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Naphthalene

(Redirected from 1-Nonylnaphthalene)
Not to be confused with naphtha, naphthene, or Naphtali.

Naphthalene is an organic compound with formula C
10H
8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass.[15] As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings. It is the main ingredient of traditional mothballs.

Naphthalene
Skeletal formula and numbering system of naphthalene
Skeletal formula and numbering system of naphthalene
Ball-and-stick model of naphthalene
Ball-and-stick model of naphthalene
Spacefill model of naphthalene
Unit cells of naphthalene
Names
IUPAC name
Naphthalene[2]
Other names
white tar, camphor tar, tar camphor, naphthalin, naphthaline, antimite, albocarbon, hexalene, mothballs, moth flakes[1]
Identifiers
3D model (JSmol)
1421310
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.863 Edit this at Wikidata
EC Number
  • 214-552-7
3347
KEGG
RTECS number
  • QJ0525000
UNII
  • InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H checkY
    Key: UFWIBTONFRDIAS-UHFFFAOYSA-N checkY
  • InChI=1/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H
    Key: UFWIBTONFRDIAS-UHFFFAOYAC
  • c1c2ccccc2ccc1
Properties
C10H8
Molar mass 128.174 g·mol−1
Appearance White solid crystals/ flakes
Odor Strong odor of coal tar or mothballs
Density 1.145 g/cm3 (15.5 °C)[3]
1.0253 g/cm3 (20 °C)[4]
0.9625 g/cm3 (100 °C)[3]
Melting point 78.2 °C (172.8 °F; 351.3 K)
80.26 °C (176.47 °F; 353.41 K)
at 760 mmHg[4]
Boiling point 217.97 °C (424.35 °F; 491.12 K)
at 760 mmHg[3][4]
19 mg/L (10 °C)
31.6 mg/L (25 °C)
43.9 mg/L (34.5 °C)
80.9 mg/L (50 °C)[4]
238.1 mg/L (73.4 °C)[5]
Solubility Soluble in alcohols, liquid ammonia, Carboxylic acids, C6H6, SO2,[5] CCl4, CS2, toluene, aniline[6]
Solubility in ethanol 5 g/100 g (0 °C)
11.3 g/100 g (25 °C)
19.5 g/100 g (40 °C)
179 g/100 g (70 °C)[6]
Solubility in acetic acid 6.8 g/100 g (6.75 °C)
13.1 g/100 g (21.5 °C)
31.1 g/100 g (42.5 °C)
111 g/100 g (60 °C)[6]
Solubility in chloroform 19.5 g/100 g (0 °C)
35.5 g/100 g (25 °C)
49.5 g/100 g (40 °C)
87.2 g/100 g (70 °C)[6]
Solubility in hexane 5.5 g/100 g (0 °C)
17.5 g/100 g (25 °C)
30.8 g/100 g (40 °C)
78.8 g/100 g (70 °C)[6]
Solubility in butyric acid 13.6 g/100 g (6.75 °C)
22.1 g/100 g (21.5 °C)
131.6 g/100 g (60 °C)[6]
log P 3.34[4]
Vapor pressure 8.64 Pa (20 °C)
23.6 Pa (30 °C)
0.93 kPa (80 °C)[5]
2.5 kPa (100 °C)[7]
0.42438 L·atm/mol[4]
-91.9·10−6 cm3/mol
Thermal conductivity 98 kPa:
0.1219 W/m·K (372.22 K)
0.1174 W/m·K (400.22 K)
0.1152 W/m·K (418.37 K)
0.1052 W/m·K (479.72 K)[8]
1.5898[4]
Viscosity 0.964 cP (80 °C)
0.761 cP (100 °C)
0.217 cP (150 °C)[9]
Structure
Monoclinic[10]
P21/b[10]
C5
2h[10]
a = 8.235 Å, b = 6.003 Å, c = 8.658 Å[10]
α = 90°, β = 122.92°, γ = 90°
Thermochemistry
165.72 J/mol·K[4]
167.39 J/mol·K[4][7]
78.53 kJ/mol[4]
201.585 kJ/mol[4]
-5156.3 kJ/mol[4]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Flammable, sensitizer, possible carcinogen.[12] Dust can form explosive mixtures with air
GHS labelling:
GHS02: FlammableGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard[11]
Danger
H228, H302, H351, H410[11]
P210, P273, P281, P501[11]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
2
0
Flash point 80 °C (176 °F; 353 K)[11]
525 °C (977 °F; 798 K)[11]
Explosive limits 5.9%[11]
10 ppm[4] (TWA), 15 ppm[4] (STEL)
Lethal dose or concentration (LD, LC):
1800 mg/kg (rat, oral)
490 mg/kg (rat, intravenous)
1200 mg/kg (guinea pig, oral)
533 mg/kg (mouse, oral)[14]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 10 ppm (50 mg/m3)[13]
REL (Recommended)
 TWA 10 ppm (50 mg/m3) ST 15 ppm (75 mg/m3)[13]
IDLH (Immediate danger)
 250 ppm[13]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

