3,5-Dimethylphenol Property

Melting point:

61-64 °C(lit.)

Boiling point:

222 °C(lit.)

Density 

1.115

vapor pressure 

5-5.4Pa at 25℃

refractive index 

1.5146 (estimate)

Flash point:

109 °C

storage temp. 

room temp

form 

Crystalline Solid

pka

pK1:10.15 (25°C)

color 

White to orange

Odor

Strong, “cresylic” odor.

Water Solubility 

5.3 g/L (25 ºC)

Sensitive 

Air & Light Sensitive

Merck 

14,10082

BRN 

774117

Exposure limits

ACGIH: TWA 1 ppm

InChIKey

TUAMRELNJMMDMT-UHFFFAOYSA-N

LogP

2.35 at 25.5℃

CAS DataBase Reference

108-68-9(CAS DataBase Reference)

NIST Chemistry Reference

Phenol, 3,5-dimethyl-(108-68-9)

EPA Substance Registry System

3,5-Dimethylphenol (108-68-9)

Safety

Hazard Codes 

T

Risk Statements 

24/25-34

Safety Statements 

26-28-36/37/39-45-28A

RIDADR 

UN 2261 6.1/PG 2

WGK Germany 

2

RTECS 

ZE6475000

TSCA 

Yes

HazardClass 

6.1

PackingGroup 

II

HS Code 

29071400

Hazardous Substances Data

108-68-9(Hazardous Substances Data)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P270Do not eat, drink or smoke when using this product.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

3,5-Dimethylphenol Chemical Properties,Usage,Production

Description

3,5-Dimethylphenol was used in simultaneous determination of urinary concentrations of phenol, o-, p-, m-cresols, 1-, 2-naphthol and xylenol isomers by capillary gas chromatography. It was used as starting reagent for total synthesis of landomycin A, most potent antitumor angucycline antibiotic and optically active polypropionate units. It also finds application as adhesives, sealant chemicals, plating and surface treating agents. It is also used as a solvent for cleaning or degreasing. Further, it is employed as a chemical intermediate for antioxidants, phenolic resins, active pharmaceutical ingredients and metaxalone (muscle relaxant).

Description

3,5-Xylenol is a crystalline solid. Molecularweight 5 122.17; Boiling point= 220℃ (sublimes);Freezing/Melting point=64℃; Flash point = 109℃.Soluble in water. Hazard Identification (based on NFPA-704 M Rating System): Health 3, Flammability 2, Reactivity0. Slightly soluble in water; solubility =0.5%.

Chemical Properties

3,5-Xylenol is a crystalline solid.

Uses

3,5-Dimethylphenol finds application as adhesives, sealant chemicals, plating and surface treating agents. It is also used as a solvent for cleaning or degreasing. Further, it is employed as a chemical intermediate for antioxidants, phenolic resins, active pharmaceutical ingredients and metaxalone (muscle relaxant).

Definition

ChEBI: A member of the class of phenols that phenol substituted by methyl groups at positions 3 and 5.

General Description

Colorless to off-white crystalline solid. Odor threshold 1 ppm. Taste threshold 0.001 mg/L.

Air & Water Reactions

3,5-Dimethylphenol is hygroscopic. Insoluble in water.

Reactivity Profile

3,5-Dimethylphenol is incompatible with bases, acid chlorides, acid anhydrides, and oxidizing agents. 3,5-Dimethylphenol corrodes steel, brass, copper, and copper alloys.

Fire Hazard

Flash point data for 3,5-Dimethylphenol are not available. 3,5-Dimethylphenol is probably combustible.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion. A severe eye irritant. Questionable carcinogen with experimental tumorigenic data. When heated to decomposition it emits acrid smoke and irritating fumes. See also other xylenol entries.

Potential Exposure

3,5-Xylenol is used as an antioxidant, solvent, plasticizer, wetting agent; and in pharmaceuticals. Xylenols are also used in pesticides, fuel, and lubricant additives; as a rubber chemical; in dyestuff manufacture. There are actually six xylenol isomers.

First aid

Get medical attention at once following exposureto this compound.Inhalation: Remove patient immediately to fresh air; irritation of nose or throat may be somewhat relieved by spraying or gargling with water until all odor is gone; 100%oxygen inhalation is indicated for cyanosis or respiratorydistress; keep patient warm but not hot.Eyes: Flood with running water for 15 min; if physician isnot immediately available, continue irrigation for another15 min; 2-3 drops of 0.5% pontocaine or equivalent maybe instilled after first 15 min; do not use oils or oily ointments unless ordered by physician.Skin: Wash affected areas with large quantities of water orsoapy water until all odor is gone; then wash with alcoholor 20% glycerin solution and more water; keep patientwarm but not hot; cover chemical burns continuously withcompresses wet with saturated solution of sodium thiosulfate; apply no salves or ointments for 24 h after injury.Ingestion: Give large quantities of liquid (saltwater, weaksodium bicarbonate solution, milk, or gruel) followed bydemulcent, such as raw egg white or corn starch paste; ifprofuse vomiting does not follow immediately, give a mildemetic (such as 1 tablespoon of mustard in glass of water)or tickle back of throat. Repeat procedure until vomitus isfree of the odor. Some demulcent should be left in stomachafter vomiting. Keep patient comfortably warm.

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, wellventilated area away from chemical oxidizers. Sources ofignition, such as smoking and open flames, are prohibitedwhere xylenols is used, handled, or stored in a manner thatcould create a potential fire or explosion hazard.

Shipping

UN 2261 Xylenols, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

Purify it as for 3,4-dimethylphenol. [Beilstein 6 IV 3141.]

Incompatibilities

A weak organic acid. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.