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2,6-Dimethylphenol structure

2,6-Dimethylphenol

  • CAS:576-26-1
  • MW:122.1644
  • MF:C8H10O
2,6-Dimethylphenol, with the chemical formula C8H10O and CAS registry number 576-26-1, is a compound known for its applications in various industries. This colorless crystalline solid, also referred to as o-Cresol, is characterized by its two methyl groups attached to the phenol ring. It is commonly used as a precursor in the production of antioxidants, fragrances, and pharmaceuticals. 2,6-Dimethylphenol is also utilized as a disinfectant and preservative in personal care products and as a chemical intermediate in the synthesis of dyes and polymers. It is important to handle this compound with caution as it can cause skin and eye irritation. Overall, 2,6-Dimethylphenol plays a significant role in various chemical processes and industries due to its versatile properties and applications.
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1. Names and Identifiers
1.1 Name
2,6-Dimethylphenol
1.2 Synonyms
1,2,6-Xylenol; 1,3-Dimethyl-2-hydroxybenzene; 2,3-Xylenol; 2,6-DIMETHYL PHENOL; 2,6-di-methyl phenol; 2,6-dimethylphenethyl chloride; 2,6-Dimethylphenethylchlorid; 2,6-Dimethyl-phenol; 2,6-DIMETHYLPHENOL PESTANAL; 2,6-DIMETHYLPHENOL, 1000MG, NEAT; 2,6-Me2C6H3OH; 2,6-Me-PhOH; 2,6-Xylenlo; 2,6-Xylenol; 2-hydroxy-1,3-dimethylbenzene; EINECS 209-400-1; MFCD00002240; Phenol, 2,6-dimethyl-; VIC-M-XYLENOL;
1.3 CAS No.
576-26-1
1.4 CID
11335
1.5 EINECS
209-400-1
1.6 Molecular Formula
C8H10O
1.7 Inchi
InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3
1.8 InChkey
NXXYKOUNUYWIHA-UHFFFAOYSA-N
1.9 Canonical Smiles
CC1=C(C(=CC=C1)C)O
1.10 Isomers Smiles
CC1=C(C(=CC=C1)C)O
2. Properties
2.1 Solubility
8g/l
2.2 Appearance
white crystal
2.3 Atmospheric OH Rate Constant
6.59e-11 cm3/molecule*sec
2.4 Storage
Light Sensitive. Ambient temperatures.
2.5 Chemical Properties
colourless crystals or white powder
2.6 Color/Form
LEAVES OR NEEDLES FROM ALCOHOL
2.7 Decomposition
When heated to decomp, it emits acrid smoke and irritating fumes.
2.8 HenrysLawConstant
6.65e-06 atm-m3/mole
2.9 Odor Threshold
0.0002 mg/cu m (detection in air)
2.10 PH
6-7 (8g/l, H2O, 20℃)
2.11 pKa
pK1:10.59 (25°C)
2.12 Water Solubility
10 g/L (20 oC)
2.13 Spectral Properties
Index of refraction: 1.5171 @ 60 deg C
MAX ABSORPTION (ALCOHOL): 271 NM (LOG E= 3.19); 275.5 NM (LOG E= 3.16); SADTLER REFERENCE NUMBER: 294 (IR, PRISM); 100 (IR, GRATING)
MASS: 4053 (National Bureau of Standards EPA-NIH Mass Spectra Data Base, NSRDS-NBS-63)
IR: 5626 (Coblentz Society Spectral Collection)
UV: 21874 (Sadtler Research Laboratories Spectral Collection)
NMR: 36 (Sadtler Research Laboratories Spectral Collection)
MASS: 509 (Atlas of Mass Spectral Data, John Wiley & Sons, New York)
2.14 Stability
Stable. Very flammable. Incompatible with oxidizing agents, acid chlorides, acid anhydrides, steel, copper, copper alloys, bases, acid chlorides.
2.15 StorageTemp
Store below +30°C.
3. Use and Manufacturing
3.1 Description

2,6-Dimethylphenol, with the chemical formula C8H10O, has the CAS number 576-26-1. It appears as a colorless to pale yellow liquid with a strong, phenolic odor. The basic structure of 2,6-Dimethylphenol consists of a phenyl ring with two methyl groups attached to the 2 and 6 positions. This compound is sparingly soluble in water, but soluble in organic solvents such as ethanol and ether. Safety information indicates that 2,6-Dimethylphenol may cause skin and eye irritation, and is harmful if swallowed or inhaled. It is important to handle this chemical with care and use appropriate protective measures to avoid exposure.