History

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In the early 1820s, two separate reports described a white solid with a pungent odor derived from the distillation of coal tar. In 1821, John Kidd cited these two disclosures and then described many of this substance's properties and the means of its production. He proposed the name naphthaline, as it had been derived from a kind of naphtha (a broad term encompassing any volatile, flammable liquid hydrocarbon mixture, including coal tar).[16] Naphthalene's chemical formula was determined by Michael Faraday in 1826. The structure of two fused benzene rings was proposed by Emil Erlenmeyer in 1866,[17] and confirmed by Carl Gräbe three years later.[18]

Physical properties

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A naphthalene molecule can be viewed as the fusion of a pair of benzene rings. (In organic chemistry, rings are fused if they share two or more atoms.) As such, naphthalene is classified as a benzenoid polycyclic aromatic hydrocarbon (PAH).[19]

The eight carbon atoms that are not shared by the two rings carry one hydrogen atom each. For purpose of the standard IUPAC nomenclature of derived compounds, those eight atoms are numbered 1 through 8 in sequence around the perimeter of the molecule, starting with a carbon atom adjacent to a shared one. The shared carbon atoms are labeled 4a (between 4 and 5) and 8a (between 8 and 1).[20]

Molecular geometry

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The molecule is planar, like benzene. Unlike benzene, the carbon–carbon bonds in naphthalene are not of the same length. The bonds C1−C2, C3−C4, C5−C6 and C7−C8 are about 1.37 Å (137 pm) in length, whereas the other carbon–carbon bonds are about 1.42 Å (142 pm) long. This difference, established by X-ray diffraction,[21] is consistent with the valence bond model in naphthalene and in particular, with the theorem of cross-conjugation. This theorem would describe naphthalene as an aromatic benzene unit bonded to a diene but not extensively conjugated to it (at least in the ground state), which is consistent with two of its three resonance structures.

 

Because of this resonance, the molecule has bilateral symmetry across the plane of the shared carbon pair, as well as across the plane that bisects bonds C2-C3 and C6-C7, and across the plane of the carbon atoms. Thus there are two sets of equivalent hydrogen atoms: the alpha positions, numbered 1, 4, 5, and 8, and the beta positions, 2, 3, 6, and 7. Two isomers are then possible for mono-substituted naphthalenes, corresponding to substitution at an alpha or beta position.

 


 
Azulene

Structural isomers of naphthalene that have two fused aromatic rings include azulene, which has a 5–7 fused ring system, and Bicyclo[6.2.0]decapentaene which has a fused 4–8 ring system.[22]

The point group symmetry of naphthalene is D2h.

Electrical conductivity

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Pure crystalline naphthalene is a moderate insulator at room temperature, with resistivity of about 1012 Ω m. The resistivity drops more than a thousandfold on melting, to about 4 × 108 Ω m. Both in the liquid and in the solid, the resistivity depends on temperature as ρ = ρ0 exp(E/(kT)), where ρ0 (Ω⋅m) and E (eV) are constant parameters, k is the Boltzmann constant (8.617 × 10−5 eV/K), and T is absolute temperature (K). The parameter E is 0.73 in the solid. However, the solid shows semiconducting character below 100 K.[23][24]

Chemical properties

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Reactions with electrophiles

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In electrophilic aromatic substitution reactions, naphthalene reacts more readily than benzene. For example, chlorination and bromination of naphthalene proceeds without a catalyst to give 1-chloronaphthalene and 1-bromonaphthalene, respectively. Likewise, whereas both benzene and naphthalene can be alkylated using Friedel–Crafts reaction conditions, naphthalene can also be easily alkylated by reaction with alkenes or alcohols, using sulfuric or phosphoric acid catalysts.[25]

In terms of regiochemistry, electrophiles attack at the alpha position. The selectivity for alpha over beta substitution can be rationalized in terms of the resonance structures of the intermediate: for the alpha substitution intermediate, seven resonance structures can be drawn, of which four preserve an aromatic ring. For beta substitution, the intermediate has only six resonance structures, and only two of these are aromatic. Sulfonation gives the "alpha" product naphthalene-1-sulfonic acid as the kinetic product but naphthalene-2-sulfonic acid as the thermodynamic product. The 1-isomer forms predominantly at 25 °C, and the 2-isomer at 160 °C. Sulfonation to give the 1- and 2-sulfonic acid occurs readily:

H2SO4 + C10H8 → C10H7SO3H + H2O

Further sulfonation give di-, tri-, and tetrasulfonic acids.

