Chinese Japanese Germany Korea


o-Cresol structure
Chemical Name:
o-Creso;O-CRESOL;2-Cresol;o-Kresol;o-toluol;FEMA 3480;ORTHO CRESO;Orthocresol;o-Oxytoluene;ortho-cresol
Molecular Formula:
Formula Weight:
MOL File:

o-Cresol Properties

Melting point:
29-31 °C (lit.)
Boiling point:
191 °C (lit.)
1.048 g/mL at 25 °C
vapor density 
3.72 (vs air)
vapor pressure 
0.3 mm Hg ( 20 °C)
refractive index 
3480 | O-CRESOL
Flash point:
178 °F
storage temp. 
under inert gas
Liquid or Low Melting Solid
10.2(at 25℃)
white to brown
4.8 (20g/l, H2O, 20℃)
explosive limit
1.47%, 148°F
Odor Threshold
Water Solubility 
20 g/L (20 ºC)
JECFA Number
Henry's Law Constant
0.34 at 5.25 °C, 0.61 at 10.00 °C, 1.57 at 20.00 °C, 2.33 at 25.00 °C (dynamic equilibrium system- GC, Feigenbrugel et al., 2004a)
Exposure limits
NIOSH REL: TWA 2.3 ppm (10 mg/m3), IDLH 250 ppm; OSHA PEL: TWA 5 ppm (22 mg/m3); ACGIH TLV: TWA for all isomers 5 ppm (adopted).
Stable, but light and air sensitive. Combustible. Incompatible with oxidizing agents, bases.
CAS DataBase Reference
95-48-7(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS)
EWG's Food Scores
NIST Chemistry Reference
Phenol, 2-methyl-(95-48-7)
EPA Substance Registry System
o-Cresol (95-48-7)
  • Risk and Safety Statements
Signal word  Danger
Hazard statements  H335-H361-H372-H401-H301-H311-H318-H301+H311-H314-H411-H225-H301+H311+H331-H370
Precautionary statements  P273-P280-P301+P310+P330-P303+P361+P353-P304+P340+P310-P305+P351+P338-P210-P260-P308+P311-P403+P233-P201-P202-P264-P270-P271-P301+P330+P331+P310-P303+P361+P353+P310+P363-P305+P351+P338+P310-P308+P313-P405-P501-P310
Hazard Codes  T
Risk Statements  24/25-34-39/23/24/25-23/24/25
Safety Statements  36/37/39-45-36/37
RIDADR  UN 3455 6.1/PG 2
WGK Germany  1
RTECS  GO6300000
Autoignition Temperature 555 °C
HazardClass  6.1
PackingGroup  II
HS Code  29071200
Toxicity LD50 orally in rats: 1.35 g/kg (Deichmann, Witherup)
NFPA 704
3 0

o-Cresol price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.09692 o-Cresol for synthesis 95-48-7 1 L $43.1 2021-03-22 Buy
Sigma-Aldrich 40250-U 2-Methylphenol solution certified reference material, 5000 μg/mL in methanol 95-48-7 u $44.6 2018-11-13 Buy
Sigma-Aldrich 40250-U 2-Methylphenol solution certified reference material, 5000?μg/mL in methanol 95-48-7 1 mL $45.6 2021-03-22 Buy
Sigma-Aldrich 8.09692 o-Cresol for synthesis 95-48-7 500 mL $46.16 2021-03-22 Buy
Sigma-Aldrich 36922 o-Cresol analytical standard 95-48-7 250mg $21.6 2021-03-22 Buy

o-Cresol Chemical Properties,Uses,Production

Chemical Properties

colourless to light yellow liquid

Chemical Properties

Cresol is a mixture of the three isomeric cresols, o-, m-, and p-cresol. Cresols are slightly soluble in water. m-Isomer: Colorless or yellow liquid with characteristic odor.

Chemical Properties

o-Cresol has a musty, phenolic aftertaste.

Physical properties

Colorless solid or liquid with a phenolic odor; darkens on exposure to air. An odor threshold concentration of 0.28 ppbv was reported by Nagata and Takeuchi (1990).


