PRODUCTS

FURFURANOL

Furfuranol is used Resin used in the foundry industry as apolymeric binder for foundry sands,
Furfuranol is used for Furan resins, Phenol resins,
Furfuranol is used Reactive diluent for phenolic and epoxyresins,

Molecular Formula: C5H6O2
EC Number: 202-626-1
CAS Number: 98-00-0

SYNONYMS:
2-(Hydroxymethyl)furan, 2-FURYLMETHANOL, 2-Furancarbinol, 2-Furane-methanol (furfurol), 2-Furanemethanol, 2-Furanmethanol (furfuryl alcohol), 2-Furanylmethanol, 2-Furfuryl alcohol, 2-Furfurylalkohol, 2-Furylcarbinol, 2-Hydroxymethylfurane, 2-hydroxymethylfuran, 5-Hydroxymethylfuran, ALPHA-FURFURYL ALCOHOL, FURYL ALCOHOL, Furan-2-methanol, Furfural alcohol, Furfuralcohol, Furfuranol, Furfurol, Furfuryl alcohol, Furylcarbinol, Methanol, (2-furyl)-, NCI-C56224, NSC 8843, Qo furfuryl alcohol, UN 2874, furanmethanol, furfuryl alcohol (furfurol), «alpha»-Furfuryl alcohol, «alpha»-Furylcarbinol, Â«alphaÂ»-Furfuryl alcohol, Â«alphaÂ»-Furylcarbinol, FA, Furfurol, 2-Furylmethanol, 2-Furan methanol, 2-furanemethanol, Furfuryl alcohol, 2-Furanylmethanol, (2-furyl)-methano, 2-Furfurylalkohol, 3-fluoro-D-alanine, 2-Furfuryl alcohol, alpha-Furylcarbinol, 2-Hydroxymethylfuran, 5-Hydroxymethylfuran, 2-hydroxymethylfurane, 2-Hydroxymethyklfuran, 2-furfur methy alcohol, 2-Furfuryl Alcohol (FA), 2-furfurylalkohol(czech), 2-Furanmethanol (furfuryl alcohol), (Furan-2-yl)methanol, Furan-2-ylmethanol, Furfuryl alcohol, 2-Furanmethanol, 2-Furancarbinol, 2-(Hydroxymethyl)furan, FURFURYL ALCOHOL, 98-00-0, 2-Furanmethanol, 2-Furylmethanol, furan-2-ylmethanol, 2-Furancarbinol, Furfural alcohol, 2-Furylcarbinol, 2-Furanylmethanol, Furfuranol, 2-Furfuryl alcohol, Furfurylalcohol, Furfuralcohol, 5-Hydroxymethylfuran, 2-(Hydroxymethyl)furan, Furyl alcohol, 2-Hydroxymethylfuran, Furylcarbinol, alpha-Furylcarbinol, Furan-2-yl-methanol, 2-Furfurylalkohol, Furfurylcarb, (2-furyl)methanol, Methanol, (2-furyl)-, 2-hydroxymethylfurane, 25212-86-6, 2-Furane-methanol, Furanmethanol, Furylcarbinol (VAN), NCI-C56224, 2-furanemethanol, FEMA No. 2491, Furan-2-methanol, NSC 8843, (furan-2-yl)methanol, CCRIS 2922, HSDB 711, DTXSID2025347, CHEBI:207496, EINECS 202-626-1, Qo furfuryl alcohol, UNII-D582054MUH, BRN 0106291, Furfurylalcohol-d2, .alpha.-Furylcarbinol, alpha-Furfuryl alcohol, AI3-01171, D582054MUH, NSC-8843, .alpha.-Furfuryl alcohol, DTXCID105347, EC 202-626-1, 5-17-03-00338 (Beilstein Handbook Reference), Furfuryl alcohol, 98%, (2-FURYL)-METHANOL (FURFURYLALCOHOL), FURFURYL ALCOHOL (IARC), FURFURYL ALCOHOL [IARC], 2-Furfurylalkohol [Czech], CAS-98-00-0, MFCD00003252, UN2874, furylmethanol, 2-Furfurylalcohol, alpha -Furylcarbinol, PFFA, methanol, 2-furyl-, (2-furyl)-Methanol, Furfuryl alcohol [UN2874], 2-Hydroxymethyl-Furan, alpha -Furfuryl alcohol, Furfuryl alcohol, 8CI, 2- FURANCARBINOL, 2- FURANYLMETHANOL, Epitope ID:136037, furfuryl alcohol (furfurol), WLN: T5OJ B1Q, CHEM-REZ 200, 2-Furane-methanol (furfurol), FURFURYL ALCOHOL [MI], FURFURYL ALCOHOL [FCC], CHEMBL308187, FURFURYL ALCOHOL [FHFI], FURFURYL ALCOHOL [HSDB], CHEBI:53371, FEMA 2491, Furfuryl alcohol, >=97%, FG, NSC8843, 2-Furanmethanol (furfuryl alcohol), 2-Furylmethanol (ACD/Name 4.0), STR01021, Tox21_202102, Tox21_303093, Furfuryl alcohol, analytical