Lithiation

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Analogous to the synthesis of phenyllithium is the conversion of 1-bromonaphthalene to 1-lithionaphthalene, by lithium–halogen exchange:

C10H7Br + BuLi → C10H7Li + BuBr

The resulting lithionaphthalene undergoes a second lithiation, in contrast to the behavior of phenyllithium. These 1,8-dilithio derivatives are precursors to a host of peri-naphthalene derivatives.[26]

Reduction and oxidation

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With alkali metals, naphthalene forms the dark blue-green radical anion salts such as sodium naphthalene, Na+C10H−
8. The naphthalene anions are strong reducing agents.

Naphthalene can be hydrogenated under high pressure in the presence of metal catalysts to give 1,2,3,4-tetrahydronaphthalene(C
10H
12), also known as tetralin. Further hydrogenation yields decahydronaphthalene or decalin (C
10H
18).

Oxidation with O
2 in the presence of vanadium pentoxide as catalyst gives phthalic anhydride:

C10H8 + 4.5 O2 → C6H4(CO)2O + 2 CO2 + 2 H2O

This reaction is the basis of the main use of naphthalene. Oxidation can also be effected using conventional stoichiometric chromate or permanganate reagents.

Production

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Naphthalene

From the 1960s until the 1990s, significant amounts of naphthalene were produced from heavy petroleum fractions during refining, but present-day production is mainly from coal tar.[citation needed] Approximately 1.3 million tons are produced annually.[citation needed]

Naphthalene is the most abundant single component of coal tar.[citation needed] The composition of coal tar varies with coal type and processing, but typical coal tar is about 10% naphthalene by weight.[citation needed] In industrial practice, distillation of coal tar yields an oil containing about 50% naphthalene, along with twelve other aromatic compounds[citation needed]. This oil, after being washed with aqueous sodium hydroxide to remove acidic components (chiefly various phenols), and with sulfuric acid to remove basic components, undergoes fractional distillation to isolate naphthalene. The crude naphthalene resulting from this process is about 95% naphthalene by weight. The chief impurities are the sulfur-containing aromatic compound benzothiophene (< 2%), indane (0.2%), indene (< 2%), and methylnaphthalene (< 2%). Petroleum-derived naphthalene is usually purer than that derived from coal tar. Where required, crude naphthalene can be further purified by recrystallization from any of a variety of solvents, resulting in 99% naphthalene by weight, referred to as 80 °C (melting point).[25]

In North America, the coal tar producers are Koppers Inc., Ruetgers Canada Inc. and Recochem Inc., and the primary petroleum producer is Monument Chemical Inc. In Western Europe the well-known producers are Koppers, Ruetgers, and Deza. In Eastern Europe, naphthalene is produced by a variety of integrated metallurgy complexes (Severstal, Evraz, Mechel, MMK) in Russia, dedicated naphthalene and phenol makers INKOR, Yenakievsky Metallurgy plant in Ukraine and ArcelorMittal Temirtau in Kazakhstan.

Other sources and occurrences

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Naphthalene and its alkyl homologs are the major constituents of creosote.

Trace amounts of naphthalene are produced by magnolias and some species of deer, as well as the Formosan subterranean termite, possibly produced by the termite as a repellant against "ants, poisonous fungi and nematode worms".[27] Some strains of the endophytic fungus Muscodor albus produce naphthalene among a range of volatile organic compounds, while Muscodor vitigenus produces naphthalene almost exclusively.[28]

Uses

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Naphthalene is used mainly as a precursor to derivative chemicals. The single largest use of naphthalene is the industrial production of phthalic anhydride, although more phthalic anhydride is made from o-xylene.

Fumigant

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Naphthalene has been used as a fumigant. It was once the primary ingredient in mothballs, although its use has largely been replaced in favor of alternatives such as 1,4-dichlorobenzene. In a sealed container containing naphthalene pellets, naphthalene vapors build up to levels toxic to both the adult and larval forms of many moths that attack textiles. Other fumigant uses of naphthalene include use in soil as a fumigant pesticide, in attic spaces to repel insects and animals such as opossums,[29] and in museum storage-drawers and cupboards to protect the contents from attack by insect pests.

