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Furan Suppliers list
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
Products Intro: Product Name:furan
Purity:99% Package:25KG;5KG;1KG
Company Name: Jiangsu Qingquan Chemical Co., Ltd.
Tel: +86-571-86589381/86589382/86589383
Products Intro: Product Name:Furan
Tel: +86-19933070948 +86-19930599843
Products Intro: Product Name:Furan
Purity:99% Package:1kg;200USD
Tel: +86 18953170293
Products Intro: Product Name:Furan
Company Name: Hubei xin bonus chemical co. LTD
Tel: 86-13657291602
Products Intro: Product Name:Furan
Purity:0.99 Package:5KG;1KG

Furan manufacturers

  • Furan
  • $200.00 / 1kg
  • 2022-11-28
  • CAS:110-00-9
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 1000kg/Month
  • Furan
  • $1.10 / 1g
  • 2022-11-25
  • CAS:110-00-9
  • Min. Order: 1g
  • Purity: 99.0% Min
  • Supply Ability: 100 Tons
  • Furan
  • $10.00 / 1KG
  • 2022-09-07
  • CAS:110-00-9
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50MT

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Question and answer

  • Q:Furan in Foods
  • A:Furan is a colorless, volatile liquid used in some chemical manufacturing industries. Furan has occasionally been reported to ....
  • Sep 20,2019
Furan Chemical Properties
Melting point -85.6 °C
Boiling point 67 °C10 mm Hg(lit.)
density 0.936 g/mL at 25 °C(lit.)
vapor density 2.35 (vs air)
vapor pressure 1672 mm Hg ( 55 °C)
refractive index n20/D 1.5070(lit.)
Fp 160 °F
storage temp. Store below +30°C.
solubility alcohols: freely soluble
form Liquid
color Clear colorless to yellow
Odor Threshold9.9ppm
explosive limit2.3-14.3%(V)
Water Solubility insoluble
Sensitive Air & Light Sensitive
Merck 14,4296
BRN 103221
Exposure limitsNIOSH: IDLH 13 ppm
Stability:Stable. Substances to be avoided include strong oxidising agents, acids, peroxides and oxygen. Highly flammable; can form explosive mixtures with air.
CAS DataBase Reference110-00-9(CAS DataBase Reference)
IARC2B (Vol. 63) 1995
NIST Chemistry ReferenceFuran(110-00-9)
EPA Substance Registry SystemFuran (110-00-9)
Safety Information
Hazard Codes T,F+
Risk Statements 45-12-19-20/22-38-48/22-52/53-68
Safety Statements 53-45-61-
RIDADR UN 2811 6.1/PG 2
WGK Germany 3
RTECS OB3870000
Autoignition Temperature390 °C
HS Code 2932 19 00
HazardClass 3
PackingGroup I
Hazardous Substances Data110-00-9(Hazardous Substances Data)
ToxicityLC (in air) in rats: 30400 ppm (Henderson)
IDLA13 ppm (35.1 mg/m3)
MSDS Information
ACROS English
SigmaAldrich English
ALFA English
Furan Usage And Synthesis
Chemical PropertiesFuran is the simplest five membered oxygen-containing heterocyclic compounds with its molecular structure containing ring diene ether. It belongs to 6π electron-based compound with all the 5 atoms being sp2-hybrid and located in the same plane. The pair of non-shared electrons of the oxygen atoms occupied p-orbital which is perpendicular to the ring plane and is parallel and overlapping with the p-orbital of the four carbons atoms, forming a five-atoms& six-electrons conjugated closed system. Therefore, it has a certain degree of aromatic nature. However, due to the electron density on the ring is not as uniform as benzene; it has a more active chemical property than benzene and can participate in many kinds of chemical reactions. It should be especially noted that, its 2, 5-position contains high electron density and prone to have nucleophilic substitution reaction. Moreover, all the derivatives of almost happens in 2-position such as furfural, furfuryl alcohol and furan carboxylic acid. Furan can also have nitrification, halogenated, sulfonated reaction. Its diene bonds can also participate in addition reaction, for example, have reaction with maleic anhydride, having diene addition reaction and generating 7-bicyclo-[2.2.1]-hept-5-ene-2, 3-dicarboxylic anhydride.
