Physical, Chemical, and Environmental Properties of Phthalates: Comparison
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Phthalic acid esters (PAEs), commonly named phthalates, are a class of dialkyl or alkyl/aryl esters of phthalic acid (1,2-benzenedicarboxylic acid) structured in one benzene ring linked with two aliphatic ester groups, most commonly in the ortho configuration.

  • phthalic acid esters
  • endocrine active substances
  • plastic pollution

1. Introduction

Phthalic acid esters (PAEs), commonly named phthalates, are a class of dialkyl or alkyl/aryl esters of phthalic acid (1,2-benzenedicarboxylic acid) structured in one benzene ring linked with two aliphatic ester groups, most commonly in the ortho configuration [1,2][1][2]. PAEs were used for the first time as additives in plastics in the 1920s and continue to be the largest plasticiser class in the 21st century [3]. Among all the possible sources of contamination, the impact of plastics in different environmental matrices has contributed to the widespread presence of phthalates. The release of chemicals associated with plastics into the marine environment is receiving increasing attention. Phthalates are biologically active compounds that dissolve in water to varying degrees depending on the physicochemical characteristics of the side chains, particularly octanol/water partitioning (Kow). Organisms can absorb these substances by ingestion, inhalation, or contact [1].
In the organisms, PAEs are metabolised into toxic compounds that can impair vital functions. Di-2-ethylhexyl phthalate (DEHP) and di-n-butyl phthalate (DnBP) are two of the most toxic and frequently used phthalates [4].
Animal experiments have shown that phthalates interfere with normal physiological processes mediated by hormones essential for reproduction, growth, and development (e.g., decreased testis weight, spermatogenesis impairment, and external genital malformations), leading to the so-called “phthalate syndrome” [5].
Based on the concentration, the nature of the compound, the physicochemical parameters of the environment, and the organism involved, exposure to PAEs leads to different effects and levels of chronic and acute toxicity [6].
Exposure to PAEs also adversely affects the behaviour and health of adults and their offspring [7,8][7][8] causing, among others, hepatotoxicity, oxidative stress, neurodevelopmental changes, genetic aberrations, and epigenetic reprogramming [7,9,10,11,12][7][9][10][11][12]. Depending on effects and exposure levels, phthalates can be considered risk factors for many multifactorial diseases (e.g., reproductive pathologies, developmental alterations and embryogenesis, including the hatching success of eggs, metabolic syndromes, and tumours) [7,13][7][13]. These effects are symptomatic of a hormone balance disorder; therefore, phthalates are endocrine active substances (EAS) that can interact or interfere with normal hormonal action, showing effects of different types and severity. For this reason, they can be called modulators, perturbators, disruptors, or endocrine destroyers.
In general, EAS can act in several ways: (i) mimic the action of the hormone naturally produced, inducing an excessive response or at the wrong times (agonistic effect); (ii) block the receptor, preventing the hormone from binding there so that it cannot act (antagonistic effect); (iii) alter the regulation of hormones, acting “upstream” on their production; (iv) alter the transport of hormones in the blood [14].
PAEs are substances of concern, as reiterated in the 2021 UN report on plastic pollution [15]; consequently, restrictive measures have been introduced, limiting their use.
The regulations on the restrictions on the use of phthalates are different between international legislations; moreover, they consider only phthalates with high rates of application, and thus, high risk of exposure, which are listed as toxic, for example, di-methyl phthalate (DMP), benzyl butylphthalate (BBzP), DEHP, DnBP, di-iso-nonyl phthalate (DiNP), di-iso-decyl phthalate (DiDP), and di-n-octyl phthalate (DnOP). The restrictions mainly concern food contacts materials (FCM), cosmetics, toys, and childcare articles [2,16,17,18][2][16][17][18].