Applicable Fields

Pharmaceuticals: 2,6-Dimethylphenol is used in the synthesis of various pharmaceutical compounds. Its purpose in this field involves its ability to act as a building block or intermediate in the production of drugs. The mechanism of action in pharmaceuticals depends on the specific compound being synthesized.

Polymer Industry: This compound is also utilized in the polymer industry. It can be used as a monomer or as a component in the synthesis of polymers. The mechanism of action in polymers involves its incorporation into the polymer chain, contributing to the desired properties of the final product.

Storage

Conditions: Store in a cool and dry place, away from direct sunlight.

3.2 General Description
Colorless to off-white crystalline solid with a sweet tarry odor. Odor threshold concentration: 0.4 mg/L .
3.3 Purification Methods
Fractionally distil 2,6-xylenol under nitrogen, crystallise it from *benzene or hexane, and sublime it at 38o/10mm. [Beilstein 6 IV 3122.] 2,6-Dimethylphenol Preparation Products And Raw materials Raw materials
3.4 Usage
CAS # : 576-26-1
4. Safety and Handling
4.1 Octanol/Water Partition Coefficient
log Kow= 2.36
4.2 Fire Hazard
2,6-Dimethylphenol is combustible.
4.3 Other Preventative Measures
SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
4.4 Cleanup Methods
FOUNDRY PLANT WASTE GASES WERE DEODORIZED WITH POTASSIUM PERMANGANATE, & DEODORIZATION EFFICIENCY WAS MEASURED BY PRESENCE OF 2,6-XYLENOL IN SCRUBBED WASTE GASES.
4.5 DisposalMethods
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Chemical Treatability of 2,6-Dimethylphenol; Concentration Process: Biological treatment; Chemical Classification: Phenols; Scale of Study: Unknown; Type of Wastewater Used: Pure compound (one solute in a solvent); Results of Study: 94.3% reduction based on chemical oxygen demand; rate of biodegradation 9 mg chemical oxygen demand/g hr (Activated sludge process).
4.6 DOT Emergency Guidelines
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Health: TOXIC; inhalation, ingestion, or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Fire or Explosion: Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors, and sewers explosion hazards. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Public Safety: CALL Emergency Response Telephone Number ... . As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Evacuation: ... Fire: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Fire: Small fires: Dry chemical, CO2 or water spray. Large fires: Dry chemical, CO2, alcohol-resistant foam or water spray. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material. Fire involving tanks or car/trailer loads: Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Spill or Leak: ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS. /Xylenols; Xylenols, liquid; Xylenols, solid/
/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ First Aid: Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves. /Xylenols; Xylenols, liquid; Xylenols, solid/
4.7 Formulations/Preparations
Pitt-Consol Xylenol 235 is a synthetic 2,6-xylenol. Homolog distribution, wt%: Ortho cresol, 0.5; 2,6-xylenols, 92; 2,4/2,5 xylenols, 0.5; meta/para cresol, 7.
Grade or purity: 99%
Pitt-Consol Xylenol 410 is a synthetic xylenol blend ... homolog distribution, wt %: 2,6-xylenol, 1; 2,4-xylenol, 42; 2,5-xylenol, 43; 2,3-xylenol group, 14. /Xylenol 410/
4.8 Protective Equipment and Clothing
Some data suggesting breakthrough times /for butyl rubber/ of approximately an hour or more. /Aromatic hydroxyl cmpd/
Breakthrough times /for neoprene/ greater than one hour reported by (normally) two or more testers. /Aromatic hydroxyl cmpd/
Breakthrough times /for polyvinyl alcohol/ less (usually significantly less) than one hour reported by (normally) two or more testers. /Aromatic hydroxyl cmpd/
4.9 Report