Under acidic condition, furan can have hydrolysis and ring open, producing 1, 4-dicarbonyl compounds. But once the furan ring has been introduced of electrophilic group, its activity can be greatly reduced and will not have diene reaction even encountering strong pro-diene compound. Although it contains certain aromatic property, but this property is very weak and there are no free hydroxyl furan or amino furan like phenol and aniline. When furan is subject to hydrogenation, it can give rise to two kinds of hydrides, namely dihydrofuran (2, 3-dihydrofuran and 2, 5-dihydrofuran) and tetrahydrofuran with the former being partially saturated cyclic enol ether and the later being saturated. Furan has a high thermal stability and is decomposed only at a temperature as high as 670 ℃ in the absence of catalyst. In the presence of a nickel catalyst, it is decomposed when heated to 360 ℃. This product is toxic and carcinogenic. The lethal concentration for Rat through oral administration is 300mg/kg. Its steam is narcotic which is similar as ether. It is easy to generate explosive peroxides in air.
Its steam encounters pine wood chip pre-soaked with hydrochloride tablets and generate green color (pine wood chip reaction). This can be used to identify the presence of furan.
The above information is edited by the chemicalbook of Dai Xiongfeng.
Raw material for organic synthesisFuran is an important raw material in organic synthesis industry and can be used in the manufacture of many kinds of industrial chemical product such as pyrrole, thiophene tetrahydrofuran and benzofuran. It can also be applied to the manufacture of drugs such as anisodamine, atropine, toluoyl pyrrole sodium acetate, thiamine furan and furadantin and so on. Furan, through oxidation and polymerization, can generate conductive poly-furan polymer with the conductivity being 18S/m (use AsF5 as the oxidant) or 2.2 × 10-4S/m (with NOSbF6 as the oxidant). Furan is unstable and prone to be subject to oxidation and polymerization. Furan, via catalytic hydrogenation, can generate tetrahydrofuran.
Many furan derivatives are drugs such as furfural, furfuryl alcohol, furan carboxylic acid, nitrofurazone, furapromide and furosemide and so on. In some monosaccharides such as fructose and ribose as well as their derivatives, there exists the cyclic structure of hydrogenated furans.
UsesIt is primarily used for the adhesive for the production of large quantities of hot-box technological cores.
Furan can be used as the raw material of organic synthesis and solvents. Furan can also be used for preparation of pyrrole, thiophene and tetrahydrofuran. Tetrahydrofuran is an important derivative of furan with many important applications. Furan, when undergoes etherfication and reduction to give 2, 5-dimethoxy dihydrofuran which is further converted to 2-hydroxy-1, 4-butanedial through hydrolysis, can be used for the production of anisodamine via synthetic approach; When furan undergoes etherfication and reduction to give 2, 5-dimethoxy tetrahydrofuran and generate butanedial via hydrolysis, is the raw material for synthesis of another kind of alkaloid, atropine. Furan is also used to produce anti-inflammatory drugs toluoyl pyrrole sodium acetate with production of each ton of this product consuming 4.75 t of furan.
Production methodFurfural is oxidized into 2-furan formic acid which undergoes decarboxylation to obtain furans. Heat the 2-furan formic acid to 200-205 ℃ (around the boiling point) so it is decomposed into carbon dioxide and furans. During the reaction process, send the sublimated 2-furan formic acid back to the reactor with the distilled furan undergoing re-distillation; collect the distillation fraction of 31-34 ℃ which is the relative pure finished product with the overall yield being about 75%. Industrially, it can be obtained through direct decarbonylation of furfural. The catalyst used in the reaction includes aluminum silicate, metal oxides or hydroxides as well as the mixtures of alloy or metals such as the mixture of zinc chromite and manganese. The reaction temperature should be about 400 ℃ with the yield being 90%. For large-scale production, the yield can be 74%.