Reported in Acacial farnesiana, ylang-ylang oil (probably as p-cresyl acetate), jasmine absolute, orange oil from leaves, the essence from flowers of Lilium candidum, anise seed oil, the essence of Artemisia santolinoflia, and some sea algae. Also reported found in asparagus, peppermint oil, cheddar cheese, provolone cheese, butter, milk, lean fish, boiled egg, smoked pork, rum, Scotch whiskey, red wine, white wine, coffee and mango.Reported found in cinnamon, coffee, Oriental tobacco, rum, sherry, tea, tomato and whiskey.


Disinfectant; phenolic resins; tricresyl phosphate; ore flotation; textile scouring agent; organic intermediate; manufacturing salicylaldehyde, coumarin, and herbicides; surfactant; synthetic food flavors (para isomer only); food antioxidant; dye, perfume, plastics, and resins manufacturing.


o-Cresol is used as a disinfectant and solvent. Lysol disinfectant is a 50% (v/v) mixed-cresol isomer in a soap emulsion formed on mixing with water. Besides disinfection products at solutions of 1–5%, the cresols are used as degreasing compounds, paintbrush cleaners, and additives in lubricating oils. Cresols were previously widely used for disinfection of poultry houses, but this use was discontinued because of their toxicity; they cause respiratory problems and abdominal edema in young chicks. o-Cresol has been used in synthetic resins, explosives, petroleum, photographic, paint, and agricultural industries.


Antiseptics; disinfectants; solvent; insecticides; resins; flame-retardant plasticizers

Production Methods

The cresols (cresylic acids) are methyl phenols and generally appear as a mixture of isomers. o-Cresol is a 2-methyl derivative of phenol and is prepared from o-toluic acid or obtained from coal tar or petroleum. Crude cresol is obtained by distilling “gray phenic acid” at a temperature of ≈180–201°C. o-Cresol may be separated from the crude or purified mixture by repeated fractional distillation in vacuo. It can also be prepared synthetically by diazotization of the specific toluidine or by fusion of the corresponding toluenesulfonic acid with sodium hydroxide.


ChEBI: A cresol that is phenol substituted by a methyl group at position 2. It is a minor urinary metabolite of toluene.

Aroma threshold values

Aroma characteristics at 1.0%: phenolic, medicinal, sweet spicy, smoky with a methyl salicylate nuance.

Taste threshold values

Taste characteristics at 2.0 ppm: sweet medicinal, phenolic and tarlike.

Synthesis Reference(s)

Tetrahedron Letters, 30, p. 5215, 1989 DOI: 10.1016/S0040-4039(01)93745-1
Chemical and Pharmaceutical Bulletin, 27, p. 816, 1979 DOI: 10.1248/cpb.27.816
Journal of the American Chemical Society, 107, p. 2571, 1985 DOI: 10.1021/ja00294a073

General Description

Colorless or yellow to brown-yellow or pinkish colored liquid with a phenol-like odor. Toxic by ingestion and/or skin absorption. May have a flash point between 100 and 199°F. Causes burns to skin, eyes and mucous membranes. Insoluble in water.

Air & Water Reactions

Sensitive to light and air. Insoluble in water.

Reactivity Profile

o-Cresol is incompatible with oxidizing agents and bases. Mixing o-Cresol with chlorosulfonic acid, nitric acid and oleum in a closed contained caused the temperature and pressure to increase.


Questionable carcinogen.

Health Hazard

The chemical is rated as a very toxic compound with a probable oral lethal dose in humans of 50-500 mg/kg, or between 1 teaspoon and 1 ounce for a 70 kg (150 lb.) person. It is a strong dermal irritant and frequently causes dermatitis. Serious or fatal poisoning may result if large areas of skin are wet with cresol, o- and the substance is not removed immediately. Ingestion of even a small amount may cause paralysis and coma. It is corrosive to body tissues, with toxicity similar to phenol.

Fire Hazard

Fire may produce irritating or poisonous gases. Runoff from fire control water may give off poisonous gases. o-Cresol may burn but does not ignite readily. Container may explode in heat of fire. Slight explosion and fire hazard in the form of vapor when exposed to heat or flame. When heated to decomposition, o-Cresol emits highly toxic fumes. Reacts violently with nitric acid, oleum, and chlorosulfonic acid. Hazardous polymerization may not occur.

