The most common solvent in everyday life is water. Most other commonly-used solvents are organic (carbon-containing) chemicals. These are called organic solvents. Solvents usually have a low boiling point and evaporate easily or can be removed by distillation, leaving the dissolved substance behind. To distinguish between solutes and solvents, solvents are usually present in the greater amount. Solvents can also be used to extract soluble compounds from a mixture, the most common example is the brewing of coffee or tea with hot water. Solvents are usually clear and colorless liquids and many have a characteristic odor. The concentration of a solution is the amount of compound that is dissolved in a certain volume of solvent. The solubility is the maximal amount of compound that is soluble in a certain volume of solvent at a specified temperature. Common uses for organic solvents are in dry cleaning (e.g. tetrachloroethylene), as paint thinners (e.g. toluene, turpentine), as nail polish removers and glue solvents (acetone, methyl acetate, ethyl acetate), in spot removers (e.g. hexane, petrol ether), in detergents (citrus terpenes), in perfumes (ethanol), and in chemical syntheses. The use of inorganic solvents (other than water) is typically limited to research chemistry and some technological processes.
Solutions and solvation
When one substance is mixed with another, a solution is formed. The mixing is referred to as miscibility. However, in addition to mixing, both substances in the solution can interact with each other in specific ways. Solvation describes these interactions. When something is dissolved, molecules of the solvent arrange itself around molecules of the solute. Heat is evolved and entropy is decreased making the solution more thermodynamically stable than the solute alone. This arranging is mediated by the respective chemical properties of the solvent and solute, such as hydrogen bonding, dipole moment and polarizability.
Solvents can be broadly classified into two categories polar/non-polar and protic/aprotic. Generally, the dielectric constant of the solvent provides a rough measure of a solvent's polarity. Solvents with a dielectric constant of less than 15 are generally considered nonpolar. Technically, the dielectric constant measures the solvent's ability to reduce the field strength of the electric field surrounding a charged particle immersed in it. This reduction is then compared to the field strength of the charged particle in a vacuum. In laymen's terms, dielectric constant of a solvent can be thought of as its ability to reduce the solute's internal charge.
Other polarity scales
Dielectric constants are not the only measure of polarity. Because solvents are used by chemists to carry out chemical reactions or observe chemical and biological phenomena, more specific measures of polarity are required.
The Grunwald Winstein mY scale measures polarity in terms of solvent influence on buildup of positive charge of a solute during a chemical reaction.
The polarity, dipole moment, polarizability and hydrogen bonding of a solvent determines what type of compounds it is able to dissolve and with what other solvents or liquid compounds it is miscible. As a rule of thumb, polar solvents dissolve polar compounds best and non-polar solvents dissolve non-polar compounds best: "like dissolves like". Strongly polar compounds like sugars (e.g. sucrose) or ionic compounds, like inorganic salts (e.g. table salt) dissolve only in very polar solvents like water, while strongly non-polar compounds like oils or waxes dissolve only in very non-polar organic solvents like hexane. Similarly, water and hexane (or vinegar and vegetable oil) are not miscible with each other and will quickly separate into two layers even after being shaken well.
Polar protic and polar a-protic
Solvents with a relative static permittivity greater than 15 can be further divided into protic and aprotic. Protic solvents solvate anions (negatively charged solutes) strongly via hydrogen bonding. Water is a protic solvent. Aprotic solvents such as acetone or dichloromethane tend to have large dipole moments (separation of partial positive and partial negative charges within the same molecule) and solvate positively charged species via their negative dipole. In chemical reactions the use of polar protic solvents favors the SN1 reaction mechanism, while polar aprotic solvents favor the SN2 reaction mechanism.
Another important property of solvents is boiling point. This also determines the speed of evaporation. Small amounts of low-boiling solvents like diethyl ether, dichloromethane, or acetone will evaporate in seconds at room temperature, while high-boiling solvents like water or dimethyl sulfoxide need higher temperatures, an air flow, or the application of vacuum for fast evaporation.
