Bronopol

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Bronopol
Bronopol
Bronopol 3D ball-and-stick.png
Names
IUPAC name
2-bromo-2-nitropropane-1,3-diol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.131
EC Number 200-143-0
KEGG
RTECS number TY3385000
UNII
UN number 3241
Properties
C3H6BrNO4
Molar mass 199.989 g/mol
Appearance white
Density 1.1
Melting point 130 °C (266 °F; 403 K)
Boiling point 140 °C (284 °F; 413 K) (decomposes)
Pharmacology
QD01AE91 (WHO)
Hazards
GHS pictograms The corrosion pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)The exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)The environment pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal word Danger
H302, H312, H315, H318, H335, H400
P261, P264, P270, P271, P273, P280, P301+312, P302+352, P304+340, P305+351+338, P310, P312, P321, P322, P330, P332+313, P362, P363, P391, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Bronopol (INN) is an organic compound that is used as an antimicrobial. It is a white solid although commercial samples appear yellow.

The first cited synthesis of 2-Bromo-2-nitro-1,3-propanediol is 1897 according to Molbase.

Bronopol was invented by The Boots Company PLC in the early 1960s and first applications were as a preservative for pharmaceuticals. Owing to its low mammalian toxicity (at in-use levels) and high activity against bacteria (especially the troublesome Gram-negative species),[1] bronopol became popular as a preservative in many consumer products such as shampoos and cosmetics. It was subsequently adopted as an antimicrobial in other industrial environments such as paper mills, oil exploration and production facilities, as well as cooling water disinfection plants.

Production[edit]

Bronopol is produced by the bromination of di(hydroxymethyl)nitromethane, which is derived from nitromethane by a nitroaldol reaction.[2] World production increased from the tens of tonnes in the late 1970s to current estimates in excess of 5,000 tonnes. Manufacturing today is the business of low cost producers, mainly in China.

Applications[edit]

Bronopol is used in consumer products as an effective preservative agent, as well as a wide variety of industrial applications (almost any industrial water system is a potential environment for bacterial growth, leading to slime and corrosion problems - in many of these systems Bronopol can be a highly effective treatment).

The use of bronopol in personal care products (cosmetics, toiletries) has declined since the late 1980s due to the potential formation of nitrosamines. While Bronopol is not in itself a nitrosating agent, under conditions where it decomposes (alkaline solution and/or elevated temperatures) it can liberate nitrite and low levels of formaldehyde and these decomposition products can react with any contaminant secondary amines or amides in a personal care formulation to produce significant levels of nitrosamines (due to the toxicity of these substances, the term 'significant' means levels as low as 10s of parts per billion).

Manufacturers of personal care products are therefore instructed by regulatory authorities to 'avoid the formation of nitrosamines' which might mean removing amines or amides from the formulation, removing Bronopol from a formulation, or using nitrosamine inhibitors.

Bronopol has been restricted for use in cosmetics in Canada.[3]

Physical and chemical properties[edit]

Appearance[edit]

Bronopol is supplied as crystals or crystalline powder, which may vary from white to pale yellow in colour depending on the grade. The yellow colouration is due to chelation of iron during the manufacturing process.

Melting point[edit]

As a pure material, Bronopol has a melting point of about 130 °C. However, due to its polymorphic characteristics, Bronopol undergoes a lattice rearrangement at 100 to 105 °C and this can often be wrongly interpreted as the melting point.

At temperatures above 140 °C, bronopol decomposes exothermically releasing hydrogen bromide and oxides of nitrogen.

Solubility[edit]

Bronopol is readily soluble in water; the dissolution process is endothermic. Solutions containing up to 28% w/v are possible at ambient temperature.

Bronopol is poorly soluble in non-polar solvents but shows a high affinity for polar organic solvents.

Solubilities at 22–25 °C
Solvent %w/v
Water 28
Methanol 89
Ethanol 56
Isopropanol 41
Liquid Paraffin <0.5

Partition coefficient[edit]

Study of the solubility data clearly shows that Bronopol has a high affinity for polar rather than non-polar environments. In two phase systems, Bronopol partitions preferentially into the polar (usually aqueous) phase.

Partition coefficients at 22–24 °C
Solvent Combination Partition Co-efficient
Hexanol/Water 0.74
Alkane|Liquid Paraffin/Water 0.043
Chloroform/Water 0.068

Stability in aqueous solution[edit]

In aqueous solutions, bronopol is most stable when the pH of the system is on the acid side of neutral. Temperature also has a significant effect on stability in alkaline systems.

Degradation[edit]

Under extreme alkaline conditions, bronopol decomposes in aqueous solution and very low levels of formaldehyde are produced.[4] Liberated formaldehyde is not responsible for the biological activity associated with bronopol. Other decomposition products detected after bronopol breakdown are bromide ion, nitrite ion, bromonitroethanol and 2-hydroxymethyl-2-nitropropane-1,3-diol.

Allergy[edit]

In 2005–06, it was the 15th-most-prevalent allergen in patch tests (3.4%) of people with suspected allergic contact dermatitis.[5] It is used as a substitute for formaldehyde, a disinfectant and preservative, in solvents. It is prevalent in skin and personal care products and topical medications.[6]

See also[edit]

References[edit]

  1. ^ Bryce, D. M.; Croshaw, B.; Hall, J. E.; Holland, V. R.; Lessel, B. (1978). "The activity and safety of the antimicrobial agent bronopol (2-bromo-2-nitropropan-1, 3-diol)" (PDF). J. Soc. Cosmet. Chem. 29: 3–24. Retrieved 5 April 2016.
  2. ^ Sheldon B. Markofsky "Nitro Compounds, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2012, Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_401.pub2
  3. ^ "Consumer product safety: Cosmetic ingredient hotlist". Health Canada. Retrieved 2017-01-24.
  4. ^ "Allergic Contact Dermatitis: Topical Preservatives, Part I".
  5. ^ Zug, KA; Warshaw, EM; Fowler, JF Jr; Maibach, HI; Belsito, DL; Pratt, MD; Sasseville, D; Storrs, FJ; Taylor, JS; Mathias, CG; Deleo, VA; Rietschel, RL; Marks, J (2009). "Patch-test results of the North American Contact Dermatitis Group 2005-2006". Dermatitis : contact, atopic, occupational, drug. 20 (3): 149–60. doi:10.2310/6620.2009.08097. PMID 19470301.
  6. ^ https://www.smartpractice.com/dermatologyallergy/pdfs/allergens/Bronopol-Patient-Info.pdf

External links[edit]