CategoryFlammable liquid
Toxicity gradingpoisoning
Acute toxicityInhalation-rat LC50: 3398 PPM/per hour; Inhalation-Mouse LC50: 120 mg/m3/per hour.
Explosive and Hazardous characteristicsMixing with air can be explosive.
Flammability and hazard characteristicsIt is flammable in case of fire, high temperature and oxidant with burning releasing irritated fume.
Storage characteristicsTreasury ventilation low-temperature and dry; store it separately from oxidants and acids.
Extinguishing agentDry powder, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent
Professional StandardsTLV-TWA 0.5 mg/m3
DescriptionFuran occurs naturally in oils distilled from rosin containing pinewood. In addition, many natural foods contain the furan ring structure and substituted furans may be formed through cooking of simple carbohydrates. Furan is also found in tobacco smoke as well as wood smoke and gas emissions from gasoline and diesel engines. Furan has also been detected in industrial effluents and can be emitted to the air from petroleum refineries and coal-mining and gasification plants.
Chemical PropertiesFuran is a colorless liquid; turns brown on standing. Strong ethereal odor.
Chemical PropertiesFuran is a cyclic dienic ether stabilized by benzene-like resonance. Because of its conjugated unsaturation and heterocyclic atom, furan will undergo many types of reactions. It is, therefore, of interest as a chemical intermediate for pharmaceuticals, insecticides and fine chemicals. The heterocyclic oxygen atom in a ring with conjugated unsaturation gives furan a combination of ether, aromatic and olefinic characteristics. This polyfunctionality permits it to undergo a variety of reactions. Compared to benzene, the furan ring has greater reactivity, and is more susceptible to cleavage, thus resembling the vinyl ethers. Like the vinyl ethers, the furan ring is cleaved by aqueous acids. This reaction is accompanied by resinification .
UsesFuran is a five-membered heterocyclic aromatic ring. Furan is used as a building block for the preparation of many heterocyclic compounds.
UsesFuran is a valuable chemical intermediate for pharmaceuticals, insecticides, and other organic compounds. The furan ring is cleaved by aqueous acid which can lead to polymer formation.
UsesIn organic syntheses.
UsesFuran is used as an intermediate in organicsynthesis.
DefinitionA heterocyclic liquid organic compound. Its five-membered ring contains four carbon atoms and one oxygen atom. The structure is characteristic of some monosaccharide sugars (furanoses).
Definitionfuran: A colourless liquid compound,C4H4O; r.d. 0.94; m.p. –86°C;b.p. 31.4°C. It has a five-memberedring consisting of four CH2 groupsand one oxygen atom.
DefinitionA heterocyclic compound.
General DescriptionFuran is a stable, colourless chemical liquid. It is highly flammable and forms explosive mixtures with air. It is incompatible with many other chemical substances, for example, strong oxidising agents, acids, peroxides, and oxygen. Furan is produced commercially by decarbonylation of furfural. It is used mainly in the production of tetrahydrofuran, thiophene, and pyrrole. It also occurs naturally in certain woods and during the combustion of coal and is found in engine exhausts, wood smoke, and tobacco smoke.
Air & Water ReactionsHighly flammable. When uninhibited, Furan forms explosive peroxides on exposure to air. Insoluble in water.
Reactivity ProfileFuran is sensitive to heat and may turn brown upon standing. Furan may be light sensitive. When uninhibited, Furan forms explosive peroxides on exposure to air. Furan may react with oxidizers, acids, peroxides and oxygen. Furan resinifies on evaporation or when in contact with mineral acids, but Furan is stable in alkalis. .
HazardFlammable, dangerous fire risk, flammable limits 2–24%, forms peroxides on exposure to air. Absorbed by skin. Possible carcinogen.
Health HazardThe vapors are narcotic. Acute exposure to Furan by inhalation may involve both reversible and irreversible changes. Acute exposure by ingestion or skin absorption, as well as chronic exposure, are associated with high toxicity.