Safety Profile

Poison by ingestion, inhalation, subcutaneous, intravenous, and intraperitoneal routes. Moderately toxic by skin contact. A severe eye and skin irritant. Human mutation data reported. Questionable carcinogen with experimental neoplastigenic data. Flammable when exposed to heat, flame, or oxidants. To fight fire, water may be used to blanket fire; foam, fog, mist, dry chemical. See also other cresol entries and PHENOL.

Potential Exposure

Cresol is used as a disinfectant and fumigant; as an ore flotation agent, and as an intermediate in the manufacture of chemicals, dyes, plastics, and antioxidants. A mixture of isomers is generally used; the concentrations of the components are determined by the source of the cresol.


Detected in distilled water-soluble fractions of 87 octane gasoline (6.61 mg/L), 94 octane gasoline (0.57 mg/L), Gasohol (1.17 mg/L), No. 2 fuel oil (2.64 mg/L), jet fuel A (0.72 mg/L), diesel fuel (1.36 mg/L), and military jet fuel JP-4 (1.51 mg/L) (Potter, 1996). o-Cresol was also detected in 82% of 65 gasoline (regular and premium) samples (62 from Switzerland, 3 from Boston, MA). At 25 °C, concentrations were from 1.1–99 mg/L in gasoline and 70–6,600 μg/L in water-soluble fractions. Average concentrations were 18 mg/L in gasoline and 1.2 mg/L in watersoluble fractions (Schmidt et al., 2002).
A high-temperature coal tar contained 2-methylphenol at an average concentration of 0.25 wt % (McNeil, 1983).
Occurs naturally in white sandlewood, sour cherries, peppermint leaves (1–10 ppb), tarragon, asparagus shoots, tea leaves, coffee beans, Japanese privet, tomatoes, licorice roots, and African palm oil (Duke, 1992).
Schauer et al. (2001) measured organic compound emission rates for volatile organic compounds, gas-phase semi-volatile organic compounds, and particle phase organic compounds from the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emission rates of 2-methylphenol were 89.6 mg/kg of pine burned, 47.7 mg/kg of oak burned, and 37.8 mg/kg of eucalyptus burned. The particle-phase emission rates were 0.018 mg/kg of oak burned and 0.006 mg/kg of eucalyptus burned.

Environmental Fate

Biological. Bacterial degradation of 2-methylphenol may introduce a hydroxyl group producing 3-methylcatechol (Chapman, 1972). In phenol-acclimated activated sludge, metabolites identified include 3-methylcatechol, 4-methylresorcinol, methylhydroquinone, α-ketobutyric acid, dihydroxybenzaldehyde, and trihydroxytoluene (Masunaga et al., 1986).
Chloroperoxidase, a fungal enzyme isolated from Caldariomyces fumago, reacted with 2- methylphenol forming 2-methyl-4-chlorophenol (38% yield) and 2-methyl-6-chlorophenol (Wannstedt et al., 1990).
Heukelekian and Rand (1955) reported a 5-d BOD value of 1.70 g/g which is 67.5% of the ThOD value of 2.72 g/g. In activated sludge inoculum, 95.0% COD removal was achieved. The average rate of biodegradation was 54.0 mg COD/g?h (Pitter, 1976).
Soil. In laboratory microcosm experiments kept under aerobic conditions, half-lives of 5.1 and 1.6 d were reported for 2-methylphenol in an acidic clay soil (<1% organic matter) and slightly basic sandy loam soil (3.25% organic matter) (Loehr and Matthews, 1992).
Surface Water. In river water, the half-life of 2-methylphenol was 2 and 4 d at 20 and 4 °C, respectively (Ludzack and Ettinger, 1960).
Groundwater. Nielsen et al. (1996) studied the degradation of 2-methylphenol in a shallow, glaciofluvial, unconfined sandy aquifer in Jutland, Denmark. As part of the in situ microcosm study, a cylinder that was open at the bottom and screened at the top was installed through a cased borehole approximately 5 m below grade. Five liters of water was aerated with atmospheric air to ensure aerobic conditions were maintained. Groundwater was analyzed weekly for approximately 3 months to determine 2-methylphenol concentrations with time. The experimentally determined first-order biodegradation rate constant and corresponding half-life were 0.2/d and 3.5 d, respectively. Groundwater contaminated with phenol and other phenols degraded in a methanogenic aquifer to methane and carbon dioxide. These results could not be duplicated in the laboratory utilizing an anaerobic digester (Godsy et al., 1983).
Photolytic. Sunlight irradiation of 2-methylphenol and nitrogen oxides in air yielded the following gas-phase products: acetaldehyde, formaldehyde, pyruvic acid, peroxyacetyl nitrate, nitrocresols, and trace levels of nitric acid and methyl nitrate. Particulate phase products were also identified and these include 2-hydroxy-3-nitrotoluene, 2-hydroxy-5-nitrotoluene, 2-hydroxy-3,5- dinitrotoluene, and tentatively identified nitrocresol isomers (Grosjean, 1984). Absorbs UV light at a maximum wavelength of 270 nm (Dohnal and Fenclová, 1995).
Chemical/Physical. Ozonation of an aqueous solution containing 2-methylphenol (200 to 600 mg/L) yielded formic, acetic, propionic, glyoxylic, oxalic, and salicylic acids (Wang, 1990). In a different experiment, however, an aqueous solution containing 2-methylphenol (1 mM) reacted with ozone (11.7 mg/min) forming 2-methylmuconic acid and hydrogen peroxide as end products. The proposed pathway of degradation involved electrophilic aromatic substitution by the first ozone molecule followed by a 1,3-dipolar addition of the second ozone molecule to the cleaved ring (Beltran et al., 1990).


