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Anthracene chemical structure, C14H10, CAS 120-12-7
2D chemical structure

Key facts

What buyers check first

Appearance
Monoclinic plates from alcohol recrystallization, when pure, colorless with violet fluor…
Melting point
216 °C
Boiling point
341.3 °C
Density
1.25-1.28 g/cm³
Flash point
121 °C
HS code
290290
Category
Aromatic building blocks
Illustrative photo, colourless crystals in small glass vials on a laboratory bench
Typical packagingIllustrative packaging image, not the actual product

What is Anthracene?

Plain description, key identifiers and synonyms

Acene is a polycyclic aromatic hydrocarbon consisting of fused benzene rings in a rectilinear arrangement. It is an ortho-fused polycyclic arene and a member of acenes.

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
anthracene
CAS number
120-12-7 CAS number cross-checkedOther or deprecated CAS: 25135-15-3, 54261-80-2
EC number
204-371-1
Molecular formula
C14H10
UNII
EH46A1TLD7
MDL number
MFCD00001240
InChIKey
MWPLVEDNUUSJAV-UHFFFAOYSA-N
InChI
InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H
SMILES (canonical and isomeric)
C1=CC=C2C=C3C=CC=CC3=CC2=C1

Synonyms

  • Paranaphthalene
  • Anthracin
  • Tetra Olive N2G
  • Anthracen
  • p-Naphthalene
  • Sterilite hop defoliant
  • Anthraxcene
  • Anthrazen
  • Acen
  • Anthracene, pure
  • Anthracene, analytical standard
  • Deuterated anthracene
  • acene
  • acenes
  • antracene
  • Azen
  • 9-Anthracene
  • Anthracene, labeled with deuterium
  • Coal tar pitch volatiles:anthracene
  • Anthracene, Reagent
  • Coal tar pitch volatiles: anthracene
  • Hracene
  • Anthracene, Practical
  • Anthracene- d10
  • A89200_aldrich
Show all 34 synonyms
  • 40076_Supelco
  • 48567_Supelco
  • 48647_Supelco
  • Anthracene, scintillator
  • 331481_Aldrich
  • 46051_Riedel
  • Anthracene, puriss., 99.0%
  • 10580_FLUKA
  • 34F - WFD F

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
Monoclinic plates from alcohol recrystallization, when pure, colorless with violet fluorescenceexp.
Odour
Weak aromatic odorexp.
Melting point
216 °Cexp.
Boiling point
341.3 °Cexp.
Density
1.25-1.28 g/cm³exp.
Flash point
121 °Cexp.
Autoignition temperature
540 °Cexp.
Solubility
In water, 4.34 × 10⁻² mg/L at 24 °Cexp.
Vapour pressure
VP: 1 mm Hg at 145 °C (sublimes)exp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
178.23 g/molcalc.
Exact mass
178.0783 Dacalc.
LogP (octanol/water)
3.99calc.
Topological polar surface area
0 Ųcalc.
Hydrogen bond donors
0calc.
Hydrogen bond acceptors
0calc.
Rotatable bonds
0calc.
Heavy atoms
14calc.
Rings
3calc.
Aromatic rings
3calc.
Fraction sp3 carbons
0calc.
Formal charge
0calc.
Stereocentres
0calc.
Lipinski rule of five
Passes (0 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Murcko scaffold

The ring system that remains when every side chain is removed

Murcko scaffold of this chemical, c1ccc2cc3ccccc3cc2c1

c1ccc2cc3ccccc3cc2c1

3 rings, 14 atoms. This chemical is the scaffold itself.

1,181 other chemicals share this scaffold

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Danger
GHS07: Harmful or irritant
Harmful or irritant
GHS08: Serious health hazard
Serious health hazard
GHS09: Hazardous to the environment
Hazardous to the environment
110NFPA 704 rating

Hazard statements

  • H315Causes skin irritation.
  • H319Causes serious eye irritation.
  • H350May cause cancer.
  • H400Very toxic to aquatic life.
  • H410Very toxic to aquatic life with long lasting effects.
Precautionary statements (15)
  • P203Obtain, read and follow all safety instructions before use.
  • P264Wash skin thoroughly after handling.
  • P264 + P265Wash skin thoroughly after handling. Do not touch eyes.
  • P273Avoid release to the environment.
  • P280Wear protective gloves, protective clothing, eye protection and face protection.
  • P302 + P352If on skin: Wash with plenty of water.
  • P305 + P351 + P338If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
  • P318If exposed or concerned, get medical advice.
  • P321Specific treatment (see supplemental first aid instructions on the label).
  • P332 + P317If skin irritation occurs: Get medical help.
  • P337 + P317If eye irritation persists: Get medical help.
  • P362 + P364Take off contaminated clothing. And wash it before reuse.
  • P391Collect spillage.
  • P405Store locked up.
  • P501Dispose of contents and container in accordance with local regulations.

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

Anthracene suppliers

Sponsored listings first, then the documented ranking: membership, verification, replies, completeness, freshness and ratings

All 112 suppliers
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Where suppliers are based

112 suppliers in 16 countries

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Anthracene price

Indicative price range per kg from live supplier offers

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Uses and applications

What the substance is used for, by industry and function

Important source of dyestuffs (manufacturing anthraquinone, alizarin dyes).