standard, AKOS000119178, UN 2874, Furfuryl alcohol [UN2874], Furfuryl alcohol, natural, >=95%, FG, NCGC00249166-01, NCGC00256987-01, NCGC00259651-01, 93793-62-5, DB-016149, DB-254877, F0076, NS00003728, EN300-19106, C20441, Q27335, A845784, J-521401, F0001-2310, Z104472794, InChI=1/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H, (2-Furyl)methanol, 2-Furancarbinol, 2-Furane-methanol, 2-Furanylmethanol, 2-Furfuryl alcohol, 2-Furylcarbinol, 2-Furylmethanol, 2-Hydroxymethylfuran, 2-Hydroxymethylfurane, 5-Hydroxymethylfuran, alpha-Furylcarbinol, Furan-2-yl-methanol, Furfural alcohol, Furfuranol, Furylcarbinol, a-Furylcarbinol, Α-furylcarbinol, 2-Furanmethanol, (2-Furyl)-methanol, (2-FURYL)-methanol (furfurylalcohol), 2-(Hydroxymethyl)furan, 2-Furane-methanol (furfurol), 2-Furanemethanol, 2-Furanmethanol (furfuryl alcohol), 2-Furanmethanol, homopolymer, 2-Furfurylalkohol, 2-Furylmethanol (acd/name 4.0), alpha -Furfuryl alcohol, alpha -Furylcarbinol, alpha-Furfuryl alcohol, FEMA 2491, Furan-2-methanol, Furan-2-ylmethanol, Furanmethanol, Furfuralcohol, Furfurol, Furfuryl alcohol (furfurol), Furfuryl alcohol, 8ci, Furfurylcarb, Furyl alcohol, qo Furfuryl alcohol, 2-Furfuryl Alcohol, Furfuryl Alcohol, 2-Hydroxymethylfuran, Furan-2-ylmethanol, Furanol, 2-Furylcarbinol, Hydroxymethylfuran, Methanol Furan-2-yl, Furfuryl alcohol, α-Furfuryl alcohol, α-Furylcarbinol, Furfuralcohol, Furyl alcohol, Furylcarbinol, 2-(Hydroxymethyl)furan, 2-Furancarbinol, 2-Furanylmethanol, 2-Furfuryl alcohol, 2-Furylcarbinol, 2-Furylmethanol, 5-Hydroxymethylfuran, Furfural alcohol, Methanol, (2-furyl)-, NCI-C56224, 2-Furfurylalkohol, UN 2874, Qo furfuryl alcohol, 2-Furanemethanol, Furfurol, 2-Hydroxymethylfurane, Furan-2-methanol, Furfuranol, NSC 8843, furfuryl alcohol (furfurol), furanmethanol, 2-Furanmethanol (furfuryl alcohol), 2-Furane-methanol (furfurol), 2-Hydroxymethylfuran, 2-Furylmethanol, 2-Furfurylalcohol, 2-Furancarbinol, 2-Furanmethanol, 2-Furanylmethanol, 2-Furfuryl alcohol, 2-Furylcarbinol, 2-Furylmethanol, 2-Hydroxymethylfuran, 5-Hydroxymethylfuran, Furfural alcohol, Furfuralcohol, Furfuranol, Furfuryl alcohol, Furfurylcarb, Furyl alcohol, Furylcarbinol (VAN), Methanol, (2-furyl)-, alpha-Furylcarbinol, [ChemIDplus] UN2874, furan-2-ylmethanol,2-Furanmethanol, 2-(Hydroxymethyl)furan, 2-Furancarbinol, 2-Furanylmethanol, 2-Furfuryl Alcohol, 2-Furylcarbinol, 2-Furylmethanol, 2-Furylmethyl Alcohol, 5-Hydroxymethylfuran, Chem-Rez 200, Furfuralcohol, Furfuranol, Furylcarbinol, NSC 8843, ?-Furfuryl Alcohol, ?-Furylcarbinol,Furfuryl Alcohol, 2-Furanmethanol, 2-(Hydroxymethyl)furan, 2-Furancarbinol, 2-Furanylmethanol, 2-Furfuryl Alcohol, 2-Furylcarbinol, 2-Furylmethanol,2-Furylmethyl Alcohol, 5-Hydroxymethylfuran, Chem-Rez 200, Furfuralcohol, Furfuranol, Furylcarbinol, NSC 8843, α-Furfuryl Alcohol, α-Furylcarbinol, 2- FURANCARBINOL, FURFURALCOHOL, alpha-FURYLCARBINOL, 2-HYDROXYMETHYLFURAN, Furfuryl Alcohol, 2-Furylmethanol, 2-Hydroxymethylfuran, Furanol, Furylcarbinol, Hydroxymethylfuran, Methanol Furan-2-yl, Furfural Alcohol, 2-furylmethanol, 2-hydroxymethylfuran, Furfural alcohol, Furfuralcohol, 2-Furanmethanol, 2-Furylcarbinol, 2-Furancarbinol, Furan-2-ylmethanol, 2-Furylmethanol, 2-Hydroxymethylfuran,