Health HazardFuran is a highly toxic compound. Inhalationof its vapors can cause acute pulmonaryedema and lung damage. The intraperitonealLD50 value in rodents is between 5 and7 mg/kg. The inhalation LC50 value in micefor a 1-hour exposure is 120 mg/m3.
Fire HazardVery dangerous, upon exposure to heat or flame. Furan may form unstable peroxides on exposure to air. Contact with acids can initiate a violent, heat producing reaction. Avoid acids, oxidizing agents. Upon standing in air, Furan may form unstable peroxides.
Flammability and ExplosibilityExtremelyflammable
Safety ProfileConfirmed carcinogen. Poison by inhalation and intraperitoneal routes. Moderately toxic by ingestion and skin contact. Experimental reproductive effects. A narcotic. Mutation data reported. The exposure concentration limit of 10 ppm together with its low boiling point requires that adequate ventilation be provided in areas where ths chemical is handled. Contact with liquid must be avoided since this chemical can be absorbed through the skin. Washing thoroughly with soap and water followed by prolonged rinsing should be done immedlatelp after accidental contact. A very dangerous fire hazard when exposed to heat or flame; can react with oxidzing materials. Unstabdized, it may form unstable peroxides on exposure to air and should always be tested before ddlation. Washing with an aqueous solution of ferrous sulfate slightly acidified with sodum bisulfate will remove these peroxides. Confirm by test. Contact with acids can initiate a violent exothermic reaction. Moderate explosion hazard when exposed to flame. Furan's low bohg point makes it easy to obtain explosive concentrations of the vapor in inadequately ventilated areas. To fight fire, use CO2, dr). chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also PEROXIDES.
Potential ExposureFuran is used as a chemical intermedi ate in the production of herbicides and pharmaceuticals; for making tetrahydrofuran; in formation of lacquers; as a sol vent for resins in organic synthesis, especially for pyrrole, thiophene.
CarcinogenicityFuran is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.
Environmental FateFuran may be released to the environment as a waste industrial product or from unintentional or accidental releases. If released to soil, it is expected to volatilize. If released to water, furan is not expected to adsorb to suspended particles and sediment and is likely to volatilize to ambient air. Sulfate-reducing bacteria can degrade furan. However, under nonsulfate-reducing conditions, biodegradation in soil and water is expected to be slow. In the air, furan will exist as a vapor and will be subject to degradation by reacting with hydroxyl radicals.
ShippingUN2389 Furan, Hazard Class: 3; Labels: 3-Flammable liquid.
Purification MethodsShake it with aqueous 5% KOH, dry it with CaSO4 or Na2SO4, then distil it under nitrogen, from KOH or sodium, immediately before use. A trace of hydroquinone could be added as an inhibitor of oxidation. [Beilstein 17 H 27, 17 I 16, 17 II 34, 17/1 V 291.]
Toxicity evaluationFuran can cause eye, skin, and mucus membrane irritation, burning sensation and, in severe cases, corrosion. If inhaled, furan may produce pulmonary edema and bronchiolar necrosis. When absorbed, furan can cause central nervous system (CNS) depression to the point of narcosis and tonic seizures.
Furan is metabolized by the cytochrome P450 enzymes in the liver and other tissues. Furan is metabolized to cis-2- butene-1,4-dial. This active metabolite is acutely toxic to liver cells. The furan ring undergoes oxidative cleavage and forms highly reactive furan radical cations or epoxides, which react directly with cellular nucleophiles. These reactive metabolites may react directly with deoxyribonucleic acid (DNA) or with cellular proteins to produce disruption of cellular functions and cell death. Chronic cell death and regeneration produced by chronic furan exposure may be a significant factor in the carcinogenicity potential of the chemical. In addition, there is some evidence to suggest that the reactive metabolites of furan may induce mutations in cellular genes.
IncompatibilitiesMay form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong acids, amines, strong bases, reducing agents. Unless stabilized with an inhibitor, air exposure forms unstable peroxides.
Waste DisposalConsult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations govern ing storage, transportation, treatment, and waste disposal.
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