o-Cresol CAS 95-48-7
Introduction：Basic information about o-Cresol CAS 95-48-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
o-Cresol Basic information
| Product Name: | o-Cresol |
| Synonyms: | O-CRESOL;O-CRESYLIC ACID;O-METHYLPHENOL;O-HYDROXYTOLUENE;FEMA 3480;2-HYDROXYTOLUENE;2-METHYLPHENOL;1-Methyl-2-hydroxybenzene |
| CAS: | 95-48-7 |
| MF: | C7H8O |
| MW: | 108.14 |
| EINECS: | 202-423-8 |
| Product Categories: | alcohol |
| Mol File: | 95-48-7.mol |
o-Cresol Chemical Properties
| Melting point | 29-31 °C (lit.) |
| Boiling point | 191 °C (lit.) |
| density | 1.048 g/mL at 25 °C |
| vapor density | 3.72 (vs air) |
| vapor pressure | 0.3 mm Hg ( 20 °C) |
| refractive index | 1.5361 |
| FEMA | 3480 | O-CRESOL |
| Fp | 178 °F |
| storage temp. | under inert gas |
| solubility | 20g/l |
| form | Liquid or Low Melting Solid |
| pka | 10.2(at 25℃) |
| color | white to brown |
| Odor | at 0.01 % in dipropylene glycol. musty phenolic plastic medicinal herbal leathery |
| PH | 4.8 (20g/l, H2O, 20℃) |
| Odor Threshold | 0.00028ppm |
| Odor Type | phenolic |
| biological source | synthetic |
| explosive limit | 1.47%, 148°F |
| Water Solubility | 20 g/L (20 ºC) |
| Merck | 14,2579 |
| JECFA Number | 691 |
| BRN | 506917 |
| 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 5ppm (22 mg/m3); ACGIH TLV: TWA for all isomers 5 ppm (adopted). |
| Dielectric constant | 5.8（-5℃） |
| Stability: | Stable, but light and air sensitive. Combustible. Incompatible with oxidizing agents, bases. |
| Major Application | agriculture cleaning products cosmetics environmental flavors and fragrances food and beverages personal care |
| Cosmetics Ingredients Functions | ANTIMICROBIAL PERFUMING |
| Cosmetic Ingredient Review (CIR) | o-Cresol (95-48-7) |
| InChI | 1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3 |
| InChIKey | QWVGKYWNOKOFNN-UHFFFAOYSA-N |
| SMILES | Cc1ccccc1O |
| LogP | 1.95 at 20℃ |
| Surface tension | 35.86mN/m at 298.15K |
| CAS DataBase Reference | 95-48-7(CAS DataBase Reference) |
| NIST Chemistry Reference | Phenol, 2-methyl-(95-48-7) |
| EPA Substance Registry System | o-Cresol (95-48-7) |
Safety Information
| 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 |
| OEB | B |
| OEL | TWA: 2.3 ppm (10 mg/m3) |
| WGK Germany | 1 |
| RTECS | GO6300000 |
| F | 8-23 |
| Autoignition Temperature | 555 °C |
| TSCA | TSCA listed |
| HazardClass | 6.1 |
| PackingGroup | II |
| HS Code | 29071200 |
| Storage Class | 6.1A - Combustible acute toxic Cat. 1 and 2 very toxic hazardous materials |
| Hazard Classifications | Acute Tox. 3 Dermal Acute Tox. 3 Oral Aquatic Chronic 3 Eye Dam. 1 Skin Corr. 1B |
| Hazardous Substances Data | 95-48-7(Hazardous Substances Data) |
| Toxicity | LD50 orally in rats: 1.35 g/kg (Deichmann, Witherup) |
| IDLA | 250 ppm |
| 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 thresholdconcentration of 0.28 ppbv was reported by Nagata and Takeuchi (1990). |
| Occurrence | Reported in Acacial farnesiana, ylang-ylang oil (probably as p-cresyl acetate), jasmine absolute, orange oilfrom 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. |
| Uses | 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 resinsmanufacturing. |
| Uses | o-Cresol is used as a disinfectant and solvent.Lysol disinfectant is a 50% (v/v) mixed-cresol isomer ina soap emulsion formed on mixing with water. Besidesdisinfection products at solutions of 1–5%, thecresols are used as degreasing compounds, paintbrush cleaners,and additives in lubricating oils. Cresols werepreviously widely used for disinfection of poultry houses, butthis use was discontinued because of their toxicity; theycause respiratory problems and abdominal edema in youngchicks. o-Cresol has been used in synthetic resins,explosives, petroleum, photographic, paint, and agriculturalindustries. |
| Uses | o-Cresol is used mostly as an intermediate for the production of pesticides, epoxy resins, dyes, and pharmaceuticals, but also as a component of disinfectants and cleaning agents. o-Cresol is readily biodegradable and has a low bioaccumulation or geoaccumulation potential. Antiseptics; disinfectants; solvent; insecticides; resins; flame-retardant plasticizers |
| Production Methods | Approximately 60% of o-cresol is obtained from coal-tar and crude oil by using classical techniques such as distillation, stripping, and liquid–liquid extraction. The remaining 40% is obtained synthetically by the alkylation of phenol with methanol. 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. |