Furfuranol belongs to the class of organic compounds known as heteroaromatic compounds.
Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
Furfuranol appears as a clear colorless liquid.

Flash point of Furfuranol is 167 °F.
Boiling point of Furfuranol is 171 °F.
Furfuranol is Denser than water.

Furfuranol is a furan bearing a hydroxymethyl substituent at the 2-position.
Furfuranol has a role as a Maillard reaction product.
Furfuranol is a primary alcohol and a member of furans.

Furfuranol has been reported in Perilla frutescens, Zea mays, and other organisms with data available.
Furfuranol is an important organic chemical raw material.
Furfuranol, also known as 2-furylcarbinol or furfural alcohol, belongs to the class of organic compounds known as heteroaromatic compounds.

Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
Furfuranol's structure is that of a furan bearing a hydroxymethyl substituent at the 2-position.
Furfuranol is a sweet, alcoholic and bitter tasting compound.

Furfuranol has been detected, but not quantified, in several different foods, such as cereals and cereal products, potato, white mustards, arabica coffee, and cocoa and cocoa products.
This could make Furfuranol a potential biomarker for the consumption of these foods.

Furfuranol, also known as 2-furylcarbinol or furfural alcohol, belongs to the class of organic compounds known as heteroaromatic compounds.
Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
Based on a literature review a significant number of articles have been published on Furfuranol.

Furfuranol is a clear colorless organic liquid when pure, but becomes amber upon prolonged exposure to light and air.
Furfuranol, produced in Argentina, is produced using a catalytic hydrogenation process at high pressure, starting from furfural.
Furfuranol has a purity of 98.5%.

Furfuranol reacts with formaldehyde and leads to the formation of resinous condensation products that are widely used in the production of thermosetting resins and is particularly resistant to chemicals and solvents.
Furfuranol (FuOH, C4H3OCH2OH, 2-furylmethanol, 2-furancarbinol) has applications in the fabrication of foundry resins, the ingredient production of P-series fuels, in liquid alkanes and in food production.

Furfuranol is also a very important intermediate in fine chemical synthesis and the polymer industry, and it is used as a chemical intermediate for the synthesis of lysine, vitamin C and levulinic acid and employed as a lubricant and as a dispersing agent.
Furfuranol is a primary organic compound containing a furan substituted with a hydroxymethyl group.

Furfuranol is an almond-scented, oily, colorless liquid that turns yellow to dark brown when exposed to air.
Therefore oxidation, esterification, and etherification are its typical reactions.
Furfuranol is miscible with but unstable in water. It is soluble in common organic solvents.