- Low Boilers: Boiling ranges below 100 °C
- Medium Boilers: Boiling ranges between 100 °C and 150 °C
- High Boilers: Boiling ranges above 150 °C
Most organic solvents have a lower density than water, which means they are lighter and will form a separate layer on top of water. An important exception: many halogenated solvents like dichloromethane or chloroform will sink to the bottom of a container, leaving water as the top layer. This is important to remember when partitioning compounds between solvents and water in a separatory funnel during chemical syntheses.
Health and safety
Most organic solvents are flammable or highly flammable, depending on their volatility. Exceptions are some chlorinated solvents like dichloromethane and chloroform. Mixtures of solvent vapors and air can explode. Solvent vapors are heavier than air, they will sink to the bottom and can travel large distances nearly undiluted. Solvent vapors can also be found in supposedly empty drums and cans, posing a flash fire hazard; hence empty containers of volatile solvents should be stored open and upside down.
Both diethyl ether and carbon disulfide have exceptionally low autoignition temperatures which increase greatly the fire risk associated with these solvents. The autoignition temperature of carbon disulfide is below 100°C (212°F), so as a result objects such as steam pipes, light bulbs, hotplates and recently extinguished bunsen burners are able to ignite its vapours.
Ethers like diethyl ether and tetrahydrofuran (THF) can form highly explosive organic peroxides upon exposure to oxygen and light, THF is normally more able to form such peroxides than diethyl ether. One of the most susceptible solvents is diisopropyl ether.
The heteroatom (oxygen) stabilizes the formation of a free radical which is formed by the abstraction of a hydrogen atom by another free radical. The carbon centred free radical thus formed is able to react with an oxygen molecule to form a peroxide compound. A range of tests can be used to detect the presence of a peroxide in an ether, one is to use a combination of iron sulfate and potassium thiocyanate. The peroxide is able to oxidize the Fe2+ ion to an Fe3+ ion which then form a deep red coordination complex with the thiocyanate. In extreme cases the peroxides can form crystalline solids within the vessel of the ether.
Unless the desiccant used can destroy the peroxides, they will concentrate during distillation due to their higher boiling point. When sufficient peroxides have formed, they can form a crystalline and shock sensitive solid precipitate. When this solid is formed at the mouth of the bottle, turning the cap may provide sufficient energy for the peroxide to detonate. Peroxide formation is not a significant problem when solvents are used up quickly; they are more of a problem for laboratories which take years to finish a single bottle. Ethers have to be stored in the dark in closed canisters in the presence of stabilizers like butylated hydroxytoluene (BHT) or over sodium hydroxide.
Peroxides may be removed by washing with acidic iron(II) sulfate, filtering through alumina, or distilling from sodium/benzophenone. Alumina does not destroy the peroxides; it merely traps them. The advantage of using sodium/benzophenone is that moisture and oxygen is removed as well.
Many solvents can lead to a sudden loss of consciousness if inhaled in large amounts. Solvents like diethyl ether and chloroform have been used in medicine as anesthetics, sedatives, and hypnotics for a long time. Ethanol is a widely used and abused psychoactive drug. Diethyl ether, chloroform, and many other solvents (e.g. from gasoline or glues) are used recreationally in glue sniffing, often with harmful long term health effects like neurotoxicity or cancer. Methanol can cause internal damage to the eyes, including permanent blindness.
It is interesting to note that ethanol has a synergistic effect when taken in combination with many solvents. For instance a combination of toluene/benzene and ethanol causes greater nausea/vomiting than either substance alone. Many chemists make a point of not drinking beer/wine/other alcoholic drinks if they know that they have been exposed to an aromatic solvent.
A major pathway to induce health effects arises from spills or leaks of solvents that reach the underlying soil. Since solvents readily migrate substantial distances, the creation of widespread soil contamination is not uncommon; there may be about 5000 sites worldwide that have major subsurface solvent contamination; this is particularly a health risk if aquifers are affected.
Chronic health effects
- Avoiding being exposed to solvent vapors by working in a fume hood, or with local exhaust ventilation (LEV), or in a well ventilated area
- Keeping the storage containers tightly closed
- Never using open flames near flammable solvents, use electrical heating instead
- Never flush flammable solvents down the drain, read safety data sheets for proper disposal information
- Avoiding the inhalation of solvent vapors
- Avoiding contact of the solvent with the skin — many solvents are easily absorbed through the skin. They also tend to dry the skin and may cause sores and wounds.