Solvent

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Molten naphthalene provides an excellent solubilizing medium for poorly soluble aromatic compounds. In many cases it is more efficient than other high-boiling solvents, such as dichlorobenzene, benzonitrile, nitrobenzene and durene. The reaction of C60 with anthracene is conveniently conducted in refluxing naphthalene to give the 1:1 Diels–Alder adduct.[30] The aromatization of hydroporphyrins has been achieved using a solution of DDQ in naphthalene.[31]

Derivative uses

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The single largest use of naphthalene is the production of phthalic anhydride, which is an intermediate used to make plasticizers for polyvinyl chloride, and to make alkyd resin polymers used in paints and varnishes.

Sulfonic acids and sulfonates

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Many naphthalenesulfonic acids and sulfonates are useful. Naphthalenesulfonic acids are used in the synthesis of 1-naphthol and 2-naphthol, precursors for various dyestuffs, pigments, rubber processing chemicals and other chemicals and pharmaceuticals.[25] They are also used as dispersants in synthetic and natural rubbers, in agricultural pesticides, in dyes, and in lead–acid battery plates. Naphthalenedisulfonic acids such as Armstrong's acid are used as precursors and to form pharmaceutical salts such as CFT.

The aminonaphthalenesulfonic acids are precursors for synthesis of many synthetic dyes.

Alkyl naphthalene sulfonates (ANS) are used in many industrial applications as nondetergent surfactants (wetting agents) that effectively disperse colloidal systems in aqueous media. The major commercial applications are in the agricultural chemical industry, which uses ANS for wettable powder and wettable granular (dry-flowable) formulations, and in the textile and fabric industry, which uses the wetting and defoaming properties of ANS for bleaching and dyeing operations.

Some naphthalenesulfonate polymers are superplasticizers used for the production of high strength concrete. They are produced by treating naphthalenesulfonic acid with formaldehyde, followed by neutralization with sodium hydroxide or calcium hydroxide.

Other derivative uses

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Propranolol is a beta blocker.

Many azo dyes are produced from naphthalene. Useful agrichemicals include naphthoxyacetic acids.[25]

Hydrogenation of naphthalene gives tetrahydronaphthalene (tetralin) and decahydronaphthalene (decalin), which are used as low-volatility solvents. Tetralin is used as a hydrogen-donor solvent.[25]

Alkylation of naphthalene with propylene gives a mixture of diisopropylnaphthalenes, which are useful as nonvolatile liquids for inks.[25]

Substituted naphthalenes serve as pharmaceuticals such as propranolol (a beta blocker) and nabumetone (a nonsteroidal anti-inflammatory drug).

Other uses

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Several uses stem from naphthalene's high volatility: it is used to create artificial pores in the manufacture of high-porosity grinding wheels; it is used in engineering studies of heat transfer using mass sublimation; and it has been explored as a sublimable propellant for cold gas satellite thrusters.[32][33]

Health effects

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Main article: Naphthalene poisoning

Exposure to large amounts of naphthalene may damage or destroy red blood cells, most commonly in people with the inherited condition known as glucose-6-phosphate dehydrogenase (G6PD) deficiency,[34] from which over 400 million people suffer.[citation needed] Humans, in particular children, have developed the condition known as hemolytic anemia, after ingesting mothballs or deodorant blocks containing naphthalene. Symptoms include fatigue, lack of appetite, restlessness, and pale skin. Exposure to large amounts of naphthalene may cause confusion, nausea, vomiting, diarrhea, blood in the urine, and jaundice (yellow coloration of the skin due to dysfunction of the liver).[35]

The US National Toxicology Program (NTP) held an experiment where male and female rats and mice were exposed to naphthalene vapors on weekdays for two years.[36] Both male and female rats exhibited evidence of carcinogenesis with increased incidences of adenoma and neuroblastoma of the nose. Female mice exhibited some evidence of carcinogenesis based on increased incidences of alveolar and bronchiolar adenomas of the lung, while male mice exhibited no evidence of carcinogenesis.

The International Agency for Research on Cancer (IARC)[37] classifies naphthalene as possibly carcinogenic to humans and animals (Group 2B). The IARC also points out that acute exposure causes cataracts in humans, rats, rabbits, and mice; and that hemolytic anemia (described above) can occur in children and infants after oral or inhalation exposure or after maternal exposure during pregnancy. Under California's Proposition 65, naphthalene is listed as "known to the State to cause cancer".[38] A probable mechanism for the carcinogenic effects of mothballs and some types of air fresheners containing naphthalene has been identified.[39][40]

Regulation

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US government agencies have set occupational exposure limits to naphthalene exposure. The Occupational Safety and Health Administration has set a permissible exposure limit at 10 ppm (50 mg/m3) over an eight-hour time-weighted average. The National Institute for Occupational Safety and Health has set a recommended exposure limit at 10 ppm (50 mg/m3) over an eight-hour time-weighted average, as well as a short-term exposure limit at 15 ppm (75 mg/m3).[41] Naphthalene's minimum odor threshold is 0.084 ppm for humans.[42]

Mothballs and other products containing naphthalene have been banned within the EU since 2008.[43][44]

In China, the use of naphthalene in mothballs is forbidden.[45] Danger to human health and the common use of natural camphor are cited as reasons for the ban.