Furfuranol can be mixed with water and many organic solvents such as Alcohol, Ether, Acetone etc but not dissolved in paraffin wax and other hydrocarbon products.
Furfuranol is produced by the hydrogenation of Furfural, bio-sourced from the bagasse of sugar cane.

Furfuranol is derived from furan and differs from the latter by an additional hydroxymethyl group.
Furfuranol forms on disproportionation of furfural and is a colorless to yellow liquid which is readily soluble in organic solvents (ethanol, benzene) but insoluble in kerosene.

Furfuranol is reactive in many ways.
Organic synthesis raw materials, can be prepared by levulinic acid (also known as acid), various properties of furan resin (such as Furfuranol resin, furan resin, II resin), Furfuranol urea formaldehyde resin, phenolic resin and anti-corrosion paint, anti-corrosion film, etc.

The cold resistance of the plasticizer made from the raw material is better than that of butyl and octanol esters.
Furan resin, varnish, pigment is a good solvent for rocket fuel.
In addition, Furfuranol is also used in synthetic fiber, rubber, pesticide and casting industry.

Furfuranol is a colorless to amber liquid with a faint, burning odor.
Furfuranol is darkens on exposure to light.
Furfuranol, also known as 2-furylcarbinol or furfural alcohol, belongs to the class of organic compounds known as heteroaromatic compounds.

Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
Furfuranol is a sweet, alcoholic, and bitter tasting compound.
Furfuranol is found, on average, in the highest concentration within beer.

Furfuranol has also been detected, but not quantified in, several different foods, such as teas (Camellia sinensis), coffee and coffee products, white mustards (Sinapis alba), herbal tea, and arabica coffees (Coffea arabica).
This could make Furfuranol a potential biomarker for the consumption of these foods.

Based on a literature review a significant number of articles have been published on Furfuranol.
Furfuranol is an organic compound containing a furan substituted with a hydroxymethyl group.
Furfuranol is a colorless liquid, but aged samples appear amber.

Furfuranol possesses a faint odor of burning and a bitter taste.
Furfuranol is miscible with but unstable in water.
Furfuranol is soluble in common organic solvents.

USES and APPLICATIONS of FURFURANOL:
The primary use of Furfuranol is as a monomer for synthesis of furan resins for bonding foundry sands for production of cores and moulds like HOT-BOX, WARM BOX and gas hardened processes as well as in the traditional FURAN-NO-BAKE system.
Secondary major use of Furfuranol is for corrosion-resistant, resinous mortars for joining corrosion- resistant tiles or bricks in the fabrication of reactors, storage tanks, fume stacks, and floors.

Furfuranol is used Solvents for dyes, resins and flavors; flavoring substances; manufacturing wetting agents, resins, polymers; aid in foundry-, dye-, varnish-, plastic- and electric- industry, corrosion-resistant sealants and cements.
Furfuranol is mainly used for the production of various properties of furan resin, furfuryl alcohol urea-.

Furfuranol is used Solvent for films, coatings and resins.
Furfuranol is used Ranitidine intermediate,etc.
Furfuranol is used as a raw material for the synthesis of various furan-type resin, anti-corrosion coatings, is also a good solvent

Furfuranol is used for manufacture of foundry resins, characterized by low viscosity, good mechanical strength at metal melting temperature and low gas emission.
Furfuranol is used for production of corrosion resistant resins with a very competitive price.

Furfuranol is used for production of abrasive wheels and adhesives based on urea-formaldehyde resin due to its wetting - dispersant properties.
Furfuranol is used for production of tetrahydrofurfuryl alcohol (THFA) used as a solvent in the pharmaceutical industry.
Furfuranol is delivered by tank trucks, in 240kg steel drums, in 1,000kg tanks and in tank container holding 21 to 23t each and by tanker (300 ~ 400t).

The packaging used is made of steel and in an inert nitrogen gas atmosphere (N2), oxygen-free to prevent oxidation during transportation.
Furfuranol is used in the production of resins (e.g., furan resins) for foundry cores and molds
Furfuranol is used intermediate in the synthesis of organic chemicals and pharmaceuticals

Furfuranol is used solvent in industrial applications, including paints and varnishes
Furfuranol is used additive in adhesives and coatings for durability and water resistance
Furfuranol is used as a solvent and for the production of furan resins and, more recently, for chemical wood modification.