Dyes, alizarin, phenanthrene, carbazole, anthraquinone, calico printing, a component of smoke screens, scintillation counting crystals, organic semiconductor research.

Intermediate for the synthesis of anthraquinone.

The use of anthracene as a plasticizer for thermosetting resins and as a light stabilizer for polymers has been proposed. The use of anthracene derivatives as building blocks for engineering plastics was also suggested.

Industrial uses: Preservative.

Pharmacology

Anthracene is anthracene, also called paranaphthalene or green oil, a solid polycyclic aromatic hydrocarbon (PAH) consisting of three benzene rings derived from coal-tar, is the simplest tricyclic aromatic hydrocarbon. It is on the EPA's priority pollutant list. It is ubiquitous in the environment as a product of incomplete combustion of fossil fuels. It has been identified in surface and drinking water, ambient air, exhaust emissions, smoke of cigarettes and cigars, and in smoked foods and edible aquatic organisms.

Read more

It is primarily used as an intermediate in the production of dyes, smoke screens, scintillation counter crystals, and in organic semiconductor research. Although a large body of literature exists on the toxicity of PAHs, data for anthracene are limited. Prolonged exposure causes variety of topical and systemic adverse reactions. Carcinogenicity bioassays with anthracene generally gave negative results.

How it is made

1) By salting out from crude anthracene oil and draining. The crude salts are purified by pressing and finally phenanthrene and carbazole are removed by the use of various solvents. 2) By distilling crude anthracene oil with alkali carbonate in iron retorts, the distillate contains only anthracene and phenanthrene. The latter is removed by carbon disulfide.

Obtained from coal tar.

High-temperature coal tar contains, on average, 1.5% of anthracene. Continuous tar distillation concentrates the anthracene in the fraction boiling between 300 and 360 °C (anthracene oil I).

Read more

This oil amounts to 15 - 20% of the raw tar and contains about 7% anthracene, it is cooled to 20 - 30 °C and then centrifuged. About 10-15 % of the crude anthracene oil I is obtained as a yellow-green crystalline material with an anthracene content of 20 - 35% (anthracene residues). These residues, which also contain 40 - 50% phenanthrene and 12-20% carbazole, are crystallized or distilled. Distillation yields a crude product containing 45 - 55% anthracene (50s anthracene). A 50s anthracene with an improved quality can be produced by two-step continuous column distillation. The crude 50s anthracene then is purified by recrystallization from selective solvents and by distillation. Repeated recrystallization from a three- to fourfold excess of pyridine produces anthracene (95% purity) from the 50s anthracene in 80% yield relative to the anthracene content. ...

Regulatory status

Inventories, regulations and trade controls that list this substance

Health and food

  • EU Cosmetics Regulation Annex II, prohibited in cosmetics
    Name: Anthracene oil, Ref no: 38, Annex ref: II/38

United States

  • TSCA inventory (USA)
    Status: Active in US commerce

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code Anthracene is traded under.

HS 2902.90Indicative HS code

Cyclic hydrocarbons, other

World exports in 2024
$612M
−6.1% vs 2023, imports $670M
2019 to 2024
Top exporters
  1. China28.0%
  2. Germany13.9%
  3. India * partner reported12.6%
Top importers
  1. Germany11.1%
  2. United States10.6%
  3. South Korea8.3%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for Anthracene is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about Anthracene, based on the data on this page

What is Anthracene?

Acene is a polycyclic aromatic hydrocarbon consisting of fused benzene rings in a rectilinear arrangement. It is an ortho-fused polycyclic arene and a member of acenes.

What is the CAS number of Anthracene?

The CAS registry number of Anthracene is 120-12-7. Other or deprecated CAS numbers: 25135-15-3, 54261-80-2.

What is the molecular formula and weight of Anthracene?

The molecular formula of Anthracene is C14H10 and its molar mass is 178.23 g/mol.

What is Anthracene used for?

Important source of dyestuffs (manufacturing anthraquinone, alizarin dyes). Dyes, alizarin, phenanthrene, carbazole, anthraquinone, calico printing, a component of smoke screens, scintillation counting crystals, organic semiconductor research. Intermediate for the synthesis of anthraquinone.

Is Anthracene hazardous?

Anthracene carries the GHS signal word "Danger". Main hazards: causes skin irritation, causes serious eye irritation, may cause cancer. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of Anthracene?

Anthracene is usually classified under HS code 290290 (Cyclic hydrocarbons, other). This is indicative, confirm it with your customs broker before shipping.

Where can I buy Anthracene?

CompoundList lists 112 suppliers of Anthracene in United States, China, India, Germany and 12 more. Send one free request to get and compare quotes. Your contact details stay private until you accept a quote.

Where can I buy Anthracene in India?

14 suppliers in India list Anthracene on CompoundList. Filter the suppliers list by country and send a request to compare prices, grades and delivery times.

What is the price of Anthracene?

Suppliers quote Anthracene on request because prices depend on grade, purity, quantity and destination. A free request on CompoundList gets you several quotes to compare.

Guides for buyers

Practical guides that help when you source, ship or handle Anthracene

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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