The IUPAC name of 2,6-Xylenol is 2,6-dimethylphenol. With the CAS registry number 576-26-1, it is also named as 1-Hydroxy-2,6-dimethylbenzene. The product's categories are aromatic phenols; phenoles and thiophenoles. It is colorless to off-white crystalline solid with a sweet tarry odor. And this chemical is soluble in alcohol, ether, chloroform, benzene and alkali solution, very slightly soluble in cold water. In addition, it is stable, very flammable, and incompatible with oxidizing agents, acid chlorides, acid anhydrides, steel, copper, copper alloys, bases, acid chlorides. Furthermore, 2,6-Xylenol should be stored away from extreme heat and away from strong oxidizing agents. 

The other characteristics of this product can be summarized as: (1)ACD/LogP: 2.40; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.4; (4)ACD/LogD (pH 7.4): 2.4; (5)ACD/BCF (pH 5.5): 39.41; (6)ACD/BCF (pH 7.4): 39.39; (7)ACD/KOC (pH 5.5): 482.78; (8)ACD/KOC (pH 7.4): 482.51; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Index of Refraction: 1.54; (13)Molar Refractivity: 37.78 cm3; (14)Molar Volume: 120.4 cm3; (15)Polarizability: 14.97×10-24 cm3; (16)Surface Tension: 37.2 dyne/cm; (17)Enthalpy of Vaporization: 45.51 kJ/mol; (18)Vapour Pressure: 0.221 mmHg at 25°C; (19)Tautomer Count: 2; (20)Exact Mass: 122.073165; (21)MonoIsotopic Mass: 122.073165; (22)Topological Polar Surface Area: 20.2; (23)Heavy Atom Count: 9; (24)Complexity: 80.6.

Preparation 2,6-Xylenol: Using phenol or orthocresol as raw material, then they have a gas phase catalytic reaction with methanol. Through distillation and purification, we can obtain the product and its purity is over 99%.

Uses of 2,6-Xylenol: It is an intermediate for the manufacture of polyphenylene oxide and modified phenolic resins and phosphate esters. And it is also used in the production of hydraulic fluids, in halogenation and aminolysis reactions.

When you are using this chemical, please be cautious about it as the following:
It is toxic in contact with skin and if swallowed. And it is also toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 

People can use the following data to convert to the molecule structure.
1. Smiles: c1(c(cccc1C)C)O;
2. InChI: InChI=1/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3.

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mammal (species unspecified) LC inhalation > 270mg/m3 (270mg/m3)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.
mouse LD50 intraperitoneal 150mg/kg (150mg/kg)   National Technical Information Service. Vol. AD691-490,
mouse LD50 intravenous 80mg/kg (80mg/kg) BEHAVIORAL: GENERAL ANESTHETIC

BEHAVIORAL: SLEEP
Journal of Medicinal Chemistry. Vol. 23, Pg. 1350, 1980.
mouse LD50 oral 450mg/kg (450mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.
mouse LD50 skin 920mg/kg (920mg/kg)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 58, 1974.
rabbit LD50 oral 700mg/kg (700mg/kg) BEHAVIORAL: ATAXIA

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Hygiene and Sanitation Vol. 33(7-9), Pg. 329, 1968.
rabbit LD50 skin 1gm/kg (1000mg/kg)   Industrial Hygiene Foundation of America, Chemical and Toxicological Series, Bulletin. Vol. 6, Pg. 1, 1967.
rat LD50 oral 296mg/kg (296mg/kg)   Gigiena Truda i Professional'naya Patologiya v Estonskoi SSR. Labor Hygiene and Occupational Pathology in the Estonian SSR. Vol. 8, Pg. 145, 1972.
rat LD50 skin 2325mg/kg (2325mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.