Furfuranol is used as a solvent and as an intermediate in the manufacturing of resins and wetting agents.
Furfuranol is used as a solvent for tanning agents, dyes, and resins.
Furfuranol is also used in sealants, cements, and furan and urea-formaldehyde polymers.

The most important use is in making poly(Furfuranol) resins to bind sand-based cores and molds in foundries and to produce plastics, cements, mortars, binders, and adhesives.
Resins made from Furfuranol are chemical-resistant and nonburning.

Furfuranol is used resins, composites.
The primary use of Furfuranol is as a monomer for the synthesis of furan resins.
These polymers are used in thermoset polymer matrix composites, cements, adhesives, coatings and casting/foundry resins.

Polymerization involves an acid-catalyzed polycondensation, usually giving a black cross-linked product.
A highly simplified representation is shown below.

Because of its low molecular weight, Furfuranol can impregnate the cells of wood, where it can be polymerized and bonded with the wood by heat, radiation, and/or catalysts or additional reactants.

The treated wood (e.g. "Kebony") has improved moisture-dimensional stability, hardness, and decay and insect resistance; catalysts can include zinc chloride, citric, and formic acid, as well as borates

-Rocket fuel uses of Furfuranol:
Furfuranol has been used in rocketry as a fuel which ignites hypergolically (immediately and energetically in contact) with white fuming nitric acid or red fuming nitric acid oxidizer.

The use of hypergolics avoids the need for an igniter. Mixtures of Furfuranol and aniline in different proportions were used in American MGM-5 Corporal ballistic missile and WAC Corporal and Aerobee sounding rockets.
Mixture of 41% of Furfuranol, 41% of xylidine and 18% of methanol, called Furaline, was used in France for experimental rocket engines for aircraft.

-Other Uses of Furfuranol:
Furfuranol is also used as a chemical building block for pharmaceutical drug synthesis, especially Ranitidine which goes into the formulation of the anti-ulcer drug.

Furfural is used as a solvent in petrochemical refining, Paint stripper and cleaning compound formulation, for refining lubricating oils, as a fungicide and weed killer.
Chemical feedstock for 5-membered oxygen heterocycles example in the production of tetrahydrofuran alcohol an important industrial solvent.

PROPERTIES OF FURFURANOL:
*High reactivity due to its hydroxymethyl group and aromatic furan ring
*Furfuranol exhibits good solvency for polar and nonpolar substances
*Thermally stable under standard conditions

BENEFITS OF FURFURANOL:
*Derived from renewable sources (furfural from biomass)
*Versatile applications in industrial and commercial processes
*Furfuranol enhances mechanical strength and thermal stability of materials

ALTERNATIVE PARENTS OF FURFURANOL:
*Furans
*Oxacyclic compounds
*Primary alcohols
*Hydrocarbon derivatives
*Aromatic alcohols

SUBSTITUENTS OF FURFURANOL:
*Heteroaromatic compound
*Furan
*Oxacycle
*Organic oxygen compound
*Hydrocarbon derivative
*Aromatic alcohol
*Primary alcohol
*Organooxygen compound
*Alcohol
*Aromatic heteromonocyclic compound

SYNTHESIS OF FURFURANOL:
Furfuranol is manufactured industrially by hydrogenation of furfural, which is itself typically produced from waste bio-mass such as corncobs or sugar cane bagasse.
As such Furfuranol may be considered a green chemical.
One-pot systems have been investigated to produce Furfuranol directly from xylose using solid acid catalysts.

REACTIONS OF FURFURANOL:
Furfuranol undergoes many reactions including Diels–Alder additions to electrophilic alkenes and alkynes.
Hydroxymethylation gives 1,5-bis(hydroxymethyl)furan.

Hydrolysis gives levulinic acid.
Upon treatment with acids, heat and/or catalysts, Furfuranol can be made to polymerize into a resin, poly(furfuryl alcohol).
Hydrogenation of Furfuranol can proceed to give hydroxymethyl derivative of tetrahydrofuran and 1,5-pentanediol.