Properties table of common solvents
The solvents are grouped into non-polar, polar aprotic, and polar protic solvents and ordered by increasing polarity. The polarity is given as the dielectric constant. The density of nonpolar solvents that are heavier than water is bolded.
|Solvent||Chemical Formula||Boiling point||Dielectric constant||Density|
|Hexane||CH3-CH2-CH2-CH2-CH2-CH3||69 °C||2.0||0.655 g/ml|
|Benzene||C6H6||80 °C||2.3||0.879 g/ml|
|Toluene||C6H5-CH3||111 °C||2.4||0.867 g/ml|
|Diethyl ether||CH3CH2-O-CH2-CH3||35 °C||4.3||0.713 g/ml|
|Chloroform||CHCl3||61 °C||4.8||1.498 g/ml|
|Ethyl acetate||CH3-C(=O)-O-CH2-CH3||77 °C||6.0||0.894 g/ml|
|Polar Aprotic Solvents|
|1,4-Dioxane||/-CH2-CH2-O-CH2-CH2-O-\||101 °C||2.3||1.033 g/ml|
|Tetrahydrofuran (THF)||/-CH2-CH2-O-CH2-CH2-\||66 °C||7.5||0.886 g/ml|
|Dichloromethane (DCM)||CH2Cl2||40 °C||9.1||1.326 g/ml|
|Acetone||CH3-C(=O)-CH3||56 °C||21||0.786 g/ml|
|Acetonitrile (MeCN)||CH3-C≡N||82 °C||37||0.786 g/ml|
|Dimethylformamide (DMF)||H-C(=O)N(CH3)2||153 °C||38||0.944 g/ml|
|Dimethyl sulfoxide (DMSO)||CH3-S(=O)-CH3||189 °C||47||1.092 g/ml|
|Polar Protic Solvents|
|Acetic acid||CH3-C(=O)OH||118 °C||6.2||1.049 g/ml|
|n-Butanol||CH3-CH2-CH2-CH2-OH||118 °C||18||0.810 g/ml|
|Isopropanol (IPA)||CH3-CH(-OH)-CH3||82 °C||18||0.785 g/ml|
|n-Propanol||CH3-CH2-CH2-OH||97 °C||20||0.803 g/ml|
|Ethanol||CH3-CH2-OH||79 °C||24||0.789 g/ml|
|Methanol||CH3-OH||65 °C||33||0.791 g/ml|
|Formic acid||H-C(=O)OH||100 °C||58||1.21 g/ml|
|Water||H-O-H||100 °C||80||1.000 g/ml|
|File:Wiktionary-logo-en-v2.svg||Look up solvent in Wiktionary, the free dictionary.|
- Partition coefficient (log P) is a measure of differential solubility of a compound in two solvents
- Solvent systems exist outside the realm of ordinary organic solvents: Supercritical fluids, ionic liquids and deep eutectic solvents
- Water pollution
- Solvents are often refluxed with an appropriate desiccant prior to distillation to remove water
- Occupational health
- Tinoco, Sauer, Wang & Puglisi, Physical Chemistry Prentice Hall 2002 p. 134
- Lowery, T.H. and Richardson, K.S., Mechanism and Theory in Organic Chemistry, Harper Collins Publishers 3rd ed. 1987 p. 181-183.
- Lowery, T.H. and Richardson, K.S., Mechanism and Theory in Organic Chemistry, Harper Collins Publishers 3rd ed. 1987 p. 177.
- Lowery, T.H. and Richardson, K.S., Mechanism and Theory in Organic Chemistry, Harper Collins Publishers 3rd ed. 1987 p. 177.
- Kosower, E.M. "An introduction to Physical Organic Chemistry" Wiley: New York, 1969 p. 293
- Gutmann, V. Coord. Chem. Rev. 1976, 18 225
- Lowery, T.H. and Richardson, K.S., Mechanism and Theory in Organic Chemistry, Harper Collins Publishers 3rd ed. 1987 p. 183.
- Table Properties of common organic solvents
- Table and text O-Chem Lecture
- Tables Properties and toxicities of organic solvents
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