2. Physical, Chemical, and Environmental Properties of Phthalates

Phthalates are formed by a reaction of phthalic anhydride with various alcohols. The number of carbon atoms present will determine the length of the lateral chains R and R’, and thus, the molecular weight of the phthalate is obtained [1]. PAEs differ chemically in the substitutions of the R1 and R2 side chains (which characterise their physicochemical properties) and are slightly volatile liquids, generally colourless, odourless, and oily liquids at room temperature [6]. In addition, their solubility in fat (lipophilic property) increases with the lengthening of the side chains R and R’ (Figure 1).
Environments 10 00099 g001 550
Figure 1.
General chemical structure of phthalate esters.
Although there is no unique classification, it is generally possible to distinguish low molecular weight PAEs (LMW PAEs) with 3–6 carbon atoms in their side chain, and high molecular weight PAEs (HMW PAEs) with R and R′ from 7 to 13 carbons [1]. LMW PAEs include DMP, diethyl phthalate (DEP), DnBP, DiBP, and dimethylglycol phthalate (DMEP) and are typically used in PVC products, medical devices, personal care products, cosmetics, adhesives, paints, printing inks, pesticides, toys, enteric-coated tablets, food packaging or bag, etc. Most of the common phthalates are reported in Table 1. PAEs with shorter alkyl chains, such as DMP and DEP, are widely used as solvents and fixatives, allowing fragrances, for example, to evaporate more slowly and to persist, thus extending product life [1,2,19][1][2][19]. HMW PAEs include BBzP, DEHP, DnOP, DiNP and DIDP, and dipropyl heptyl phthalate (DPHP), which are most commonly used as plasticisers to provide the plastic vinyl its flexibility [1]. PAEs have a relatively high boiling point and low melting point, which confers properties particularly suitable for use as plasticisers, heat transfer fluids, and carriers in the polymer industry [1]. Linear esters offer superior flexibility at low temperatures and have lower volatility than branched esters [1]. As a result of these characteristics, PAEs are widely used both as plasticisers and also as non-plasticising agents [20] in large quantities. In fact, some products may consist, by weight, of up to 40% of phthalates [21]. Despite their favourable physicochemical properties and their versatility of application in several fields that have provided numerous benefits to society, PAEs have instead demonstrated several adverse health effects of exposed organisms in all environments, especially in aquatic ones [22]. Since phthalates are not chemically bound to the polymers in which they are mixed, they can be released (for example, by contact, leaching, migration, or evaporation) in the environment, leading to exposure to the organisms present therein [22,23,24][22][23][24]. PAE residues have been detected in all environmental compartments. Extensive production, the storage of waste containing PAE in the environment, the inefficiency of traditional waste plants on the complete degradation, and the possible negative effects of PAEs on human health pose great global environmental and health risks for long durations [25]. Different reservoirs depend on different physicochemical properties, including water solubility (Sw), vapour pressure (Vp), Henry’s constant (KH), air/water partitioning, octanol/air partitioning (Koa), octanol/water partitioning (Kow), organic carbon partitioning (Koc), and abiotic degradation/biodegradation processes [1]. In the aquatic environment, among all the possible sources of contamination, certainly, the impact of plastics (a major source of contamination) in different environmental matrices has contributed and is contributing to their ubiquitous diffusion (due to their ability to float and resist degradation). Phthalates, favoured by the size of micro- and nano-plastics, can easily pass from low trophic levels of the food chain such as plankton and fish and then up to top predators and humans [26]. In addition, it has been shown that microplastics [27] and therefore PAEs [9] can pass through the placenta, causing exposure of the foetus to these pollutants. PAEs’ presence has also been documented in regions far from the production areas due to the atmospheric and oceanic transport that contributes significantly to their spread [28]. This is particularly the case for short-chain phthalates, which are more susceptible to long-distance transport phenomena. As a result, they can also be found all over the world in regions where they have never been used or produced and it is very difficult to trace the source of origin [28]. To this, bioaccumulation and trophic transfer phenomena are added, further amplifying their diffusion. The PAEs’ fate and toxicity are correlated with the wide variety of environmental and biological transformations in different compartments, which depend on the structure and the physicochemical properties of the specific PAEs, the chemical nature of the investigated matrix, as well as different environmental conditions, including organic carbon content, pH, salinity, enzyme activities, etc. [29,30,31][29][30][31]. PAEs, similar to other persistent organic pollutants (POPs), are subject to biomagnification phenomena with potential negative impacts on the food chain, human health, and the environment [32].
Table 1.
Most common phthalates with acronyms, molecular formulas, CAS, R1, and R2 chains and their log K
ow.
.
PAE Congeners Acronym Molecular Formula CAS R1 R2 Log Kow
dimethyl phthalate DMP C10H10O4 131-11-3 CH3 CH3 1.60
diethyl phthalate DEP C12H14O4 84-66-2 CH2CH3 CH2CH3 2.47
diisobutyl phthalate DiBP C16H22O4 84-69-5 CH2CH(CH3)2 CH2CH(CH3)2 4.11
dibutyl phthalate DnBP C16H22O4 84-74-2 CH2CH2CH2CH3 CH2CH2CH2CH3 4.50
dimethylglycol phthalate DMEP C14H18O6 117-82-8 CH2CH2OCH3 CH2CH2OCH3 1.11 *
benzyl butyl phthalate BBzP C19H20O4 85-68-7 CH2C6H5 CH2C6H5 4.73
dicyclohexyl phthalate DCHP C20H26O4 84-61-7 CH(CH2)5 CH(CH2)5 5.6
di-n-pentyl phthalate DnPP C18H26O4 131-18-0 CH2(CH2)3CH3 CH2(CH2)3CH3 5.62
bis (2-n-butoxyethyl) phthalate DBEP C20H30O6 117-83-9 CH2CH2O(CH2)3CH3 CH2CH2O(CH2)3CH3 4.06 *
diphenyl phthalate DPhP C24H38O4 84-62-8 C6H5 C6H5 n.a.
di(2-ethylhexyl) phthalate DEHP C20H14O4 117-81-7 CH(CH2)5(CH3)2 CH(CH2)5(CH3)2 7.60
di-n-octyl phthalate DnOP C24H38O4 117-84-0 (CH2)7CH3 (CH2)7CH3 8.10
diisononyl phthalate DiNP C26H42O4 28553-12-0 C9H19 C9H19 8.8
dinonyl phthalate DnNP C26H42O4 84-76-4 C9H19 C9H19 9.52 *
Log Kow values were obtained from PubChem [33]; when the calculated value was not present, the estimated value was added *; n.a.: not available.
The danger of phthalates derives from their ability to interact with cell membranes, which is justified by their affinity towards organic portions. This property can be represented by the partition coefficient octanol/water, log Kow, i.e., the concentration ratio of a solute between octanol and water. Kow provides an estimate of the hydrophobicity of a given molecule and can predict the tendency of the breakdown of a chemical in water, lipids, sediments, and soil organic matter.

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