4.10 Skin, Eye, and Respiratory Irritations
An eye irritant.
4.11 Specification

The IUPAC name of 2,6-Xylenol is 2,6-dimethylphenol. With the CAS registry number 576-26-1, it is also named as 1-Hydroxy-2,6-dimethylbenzene. The product's categories are aromatic phenols; phenoles and thiophenoles. It is colorless to off-white crystalline solid with a sweet tarry odor. And this chemical is soluble in alcohol, ether, chloroform, benzene and alkali solution, very slightly soluble in cold water. In addition, it is stable, very flammable, and incompatible with oxidizing agents, acid chlorides, acid anhydrides, steel, copper, copper alloys, bases, acid chlorides. Furthermore, 2,6-Xylenol should be stored away from extreme heat and away from strong oxidizing agents. 

The other characteristics of this product can be summarized as: (1)ACD/LogP: 2.40; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.4; (4)ACD/LogD (pH 7.4): 2.4; (5)ACD/BCF (pH 5.5): 39.41; (6)ACD/BCF (pH 7.4): 39.39; (7)ACD/KOC (pH 5.5): 482.78; (8)ACD/KOC (pH 7.4): 482.51; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Index of Refraction: 1.54; (13)Molar Refractivity: 37.78 cm3; (14)Molar Volume: 120.4 cm3; (15)Polarizability: 14.97×10-24 cm3; (16)Surface Tension: 37.2 dyne/cm; (17)Enthalpy of Vaporization: 45.51 kJ/mol; (18)Vapour Pressure: 0.221 mmHg at 25°C; (19)Tautomer Count: 2; (20)Exact Mass: 122.073165; (21)MonoIsotopic Mass: 122.073165; (22)Topological Polar Surface Area: 20.2; (23)Heavy Atom Count: 9; (24)Complexity: 80.6.

Preparation 2,6-Xylenol: Using phenol or orthocresol as raw material, then they have a gas phase catalytic reaction with methanol. Through distillation and purification, we can obtain the product and its purity is over 99%.

Uses of 2,6-Xylenol: It is an intermediate for the manufacture of polyphenylene oxide and modified phenolic resins and phosphate esters. And it is also used in the production of hydraulic fluids, in halogenation and aminolysis reactions.

When you are using this chemical, please be cautious about it as the following:
It is toxic in contact with skin and if swallowed. And it is also toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 

People can use the following data to convert to the molecule structure.
1. Smiles: c1(c(cccc1C)C)O;
2. InChI: InChI=1/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3.

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mammal (species unspecified) LC inhalation > 270mg/m3 (270mg/m3)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.
mouse LD50 intraperitoneal 150mg/kg (150mg/kg)   National Technical Information Service. Vol. AD691-490,
mouse LD50 intravenous 80mg/kg (80mg/kg) BEHAVIORAL: GENERAL ANESTHETIC

BEHAVIORAL: SLEEP
Journal of Medicinal Chemistry. Vol. 23, Pg. 1350, 1980.
mouse LD50 oral 450mg/kg (450mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.
mouse LD50 skin 920mg/kg (920mg/kg)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 58, 1974.
rabbit LD50 oral 700mg/kg (700mg/kg) BEHAVIORAL: ATAXIA

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Hygiene and Sanitation Vol. 33(7-9), Pg. 329, 1968.
rabbit LD50 skin 1gm/kg (1000mg/kg)   Industrial Hygiene Foundation of America, Chemical and Toxicological Series, Bulletin. Vol. 6, Pg. 1, 1967.
rat LD50 oral 296mg/kg (296mg/kg)   Gigiena Truda i Professional'naya Patologiya v Estonskoi SSR. Labor Hygiene and Occupational Pathology in the Estonian SSR. Vol. 8, Pg. 145, 1972.
rat LD50 skin 2325mg/kg (2325mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 20(4), Pg. 43, 1976.

4.12 Toxicity
LD50 orally in Rabbit: 296 mg/kg LD50 dermal Rabbit 1000 mg/kg
5. MSDS

2.Hazard identification

2.1 Classification of the substance or mixture

Acute toxicity - Oral, Category 3

Acute toxicity - Dermal, Category 3

Skin corrosion, Category 1B

Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 2

2.2 GHS label elements, including precautionary statements

Pictogram(s)
Signal word

Danger

Hazard statement(s)

H301 Toxic if swallowed

H311 Toxic in contact with skin

H314 Causes severe skin burns and eye damage

H411 Toxic to aquatic life with long lasting effects

Precautionary statement(s)
Prevention

P264 Wash ... thoroughly after handling.