| Definition | 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. |
| Hazard | 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. |
| Flammability and Explosibility | Not classified |
| 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. |
| Source | Detected in distilled water-soluble fractions of 87 octane gasoline (6.61 mg/L), 94 octanegasoline (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 alsodetected in 82% of 65 gasoline (regular and premium) samples (62 from Switzerland, 3 fromBoston, MA). At 25 °C, concentrations were from 1.1–99 mg/L in gasoline and 70–6,600 μg/L inwater-soluble fractions. Average concentrations were 18 mg/L in gasoline and 1.2 mg/L in watersolublefractions (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 Africanpalm oil (Duke, 1992). Schauer et al. (2001) measured organic compound emission rates for volatile organiccompounds, gas-phase semi-volatile organic compounds, and particle phase organic compoundsfrom the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emissionrates of 2-methylphenol were 89.6 mg/kg of pine burned, 47.7 mg/kg of oak burned, and 37.8mg/kg of eucalyptus burned. The particle-phase emission rates were 0.018 mg/kg of oak burnedand 0.006 mg/kg of eucalyptus burned. |
| Environmental fate | Biological. Bacterial degradation of 2-methylphenol may introduce a hydroxyl group producing3-methylcatechol (Chapman, 1972). In phenol-acclimated activated sludge, metabolites identifiedinclude 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 theThOD 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 and1.6 d were reported for 2-methylphenol in an acidic clay soil (<1% organic matter) and slightlybasic 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 microcosmstudy, a cylinder that was open at the bottom and screened at the top was installed through a casedborehole approximately 5 m below grade. Five liters of water was aerated with atmospheric air toensure aerobic conditions were maintained. Groundwater was analyzed weekly for approximately3 months to determine 2-methylphenol concentrations with time. The experimentally determinedfirst-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 amethanogenic aquifer to methane and carbon dioxide. These results could not be duplicated in thelaboratory utilizing an anaerobic digester (Godsy et al., 1983). Photolytic. Sunlight irradiation of 2-methylphenol and nitrogen oxides in air yielded thefollowing gas-phase products: acetaldehyde, formaldehyde, pyruvic acid, peroxyacetyl nitrate,nitrocresols, and trace levels of nitric acid and methyl nitrate. Particulate phase products were alsoidentified 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 lightat a maximum wavelength of 270 nm (Dohnal and Fenclová, 1995). Chemical/Physical. Ozonation of an aqueous solution containing 2-methylphenol (200 to 600mg/L) yielded formic, acetic, propionic, glyoxylic, oxalic, and salicylic acids (Wang, 1990). In adifferent experiment, however, an aqueous solution containing 2-methylphenol (1 mM) reactedwith 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 firstozone molecule followed by a 1,3-dipolar addition of the second ozone molecule to the cleavedring (Beltran et al., 1990). |
| Shipping | 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.] |
| Incompatibilities | 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. |
| Toxics Screening Level | The initial threshold screening level (ITSL) for o-cresol is 100 μg/m3 based on an 8 hour averaging time. |
| 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 | Magnesium oxide-->o-Toluidine-->m-Cresol-->Ferric oxide-->Vanadium(V) oxide-->Column plate-->Phenol crude-->Xylenol-->2,6-Dimethylphenol-->Phenol oil |
| Preparation Products | m-Cresol-->Bensulfuron methyl-->Salicylaldehyde-->p-Cresol-->Coumarin-->2,6-Dimethylphenol-->2-Methyl-4-chlorophenoxyacetic acid-->Antioxidant AM-->2-Methylanisole-->o-Cresolphthalein-->Bromocresol Purple-->4-HYDROXY-3-METHYLBENZOIC ACID-->3,3-Bis(3-methyl-4-hydroxyphenyl)indoline-2-on-->Tri-o-cresyl Phosphate-->3-Methylsalicylic acid-->Cresol Red-->4-Chloroanisole-->ACID ORANGE 51-->4-Amino-3-[(2,5-dichlorophenyl)azo]-6-[[4'-[(3-methyl-4-hydroxyphenyl)azo]-1,1'-biphenyl-4-yl]azo]-5-hydroxy-2,7-naphthalenedisulfonic acid disodium salt |