The etherification reaction of Furfuranol with alkyl or aryl halide (e.g. benzyl chloride) in the liquid-liquid-liquid triphase system with the help of a phase transfer catalyst also reported.
In the Achmatowicz reaction, also known as the Achmatowicz rearrangement, Furfuranol is converted to a dihydropyran.

PHYSICAL AND CHEMICAL PROPERTIES OF FURFURANOL:
Character: a colorless, flowable liquid that turns brown or deep red when exposed to sunlight or air.
Bitter taste.
boiling point 171 ℃
freezing point -29 ℃
relative density 1.1296
refractive index 1.4868
flash point 75 ℃
solubility is miscible with water, but unstable in water, soluble in ethanol, ether, benzene and chloroform, insoluble in petroleum hydrocarbons.

NATURE OF FURFURANOL:
Furfuranol is a colorless, flowable liquid that turns brown or deep red when exposed to sunlight or air, is flammable and has a bitter taste.
Furfuranol is miscible with water, but unstable in water, soluble in ethanol, ether, benzene and chloroform, insoluble in petroleum hydrocarbons.
The vapor forms an explosive mixture with air.

Acid exposure
Easy to merge the occurrence of a severe explosion, the formation of insoluble resin.
The relative density was 1.1296.

Freezing point -29 °c.
Boiling Point (look kPa) 171 °c.
Refractive index 4868.

Spontaneous ignition point 490.5.
Flash point 75 °c.

PREPARATION METHOD OF FURFURANOL:
The catalytic hydrogenation of furfural to Furfuranol includes a liquid phase hydrogenation (medium pressure or high pressure) method, a gas phase hydrogenation method and a konizaro method.

liquid phase hydrogenation method this method is to use a bubbling reactor to suspend the catalyst in furfural, using Cu-CrCa series catalyst, chromium calcium from copper nitrate [Cu(N03)2.3H2 0], chromic ammonium acid [(NH4)2 Cr04], calcium nitrate [Ca(N03)2- 4H2 0] and NH3-H20, at 190~210 ℃, medium pressure (5 ~ 8MPa), obtained by hydrogenation reaction.

the reaction temperature of gas phase hydrogenation method is low, and the length-diameter ratio of the tubular reactor used can reach 100; The material passes through the bottom layer of the catalyst with piston flow pattern, which is beneficial to the inhibition of secondary hydrogenation, because of the high selectivity of the reaction, low consumption, basically eliminate the chromium pollution.

konizarol method (self-oxidation-reduction method) furfural reacts with sodium hydroxide, half is reduced to Furfuranol, and the other half is oxidized to the sodium salt of furoic acid.
This method does not need hydrogen, the equipment is simple; The disadvantage is that the main by-products each account for half, consume more solvent, separation trouble.

PHYSICAL and CHEMICAL PROPERTIES of FURFURANOL:
Chemical Name: Furfuranol
Molecular Formula: C5H6O2
Molecular Weight: 98.10 g/mol
EC Number: 202-626-1
CAS Number: 98-00-0
Appearance: Colorless to pale yellow liquid
Density: ~1.13 g/cm³ at 20°C
Melting Point: -29°C
Boiling Point: 171°C
Flash Point: 66°C (closed cup)
Solubility: Soluble in water and organic solvents like ethanol and ether
Odor: Characteristic, sweet, and slightly burnt odor

Systematic Name:Furfuranol
EPA Registry Name:Furfuranol
IUPAC Name:(Furan-2-yl)methanol
Comptox DTXSID:DTXSID2025347
Internal Tracking Number:17681
CAS Number:98-00-0
Substance Type:Chemical Substance
Molecular Formula:C5H6O2
Molecular Weight:98.1 g/mol
Chemical Formula: C5H6O2
Average Molecular Weight: 98.0999

Monoisotopic Molecular Weight: 98.036779436
IUPAC Name: (furan-2-yl)methanol
Traditional Name: furfuryl alcohol
CAS Registry Number: 98-00-0
SMILES: OCC1=CC=CO1
InChI Identifier: InChI=1S/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2
InChI Key: XPFVYQJUAUNWIW-UHFFFAOYSA-N
CAS: 98-00-0
EINECS: 202-626-1
InChI: InChI=1/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2
Molecular Formula: C5H6O2