P270 Do not eat, drink or smoke when using this product.

P280 Wear protective gloves/protective clothing/eye protection/face protection.

P260 Do not breathe dust/fume/gas/mist/vapours/spray.

P273 Avoid release to the environment.

Response

P301+P310 IF SWALLOWED: Immediately call a POISON CENTER/doctor/\u2026

P321 Specific treatment (see ... on this label).

P330 Rinse mouth.

P302+P352 IF ON SKIN: Wash with plenty of water/...

P312 Call a POISON CENTER/doctor/\u2026if you feel unwell.

P361+P364 Take off immediately all contaminated clothing and wash it before reuse.

P301+P330+P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower].

P363 Wash contaminated clothing before reuse.

P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P310 Immediately call a POISON CENTER/doctor/\u2026

P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

P391 Collect spillage.

Storage

P405 Store locked up.

Disposal

P501 Dispose of contents/container to ...

2.3 Other hazards which do not result in classification

none

6. NMR Spectrum
13C NMR : in CDCl3  
1H NMR : 90 MHz in CDCl3  
gas  
IR : KBr disc  
SOLUTION (10% CCl4 FOR 2.6-7.5, 10% CS2 FOR 7.5-24)  
Raman : 4880 A,200 M,powder  
Mass  
7. Synthesis Route
576-26-1Total: 125 Synthesis Route
 
87-62-7
87-62-7 160 Suppliers
 
576-26-1
576-26-1 94 Suppliers
 
95-48-7
95-48-7 135 Suppliers
 
576-26-1
576-26-1 94 Suppliers
8. Precursor and Product
precursor:
product:
9. Computed Properties
10.Other Information
Usage
2,6-dimethylphenol is used in the synthesis of anti-oxidant compounds due to the phenol moiety in the structure. In addition, this compound is used as a reactant in the synthesis of polyphenylene ether polymers.
Merck
14,10082
BRN
1446677
Chemical Properties
colourless crystals or white powder
Occurrence
Reported found in smoked fatty fish, boiled and cooked cured pork, rum, malt whiskey, Japanese whiskey, coffee, katsuobushi (dried bonito) and lamb’s lettuce (Valerianella locusta).
Uses
CAS # : 576-26-1
Uses
Intermediate for Plastics, Agrochemicals, Pharmaceuticals, and is used as a solvent.
Uses
Similar to other xylenol compounds, 2,6-dimethylphenol is used in the synthesis of anti-oxidant compounds due to the phenol moiety in the structure. In addition, this compound is used as a a reactant in the synthesis of polyphenylene ether polymers.
Preparation
From coal tar oil or coal hydrogenation.
Aroma threshold values
Detection: 400 ppb
General Description
Colorless to off-white crystalline solid with a sweet tarry odor. Odor threshold concentration: 0.4 mg/L .
Air & Water Reactions
Insoluble in water
Reactivity Profile
2,6-Dimethylphenol is incompatible with bases, acid chlorides, acid anhydrides, and oxidizing agents. Corrodes steel, brass, copper, and copper alloys.
Fire Hazard
2,6-Dimethylphenol is combustible.
Purification Methods
Fractionally distil 2,6-xylenol under nitrogen, crystallise it from *benzene or hexane, and sublime it at 38o/10mm. [Beilstein 6 IV 3122.]
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12. Related Questions
How is 2,6-Dimethylphenol synthesized?2,6-Dimethylphenol, also known as DMP, is one of the six isomers of dimethylphenol. Applications 2,6-Dimethylphenol is widely used in the synthesis of polyphenylene ether resin (PPE), photographic age..
What are the applications of 2,6-Dimethylphenol?2,6-Dimethylphenol, also known as 2,6-Dimethylphenol, is a leaf-like or needle-like crystalline or colorless solid at room temperature and pressure. It is slightly soluble in water but easily soluble ..
13. Realated Product Infomation
 
 
 
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