating a decreased electron flow from substrate dehydrogenases to ubiquinone that in turn increases free electron “leakage” from the respiratory chain, electrons that then combine with molecular oxygen to produce superoxide (O2??). A number of other moderately lipophilic compounds of food and drink relevance, notably ethanol and certain plant essential oils, including the widely used menthol generate ROS in a similar manner.

Physical properties

Colorless or white crystalline solid; density 1.36 g/cm3; decomposes at 270°C; soluble in water, 58 g/100 g solution; moderately soluble in alcohol.

Definition

ChEBI: A potassium salt having sorbate as the counterion.

Production Methods

Potassium sorbate is prepared from sorbic acid and potassium hydroxide.

Preparation

Potassium sorbate is prepared by reacting potassium hydroxide with sorbic acid, followed by evaporation and crystallization:CH3CH=CHCH=CHCOOH + KOH →CH3CH=CHCH=CHCOOK + H2O.

General Description

Sorbates have been reported to be less toxic than benzoate and have been classified as “Generally Recognized as Safe” (GRAS) additives by the U.S. Food and Drug Administration (FDA).Sorbic acid is metabolised to mainly to carbon dioxide. While the minor amounts are converted to trans,trans-muconic acid (ttMA), which is excreted unchanged into the urine. Urinary ttMA is a biomarker for the occupational and environmental exposure to benzene. Ability of trans,trans-2,4-Hexadienoic acid potassium salt (Sorbic acid potassium salt, Potassium sorbate) to induce chromosome aberrations, sister chromatid exchanges (SCE) and gene mutations in cultured Chinese hamster V79 cells has been examined.Potassium sorbate is reported to be less genotoxic than the sodium salt analog.

Pharmaceutical Applications

Potassium sorbate is an antimicrobial preservative, with antibacterial and antifungal properties used in pharmaceuticals, foods, enteral preparations, and cosmetics. Generally, it is used at concentrations of 0.1–0.2% in oral and topical formulations, especially those containing nonionic surfactants. Potassium sorbate has been used to enhance the ocular bioavailability of timolol. Potassium sorbate is used in approximately twice as many pharmaceutical formulations as is sorbic acid owing to its greater solubility and stability in water. Like sorbic acid, potassium sorbate has minimal antibacterial properties in formulations above pH 6.

Toxicology

Potassium sorbate is a skin, eye and respiratory irritant. Although some research implies it has a long term safety record, in vitro studies have shown that it is both genotoxic and mutagenic to human blood cells. Potassium sorbate is found to be toxic to human DNA in peripheral blood lymphocytes (type of white blood cells), and hence found that it negatively affects immunity. It is often used with ascorbic acid and iron salts as they increase its effectiveness but this tends to form mutagenic compounds that damage DNA molecules. Potassium sorbate exhibits low toxicity with LD50 (rat, oral) of 4.92 g / kg, similar to that of table salt . Typical usage rates of potassium sorbate are 0.025 % to 0.1 % (see sorbic acid), which in a 100 g serving yields intake of 25 mg to 100 mg. Acceptable daily intakes for human is 12.5 mg / kg, or 875 mg daily for an average adult (70 kg), according to FAO/World Health Organization Expert Committee on Food Additives.

Safety

Potassium sorbate is used as an antimicrobial preservative in oral and topical pharmaceutical formulations and is generally regarded as a relatively nontoxic material. However, some adverse reactions to potassium sorbate have been reported, including irritant skin reactions which may be of the allergic, hypersensitive type. There have been no reports of adverse systemic reactions following oral consumption of potassium sorbate. The WHO has set an estimated total acceptable daily intake for sorbic acid, calcium sorbate, potassium sorbate, and sodium sorbate expressed as sorbic acid at up to 25 mg/kg body-weight. (mouse, IP): 1.3 g/kg (rat, oral): 4.92 g/kg See also Sorbic Acid.

storage

Potassium sorbate is more stable in aqueous solution than sorbic acid; aqueous solutions may be sterilized by autoclaving. The bulk material should be stored in a well-closed container, protected from light, at a temperature not exceeding 40°C.

Incompatibilities

Some loss of antimicrobial activity occurs in the presence of nonionic surfactants and some plastics.

Regulatory Status

GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (nasal sprays; oral capsules, solutions, suspensions, syrups, tablets; topical creams and lotions). Included in nonparenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

InChI:InChI=1/C6H8O2.K/c1-2-3-4-5-6(7)8;/h2-5H,1H3,(H,7,8);/q;+1/p-1/b3-2-,5-4-;

24634-61-5 Relevant articles

Drying granulation method of potassium sorbate granules

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Paragraph 0022-0065, (2017/06/23)

The invention discloses a dry granulatio...

Method using ceramic membrane reactor to prepare potassium sorbate

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Paragraph 0022-0024, (2017/03/17)

The invention belongs to the field of po...

Process for producing sorbic acid or salts thereof

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, (2008/06/13)

A process produces sorbic acid or its sa...

24634-61-5 Process route

sorbic Acid
110-44-1,91751-55-2

sorbic Acid

potassium sorbate
24634-61-5

potassium sorbate

Conditions
Conditions Yield
With potassium hydroxide; In water; at 55 ℃; for 0.5h; Temperature;
91.5%
In ethanol; water;
With potassium carbonate; In ethanol; for 0.666667h; Time;
1-bromo-butane
109-65-9

1-bromo-butane

potassium sorbate
24634-61-5

potassium sorbate

n-butyl 2(E),4(E)-hexadienoate
7367-78-4

n-butyl 2(E),4(E)-hexadienoate

Conditions
Conditions Yield
With Aliquat 336; for 6h; Heating;
95%

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    Sorbyl alcohol

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