Molar Mass: 98.1
Density: 1.135 g/mL at 25 °C (lit.)
Melting Point: -29 °C (lit.)
Boling Point: 170 °C (lit.)
Flash Point: 149°F
JECFA Number: 451
Water Solubility: MISCIBLE
Solubility: alcohol: soluble
Vapor Presure: 0.5 mm Hg (20 °C)
Vapor Density: 3.4 (vs air)
Appearance: Liquid
Color: Clear yellow

Odor: Mildly irritating.
Merck: 14,4305
BRN: 106291
pKa: 14.02±0.10 (Predicted)
PH: 6 (300 g/l, H2O, 20 °C)
Storage Condition: Store below +30 °C.
Explosive Limit: 1.8-16.3% (V)
Refractive Index: n20/D 1.486 (lit.)
Chemical formula: C5H6O2
Molar mass: 98.10 g/mol
Appearance: colorless liquid
Odor: burning odor

Density: 1.128 g/cm3
Melting point: −29 °C (−20 °F; 244 K)
Boiling point: 170 °C (338 °F; 443 K)
Solubility in water: miscible
Water Solubility: 34.3 g/L
logP: 0.25
logP: 0.27
logS: -0.46
pKa (Strongest Acidic): 13.75
pKa (Strongest Basic): -2.9
Physiological Charge: 0

Hydrogen Acceptor Count: 1
Hydrogen Donor Count: 1
Polar Surface Area: 33.37 Å²
Rotatable Bond Count: 1
Refractivity: 25.26 m³•mol⁻¹
Polarizability: 9.76 Å³
Number of Rings: 1
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: No

Veber's Rule: Yes
MDDR-like Rule: No
Chemical Formula: C5H6O2
IUPAC name: (furan-2-yl)methanol
InChI Identifier: InChI=1S/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2
InChI Key: XPFVYQJUAUNWIW-UHFFFAOYSA-N
Isomeric SMILES: OCC1=CC=CO1
Average Molecular Weight: 98.0999
Monoisotopic Molecular Weight: 98.036779436
Appearance: Colorless to light yellow color, transparent liquid

Molecular formula: C5H6O2
Molecular weight: 98.10
CAS No.: 98-00-0
Molecular Weight: 98.10 g/mol
XLogP3: 0.3
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 1
Exact Mass: 98.036779430 g/mol
Monoisotopic Mass: 98.036779430 g/mol
Topological Polar Surface Area: 33.4 Å²
Heavy Atom Count: 7

Formal Charge: 0
Complexity: 54
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Molecular form: C5H6O2
Appearance: Yellow Oil
Mol. Weight: 98.1
Storage: 2-8°C Refrigerator
Shipping Conditions: Ambient
Applications: NA
Chemical Name: Furfuryl Alcohol
Molecular Formula: C5H6O2
Molecular Weight: 98.10 g/mol
EC Number: 202-626-1
CAS Number: 98-00-0

Appearance: Clear to pale yellow liquid
Density: ~1.13 g/cm³ at 20°C
Melting Point: -29°C
Boiling Point: 171°C
Flash Point: 75°C (closed cup)
Solubility: Soluble in water, ethanol, and ether
Odor: Characteristic faintly sweet, smoky odor
Chemical name: Furfuranol
CAS number: 98-00-0
Furfuryl Alcohol purity (%): min. 98.0

Furfural content (%): max. 0.7
Moisture content (%): max. 0.3
Cloud Point (%): max. 10
Physical description: Colorless to amber liquid with a faint,
burning odor.
Boiling point: 338°F
Molecular weight: 98.1
Freezing point/melting point: -24°F
Vapor pressure: 0.6 mmHg at 77°F

Flash point: 167°F
Vapor density: 3.4
Specific gravity: 1.13
Ionization potential:
Lower explosive limit (LEL): 1.8%
Upper explosive limit (UEL): 16.3%
NFPA health rating: 3
NFPA fire rating: 2
NFPA reactivity rating: 1

FIRST AID MEASURES of FURFURANOL:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of FURFURANOL:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of FURFURANOL:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of FURFURANOL:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of FURFURANOL:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.

STABILITY and REACTIVITY of FURFURANOL:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available