Naphthalene derivatives

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The partial list of naphthalene derivatives includes the following compounds:

Name Chemical formula Molar mass [g/mol] Melting point [°C] Boiling point [°C] Density [g/cm3] Refractive index
1-Naphthoic acid C11H8O2 172.18 157 300 —
2-Naphthoic acid C11H8O2 172.18 185.5 —
1-Naphthoyl chloride C11H7ClO 190.63 16–19 190 (35 Torr) 1.265 1.6552
1-Naphthol C10H8O 144,17 94–96 278 1.224 —
1-Naphthaldehyde C11H8O 156,18 1–2 160 (15 Torr)
1-Nitronaphthalene C10H7NO2 173.17 53–57 340 1.22 —
1-Fluoronaphthalene C10H7F 146.16 −19 215 1.323 1.593
1-Chloronaphthalene C10H7Cl 162.62 −6 259 1.194 1.632
2-Chloronaphthalene C10H7Cl 162.62 59.5 256 1.138 1.643
1-Bromonaphthalene C10H7Br 207.07 −2 279 1.489 1.670
1,2,7-Trimethylnaphthalene (Sapotalin) C13H14 170.25 143 128 0.987  
1-Nonylnaphthalene[46] C19H26 254.417 8 115 0.9371
Naphthalene-2-sulfonic acid

See also

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References

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  1. ^ Naphthalene: trade names
  2. ^ Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 13, 35, 204, 207, 221–222, 302, 457, 461, 469, 601, 650. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
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  4. ^ a b c d e f g h i j k l m n Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
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  11. ^ a b c d e f Sigma-Aldrich Co., Naphthalene.
  12. ^ Naphthalene carcinogenicity
  13. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0439". National Institute for Occupational Safety and Health (NIOSH).
  14. ^ "Naphthalene". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
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  20. ^ Blue Book, P-14.4 NUMBERING
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  26. ^ van Soolingen J, de Lang RJ, den Besten R, et al. (1995). "A simple procedure for the preparation of 1,8-bis(diphenylphosphino)naphthalene". Synthetic Communications. 25 (11): 1741–1744. doi:10.1080/00397919508015858.
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  28. ^ Daisy BH, Strobel GA, Castillo U, et al. (November 2002). "Naphthalene, an insect repellent, is produced by Muscodor vitigenus, a novel endophytic fungus". Microbiology. 148 (Pt 11): 3737–41. doi:10.1099/00221287-148-11-3737. PMID 12427963.
  29. ^ "Summary of Possum Repellent Study". Archived from the original on September 28, 2013.
  30. ^ K. Komatsua; Y. Murataa; N. Sugitaa; et al. (1993). "Use of naphthalene as a solvent for selective formation of the 1:1 Diels–Alder adduct of C60 with anthracene". Tetrahedron Letters. 34 (52): 8473–8476. doi:10.1016/S0040-4039(00)61362-X.
  31. ^ M.A. Filatov; A.V. Cheprakov (2011). "The synthesis of new tetrabenzo- and tetranaphthoporphyrins via the addition reactions of 4,7-dihydroisoindole". Tetrahedron. 67 (19): 3559–3566. doi:10.1016/j.tet.2011.01.052.
  32. ^ Tsifakis, Dimitrios; Charles, Christine; Boswell, Rod (2020-09-23). "Naphthalene as a Cubesat Cold Gas Thruster Propellant". Frontiers in Physics. 8: 389. Bibcode:2020FrP.....8..389T. doi:10.3389/fphy.2020.00389. hdl:1885/229663.
  33. ^ "New propulsion system using the key ingredient in moth balls could propel satellites through space". Australian Broadcasting Corporation. 8 December 2021. Retrieved December 11, 2021.
  34. ^ Santucci K, Shah B (Jan 2000). "Association of naphthalene with acute hemolytic anemia". Acad Emerg Med. 7 (1): 42–7. doi:10.1111/j.1553-2712.2000.tb01889.x. PMID 10894241.
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  36. ^ "NTP Technical Reports 410 and 500". NTP Technical Reports 410 and 500, available from NTP: Long-Term Abstracts & Reports. Archived from the original on October 24, 2004. Retrieved March 6, 2005.
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