UN2076 Cresols, liquid, Hazard class: 6.1; Labels: 6.1-Poisonous materials, 8-Corrosive material. UN3455 Cresols, solid, Hazard class: 6.1; Labels: 6.1- Poisonous materials, 8-Corrosive material.

Purification Methods

It can be freed from m-and p-isomers by repeated fractional distillation, It crystallises from *benzene by addition of pet ether. It has been fractionallly crystallised by partial freezing of its melt. The 3,5-dinitrobenzoate (prepared with 3,5-dinitrobenzoyl chloride in dry pyridine, and recrystallised from EtOH or aqueous Me2CO) has m 138o. [Beilstein 6 IV 1940.]


Vapors may form explosive mixture with air. Incompatible with strong acids; oxidizers, alkalies, aliphatic amines; amides, chlorosulfonic acid; oleum. Decomposes on heating, producing strong acids and bases, causing fire and explosion hazard. Liquid attacks some plastics and rubber. Attacks many metals.

Waste Disposal

Wastewaters may be subjected to biological treatment. Concentrations may be further reduced by ozone treatment. High concentration wastes may be destroyed in special waste incinerators.

o-Cresol Preparation Products And Raw materials

Raw materials

Preparation Products

o-Cresol Suppliers

Global( 327)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
+86(0)13336195806 +86-571-85586718
+86-571-85864795 China 20012 60
Henan DaKen Chemical CO.,LTD.
+86-371-66670886 China 20898 58
Henan Tianfu Chemical Co.,Ltd.
0371-55170693 CHINA 22607 55
Anhui Royal Chemical Co., Ltd.
+86-025-86655873 CHINA 536 55
career henan chemical co
+86-371-86658258 CHINA 29954 58
+86 18953170293
+86 0531-67809011 CHINA 2941 58
Hubei Jusheng Technology Co.,Ltd.
027-59599243 CHINA 28229 58
Hebei Guanlang Biotechnology Co., Ltd.
+8619930503282 China 5930 58
Hubei xin bonus chemical co. LTD
027-59338440 CHINA 23035 58
Shandong chuangyingchemical Co., Ltd.
18853181302 CHINA 5917 58

View Lastest Price from o-Cresol manufacturers

Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
2021-07-28 o-Cresol
US $1.00 / KG 1KG 99% 10 mt Hebei Guanlang Biotechnology Co., Ltd.
2021-07-13 o-Cresol
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
2021-07-10 o-Cresol
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd

o-Cresol Spectrum

95-48-7(o-Cresol)Related Search:

Copyright 2017 © ChemicalBook. All rights reserved